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Phenylacetic acid derivatives, preparation thereof and intermediates therefor, and compositions containing them
RE37873 Phenylacetic acid derivatives, preparation thereof and intermediates therefor, and compositions containing them
Patent Drawings:

Inventor: Bayer, et al.
Date Issued: October 8, 2002
Application: 09/834,711
Filed: April 16, 2001
Inventors: Ammermann; Eberhard (Heppenheim, DE)
Bayer; Herbert (Mannheim, DE)
Grammenos; Wassilios (Ludwigshafen, DE)
Harreus; Albrecht (Ludwigshafen, DE)
Kirstgen; Reinhard (Neustadt, DE)
Lorenz; Gisela (Hambach, DE)
Muller; Ruth (Andernach, DE)
Rohl; Franz (Schifferstadt, DE)
Sauter; Hubert (Mannheim, DE)
Assignee: BASF Aktiengesellschaft (Ludwigshafen, DE)
Primary Examiner: Raymond; Richard L.
Assistant Examiner:
Attorney Or Agent: Keil & Weinkauf
U.S. Class: 514/522; 514/542; 514/599; 514/616; 514/618; 514/620; 514/622; 558/414; 560/18; 560/35; 564/153; 564/154; 564/162; 564/164; 564/165; 564/74
Field Of Search: 558/414; 560/18; 560/35; 564/74; 564/153; 564/154; 564/162; 564/164; 564/165; 514/522; 514/542; 514/599; 514/616; 514/618; 514/620; 514/622
International Class:
U.S Patent Documents: 5194662; 5221691; 5393782; 5756426
Foreign Patent Documents: 2104806; 398692; 513580; 528682; 567828; 94/26700; 95/18789
Other References: Pat. Abst. of Japan, vol. 17, No. 644 (C-1134); (JP 5201946, Aug. 10, 1993)..
Pat. Abst. of Japan, vol. 18, No. 19 (C-1152); (JP 5255012, May 10, 1993)..
Pat. Abst. of Japan, vol. 18, No. 93 (C-1166); (JP 5294948, Sep. 11, 1993)..









Abstract: Phenylacetic acid derivatives of the formula I ##STR1##
Claim: We claim:

1. A phenylacetic acid derivative of the formula I ##STR28##

where the substituents and the index have the following meanings: X is oxygen or sulfur; R is hydrogen or C.sub.1 -C.sub.4 -alkyl; R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl; R.sup.2 is cyano, nitro, trifluoromethyl, halogen, C.sub.1-C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy; m is 0, 1 or 2, it being possible for the R.sup.2 radicals to be different if m is 2; R.sup.3 is hydrogen, cyano, nitro, hydroxyl, amino, .Iadd.cyclopropyl, .Iaddend.halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1-C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.3 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.1 -C.sub.4 -alkylamino or di-C.sub.1 -C.sub.4 -alkylamino; R.sup.4 is hydroxyl, amino, halogen, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6-alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.2 -C.sub.6 -alkenylthio, C.sub.2 -C.sub.6 -alkenylamino, N-C.sub.2 -C.sub.6 -alkenyl-N-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6-alkynyloxy, C.sub.2 -C.sub.6 -alkynylthio, C.sub.2 -C.sub.6 -alkynylamino, N-C.sub.2 -C.sub.6 -alkynyl-N-C.sub.1 -C.sub.6 -alkylamino, it being possible for the hydrocarbon radicals of these groups to be partly or completely halogenated or to carry oneto three of the following radicals: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl,di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6-alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, aryl, aryloxy, aryl-C.sub.1 -C.sub.4 -alkoxy, arylthio and aryl-C.sub.1 -C.sub.4 -alkylthio, it being possible forthe cyclic radicals in turn to be partly or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6-haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6-alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2-C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio and C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; C.sub.3 -C.sub.6 -cycloalkoxy, C.sub.3 -C.sub.6 -cycloalkylthio, C.sub.3 -C.sub.6 -cycloalkylamino, N-C.sub.3 -C.sub.6 -cycloalkyl-N-C.sub.1-C.sub.6 -alkylamino, C.sub.3 -C.sub.6 -cycloalkenyloxy, C.sub.3 -C.sub.6 -cycloalkenylthio, C.sub.3 -C.sub.6 -cycloalkenylamino, N-C.sub.3 -C.sub.6 -cycloalkenyl-N-C.sub.1 -C.sub.6 -alkylamino, aryloxy, arylthio, arylamino and N-aryl-N-C.sub.1 -C.sub.6-alkylamino, it being possible for the cyclic radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6-alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio,C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6-alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl and aryloxy; R.sup.5 is hydrogen, C.sub.1 -C.sub.10 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.2 -C.sub.10 -alkenyl, C.sub.2 -C.sub.10 -alkynyl, C.sub.1 -C.sub.10 -alkylcarbonyl, C.sub.2-C.sub.10 -alkenylcarbonyl, C.sub.3 -C.sub.10 -alkynylcarbonyl or C.sub.1 -C.sub.10 -alkylsulfonyl, it being possible for these radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl,mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1-C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1-C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, benzyl, benzyloxy, aryl, aryloxy and arylthio, it being possible for the cyclic groups in turn to be partly or completelyhalogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1-C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6-alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio orC(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; aryl, arylcarbonyl and arylsulfonyl, it being possible for these radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl,aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy,C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6-alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl and aryloxy or C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; where A is oxygen, sulfur or nitrogen and wherethe nitrogen carries hydrogen or C.sub.1 -C.sub.6 -alkyl; n is 0 or 1; R.sup.6 is hydrogen or C.sub.1 -C.sub.6 -alkyl and R.sup.7 is hydrogen or C.sub.1 -C.sub.6 -alkyl,

.[.and.]. .Iadd.or .Iaddend.its .[.salts.]. .Iadd.salt.Iaddend..

2. A compound of the formula I as claimed in claim 1, in which R.sup.3, R.sup.4 and R.sup.5 have the following meanings: R.sup.3 is hydrogen, hydroxyl, cyclopropyl, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4-alkylthio, R.sup.4 is hydroxyl, halogen, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -alkylthio, R.sup.5 is hydrogen, C.sub.1 -C.sub.10 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.2 -C.sub.10 -alkenyl, C.sub.2 -C.sub.10 -alkynyl, C.sub.1 -C.sub.10-alkylcarbonyl, C.sub.2 -C.sub.10 -alkenylcarbonyl, C.sub.3 -C.sub.10 -alkynyl carbonyl or C.sub.1 -C.sub.10 -alkylsulfonyl, it being possible for these groups to be partly or completely halogenated or to carry one to 3 of the following groups: cyano,nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6-alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkyl amino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1-C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy and arylthio, it being possible for the aromatic radicals in turn, to be partly orcompletely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, halogen, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6-alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6-alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy,aryl, aryloxy, arylthio or C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; aryl, arylcarbonyl, and arylsulfonyl, it being possible for these groups to be partly or completely halogenated or to carry one to 3 of the following groups: cyano, nitro, hydroxyl,mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl,C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6-alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy or C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; where A isoxygen, sulfur or nitrogen and where the nitrogen carries hydrogen or C.sub.1 -C.sub.6 -alkyl n is 0 or 1; R.sup.6 is hydrogen or C.sub.1 -C.sub.6 -alkyl and R.sup.7 is hydrogen or C.sub.1 -C.sub.6 -alkyl,

and its salts.

3. A compound of the formula I as claimed in claim 1, in which m is 0.

4. A compound of the formula I as claimed in claim 1, in which R.sup.1 is methyl.

5. The compound defined in claim 1, wherein R.sup.4 denotes one of the following: halogen, or C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.2 -C.sub.6 -alkenylamino,N-C.sub.2 -C.sub.6 -alkenyl-N-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkynyloxy, C.sub.2 -C.sub.6 -alkynylamino and N-C.sub.2 -C.sub.6 -alkynyl-N-C.sub.1 -C.sub.6 -alkylamino, it being possible for the hydrocarbon radicals of these groups to bepartly or completely halogenated or to carry one to three of the following radicals: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6-alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6-alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, aryl, aryloxy, aryl-C.sub.1 -C.sub.4 -alkoxy, arylthioand aryl-C.sub.1 -C.sub.4 -alkylthio, it being possible for the cyclic radicals in turn to be partly or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl,aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6-alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6-alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio and C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; C.sub.3 -C.sub.6 -cycloalkoxy, C.sub.3 -C.sub.6 -cycloalkylamino, N-C.sub.3 -C.sub.6-cycloalkyl-N-C.sub.1 -C.sub.6 -alkylamino, C.sub.3 -C.sub.6 -cycloalkenyloxy, C.sub.3 -C.sub.6 -cycloalkenylamino, N-C.sub.3 -C.sub.6 -cycloalkenyl-N-C.sub.1 -C.sub.6 -alkylamino, aryloxy, arylamino and N-aryl-N-C.sub.1 -C.sub.6 -alkylamino, it beingpossible for the cyclic radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1-C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6-alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2-C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl and aryloxy.

6. The compound defined in claim 1, wherein R.sup.4 denotes one of the following: C.sub.1 -C.sub.6 -alkoxy, C.sub.2 -C.sub.6 -alkenyloxy and C.sub.2 -C.sub.6 -alkynyloxy, it being possible for the hydrocarbon radicals of these groups to bepartly or completely halogenated or to carry one to three of the following radicals: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6-alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6-alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, aryl, aryloxy, aryl-C.sub.1 -C.sub.4 -alkoxy, arylthioand aryl-C.sub.1 -C.sub.4 -alkylthio, it being possible for the cyclic radicals in turn to be partly or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl,aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6-alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6-alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio and C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; C.sub.3 -C.sub.6 -cycloalkoxy, C.sub.3 -C.sub.6 -cycloalkenyloxy, and aryloxy, itbeing possible for the cyclic radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1-C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkulsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6-alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6-alkenyloxy, benzyl, benzyloxy, aryl and aryloxy.

7. The compound defined in claim 1, wherein R.sup.4 denotes one of the following: C.sub.1 -C.sub.6 -alkoxy, it being possible for the hydrocarbon radicals of these groups to be partly or completely halogenated or to carry one to three of thefollowing radicals: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6-alkylaminothiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1-C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, aryl, aryloxy, aryl-C.sub.1 -C.sub.4 -alkoxy, arylthio and aryl-C.sub.1 -C.sub.4 -alkylthio, it being possible for the cyclic radicals in turnto be partly or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6-alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6-alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy,aryl, aryloxy, arylthio and C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7.

8. A composition against animal pests or harmful fungi, containing customary additives and an effective amount of a compound of the formula I as defined in claim 1.

9. A method for controlling animal pests or harmful fungi, which comprises treating the pests or harmful fungi, their environment of the plants, surfaces, materials or spaces to be kept free from them with an effective amount of a compound ofthe formula I as defined in claim 1.
Description: The present invention relates to phenylacetic acid derivatives of the formula I ##STR2##

where the substituents and the index have the following meanings: X is oxygen or sulfur: R is hydrogen .[.and [sic].]. .Iadd.or .Iaddend.C.sub.1 -C.sub.4 -alkyl; R.sup.1 is hydrogen .[.and [sic].]. .Iadd.or .Iaddend.C.sub.1 -C.sub.4 -alkyl;R.sup.2 is cyano, nitro, trifluoromethyl, halogen, C.sub.1 -C.sub.4 -alkyl .[.and [sic].]. .Iadd.or .Iaddend.C.sub.1 -C.sub.4 -alkoxy; m is 0, 1 or 2, it being possible for the R.sup.2 radicals to be different if m is 2; R.sup.3 is hydrogen, cyano,nitro, hydroxyl, amino, .Iadd.cyclopropyl, .Iaddend.halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.1 -C.sub.4 -alkylamino or di-C.sub.1 -C.sub.4-alkylamino; R.sup.4 is hydrogen, cyano, nitro, hydroxyl, amino, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyl, C.sub.2-C.sub.6 -alkenyloxy, C.sub.2 -C.sub.6 -alkenylthio, C.sub.2 -C.sub.6 -alkenylamino, N-C.sub.2 -C.sub.6 -alkenyl-N-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkynyl, C.sub.2 -C.sub.6 -alkynyloxy, C.sub.2 -C.sub.6 -alkynylthio, C.sub.2 -C.sub.6-alkynylamino, N-C.sub.2 -C.sub.6 -alkynyl-N-C.sub.1 -C.sub.6 -alkylamino, it being possible for the hydrocarbon radicals of these groups to be partly or completely halogenated or to carry one to three of the following radicals; cyano, nitro, hydroxyl,mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.1 -C.sub.6-alkylfulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6-alkenyloxy, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, heterocyclyl, heterocyclyloxy, aryl, aryloxy, aryl-C.sub.1 -C.sub.4 -alkoxy, arylthio, aryl-C.sub.1 -C.sub.4 -alkylthio, hetaryl, hetaryloxy, hetaryl-C.sub.1 -C.sub.4 -alkoxy,hetarylthio, hetaryl-C.sub.1 -C.sub.4 -alkylthio, it being possible for the cyclic radicals in turn to be partly or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl,aminocarbonyl, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1-C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6-alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio, hetaryl, hetaryloxy, hetarylthio and C(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkoxy, C.sub.3 -C.sub.6 -cycloalkylthio, C.sub.3 -C.sub.6-cycloalkylamino, N-C.sub.3 -C.sub.6 -cycloalkyl-N-C.sub.1 -C.sub.6 -alkylamino, C.sub.3 -C.sub.6 -cycloalkenyl, C.sub.3 -C.sub.6 -cycloalkenyloxy, C.sub.3 -C.sub.6 -cycloalkenylthio, C.sub.3 -C.sub.6 -cycloalkenylamino, N-C.sub.3 -C.sub.6-cycloalkenyl-N-C.sub.1 -C.sub.6 -alkylamino, heterocyclyl, heterocyclyloxy, heterocyclylthio, heterocyclylamino, N-heterocyclyl-N-C.sub.1 -C.sub.6 -alkylamino, aryl, aryloxy, arylthio, arylamino, N-aryl-N-C.sub.1 -C.sub.6 -alkylamino, hetaryl,hetaryloxy, hetarylthio, hetarylamino, N-hetaryl-N-C.sub.1 -C.sub.6 -alkylamino, it being possible for the cyclic radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino,carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6-haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -CV.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6-alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, hetaryl and hetaryloxy; R.sup.5 is hydrogen, C.sub.1 -C.sub.10 -alkyl, C.sub.3 -C.sub.6-cycloalkyl, C.sub.2 -C.sub.10 -alkenyl, C.sub.2 -C.sub.10 -alkynyl, C.sub.1 -C.sub.10 -alkylcarbonyl, C.sub.2 -C.sub.10 -alkenylcarbonyl, C.sub.3 -C.sub.10 -alkynylcarbonyl or C.sub.1 -C.sub.10 -alkylsulfonyl, it being possible for these radicals to bepartly or completely halogenated or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6-alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6-alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6-cycloalkoxy, heterocyclyl, heterocyclyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio, hetaryl, hetaryloxy and hetarylthio, it being possible for the cyclic groups in turn to be partly or completely halogenated or to carry one to three of the followinggroups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl,C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkoxycarbonyl C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6-alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio, hetaryl, hetaryloxy, hetarylthio orC(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; aryl, arylcarbonyl, arylsulfonyl, hetaryl, hetarylcarbonyl or hetarylsulfonyl, it being possible for these radicals to be partly or completely halogenated or to carry one to three of the following groups: cyano,nitro, hydroxyl, mercapto, amino, carbonyl, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3-C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1-C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, hetaryl, hetaryloxy orC(.dbd.NOR.sup.6)--A.sub.n --R.sup.7 ; where A is oxygen, sulfur or nitrogen and where the nitrogen carries hydrogen or C.sub.1 -C.sub.6 -alkyl; n is 0 or 1; R.sup.6 is hydrogen or C.sub.1 -C.sub.6 -alkyl and R.sup.7 is hydrogen or C.sub.1 -C.sub.6-alkyl,

and their salts.

The invention additionally relates to processes and intermediates for preparing these compounds and compositions containing them for controlling animals pests and harmful fungi.

Phenylacetic acid derivatives for pest control are disclosed in the literature (EP-A 398 692, EP-A 477 631, EP-A 513 580, EP-A 567 828, EP-A 528 682, EP-A 463 488, WO-A 92/13,830).

It is an object of the present invention to provide novel compounds having improved action.

We have found that this object is achieved by the phenylacetic acid derivatives I defined at the outset. We have additionally found processes and intermediates for their preparation and compositions containing them for controlling animal pestsand harmful fungi and their use within this context.

The compounds I are obtainable in various ways by processes known per se in the literature.

Fundamentally, it is insignificant in the synthesis of the compounds I where the group .sup..circle-w/dot. C(NOCH.sub.3)--CONRR.sup.1 or the group --CH.sub.2 ON.dbd.C(R.sup.3)--C(R.sup.4).dbd.NOR.sup.5 is constructed first.

The construction of the group --C(NOCH.sub.3)--CONRR.sup.1 is disclosed, for example, in the literature cited at the outset.

The manner of the synthesis of the --CH.sub.2 ON.dbd.C(R.sup.3)--C(R.sup.4).dbd.NOR.sup.5 side chain essentially depends on the nature of the substituents R.sup.3 and R.sup.4.

1. In the case in which R.sup.3 and R.sup.4 are not halogen, the construction of the group --CH.sub.2 ON.dbd.C(R.sup.3)--C(R.sup.4).dbd.NOR.sup.5 in general proceeds by reacting a benzyl derivative of the formula II with a hydroxyimine of theformula III. ##STR3##

L.sup.1 in the formula II is a nucleophilically replaceable leaving group, eg. halogen or sulfonate groups, preferably chlorine, bromine, iodine, mesylate, tosylate or triflate.

The reaction is carried out in a manner known per se in an inert organic solvent in the presence of a base, eg. sodium hydride, potassium hydroxide, potassium carbonate or triethylamine according to the methods described in Houben-Weyl, Vol. E14b, p. 370 ff and Houben-Weyl, Vol. 10/1, p. 1189 ff.

The hydroxyimine III required is obtained, for example, by reaction of a corresponding dihydroxyimine IV with a nucleophilically substituted reagent VI. ##STR4##

L.sup.2 in the formula VI is a nucleophilically replaceable leaving group, eg. halogen or sulfonate groups, preferably chlorine, bromine, iodine, mesylate, tosylate or triflate.

The reaction is carried out in a manner known per se in an inert organic solvent in the presence of a base, eg. potassium carbonate, potassium hydroxide, sodium hydride, pyridine or triethylamine according to the methods described inHouben-Weyl, Vol. E 14b, p. 307 ff, p. 370 ff and p. 385 ff; Houben-Weyl, Vol. 10/4, p. 55 ff, p. 180 ff and p. 217 ff; Houben-Weyl, Vol. E5, p. 780 ff.

1.1 Alternatively, the compounds I can also be obtained by converting the benzyl derivative II first to a corresponding benzyl oxime of the formula V using the dihydroxyimine IV. V then being reacted with the nucleophilically substituted reagentVI to give I. ##STR5##

The reaction is carried out in a manner known per se in an inert organic solvent in the presence of a base, eg. potassium carbonate, potassium hydroxide, sodium hydride, pyridine or triethylamine according to the methods described inHouben-Weyl, Vol. 10/1, p. 1189 ff; Houben-Weyl, Vol. E 14b, p. 307 ff. p. 370 ff and p. 385 ff; Houben-Weyl, Vol. 10/4, p. 55 ff, p. 180 ff and p. 217 ff; Houben-Weyl, Vol. E5, p. 780 ff.

1.2 In a similar manner, it is also possible to prepare the required hydroxyimine of the formula III from a carbonylhydroxyimine VII by reaction with a hydroxylamine IXa or its salt IXb. ##STR6##

Q.sup..crclbar. in the formula IXb is the anion of an acid, in particular of an inorganic acid, eg. halide such as chloride.

The reaction is carried out in a manner known per se in an inert organic solvent according to the methods described in EP-A 513 580; Houben-Weyl, Volume 10/4, p. 73 ff; Houben-Weyl, Vol. E14b, p. 369 ff and p. 385 ff.

1.3 Alternatively, the compounds I can also be obtained by converting the benzyl derivative II first to a corresponding benzylketoxyimine of the formula VIII using the carbonylhydroxyimine VII. VIII then being reacted with the hydroxylamine IXaor its salt IXb to give I. ##STR7##

The reaction is carried out in a manner known per se in an inert organic solvent according to the methods described in Houben-Weyl, Vol. E14b, p. 369 ff; Houben-Weyl, Vol. 10/1, p. 1189 ff and Houben-Weyl, Vol. 10/4, p. 73 ff or EP-A 513 580.

1.4 another possibility for preparing the compounds I is the reaction of the benzyl derivative II with N-hydroxyphthalimide and subsequent hydrazinolysis to the benzylhydroxylamine IIa and the further reaction of IIa with a carbonyl compound X.##STR8##

The reaction is carried out in a manner known per se in an inert organic solvent according to the methods described in EP-A 463 488 and German Appl. No. 42 28 867.3.

The carbonyl compound X required is obtained, for example, by reaction of a corresponding hydroxyiminocarbonyl VIIa with a nucleophilically substituted reagent VI ##STR9##

or by reaction of a corresponding dicarbonyl XI with a hydroxylamine IXa or its salt IXb ##STR10##

The reactions are carried out in a manner known per se in an inert organic solvent according to the methods described in EP-A 513 580, Houben-Weyl, Vol. 10/4, p. 55 ff, p. 73 ff, p. 180 ff and p. 217 ff, Houben-Weyl, Vol. E14b, p. 307 ff and 369ff. Houben-Weyl, Vol. E5, p. 780 ff.

1.5 Correspondingly, the compounds I can also be obtained by converting the benzylhydroxylamine IIa first to the corresponding benzyloxyimine of the formula V using the hydroxyiminocarbonyl VIIa. V then being reacted with the nucleophilicallysubstituted reagent VI to give I as described above. ##STR11##

1.6 In a similar manner, the compounds I can also be prepared by converting the benzylhydroxylamine IIa first to the benzyloxyimine VIII using the dicarbonyl of the formula XI and then reacting VIII with the hydroxylamine IXa or its salt IXb togive I as described above. ##STR12##

2. Compounds in which R.sup.3 and/or R.sup.4 are a halogen atom are obtained by methods known per se from the corresponding precursors in which the radical concerned is a hydroxyl group (cf. Houben-Weyl, Vol. E5, p. 631; J. Org. Chem. 36(1971), 233; J. Org. Chem. 57 (1992), 3245). Preferably, the corresponding reactions to give the halogen derivative are performed in stages I and VIII.

3. Compounds in which R.sup.3 and/or R.sup.4 are bonded to the structure via an O, S or N atom are obtained by methods known per se from the corresponding precursors in which the radical concerned is a halogen atom (cf. Houben-Weyl, Vol. E5, p.826 ff and ;1280 ff. J. Org. Chem. 36 (1971), 233, J. Org. Chem. 46 (1981), 3623). Preferably, the corresponding conversions of the halogen derivative are performed in stages I and VIII.

4. Compounds in which R.sup.3 and/or R.sup.4 are bonded to the structure via an oxygen atom are in some cases also obtained by methods known per se from the corresponding precursors in which the radical concerned is a hydroxyl group (cf. Houben-Weyl, Vol. E5, p. 826-829, Aust. J. Chem. 27 give the alkoxy derivatives are performed in stages I and VIII.

5. Compounds in which R.sup.3 is not halogen are preferably obtained by first converting a compound X to the corresponding benzoic acid XIII according to the methods described in EP-A 493 711 using a lactone XII and converting XIII via thecorresponding halides to the cyanocarboxylic acids XIV, which are then converted by way of the Pinner reaction (Angew. Chem. 94 (1982). 1) to the .alpha.-keto esters XV. The corresponding carboxamides, which are subsequently converted to the compoundsI, are obtained from the derivatives XV by amidation. ##STR13##

6. The compounds XVI in which R is hydrogen can also be obtained directly from the carbonyl halides by reaction with isocyanates and subsequent hydrolysis by modifying the process described in 5. (EP 547 825). ##STR14##

7. In another variant, compounds XVI are obtained by converting an ortho halogen compound, after metallation with oxalyl chloride, to the corresponding keto acid chloride, which is subsequently converted with an amine to the corresponding amideXVI (cf. J. Org. Chem. 46 (1981), 46, 212 ff; DE-A 40 42 280; Houben-Weyl, Vol. E5, p. 972 ff). ##STR15##

8. In another variant, the compounds I in which X is oxygen are obtained, starting from the keto esters XV, by first converting the keto function to the oxime .[.ether [sic].]. .Iadd.ester .Iaddend.and converting the oxime ester thus obtainedto I using an appropriate amine (Houben-Weyl, Vol. E5, p. 941 ff). ##STR16##

9. The compounds I in which X is sulfur are obtained from the corresponding amides I by reaction with a sulfurizing reagent (eg. phosphorus sulfide or .[.Zawesson's [sic].]. .Iadd.Lawesson's reagent; cf. Houben-Weyl, Vol. IX, 764ff)..Iaddend. ##STR17##

The compounds II are known (EP-A 477 631, EP-A 463 488) or can be prepared by the methods described there.

On account of their C.dbd.C and C.dbd.N double bonds, the compounds I can be obtained during preparation as E/Z isomer mixtures which can be separated into the individual compounds in a customary manner, eg. by crystallization or chromatography.

If isomer mixtures are obtained during the synthesis, in general, however, a separation is not absolutely necessary, as the individual isomers can in some cases be converted to one another during preparation for application or during application(eg. under the action of light, acid or base). Corresponding conversions can also take place after application, for example during the treatment of plants in the treated plant or in the harmful fungus or animal pest to be controlled.

With reference to the C.dbd.NOCH.sub.3 double bond, the cis isomers of the compounds I are preferred with respect to their activity (configuration based on the --OCH.sub.3 group in relation to the --CXNRR.sup.1 group).

With reference to the --C(R.sup.3).dbd.NOCH.sub.2 -- double bond, the Z isomers of the compounds I are preferred with respect to their activity (configuration based on the radical R.sup.3 in relation to the --OCH.sub.2 -- group).

In the definitions of the compounds I given at the outset, collective terms were used which are generally representative of the following groups: halogen: fluorine, chlorine, bromine and iodine; alkyl: straight-chain or branched alkyl groupshaving 1 to 4, 6 or 10 carbon atoms, eg. C.sub.1 -C.sub.6 -alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylopropyl,1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl; alkylamino: an amino group which carries a straight-chain or branched alkyl group having 1 to 6 carbon atoms as mentioned above; dialkylamino:an amino group which carries two straight-chain or branched alkyl groups which are independent of one another and each have 1 to 6 carbon atoms as mentioned above; alkylcarbonyl: straight-chain or branched alkyl groups having 1 to 10 carbon atoms, whichare bonded to the structure via a carbonyl group (--CO--); alkylsulfonyl: straight-chain or branched alkyl groups having 1 to 6 or 10 carbon atoms, which are bonded to the structure via a sulfonyl group (--S(.dbd.O).sub.2 --); alkylsulfoxyl:straight-chain or branched alkyl groups having 1 to 6 carbon atoms, which are bonded to the structure via a sulfoxyl group (--S(--O)--); alkylaminocarbonyl: alkylamino groups having 1 to 6 carbon atoms as mentioned above, which are bonded to thestructure via a carbonyl group (--CO--); dialkylaminocarbonyl: dialkylamino groups in each case having 1 to 6 carbon atoms per alkyl radical as mentioned above, which are bonded to the structure via a carbonyl group (--CO--); alkylaminothiocarbonyl:alkylamino groups having 1 to 6 carbon atoms as mentioned above, which are bonded to the structure via a thiocarbonyl group (--CS--); dialkylaminothiocarbonyl: dialkylamino groups in each case having 1 to 6 carbon atoms per alkyl radical as mentionedabove, which are bonded to the structure via a thiocarbonyl group (--CS--); haloalkyl: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, it being possible for the hydrogen atoms in these groups to be partly or completely replaced byhalogen atoms as mentioned above, eg. C.sub.1 -C.sub.2 -haloalkyl such as chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-fluoroethyl,2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl; alkoxy: straight-chain or branched alkyl groups having 1 to 4 or 6 carbonatoms as mentioned above, which are bonded to the structure via an oxygen atom (--O--), eg. C.sub.1 -C.sub.6 -alkoxy such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy, 1,1-dimethylethoxy, pentoxy, 1-methylbutoxy,2-methylbutoxy, 3-methylbutoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexyloxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy,2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy and 1-ethyl-2-methylpropoxy;

alkoxycarbonyl: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, which are bonded to the structure via an oxycarbonyl group (--OC(.dbd.O)--);

haloalkoxy: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, it being possible for the hydrogen atoms in these groups to be partly or completely replaced by halogen atoms as mentioned above, and these groups being bonded to thestructure via an oxygen atom;

alkylthio: straight-chain or branched alkyl groups having 1 to 4 or 6 carbon atoms as mentioned above, which are bonded to the structure via a sulfur atom (--S--), eg. C.sub.1 -C.sub.6 -alkylthio such as methylthio, ethylthio, propylthio,1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio, 1,1-dimethylethylthio, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio, 1,1-dimethylpropylthio,1,2-dimethylpropylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio,1-ethylbutylthio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio, 1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio and 1-ethyl-2-methylpropylthio;

cycloalkyl: monocyclic alkyl groups having 3 to 6 carbon ring members, eg. cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl;

alkenyl: straight-chain or branched alkenyl groups having 2 to 6 or 10 carbon atoms and a double bond in any desired position, eg. C.sub.2 -C.sub.6 -alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl,3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl,3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl,1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl,1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl,1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl,2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl;

alkenyloxy: straight-chain or branched alkenyl groups having 2 to 6 carbon atoms and a double bond in any desired position, which are bonded to the structure via an oxygen atom (--O--);

alkenylcarbonyl: straight-chain or branched alkenyl groups having 2 to 10 carbon atoms and a double bond in any desired position, which are bonded to the structure via a carbonyl group (--CO--);

alkenylthio or alkenylamino: straight-chain or branched alkenyl groups having 2 to 6 carbon atoms and a double bond in any desired position, which are bonded to the structure (alkenylthio) via a sulfur atom or (alkenylamino) a nitrogen atom;

alkenyl: straight-chain or branched alkynyl groups having 2 to 10 carbon atoms and a triple bond-in any desired position, eg. C.sub.2 -C.sub.6 -alkynyl such as ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentynyl,3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl,2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-2-pentynyl, 1,1-di-methyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and1-ethyl-1-methyl-2-propynyl;

alkynylcarbonyl: straight-chain or branched alkynyl groups having 3 to 10 carbon atoms and a triple bond in any desired position, which are bonded to the structure via a carbonyl group (--CO--);

alkynyloxy or alkynylthio and alkynylamino: straight-chain or branched alkynyl groups having 2 to 6 carbon atoms and a triple bond in any desired position, which are bonded to the structure (alkynyloxy) via an oxygen atom or (alkynylthio) via asulfur atom or (alkynylamino) via a nitrogen atom;

cycloalkenyl or cycloalkenyloxy, cycloalkenylthio and cycloalkylamino [sic]: monocyclic alkenyl groups having 3 to 6 carbon ring members, which are bonded to the structure directly or (cycloalkenyloxy) via an oxygen atom or (cycloalkenylthio) asulfur atom or (cycloalkenylamino) via a nitrogen atom, eg. cyclopropenyl, cyclobutenyl, cyclopentenyl or cyclohexenyl;

cycloalkoxy or cycloalkylthio and cycloalkylamino: monocyclic alkenyl groups having 3 to 6 carbon ring members, which are bonded to the structure (cycloalkoxy) via an oxygen atom or (cycloalkylthio) a sulfur atom or (cycloalkylamino) via anitrogen atom, eg. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

heterocyclyl or heterocyclyloxy, heterocyclythio and hoterocyclylamino: three- to six-membered, saturated or partly unsaturated mono- or polycyclic heterocycles, which contain one to three heteroatoms selected from a group consisting of oxygen,nitrogen and sulfur, and which are bonded to the structure directly or (heterocyclyloxy) via an oxygen atom or (heterocyclylthio) via a sulfur atom or (heterocyclylamino) via a nitrogen atom, such as eg. 2-tetrhydrofuranyl, oxiranyl,3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazoldinyl [sic], 4-isoxazolidinyl, 5-isoxazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl,5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl, 1,2,4-thiadiazolidin-3-yl,1,2,4-thiadiazolidin-5-yl, 1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl, 1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-2-yl, 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,3-dihydrofur-4-yl, 2,3-dihydrofur-5-yl, 2,5-dihydrofur-2-yl, 2,5-dihydrofur-3-yl,2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,3-dihydrothien-4-yl, 2,3-dihydrothien-5-yl, 2,5-dihydrothien-2-yl, 2,5-dihydrothien-3-yl, 2,3-dihydropyrrol-2-yl, 2,3-dihydropyrrol-3-yl, 2,3-dihydropyrrol-4-yl, 2,3-dihydropyrrol-5-yl,2,5-dihydropyrrol-2-yl, 2,5-dihydropyrrol-3-yl, 2,3-dihydroisoxazol-3-yl, 2,3-dihydroisoxazol-4-yl, 2,3-dihydroisoxazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl, 2,5-dihydroisothiazol-3-yl,2,5-dihydroisothiazol-4-yl, 2,5-dihydroisothiazol-5-yl, 2,3-dihydroisopyrazol-3-yl, 2,3-dihydroisopyrazol-4-yl, 2,3-dihydroisopyrazol-5-yl, 4,5-dihydroisopyrazol-3-yl, 4,5-dihydroisopyrazol-4-yl, 4,5-dihydroisopyrazol-5-yl, 2,5-dihydroisopyrazol-3-yl,2,5-dihydroisopyrazol-4-yl, 2,5-dihydroisopyrazol-5-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 4,5-dihydrooxazol-3-yl, 4,5-dihydrooxazol-4-yl, 4,5-dihydrooxazol-5-yl, 2,5-dihydrooxazol-3-yl, 2,5-dihydrooxazol-4-yl, 2,5-dihydrooxazol, 5-yl, 2,3-dihydrothiazol-2-yl, 2,3-dihydrothiazol-4-yl, 2,3-dihydrothiazol-5-yl, 4,5-dihydrothiazol-2-yl, 4,5-dihydrothiazol-4-yl, 4,5-dihydrothiazol-5-yl, 2,5-dihydrothiazol-2-yl, 2,5-dihydrothiazol-4-yl, 2,5-dihydrothiazol-5-yl,2,3-dihydroimidazol-2-yl, 2,3-dihydroimidazol-4-yl, 2,3-dihydroimidazol-5-yl, 4,5-dihydroimidazol-2-yl, 4,5-dihydroimidazol-4-yl, 4,5-dihydroimidazol-5-yl, 2,5-dihydroimidazol-2-yl, 2,5-dihydroimidazol-4-yl, 2,5-dihydroimidazol-5-yl, 2-morpholinyl,3-morpholinyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 3-tetrahydropyridazinyl, 4-tetrahydropyridazinyl, 2-tetrahydropyrimidinyl, 4-tetrahydropyrimidinyl, 5-tetrahydropyrimidinyl, 2-tetrahydropyridazinyl, 1,3,5-tetrahydrotriazin-2-yl,1,2,4-tetrahydrotriazin-3-yl, 1,3-dihydrooxazin-2-yl, 1,3-dithian-2-yl, 2-tetrahydropyranyl, 1,3-dioxolan-2-yl, 3,4,5,6-tetrahydropyridin-2-yl, 4H-1,3-thiazin-2-yl, 4H-3,1-benzothiazin-2-yl, 1,1-dioxo-2,3,4,5-tetrahydrothien-2-yl,2H-1,4-benzothiazin-3-yl, 2H,1,4-benzoxazin-3-yl, 1,3-dihydrooxazin-2-yl, 1,3-dithian-2-yl;

aryl or aryloxy, arylthio, arylcarbonyl and arylsulfonyl: aromatic mono- or polycyclic hydrocarbon radicals which are bonded to the structure directly or (aryloxy) via an oxygen atom (--O--) or (arylthio) a sulfur atom (--S--), (arylcarbonyl) viaa carbonyl group (--CO--) or (arylsulfonyl) via a sulfonyl group (--SO.sub.2 --), eg. phenyl, naphthyl and phenanthrenyl or phenoxy, naphthyloxy and phenanthrenyloxy and the corresponding carbonyl and sulfonyl radicals;

arylamino: aromatic mono- or polycyclic hydrocarbon radicals which are bonded to the structure via nitrogen atom; hetaryl or hetaryloxy, hetarylthio, hetarylcarbonyl and hetarylsulfonyl: aromatic mono- or polycyclic radicals which, in addition tocarbon ring members, additionally can contain one to four nitrogen atoms or one to three nitrogen atoms and an oxygen or a sulfur atom or an oxygen or a sulfur atom and which are bonded to the structure directly or (hetaryloxy) via an oxygen atom (--O--)or (hetarylthio) a sulfur atom .[.(--s--) [sic].]. .Iadd.(--S--), .Iaddend.(hetarylcarbonyl) via a carbonyl group (--CO--) or (getarylsulfonyl) via a sulfonyl group .[.(--SO--) [sic].]. .Iadd.(--SO.sub.2 --).Iaddend., eg. 5-membered heteroaryl,containing one to three nitrogen atoms: 5-membered ring heteroaryl groups which, in addition to carbon atoms, can contain one to three nitrogen atoms as ring members, eg. 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-imidazolyl,4-imidazolyl, 1,2,4-triazol-3-yl and 1,3,4-triazol-2-yl; 5-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and a sulfur or oxygen atom or an oxygen or a sulfur atom: 5-membered ring heteroaryl groups which, inaddition to carbon atoms, can contain one to four nitrogen atoms or one to three nitrogen atoms and a sulfur or oxygen atom or an oxygen or sulfur atom as ring members, eg. 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl,4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 3-pyrazolyl, 5-pyrazolyl, 5-pyrazolyl, 4-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-imidazolyl, 4-imidizolyl, 1,2,4-oxadiazol-3-yl,1,2,4-oxadiazol-5-yl, 1,2,4-thi adiazol-3-yl, 1,2,4-thi adiazol-5-yl, 1,2,4-triazol-3-yl, 1,3,4-oxadiazol-2-yl, 1,3,4-thiadiazol-2-yl, 1,3,4-thiazol-2-yl; benzo-fused 5-membered heteroaryl, containing one to three nitrogen atoms or one nitrogen atomand/or an oxygen or sulfur atom: 5-membered ring heteroaryl groups which, in addition to carbon atoms, can contain one to four nitrogen atoms or one to three nitrogen atoms and a sulfur or oxygen atom or an oxygen or a sulfur atoms as ring members, andin which two adjacent carbon ring members or a nitrogen and an adjacent carbon ring member can be bridged by a buta-1,3-diene-1,4-diyl group; 5-membered heteroaryl bonded via nitrogen, containing one to four nitrogen atoms, or benzo-fused 5-memberedheteroaryl bonded via nitrogen, containing one to three nitrogen atoms: 5-membered ring heteroaryl groups which, in addition to carbon atoms, can contain one to four nitrogen atoms or one to three nitrogen atoms as ring members, and in which two adjacentcarbon ring members or a nitrogen and an adjacent carbon ring member can be bridged by a buta-1,3-diene-1,4-diyl group, these rings being bonded to the structure via one of the nitrogen ring members; 6-membered heteroaryl, containing one to three or oneto four nitrogen atoms: 6-membered ring heteroaryl groups which, in addition to carbon atoms, can contain one to three or one to four nitrogen atoms as ring members, eg. 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl,4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl, 1,3,5-triazin-2-yl, 1,2,4-triazin-3-yl and 1,2,4,5-tetrazinyl; benzo-fused 6-membered heteroaryl, containing one to four nitrogen atoms: 6-membered ring heteroaryl groups in which two adjacent carbon ringmembers can be bridged by a buta-1,3-diene-1,4-diyl group, eg. quinoline, isoquinoline, quinazoline and quinoxaline,

or the corresponding oxy, thio, carbonyl or sulfonyl groups; hetarylamino: aromatic mono- or polycyclic radicals which, in addition to carbon ring members, can additionally contain one to four nitrogen atoms or one to three nitrogen atoms and anyoxygen or a sulfur atom or an oxygen or a sulfur atom and which are bonded to the structure via a nitrogen atom.

The statement partly or completely halogenated is intended to express that in the groups characterized in this way the hydrogen atoms can be partly or completely replaced by identical or different halogen atoms as mentioned above.

With respect to their biological action, compounds of the formula I are preferred in which m is 0.

Equally preferred are compounds of the formula I in which R is hydrogen or methyl.

Equally preferred are compounds of the formula I in which R.sup.1 is hydrogen or methyl.

Compounds of the formula I are particularly preferred in which R is hydrogen and R.sup.1 is hydrogen or methyl.

Compounds of the formula I are particularly preferred in which R and R.sup.1 are simultaneously hydrogen or methyl.

In addition, compounds I are preferred in which R.sup.3 is hydrogen, hydroxyl, cyclopropyl, chlorine, methyl, methoxy, methylthio or phenyl.

Compounds I are additionally preferred in which R.sup.3 is methyl.

In addition, compounds I are preferred in which R.sup.3 is methoxy.

Compounds I are additionally preferred in which R.sup.3 is hydroxyl.

In addition, compounds I are preferred in which R.sup.3 is chlorine.

In addition, compounds I are preferred in which R.sup.4 is hydrogen, hydroxyl, cyclopropyl, chlorine, methyl, ethyl, isopropyl, methoxy or methylthio.

Compounds I are additionally preferred in which R.sup.4 is methyl.

In addition, compounds I are preferred in which R.sup.4 is methoxy.

Compounds I are additionally preferred in which R.sup.4 is hydroxyl.

In addition, compounds I are preferred in which R.sup.4 is ethyl.

Compounds I are additionally preferred in which R.sup.4 is isopropyl.

Compounds I are additionally preferred in which R.sup.4 is cyclopropyl.

In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted aryl or hetaryl.

In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted pyridyl, pyrimidyl, pyrazinyl, pyridazinyl or triazinyl.

In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted furyl, thienyl or pyrrolyl.

In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, pyrazolyl or imidazolyl.

In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted .[.oxidiazolyl [sic].]. .Iadd.oxadiazolyl.Iaddend., thiadiazolyl or triazolyl.

Compounds I are additionally preferred in which R.sup.4 is phenyl, which is unsubstituted or carries one or two of the following groups: nitro, cyano, hydroxyl, amino, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1-C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylamino, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylsulfonyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, C.sub.1 -C.sub.4 -alkylaminocarbonyl ordi-C.sub.1 -C.sub.4 -alkylaminocarbonyl.

Compounds I are additionally preferred in which R.sup.5 is hydrogen, C.sub.1 -C.sub.6 -alkyl, arylalkyl, heteraylalkyl, aryloxyalkyl, hetaryloxyalkyl, aryl or hetaryl.

In addition, compounds I are preferred in which R.sup.5 is C.sub.1 -C.sub.6 -alkyl.

Compounds I are additionally preferred in which R.sup.5 is methyl or ethyl.

In addition, compounds I are preferred in which R.sup.5 is arylalkyl or heterarylalkyl.

Compounds I are additionally preferred in which R.sup.5 is aryloxyalkyl or hetaryloxyalkyl.

Compounds I are additionally preferred in which R.sup.5 is aryl or hetaryl.

In addition, compounds of the formula I are preferred in which X is O.

In addition, compounds of the formula I are preferred in which X is S.

The compounds I compiled in the following tables are particularly preferred with respect to their use.

TABLE 1 Compounds of the general formula 1.1 in which (R.sup.2).sub.m is hydrogen and the combination of the substituents R.sup.3 . R.sup.4 and R.sup.5 for a compound in each case corresponds to one line of Table A ##STR18##

TABLE 2 Compounds of the general formula I.1 in which (R.sup.2).sub.m is chlorine and the combination of the substituents R.sup.3, R.sup.4 and R.sup.5 for a com- pound in each case corresponds to one line of Table A.

TABLE 3 Compounds of the general formula 1.2 in which (R.sup.2).sub.m is hydrogen and the combination of the substituents R.sup.3 . R.sup.4 and R.sup.5 for a compound in each case corresponds to one line of Table A ##STR19##

TABLE 4 Compounds of the general formula I.2 in which (R.sup.2).sub.m is chlorine and the combination of the substituents R.sup.3, R.sup.4 R.sup.5 for a com- pound in each case corresponds to one line of Table A.

TABLE 5 Compounds of the general formula 1.3 in which (R.sup.2).sub.m is hydrogen and the combination of the substituents R.sup.3 . R.sup.4 and R.sup.5 for a compound in each case corresponds to one line of Table A ##STR20##

TABLE 6 Compounds of the general formula I.3 in which (R.sup.2).sub.m is chlorine and the combination of the substituents R.sup.3, R.sup.4 and R.sup.5 for a com- pond in each case correspond to one line of Table A.

TABLE 7 Compounds of the general formula 1.4 in which (R.sup.2).sub.m is hydrogen and the combination of the substituents R.sup.3 . R.sup.4 and R.sup.5 for a compound in each case corresponds to one line of Table A ##STR21##

TABLE 8 Compounds of the general formula I.4 in which (R.sup.2).sub.m is chlorime and the combination of the substituents R.sup.3, R.sup.4 and R.sup.5 for a com- pound in each case corresponds to one line of Table A.

TABLE 9 Compounds of the general formula 1.5 in which (R.sup.2).sub.m is hydrogen and the combination of the substituents R.sup.3 . R.sup.4 and R.sup.5 for a compound in each case corresponds to one line of Table A ##STR22##

TABLE 10 Compounds of the general formula I.5 in which (R.sup.2).sub.m is chlorine and the combination of the substituents R.sup.3, R.sup.4 and R.sup.5 for a com- pound in cach case corresponds to one line of Table A.

TABLE 11 Compounds of the general formula 1.6 in which (R.sup.2).sub.m is hydrogen and the combination of the substituents R.sup.3 . R.sup.4 and R.sup.5 for a compound in each case corresponds to one line of Table A ##STR23##

TABLE 12 Compounds of the general formula I.6 in which (R.sup.2).sub.m is a chlorine and the combination of the substituents R.sup.3, R.sup.4 and R.sup.5 for a com- pound in each case corresponds to one line of Table A.

TABLE A No. R.sup.3 R.sup.4 R.sup.5 1 CH.sub.3 CH.sub.3 H 2 CH.sub.3 CH.sub.3 CH.sub.3 3 CH.sub.3 CH.sub.3 C.sub.2 H.sub.5 4 CH.sub.3 CH.sub.3 n-C.sub.3 H.sub.7 5 CH.sub.3 CH.sub.3 i-C.sub.3 H.sub.7 6 CH.sub.3 CH.sub.3 Cyclopropyl 7CH.sub.3 CH.sub.3 n-C.sub.4 H.sub.9 8 CH.sub.3 CH.sub.3 s-C.sub.4 H.sub.9 9 CH.sub.3 CH.sub.3 i-C.sub.4 H.sub.9 10 CH.sub.3 CH.sub.3 t-C.sub.4 H.sub.9 11 CH.sub.3 CH.sub.3 n-C.sub.5 H.sub.11 12 CH.sub.3 CH.sub.3 i-C.sub.5 H.sub.11 13 CH.sub.3CH.sub.3 neo-C.sub.5 H.sub.11 14 CH.sub.3 CH.sub.3 Cyclopentyl 15 CH.sub.3 CH.sub.3 n-C.sub.6 H.sub.13 16 CH.sub.3 CH.sub.3 Cyclohexyl 17 CH.sub.3 CH.sub.3 n-C.sub.8 H.sub.17 18 CH.sub.3 CH.sub.3 CH.sub.2 CH.sub.2 Cl 19 CH.sub.3 CH.sub.3(CH.sub.2).sub.4 Cl 20 CH.sub.3 CH.sub.3 CH.sub.2 CN 21 CH.sub.3 CH.sub.3 CH.sub.2 CH.sub.2 CN 22 CH.sub.3 CH.sub.3 (CH.sub.2).sub.3 CN 23 CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 CN 24 CH.sub.3 CH.sub.3 (CH.sub.2).sub.6 CN 25 CH.sub.3 CH.sub.3Cyclohexylmethyl 26 CH.sub.3 CH.sub.3 2-Cyclohexyleth-1-yl 27 CH.sub.3 CH.sub.3 Cyclopropylmethyl 28 CH.sub.3 CH.sub.3 2-Cyclopropyleth-1-yl 29 CH.sub.3 CH.sub.3 2-Methoxyeth-1-yl 30 CH.sub.3 CH.sub.3 2-Ethoxyeth-1-yl 31 CH.sub.3 CH.sub.32-Isopropoxyeth-1-yl 32 CH.sub.3 CH.sub.3 3-Methoxyprop-1-yl 33 CH.sub.3 CH.sub.3 3-Ethoxyprop-1-yl 34 CH.sub.3 CH.sub.3 3-Isopropoxyprop-1-yl 35 CH.sub.3 CH.sub.3 4-Methoxybut-1-yl 36 CH.sub.3 CH.sub.3 4-Isopropoxybut-1-yl 37 CH.sub.3 CH.sub.3Propen-3-yl 38 CH.sub.3 CH.sub.3 But-2-en-1-yl 39 CH.sub.3 CH.sub.3 3-Methylbut-2-en-1-yl 40 CH.sub.3 CH.sub.3 2-Vinyloxyeth-1-yl 41 CH.sub.3 CH.sub.3 Allyloxyeth-1-yl 42 CH.sub.3 CH.sub.3 2-Trifluoromethoxyeth-1-yl 43 CH.sub.3 CH.sub.33-Trifluoromethoxyprop-1-yl 44 CH.sub.3 CH.sub.3 4-Difluoromethoxybut-1-yl 45 CH.sub.3 CH.sub.3 Hydroxycarbonylmethyl 46 CH.sub.3 CH.sub.3 Methoxycarbonylmethyl 47 CH.sub.3 CH.sub.3 Aminocarbonylmethyl 48 CH.sub.3 CH.sub.3N-Methylaminocarbonylmethyl 49 CH.sub.3 CH.sub.3 N,N-Dimethylaminocarbonyl- methyl 50 CH.sub.3 CH.sub.3 2-Hydroxycarbonyleth-1-yl 51 CH.sub.3 CH.sub.3 2-Methoxycarbonyleth-1-yl 52 CH.sub.3 CH.sub.3 2-Aminocarbonyleth-1-yl 53 CH.sub.3 CH.sub.32-N-Methylaminocarbon- yleth-1-yl 54 CH.sub.3 CH.sub.3 2-Dimethylaminocarbon- yleth-1-yl 55 CH.sub.3 CH.sub.3 2-Aminoeth-1-yl 56 CH.sub.3 CH.sub.3 2-Aminoprop-1-yl 57 CH.sub.3 CH.sub.3 4-Aminobut-1-yl 58 CH.sub.3 CH.sub.3 3-Dimethylaminoprop-1-yl 59 CH.sub.3 CH.sub.3 4-Aminothiocarbonylbut-1-yl 60 CH.sub.3 CH.sub.3 2-Oxopropyl 61 CH.sub.3 CH.sub.3 Cyclohexyl 62 CH.sub.3 CH.sub.3 Cyclopropyl 63 CH.sub.3 CH.sub.3 Cyclopentyl 64 CH.sub.3 CH.sub.3 2-Methoxyiminoprop-1-yl 65 CH.sub.3 CH.sub.32-Methoxyiminoeth-1-yl 66 CH.sub.3 CH.sub.3 6-Aminocarbonylhex-1-yl 67 CH.sub.3 CH.sub.3 3-Aminothiocarbonyl- prop-1-yl 68 CH.sub.3 CH.sub.3 2-Aminothiocarbonyleth-1-yl 69 CH.sub.3 CH.sub.3 Aminothiocarbonylmethyl 70 CH.sub.3 CH.sub.34-(N,N-Dimethylamino)- but-1-yl 71 CH.sub.3 CH.sub.3 2-(Methylthio)eth-1-yl 72 CH.sub.3 CH.sub.3 2-(Methylsulfonyl)eth-1-yl 73 CH.sub.3 CH.sub.3 4-(Methylthio)prop-1-yl 74 CH.sub.3 CH.sub.3 4-(Methylsulfonyl)prop-1-yl 75 CH.sub.3 CH.sub.3 Benyzl 76 CH.sub.3 CH.sub.3 2-F--C.sub.6 H.sub.4 --CH.sub.2 77 CH.sub.3 CH.sub.3 3-F--C.sub.6 H.sub.4 --CH.sub.2 78 CH.sub.3 CH.sub.3 4-F--C.sub.6 H.sub.4 --CH.sub.2 79 CH.sub.3 CH.sub.3 2,3-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 80 CH.sub.3 CH.sub.32,4-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 81 CH.sub.3 CH.sub.3 2,5-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 82 CH.sub.3 CH.sub.3 2,6-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 83 CH.sub.3 CH.sub.3 3,4-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 84 CH.sub.3 CH.sub.33,5-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 85 CH.sub.3 CH.sub.3 2-Cl--C.sub.6 H.sub.4 --CH.sub.2 86 CH.sub.3 CH.sub.3 3-Cl--C.sub.6 H.sub.4 --CH.sub.2 87 CH.sub.3 CH.sub.3 4-Cl--C.sub.6 H.sub.4 --CH.sub.2 88 CH.sub.3 CH.sub.3 2,3-Cl.sub.2 --C.sub.6H.sub.3 --CH.sub.2 89 CH.sub.3 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 90 CH.sub.3 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 91 CH.sub.3 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 92 CH.sub.3 CH.sub.3 3,4-Cl.sub.2--C.sub.6 H.sub.3 --CH.sub.2 93 CH.sub.3 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 94 CH.sub.3 CH.sub.3 2,3,4-Cl.sub.3 --C.sub.6 H.sub.3 --CH.sub.2 95 CH.sub.3 CH.sub.3 2,3,5-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 96 CH.sub.3 CH.sub.32,3,6-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 97 CH.sub.3 CH.sub.3 2,4,5-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 98 CH.sub.3 CH.sub.3 2,4,6-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 99 CH.sub.3 CH.sub.3 3,4,5-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 100CH.sub.3 CH.sub.3 2-Br--C.sub.6 H.sub.4 --CH.sub.2 101 CH.sub.3 CH.sub.3 3-Br--C.sub.6 H.sub.4 --CH.sub.2 102 CH.sub.3 CH.sub.3 4-Br--C.sub.6 H.sub.4 --CH.sub.2 103 CH.sub.3 CH.sub.3 2,3-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 104 CH.sub.3 CH.sub.32,4-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 105 CH.sub.3 CH.sub.3 2,5-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 106 CH.sub.3 CH.sub.3 2,6-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 107 CH.sub.3 CH.sub.3 3,4-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 108 CH.sub.3CH.sub.3 3,5-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 109 CH.sub.3 CH.sub.3 2-F, 3-Cl--C.sub.6 H.sub.3 --CH.sub.2 110 CH.sub.3 CH.sub.3 2-F, 4-Cl--C.sub.6 H.sub.3 --CH.sub.2 111 CH.sub.3 CH.sub.3 2-F, 5-Cl--C.sub.6 H.sub.3 --CH.sub.2 112 CH.sub.3CH.sub.3 2-F, 3-Br--C.sub.6 H.sub.3 --CH.sub.2 113 CH.sub.3 CH.sub.3 2-F, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 114 CH.sub.3 CH.sub.3 2-F, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 115 CH.sub.3 CH.sub.3 2-Cl, 3-Br--C.sub.6 H.sub.3 --CH.sub.2 116 CH.sub.3 CH.sub.32-Cl, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 117 CH.sub.3 CH.sub.3 2-Cl, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 118 CH.sub.3 CH.sub.3 3-F, 4-Cl--C.sub.6 H.sub.3 --CH.sub.2 119 CH.sub.3 CH.sub.3 3-F, 5-Cl--C.sub.6 H.sub.3 --CH.sub.2 120 CH.sub.3 CH.sub.3 3-F,6-Cl--C.sub.6 H.sub.3 --CH.sub.2 121 CH.sub.3 CH.sub.3 3-F, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 122 CH.sub.3 CH.sub.3 3-F, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 123 CH.sub.3 CH.sub.3 3-F, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 124 CH.sub.3 CH.sub.3 3-Cl,4-Br--C.sub.6 H.sub.3 --CH.sub.2 125 CH.sub.3 CH.sub.3 3-Cl, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 126 CH.sub.3 CH.sub.3 3-Cl, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 127 CH.sub.3 CH.sub.3 4-F, 5-Cl--C.sub.6 H.sub.3 --CH.sub.2 128 CH.sub.3 CH.sub.3 4-F,6-Cl--C.sub.6 H.sub.3 --CH.sub.2 129 CH.sub.3 CH.sub.3 4-F, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 130 CH.sub.3 CH.sub.3 4-F, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 131 CH.sub.3 CH.sub.3 4-Cl, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 132 CH.sub.3 CH.sub.3 5-F,6-Cl--C.sub.6 H.sub.3 --CH.sub.2 133 CH.sub.3 CH.sub.3 5-F, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 134 CH.sub.3 CH.sub.3 5-Cl, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 135 CH.sub.3 CH.sub.3 3-Br, 4-Cl, 5-Br--C.sub.6 H.sub.2 --CH.sub.2 136 CH.sub.3 CH.sub.32-CN--C.sub.6 H.sub.4 --CH.sub.2 137 CH.sub.3 CH.sub.3 3-CN--C.sub.6 H.sub.4 --CH.sub.2 138 CH.sub.3 CH.sub.3 4-CN--C.sub.6 H.sub.4 --CH.sub.2 139 CH.sub.3 CH.sub.3 2-NO.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 140 CH.sub.3 CH.sub.3 3-NO.sub.2 --C.sub.6H.sub.4 --CH.sub.2 141 CH.sub.3 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 142 CH.sub.3 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 143 CH.sub.3 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 144 CH.sub.3 CH.sub.3 4-CH.sub.3 --C.sub.6H.sub.4 --CH.sub.2 145 CH.sub.3 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 146 CH.sub.3 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 147 CH.sub.3 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 148 CH.sub.3CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 149 CH.sub.3 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 150 CH.sub.3 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 151 CH.sub.3 CH.sub.3 2-C.sub.2 H.sub.5--C.sub.6 H.sub.4 --CH.sub.2 152 CH.sub.3 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 153 CH.sub.3 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 154 CH.sub.3 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 --CH.sub.2 155CH.sub.3 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 --CH.sub.2 156 CH.sub.3 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 --CH.sub.2 157 CH.sub.3 CH.sub.3 2-Cyclohexyl-C.sub.6 H.sub.4 --CH.sub.2 158 CH.sub.3 CH.sub.3 3-Cyclohexyl-C.sub.6H.sub.4 --CH.sub.2 159 CH.sub.3 CH.sub.3 4-Cyclohexyl-C.sub.6 H.sub.4 --CH.sub.2 160 CH.sub.3 CH.sub.3 2-Vinyl-C.sub.6 H.sub.4 --CH.sub.2 161 CH.sub.3 CH.sub.3 3-Vinyl-C.sub.6 H.sub.4 --CH.sub.2 162 CH.sub.3 CH.sub.3 4-Vinyl-C.sub.6 H.sub.4--CH.sub.2 163 CH.sub.3 CH.sub.3 2-Allyl-C.sub.6 H.sub.4 --CH.sub.2 164 CH.sub.3 CH.sub.3 3-Allyl-C.sub.6 H.sub.4 --CH.sub.2 165 CH.sub.3 CH.sub.3 4-Allyl-C.sub.6 H.sub.4 --CH.sub.2 166 CH.sub.3 CH.sub.3 2-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 167 CH.sub.3 CH.sub.3 3-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 168 CH.sub.3 CH.sub.3 4-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 169 CH.sub.3 CH.sub.3 3-CH.sub.3, 5-i-C.sub.4 H.sub.9 --C.sub.6 H.sub.3 --CH.sub.2 170 CH.sub.3CH.sub.3 2-OH--C.sub.6 H.sub.4 --CH.sub.2 171 CH.sub.3 CH.sub.3 3-OH--C.sub.6 H.sub.4 --CH.sub.2 172 CH.sub.3 CH.sub.3 4-OH--C.sub.6 H.sub.4 --CH.sub.2 173 CH.sub.3 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 174 CH.sub.3 CH.sub.3 3-OCH.sub.3--C.sub.6 H.sub.4 --CH.sub.2 175 CH.sub.3 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 176 CH.sub.3 CH.sub.3 2,3-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 177 CH.sub.3 CH.sub.3 2,4-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 178CH.sub.3 CH.sub.3 2-5-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 179 CH.sub.3 CH.sub.3 3,4-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 180 CH.sub.3 CH.sub.3 3,5-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 181 CH.sub.3 CH.sub.33,4,5-(OCH.sub.3).sub.3 --C.sub.6 H.sub.2 --CH.sub.2 182 CH.sub.3 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 183 CH.sub.3 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 184 CH.sub.3 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6H.sub.4 --CH.sub.2 185 CH.sub.3 CH.sub.3 2-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 186 CH.sub.3 CH.sub.3 3-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 187 CH.sub.3 CH.sub.3 4-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 188CH.sub.3 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 189 CH.sub.3 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 190 CH.sub.3 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 191 CH.sub.3 CH.sub.34-O-(n-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 --CH.sub.2 192 CH.sub.3 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 --CH.sub.2

193 CH.sub.3 CH.sub.3 4-O-(n-C.sub.6 H.sub.13)--C.sub.6 H.sub.4 --CH.sub.2 194 CH.sub.3 CH.sub.3 2-O-Allyl-C.sub.6 H.sub.4 --CH.sub.2 195 CH.sub.3 CH.sub.3 3-O-Allyl-C.sub.6 H.sub.4 --CH.sub.2 196 CH.sub.3 CH.sub.3 4-O-Allyl-C.sub.6 H.sub.4--CH.sub.2 197 CH.sub.3 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 198 CH.sub.3 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 199 CH.sub.3 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 200 CH.sub.3 CH.sub.3 2-Acetyl-C.sub.6 H.sub.4--CH.sub.2 201 CH.sub.3 CH.sub.3 3-Acetyl-C.sub.6 H.sub.4 --CH.sub.2 202 CH.sub.3 CH.sub.3 4-Acetyl-C.sub.6 H.sub.4 --CH.sub.2 203 CH.sub.3 CH.sub.3 2-Methoxycarbonyl-C.sub.6 H.sub.4 --CH.sub.2 204 CH.sub.3 CH.sub.3 3-Methoxycarbonyl-C.sub.6 H.sub.4 --CH.sub.2 205 CH.sub.3 CH.sub.3 4-Methoxycarbonyl-C.sub.6 H.sub.4 --CH.sub.2 206 CH.sub.3 CH.sub.3 2-Aminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 207 CH.sub.3 CH.sub.3 3-Aminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 208 CH.sub.3 CH.sub.34-Aminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 209 CH.sub.3 CH.sub.3 2-Dimethylaminocarbo- nyl-C.sub.6 H.sub.4 --CH.sub.2 210 CH.sub.3 CH.sub.3 3-Dimethylaminocarbo- nyl-C.sub.6 H.sub.4 --CH.sub.2 211 CH.sub.3 CH.sub.3 4-Dimethylaminocarbo- nyl-C.sub.6 H.sub.4 --CH.sub.2 212 CH.sub.3 CH.sub.3 2-(N-Methylaminocarbo- nyl)-C.sub.6 H.sub.4 --CH.sub.2 213 CH.sub.3 CH.sub.3 3-(N-Methylaminocarbo- nyl)-C.sub.6 H.sub.4 --CH.sub.2 214 CH.sub.3 CH.sub.3 4-(N-Methylaminocarbo- nyl)-C.sub.6H.sub.4 --CH.sub.2 215 CH.sub.3 CH.sub.3 2-H.sub.2 N--C.sub.6 H.sub.4 --CH.sub.2 216 CH.sub.3 CH.sub.3 3-H.sub.2 N--C.sub.6 H.sub.4 --CH.sub.2 217 CH.sub.3 CH.sub.3 4-H.sub.2 N--C.sub.6 H.sub.4 --CH.sub.2 218 CH.sub.3 CH.sub.3 2-Amino- thiocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 219 CH.sub.3 CH.sub.3 3-Amino- thiocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 220 CH.sub.3 CH.sub.3 4-Amino- thiocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 221 CH.sub.3 CH.sub.3 2-Methoxyiminomethyl- C.sub.6 H.sub.4--CH.sub.2 222 CH.sub.3 CH.sub.3 3-Methoxyiminomethyl- C.sub.6 H.sub.4 --CH.sub.2 223 CH.sub.3 CH.sub.3 4-Methoxyiminomethyl- C.sub.6 H.sub.4 --CH.sub.2 224 CH.sub.3 CH.sub.3 2-Formyl-C.sub.6 H.sub.4 --CH.sub.2 225 CH.sub.3 CH.sub.33-Formyl-C.sub.6 H.sub.4 --CH.sub.2 226 CH.sub.3 CH.sub.3 4-Formyl-C.sub.6 H.sub.4 --CH.sub.2 227 CH.sub.3 CH.sub.3 2-(1'-Methoxyiminoeth- 1'-yl)-C.sub.6 H.sub.4 --CH.sub.2 228 CH.sub.3 CH.sub.3 3-(1'-Methoxyiminoeth- 1'-yl)-C.sub.6 H.sub.4--CH.sub.2 229 CH.sub.3 CH.sub.3 4-(1'-Methoxyiminoeth- 1'-yl)-C.sub.6 H.sub.4 --CH.sub.2 230 CH.sub.3 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 231 CH.sub.3 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 232 CH.sub.3 CH.sub.3 4-SCH.sub.3--C.sub.6 H.sub.4 --CH.sub.2 233 CH.sub.3 CH.sub.3 2-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 234 CH.sub.3 CH.sub.3 3-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 235 CH.sub.3 CH.sub.3 4-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 236CH.sub.3 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 237 CH.sub.3 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 238 CH.sub.3 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 239 CH.sub.3 CH.sub.3 2-OCHF.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 240 CH.sub.3 CH.sub.3 3-OCHF.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 241 CH.sub.3 CH.sub.3 4-OCHF.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 242 CH.sub.3 CH.sub.3 3-CF.sub.3, 4-OCF.sub.3 --C.sub.6 H.sub.3 --CH.sub.2 243 CH.sub.3 CH.sub.3 1-Naphthyl-CH.sub.2 244 CH.sub.3 CH.sub.3 2-Naphthyl-CH.sub.2 245 CH.sub.3 CH.sub.3 2-Phenoxyeth-1-yl 246 CH.sub.3 CH.sub.3 2-(2'-Chlorophenoxy)eth-1- yl 247 CH.sub.3 CH.sub.3 3-(2'-Chlorophenoxy)eth-1- yl 248 CH.sub.3 CH.sub.3 2-(4'-Chlorophenoxy)eth-1- yl 249CH.sub.3 CH.sub.3 2-(3',5'-Dichlorophenoxy)- eth-1-yl 250 CH.sub.3 CH.sub.3 2-(2'-Cyanophenoxy)eth-1-yl 251 CH.sub.3 CH.sub.3 2-(3'-Cyanophenoxy)eth-1-yl 252 CH.sub.3 CH.sub.3 2-(4'-Cyanophenoxy)eth-1-yl 253 CH.sub.3 CH.sub.3 2-(2'-Methyl- phenoxy)eth-1-yl 254 CH.sub.3 CH.sub.3 2-(3'-Methyl- phenoxy)eth-1-yl 255 CH.sub.3 CH.sub.3 2-(4'-Methyl- phenoxy)eth-1-yl 256 CH.sub.3 CH.sub.3 2-(3'-t-Butylphe- noxy)eth-1-yl 257 CH.sub.3 CH.sub.3 2-(4'-t-Butylphe- noxy)eth-1-yl 258 CH.sub.3CH.sub.3 2-(2'-Nitrophenoxy)eth-1-yl 259 CH.sub.3 CH.sub.3 2-(3'-Nitrophenoxy)eth-1-yl 260 CH.sub.3 CH.sub.3 2-(4'-Nitrophenoxy)eth-1-yl 261 CH.sub.3 CH.sub.3 2-(2'-Methoxyphen- oxy)eth-1-yl 262 CH.sub.3 CH.sub.3 2-(3'-Methoxyphen- oxy)eth-1-yl 263 CH.sub.3 CH.sub.3 2-(4'-Methoxyphen- oxy)eth-1-yl 264 CH.sub.3 CH.sub.3 2-(2'-Trifluoromethylphen- oxy)eth-1-yl 265 CH.sub.3 CH.sub.3 2-(3'-Trifluoromethylphen- oxy)eth-1-yl 266 CH.sub.3 CH.sub.3 2 (4'-Trifluoromethylphen- oxy)eth-1-yl 267CH.sub.3 CH.sub.3 2-(2'-Acetylphenoxy)- eth-1-yl 268 CH.sub.3 CH.sub.3 3-(2'-Acetylphenoxy)- eth-1-yl 269 CH.sub.3 CH.sub.3 4-(2'-Acetylphenoxy)- eth-1-yl 270 CH.sub.3 CH.sub.3 2-(2'-Methoxy- carbonyl)eth-1-yl 271 CH.sub.3 CH.sub.3 2-(3'-Methoxy- carbonyl)eth-1-yl 272 CH.sub.3 CH.sub.3 2-(4'-Methoxy- carbonyl)eth-1-yl 273 CH.sub.3 CH.sub.3 2-(2'-Dimethylamino- carbonyl)eth-1-yl 274 CH.sub.3 CH.sub.3 2-(3'-Dimethylamino- carbonyl)eth-1-yl 275 CH.sub.3 CH.sub.3 2-(3'-Dimethylamino- carbonyl)eth-1-yl 276 CH.sub.3 CH.sub.3 2-(2'-Aminothiocarbo- nyl)eth-1-yl 277 CH.sub.3 CH.sub.3 2-(3'-Aminothiocarbo- nyl)eth-1-yl 278 CH.sub.3 CH.sub.3 2-(4'-Aminothiocarbo- nyl)eth-1-yl 279 CH.sub.3 CH.sub.3 2-(2'-Methyl- sulfonyl)eth-1-yl 280 CH.sub.3 CH.sub.3 2-(3'-Methyl- sulfonyl)eth-1-yl 281 CH.sub.3 CH.sub.3 2-(4'-Methyl- sulfonyl)eth-1-yl 282 CH.sub.3 CH.sub.3 3-Phenoxyprop-1-yl 283 CH.sub.3 CH.sub.3 3-(2'-Chlorophenoxy)prop-1- yl 284 CH.sub.3 CH.sub.33-(3'-Chlorophenoxy)prop-1- yl 285 CH.sub.3 CH.sub.3 3-(4'-Chlorophenoxy)prop-1- yl 286 CH.sub.3 CH.sub.3 3-(3',5'-Dichlorophenoxy)- prop-1-yl 287 CH.sub.3 CH.sub.3 3-(2'-Cyanophen- oxy)prop-1-yl 288 CH.sub.3 CH.sub.3 3-(3'-Cyanophen- oxy)prop-1-yl 289 CH.sub.3 CH.sub.3 3-(4'-Cyanophen- oxy)prop-1-yl 290 CH.sub.3 CH.sub.3 3-(2'-Methyl- phenoxy)prop-1-yl 291 CH.sub.3 CH.sub.3 3-(3'-Methyl- phenoxy)prop-1-yl 292 CH.sub.3 CH.sub.3 3-(4'-Methyl- phenoxy)prop-1-yl 293 CH.sub.3CH.sub.3 3-(2'-Methoxyphenoxy)prop- 1-yl 294 CH.sub.3 CH.sub.3 3-(3'-Methoxyphenoxy)prop- 1-yl 295 CH.sub.3 CH.sub.3 3-(4'-Methoxyphenoxy)prop- 1-yl 296 CH.sub.3 CH.sub.3 3-(2'-Trifluoromethyl- phenoxy)prop-1-yl 297 CH.sub.3 CH.sub.33-(3'-Trifluoromethyl- phenoxy)prop-1-yl 298 CH.sub.3 CH.sub.3 3-(4'-Trifluoromethyl- phenoxy)prop-1-yl 299 CH.sub.3 CH.sub.3 4-Phenoxybut-1-yl 300 CH.sub.3 CH.sub.3 2-Phenyleth-1-yl 301 CH.sub.3 CH.sub.3 2-(2'-Chlorophenyl)eth-1-yl 302 CH.sub.3CH.sub.3 2-(3'-Chlorophenyl)eth-1-yl 303 CH.sub.3 CH.sub.3 2-(4'-Chlorophenyl)eth-1-yl 304 CH.sub.3 CH.sub.3 2-(3',5'-Dichlorophenyl)eth- 1-yl 305 CH.sub.3 CH.sub.3 2-(2'-Cyanophenyl)eth-1-yl 306 CH.sub.3 CH.sub.3 2-(3'-Cyanophenyl)eth-1-yl 307CH.sub.3 CH.sub.3 2-(4'-Cyanophenyl)eth-1-yl 308 CH.sub.3 CH.sub.3 2-(2'-Methylphenyl)eth-1-yl 309 CH.sub.3 CH.sub.3 2-(3'-Methylphenyl)eth-1-yl 310 CH.sub.3 CH.sub.3 2-(4'-Methylphenyl)eth-1-yl 311 CH.sub.3 CH.sub.3 2-(2'-Methoxy- phenyl)eth-1-yl 312 CH.sub.3 CH.sub.3 2-(3'-Methoxy- phenyl)eth-1-yl 313 CH.sub.3 CH.sub.3 2-(4'-Methoxy- phenyl)eth-1-yl 314 CH.sub.3 CH.sub.3 2-(2'-Trifluoromethyl- phenyl)eth-1-yl 315 CH.sub.3 CH.sub.3 2-(3'-Trifluoromethyl- phenyl)eth-1-yl 316 CH.sub.3CH.sub.3 2-(4'-Trifluoromethyl- phenyl)eth-1-yl 317 CH.sub.3 CH.sub.3 3-Phenylprop-1-yl 318 CH.sub.3 CH.sub.3 3-(2'-Chlorophenyl)prop-1- yl 319 CH.sub.3 CH.sub.3 3-(3'-Chlorophenyl)prop-1- yl 320 CH.sub.3 CH.sub.3 3-(4'-Chlorophenyl)prop-1- yl 321 CH.sub.3 CH.sub.3 3-(2'-Cyanophenyl)prop-1-yl 322 CH.sub.3 CH.sub.3 3-(3'-Cyanophenyl)prop-1-yl 323 CH.sub.3 CH.sub.3 3-(4'-Cyanophenyl)prop-1-yl 324 CH.sub.3 CH.sub.3 3-(2'-Trifluoromethyl- phenyl)prop-1-yl 325 CH.sub.3 CH.sub.34-Phenylbut-1-yl 326 CH.sub.3 CH.sub.3 4-(4'-Chlorophenyl)but-1-yl 327 CH.sub.3 CH.sub.3 6-(4'-Chlorophenyl)hex-1-yl 328 CH.sub.3 CH.sub.3 2-Pyridylmethyl 329 CH.sub.3 CH.sub.3 3-Pyridylmethyl 330 CH.sub.3 CH.sub.3 4-Pyridylmethyl 331 CH.sub.3CH.sub.3 4-Chloropyridin-2-ylmethyl 332 CH.sub.3 CH.sub.3 5-Chloropyridin-2-ylmethyl 333 CH.sub.3 CH.sub.3 6-Chloropyridin-2-ylmethyl 334 CH.sub.3 CH.sub.3 5-Chloropyridin-3-ylmethyl 335 CH.sub.3 CH.sub.3 6-Chloropyridin-3-ylmethyl 336 CH.sub.3CH.sub.3 2-Chloropyridin-4-ylmethyl 337 CH.sub.3 CH.sub.3 2-Pyrimidinylmethyl 338 CH.sub.3 CH.sub.3 4-Chloropyrimidin-2-yl- methyl 339 CH.sub.3 CH.sub.3 5-Chloropyrimidin-2-yl- methyl 340 CH.sub.3 CH.sub.3 6-Chloropyrimidin-4-yl- methyl 341CH.sub.3 CH.sub.3 6-Chloropyrimidin-5-yl- methyl 342 CH.sub.3 CH.sub.3 2-Chloropyrimidin-5-yl- methyl 343 CH.sub.3 CH.sub.3 4-Pyridazinylmethyl 344 CH.sub.3 CH.sub.3 2-Pyrazinylmethyl 345 CH.sub.3 CH.sub.3 5-Chloropyrazin-2-ylmethyl 346 CH.sub.3CH.sub.3 6-Chloropyrazin-2-ylmethyl 347 CH.sub.3 CH.sub.3 3-Pyridazinylmethyl 348 CH.sub.3 CH.sub.3 6-Chloropyridazin-3-yl- methyl 349 CH.sub.3 CH.sub.3 1,3,5-Triazinylmethyl 350 CH.sub.3 CH.sub.3 2-Furylmethyl 351 CH.sub.3 CH.sub.3 3-Furylmethyl

352 CH.sub.3 CH.sub.3 4-Bromofur-2-ylmethyl 353 CH.sub.3 CH.sub.3 5-Chlorofur-2-ylmethyl 354 CH.sub.3 CH.sub.3 2-Thienylmethyl 355 CH.sub.3 CH.sub.3 3-Thienylmethyl 356 CH.sub.3 CH.sub.3 5-Methylthien-3-ylmethyl 357 CH.sub.3 CH.sub.35-Chlorothien-2-ylmethyl 358 CH.sub.3 CH.sub.3 2-Chlorothien-4-ylmethyl 359 CH.sub.3 CH.sub.3 2-Pyrrolylmethyl 360 CH.sub.3 CH.sub.3 3-Pyrrolylmethyl 361 CH.sub.3 CH.sub.3 2-Oxazolylmethyl 362 CH.sub.3 CH.sub.3 4-Methyloxazol-2-ylmethyl 363CH.sub.3 CH.sub.3 5-Methyloxazol-2-ylmethyl 364 CH.sub.3 CH.sub.3 4-Chlorooxazol-2-ylmethyl 365 CH.sub.3 CH.sub.3 5-Chlorooxazol-2-ylmethyl 366 CH.sub.3 CH.sub.3 4-Oxazolylmethyl 367 CH.sub.3 CH.sub.3 2-Methyloxazol-4-ylmethyl 368 CH.sub.3 CH.sub.35-Methyloxazol-4-ylmethyl 369 CH.sub.3 CH.sub.3 2-Chlorooxazol-4-ylmethyl 370 CH.sub.3 CH.sub.3 5-Chlorooxazol-4-ylmethyl 371 CH.sub.3 CH.sub.3 5-Oxazolylmethyl 372 CH.sub.3 CH.sub.3 2-Methyloxazol-5-ylmethyl 373 CH.sub.3 CH.sub.34-Methyloxazol-5-ylmethyl 374 CH.sub.3 CH.sub.3 2-Chlorooxazol-5-ylmethyl 375 CH.sub.3 CH.sub.3 4-Chlorooxazol-5-ylmethyl 376 CH.sub.3 CH.sub.3 2-Thiazolylmethyl 377 CH.sub.3 CH.sub.3 4-Methylthiazol-2-ylmethyl 378 CH.sub.3 CH.sub.35-Methylthiazol-2-ylmethyl 379 CH.sub.3 CH.sub.3 4-Chlorothiazol-2-ylmethyl 380 CH.sub.3 CH.sub.3 5-Chlorothiazol-2-ylmethyl 381 CH.sub.3 CH.sub.3 4-Thiazolylmethyl 382 CH.sub.3 CH.sub.3 2-Methylthiazol-4-ylmethyl 383 CH.sub.3 CH.sub.35-Methylthiazol-4-ylmethyl 384 CH.sub.3 CH.sub.3 2-Chlorothiazol-4-ylmethyl 385 CH.sub.3 CH.sub.3 5-Chlorothiazol-4-ylmethyl 386 CH.sub.3 CH.sub.3 5-Thiazolylmethyl 387 CH.sub.3 CH.sub.3 2-Methylthiazol-5-ylmethyl 388 CH.sub.3 CH.sub.34-Methylthiazol-5-ylmethyl 389 CH.sub.3 CH.sub.3 2-Chlorothiazol-5-ylmethyl 390 CH.sub.3 CH.sub.3 4-Chlorothiazol-5-ylmethyl 391 CH.sub.3 CH.sub.3 3-Isoxazolylmethyl 392 CH.sub.3 CH.sub.3 4-Methylisoxazol-3-ylmethyl 393 CH.sub.3 CH.sub.35-Methylisoxazol-3-ylmethyl 394 CH.sub.3 CH.sub.3 4-Chloroisoxazol-3-ylmethyl 395 CH.sub.3 CH.sub.3 5-Chloroisoxazol-3-ylmethyl 396 CH.sub.3 CH.sub.3 4-Isoxazolylmethyl 397 CH.sub.3 CH.sub.3 3-Methylisoxazol-4-ylmethyl 398 CH.sub.3 CH.sub.35-Methylisoxazol-4-ylmethyl 399 CH.sub.3 CH.sub.3 3-Chloroisoxazol-4-ylmethyl 400 CH.sub.3 CH.sub.3 5-Chloroisoxazol-4-ylmethyl 401 CH.sub.3 CH.sub.3 5-Isoxazolylmethyl 402 CH.sub.3 CH.sub.3 3-Methylisoxazol-5-ylmethyl 403 CH.sub.3 CH.sub.34-Methylisoxazol-5-ylmethyl 404 CH.sub.3 CH.sub.3 3-Chloroisoxazol-5-ylmethyl 405 CH.sub.3 CH.sub.3 4-Chloroisoxazol-5-ylmethyl 406 CH.sub.3 CH.sub.3 3-Isothiazolylmethyl 407 CH.sub.3 CH.sub.3 4-Methylisothiazol-3-yl- methyl 408 CH.sub.3 CH.sub.35-Methylisothiazol-3-yl- methyl 409 CH.sub.3 CH.sub.3 4-Chloroisothiazol-3-yl- methyl 410 CH.sub.3 CH.sub.3 5-Chloroisothiazol-3-yl- methyl 411 CH.sub.3 CH.sub.3 4-Isothiazolylmethyl 412 CH.sub.3 CH.sub.3 3-Methylisothiazol-4-yl- methyl 413CH.sub.3 CH.sub.3 5-Methylisothiazol-4-yl- methyl 414 CH.sub.3 CH.sub.3 3-Chloroisothiazol-4-yl- methyl 415 CH.sub.3 CH.sub.3 5-Chloroisothiazol-4-yl- methyl 416 CH.sub.3 CH.sub.3 5-Isothiazolylmethyl 417 CH.sub.3 CH.sub.3 3-Methylisothiazol-5-yl- methyl 418 CH.sub.3 CH.sub.3 4-Methylisothiazol-5-yl- methyl 419 CH.sub.3 CH.sub.3 3-Chloroisothiazol-5-yl- methyl 420 CH.sub.3 CH.sub.3 4-Chloroisothiazol-5-yl- methyl 421 CH.sub.3 CH.sub.3 4-Imidazolylmethyl 422 CH.sub.3 CH.sub.31-Phenylpyrazol-3-ylmethyl 423 CH.sub.3 CH.sub.3 1-Methylimidazol-4-ylmethyl 424 CH.sub.3 CH.sub.3 1-Phemyl-1,2,4-tri- azol-3-ylmethyl 425 CH.sub.3 CH.sub.3 1,2,4-Oxadiazol-3-ylmethyl 426 CH.sub.3 CH.sub.3 5-Chloro-1,2,4-oxadiazol-3- ylmethyl 427CH.sub.3 CH.sub.3 5-Methyl-1,2,4-oxadiazol-3- ylmethyl 428 CH.sub.3 CH.sub.3 5-Trifluoromethyl-1,2,4- oxadiazol-3-ylmethyl 429 CH.sub.3 CH.sub.3 1,3,4-Oxadiazol-2-ylmethyl 430 CH.sub.3 CH.sub.3 5-Chloro-1,3,4-oxadiazol-2- ylmethyl 431 CH.sub.3CH.sub.3 5-Methyl-1,3,4-oxadaizol-2- ylmethyl 432 CH.sub.3 CH.sub.3 5-Methoxy-1,3,4-oxadiazol-2- ylmethyl 433 CH.sub.3 CH.sub.3 1,2,4-Thiadiazol-3-ylmethyl 434 CH.sub.3 CH.sub.3 5-Chloro-1,2,4-thiadiazol-3- ylmethyl 435 CH.sub.3 CH.sub.35-Methyl-1,2,4-thiadiazol-3- ylmethyl 436 CH.sub.3 CH.sub.3 1,3,4-Thiadiazol-2-ylmethyl 437 CH.sub.3 CH.sub.3 5-Chloro-1,3,4-thiadiazol-2- ylmethyl 438 CH.sub.3 CH.sub.3 5-Methyl-1,3,4-thiadiazol-2- ylmethyl 439 CH.sub.3 CH.sub.35-Cyano-1,3,4-thiadiazol-2- ylmethyl 440 CH.sub.3 CH.sub.3 2-(2'-Pyridinyloxy)eth-1-yl 441 CH.sub.3 CH.sub.3 2-(3'-Pyridinyloxy)eth-1-yl 442 CH.sub.3 CH.sub.3 2-(4'-Pyridinyloxy)eth-1-yl 443 CH.sub.3 CH.sub.3 2-(2'-Pyrimidinyl- loxy)eth-1-yl 444CH.sub.3 CH.sub.3 2-(4'-Pyrimidinyl- loxy)eth-1-yl 445 CH.sub.3 CH.sub.3 2-(5'-Pyrimidinyl- loxy)eth-1-yl 446 CH.sub.3 CH.sub.3 2-(2'-Pyrazinyloxy)eth-1-yl 447 CH.sub.3 CH.sub.3 2-(2'-Pyridazinyl- loxy)eth-1-yl 448 CH.sub.3 CH.sub.32-(3'-Pyridazinyl- loxy)eth-1-yl 449 CH.sub.3 CH.sub.3 2-(1',3',5'-Triazin- yloxy)eth-1-yl 450 CH.sub.3 CH.sub.3 2-(5'-Methylisoxazol-3'-yl- oxy)eth-1-yl 451 CH.sub.3 CH.sub.3 2-(5'Chloroisoxazol-3'-yl- oxy)eth-1-yl 452 CH.sub.3 CH.sub.32-(2'-Methoxythiazol-4'-yl- oxy)eth-1-yl 453 CH.sub.3 CH.sub.3 2-(4'-Chlomoxazol-2'-yl- oxy)eth-1-yl 454 CH.sub.3 CH.sub.3 2-(1'-Phenyl-1'H-1',2',4'- triazol-3'-yloxy)eth-1-yl 455 CH.sub.3 CH.sub.3 2-(1'-Phenylpyrazol-3'-yl- oxy)eth-1-yl 456CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 457 CH.sub.3 CH.sub.3 2-Cl--C.sub.6 H.sub.4 458 CH.sub.3 CH.sub.3 3-Cl--C.sub.6 H.sub.4 459 CH.sub.3 CH.sub.3 4-Cl--C.sub.6 H.sub.4 460 CH.sub.3 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 461 CH.sub.3 CH.sub.32,4-Cl.sub.2 --C.sub.6 H.sub.3 462 CH.sub.3 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 463 CH.sub.3 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 464 CH.sub.3 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 465 CH.sub.3 CH.sub.3 4-CN--C.sub.6 H.sub.4 466 CH.sub.3CH.sub.3 2-NO.sub.2 --C.sub.6 H.sub.4 467 CH.sub.3 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 468 CH.sub.3 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 469 CH.sub.3 CH.sub.3 2,4-(NO.sub.2).sub.2 --C.sub.6 H.sub.3 470 CH.sub.3 CH.sub.3 2-CH.sub.3 --C.sub.6H.sub.4 471 CH.sub.3 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 472 CH.sub.3 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.3 473 CH.sub.3 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 474 CH.sub.3 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 435 CH.sub.3CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 476 CH.sub.3 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 477 CH.sub.3 CH.sub.3 2-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 478 CH.sub.3 CH.sub.3 3-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 479 CH.sub.3 CH.sub.34-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 480 CH.sub.3 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 481 CH.sub.3 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 482 CH.sub.3 CH.sub.3 3-Acetyl-C.sub.6 H.sub.4 483 CH.sub.3 CH.sub.3 4-Acetyl-C.sub.6 H.sub.4 484 CH.sub.3CH.sub.3 3-Methoxycarbonyl-C.sub.6 H.sub.4 485 CH.sub.3 CH.sub.3 4-Methoxycarbonyl-C.sub.6 H.sub.4 486 CH.sub.3 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 487 CH.sub.3 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 488 CH.sub.3 CH.sub.3 2-Naphthyl 489 CH.sub.3CH.sub.3 6-Chloropyridazin-3-yl 490 CH.sub.3 CH.sub.3 5-Chloropyrazin-2-yl 491 CH.sub.3 CH.sub.3 Quinotin-2-yl 492 CH.sub.3 CH.sub.3 2,5-Dimethylpyrazin-3-yl 493 CH.sub.3 CH.sub.3 Pyrazin-2-yl 494 CH.sub.3 CH.sub.3 3-Chloropyrid-2-yl 495 CH.sub.3CH.sub.3 6-Chloropyrid-2-yl 496 CH.sub.3 CH.sub.3 4-Trifluoromethy [sic], 6-Chloropyrid-2-yl 497 CH.sub.3 CH.sub.3 4-Trifluoromethylpyrid-2-yl 498 CH.sub.3 CH.sub.3 6-Trifluoromethylpyrid-2-yl 499 CH.sub.3 CH.sub.3 6-Methoxypyrid-2-yl 500 CH.sub.3CH.sub.3 5-Chloropyrid-2-yl 501 CH.sub.3 CH.sub.3 Pyrid-2-yl 502 CH.sub.3 CH.sub.3 Benzothiazol-2-yl 503 CH.sub.3 CH.sub.3 7-Chloroquinolin-4-yl 504 CH.sub.3 CH.sub.3 3-Nitropyrid-2-yl 505 CH.sub.3 CH.sub.3 Pyrrol-3-yl 506 CH.sub.3 CH.sub.3Pyrrol-2-yl 507 CH.sub.3 CH.sub.3 2,6-Dioctylpyrid-4-yl 508 CH.sub.3 CH.sub.3 5-Nitropyrid-2-yl 509 CH.sub.3 CH.sub.3 Pyrid-4-yl 510 CH.sub.3 CH.sub.3 Pyrid-3-yl 511 CH.sub.3 CH.sub.3 Pyrimidin-2-yl 512 CH.sub.3 CH.sub.3 Pyrimidin-4-yl 513CH.sub.3 CH.sub.3 Quinazolin-4-yl 514 CH.sub.3 CH.sub.3 6-Chloropyrimidin-4-yl 515 CH.sub.3 CH.sub.3 6-Methoxypyrimidin-4-yl 516 CH.sub.3 CH.sub.3 2,5,6-Trichloropyrimidin-4- yl 517 CH.sub.3 CH.sub.3 2,6-Dimethylpyrimidin-4-yl 518 CH.sub.3 CH.sub.32-Methyl, 6-Chloropyrimidin-4-yl 519 CH.sub.3 CH.sub.3 2-Methyl, 6-Ethoxypyrimidin-4-yl 520 CH.sub.3 CH.sub.3 4,5,6-Trichloropyrimidin-2- yl 521 CH.sub.3 CH.sub.3 4,6-Dimethoxypyrimidin-2-yl 522 CH.sub.3 CH.sub.3 4,6-Dimethylpyrimidin-2-yl 523CH.sub.3 CH.sub.3 4,6-Dichloropyrimidin-2-yl 524 CH.sub.3 CH.sub.3 4-Methyl, 6-methoxypyrimi- din-2-yl 525 CH.sub.3 CH.sub.3 4-Chloro, 6-methoxypyrimi- din-2-yl 526 CH.sub.3 CH.sub.3 6-Chloroquinoxalin-2-yl 527 CH.sub.3 CH.sub.33,6-Dichloro-1,2,4-tri- azin-5-yl 528 CH.sub.3 CH.sub.3 4-Methoxy-1,3,5-tri- azin-2-yl 529 CH.sub.3 CH.sub.3 3-Ethoxy-1,3,5-triazin-2-yl 530 CH.sub.3 CH.sub.3 4,6-Dichlor-1,3,5-tri- azin-2-yl 531 CH.sub.3 CH.sub.3 4-Ethoxy, 6-Chloro-1,3,5-triazin-2-yl 532 CH.sub.3 CH.sub.3 Isoxazol-3-yl 533 CH.sub.3 CH.sub.3 Thien-2-yl 534 CH.sub.3 CH.sub.3 Fur-2-yl 535 CH.sub.3 CH.sub.3 Thiatriazol-5-yl 536 CH.sub.3 CH.sub.3 (E)-1-Chloropropen-3-yl 537 CH.sub.3 CH.sub.3(E)-4-(4'-Chlorophenyl)but- 2-en-1-yl 538 CH.sub.3 CH.sub.3 Propyn-3-yl 539 CH.sub.3 CH.sub.3 Methylcarbonyl 540 CH.sub.3 CH.sub.3 Ethylcarbonyl 541 CH.sub.3 CH.sub.3 n-Propylcarbonyl 542 CH.sub.3 CH.sub.3 i-Propylcarbonyl 543 CH.sub.3 CH.sub.3n-Butylcarbonyl 544 CH.sub.3 CH.sub.3 s-Butylcacbonyl 545 CH.sub.3 CH.sub.3 i-Butylcarbonyl 546 CH.sub.3 CH.sub.3 i-Butylcarbonyl 547 CH.sub.3 CH.sub.3 n-Pentylcarbonyl 548 CH.sub.3 CH.sub.3 i-Pentylcarbonyl 549 CH.sub.3 CH.sub.3 neo-Pentylcarbonyl 550 CH.sub.3 CH.sub.3 n-Hexylcarbonyl 551 CH.sub.3 CH.sub.3 n-Octylcarbonyl 552 CH.sub.3 CH.sub.3 1-Propenylcarbonyl 553 CH.sub.3 CH.sub.3 2-Penten-1-yl-carbonyl 554 CH.sub.3 CH.sub.3 2,5-Heptadien-1-yl-carbonyl

555 CH.sub.3 CH.sub.3 Benzoyl 556 CH.sub.3 CH.sub.3 2-Chlorobenzoyl 557 CH.sub.3 CH.sub.3 3-Chlorobenzoyl 558 CH.sub.3 CH.sub.3 4-Chlorobenzoyl 559 CH.sub.3 CH.sub.3 2-Cyanobenzoyl 560 CH.sub.3 CH.sub.3 3-Cyanobenzoyl 561 CH.sub.3 CH.sub.34-Cyanobenzoyl 562 CH.sub.3 CH.sub.3 4-Methoxybenzoyl 563 CH.sub.3 CH.sub.3 2-Pyridylcarbonyl 564 CH.sub.3 CH.sub.3 3-Pyridylcarbonyl 565 CH.sub.3 CH.sub.3 4-Pyridylcarbonyl 566 CH.sub.3 CH.sub.3 2-Pyrimidinylcarbonyl 567 CH.sub.3 CH.sub.32-Oxazolylcarbonyl 568 CH.sub.3 CH.sub.3 4-Methylisoxazol-5-yl- carbonyl 569 CH.sub.3 CH.sub.3 Methylsulfonyl 570 CH.sub.3 CH.sub.3 Ethylsulfonyl 571 CH.sub.3 CH.sub.3 n-Propylsulfonyl 572 CH.sub.3 CH.sub.3 i-Propylsulfonyl 573 CH.sub.3 CH.sub.3n-Butylsulfonyl 574 CH.sub.3 CH.sub.3 t-Butylsulfonyl 575 CH.sub.3 CH.sub.3 n-Pentylsulfonyl 576 CH.sub.3 CH.sub.3 neo-Pentylsulfonyl 577 CH.sub.3 CH.sub.3 n-Hexylsulfonyl 578 CH.sub.3 CH.sub.3 n-Octylsulfonyl 579 CH.sub.3 CH.sub.3 Phenylsulfonyl 580 CH.sub.3 CH.sub.3 2-Chlorophenylsulfonyl 581 CH.sub.3 CH.sub.3 3-Chlorophenylsulfonyl 582 CH.sub.3 CH.sub.3 4-Chlorophenylsulfonyl 583 CH.sub.3 CH.sub.3 2-Cyanophenylsulfonyl 584 CH.sub.3 CH.sub.3 3-Cyanophenylsulfonyl 585 CH.sub.3 CH.sub.34-Cyanophenylsulfonyl 586 CH.sub.3 CH.sub.3 2-Pyridylsulfonyl 587 CH.sub.3 CH.sub.3 3-Pyridylsulfonyl 588 CH.sub.3 CH.sub.3 4-Pyridylsulfonyl 589 CH.sub.3 CH.sub.3 2-Pyrimidinylsulfonyl 590 CH.sub.3 CH.sub.3 4-Oxazolylsulfonyl 591 CH.sub.3 CH.sub.35-Chlorothiazol-2-yl- sulfonyl 592 CH.sub.3 CH.sub.3 2-t-C.sub.4 H.sub.9 --C.sub.6 H.sub.4 --CH.sub.2 593 CH.sub.3 CH.sub.3 3-t-C.sub.4 H.sub.9 --C.sub.6 H.sub.4 --CH.sub.2 594 CH.sub.3 CH.sub.3 4-t-C.sub.4 H.sub.9 --C.sub.6 H.sub.4 --CH.sub.2 595 CH.sub.3 CH.sub.3 2-(4'-Chlorothiazol-2'-yl- oxy)3th-1-yl 596 CH.sub.3 CH.sub.3 2-(1'-Methylpyrazo-4'-yl- oxy)eth-1-yl 597 CH.sub.3 CH.sub.3 4-Br--C.sub.6 H.sub.4 598 CH.sub.3 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 599 CH.sub.3CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 600 CH.sub.3 CH.sub.3 3-Dimethylaminocarbonyl-C.sub.6 H.sub.4 601 CH.sub.3 CH.sub.3 4-Dimethylaminocarbonyl-C.sub.6 H.sub.4 602 CH.sub.3 CH.sub.3 2-Hydroxyprop-1-yl 603 CH.sub.3 CH.sub.36-Hydroxy-2-methyl- pyrimidin-4-ylmethyl 604 CH.sub.3 CH.sub.3 [6-OH,2-CH(CH.sub.2).sub.2 -pyrimidin- 4-yl]-CH.sub.2 605 CH.sub.3 CH.sub.3 [6-OH,2-CH(CH.sub.2).sub.2 -pyrimidin- 4-yl]-CH.sub.2 606 CH.sub.3 CH.sub.3 5-(2'-Furan)-pent-1-yl 607CH.sub.3 CH.sub.3 5-(2'-N-Methylpyr- rol)-pent-1-yl 608 CH.sub.3 CH.sub.3 [2-(4-Cl--C.sub.6 H.sub.4)-oxazol-4-yl]- CH.sub.2 609 CH.sub.3 CH.sub.3 3-CF.sub.3 -pyridin-2-yl 610 CH.sub.3 CH.sub.3 5-CF.sub.3 -pyridin-2-yl 611 CH.sub.3 CH.sub.36-(2'-Thienyl)hex-1-yl 612 CH.sub.3 t-C.sub.4 H.sub.9 H 613 CH.sub.3 t-C.sub.4 H.sub.9 CH.sub.3 614 CH.sub.3 t-C.sub.4 H.sub.9 C.sub.2 H.sub.5 615 CH.sub.3 t-C.sub.4 H.sub.9 n-C.sub.3 H.sub.7 616 CH.sub.3 t-C.sub.4 H.sub.9 i-C.sub.3 H.sub.7 617CH.sub.3 t-C.sub.4 H.sub.9 Cyclopropyl 618 CH.sub.3 t-C.sub.4 H.sub.9 n-C.sub.4 H.sub.9 619 CH.sub.3 t-C.sub.4 H.sub.9 t-C.sub.4 H.sub.9 620 CH.sub.3 t-C.sub.4 H.sub.9 n-C.sub.6 H.sub.13 621 CH.sub.3 t-C.sub.4 H.sub.9 (E)-1-Chloropropen-3-yl 622CH.sub.3 t-C.sub.4 H.sub.9 Propyn-3-yl 623 CH.sub.3 t-C.sub.4 H.sub.9 3-Methylbut-2-en-1-yl 624 CH.sub.3 t-C.sub.4 H.sub.9 2-Naphthyl-CH.sub.2 625 CH.sub.3 t-C.sub.4 H.sub.9 4-Cl--C.sub.6 H.sub.4 --CH.sub.2 626 CH.sub.3 t-C.sub.4 H.sub.9(E)-4-(4'-Chlorophenyl)but- 2-en-1-yl 627 CH.sub.3 t-C.sub.4 H.sub.9 6-(4'-Chlorophenyl)hex-1-yl 628 CH.sub.3 t-C.sub.4 H.sub.9 3-CF.sub.3 --C.sub.6 H.sub.4 629 CH.sub.3 C.sub.6 H.sub.5 H 630 CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 631 CH.sub.3 C.sub.6H.sub.5 C.sub.2 H.sub.5 632 CH.sub.3 C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 633 CH.sub.3 C.sub.6 H.sub.5 i-C.sub.3 H.sub.7 634 CH.sub.3 C.sub.6 H.sub.5 Cyclopropyl 635 CH.sub.3 C.sub.6 H.sub.5 n-C.sub.4 H.sub.9 636 CH.sub.3 C.sub.6 H.sub.5 t-C.sub.4H.sub.9 637 CH.sub.3 C.sub.6 H.sub.5 n-C.sub.6 H.sub.13 638 CH.sub.3 C.sub.6 H.sub.5 4-Cl--C.sub.6 H.sub.4 --CH.sub.2 639 CH3 C.sub.6 H.sub.5 3-CF.sub.3 --C.sub.6 H.sub.4 640 CH.sub.3 C.sub.6 H.sub.5 6-(4'-Chlorophenyl)hex-1-yl 641 CH.sub.3 C.sub.6H.sub.5 (E)-4-(4'-Chlorophenyl)but- 2-en-1-yl 642 CH.sub.3 H H 643 CH.sub.3 H CH.sub.3 644 CH3 H C.sub.2 H.sub.5 645 CH.sub.3 H n-C.sub.3 H.sub.7 646 CH3 H C.sub.3 H.sub.7 647 CH.sub.3 OH H 648 CH.sub.3 OH CH.sub.3 649 CH.sub.3 OH C.sub.2H.sub.5 650 CH.sub.3 OH n-C.sub.3 H.sub.7 651 CH.sub.3 OH t-C.sub.3 H.sub.7 652 CH.sub.3 Cl CH.sub.3 653 CH.sub.3 Cl C.sub.2 H.sub.5 654 CH.sub.3 Cl n-C.sub.3 H.sub.7 655 CH.sub.3 Cl i-C.sub.3 H.sub.7 656 CH.sub.3 OCH.sub.3 H 657 CH.sub.3OCH.sub.3 CH.sub.3 658 CH.sub.3 OCH.sub.3 C.sub.2 H.sub.5 659 CH.sub.3 OCH.sub.3 n-C.sub.3 H.sub.7 660 CH.sub.3 OCH.sub.3 i-C.sub.3 H.sub.7 661 CH.sub.3 SCH.sub.3 H 662 CH.sub.3 SCH.sub.3 CH.sub.3 663 CH.sub.3 SCH.sub.3 C.sub.2 H.sub.5 664CH.sub.3 SCH.sub.3 n-C.sub.3 H.sub.7 665 CH.sub.3 SCH.sub.3 i-C.sub.3 H.sub.7 666 CH.sub.3 Cyclopropyl H 667 CH.sub.3 Cyclopropyl CH.sub.3 668 CH.sub.3 Cyclopropyl C.sub.2 H.sub.5 669 CH.sub.3 Cyclopropyl n-C.sub.3 H.sub.7 670 CH.sub.3 Cyclopropyli-C.sub.3 H.sub.7 671 CH.sub.3 2-Pyridyl H 672 CH.sub.3 2-Pyridyl CH.sub.3 673 CH.sub.3 2-Pyridyl C.sub.2 H.sub.5 674 CH.sub.3 2-Pyridyl n-C.sub.3 H.sub.7 675 CH.sub.3 2-Pyridyl i-C.sub.3 H.sub.7 676 CH.sub.3 3-Pyridyl H 677 CH.sub.3 3-PyridylCH.sub.3 678 CH.sub.3 3-Pyridyl C.sub.2 H.sub.5 679 CH.sub.3 3-Pyridyl n-C.sub.3 H.sub.7 680 CH.sub.3 3-Pyridyl i-C.sub.3 H.sub.7 681 CH.sub.3 4-Pyridyl H 682 CH.sub.3 4-Pyridyl CH.sub.3 683 CH.sub.3 4-Pyridyl C.sub.2 H.sub.5 684 CH.sub.34-Pyridyl n-C.sub.3 H.sub.7 685 CH.sub.3 4-Pyridyl i-C.sub.3 H.sub.7 686 CH.sub.3 2-Pyridimidyl H 687 CH.sub.3 2-Pyridimidyl CH.sub.3 688 CH.sub.3 2-Pyridimidyl C.sub.2 H.sub.5 689 CH.sub.3 2-Pyridimidyl n-C.sub.3 H.sub.7 690 CH.sub.3 2-Pyridimidyli-C.sub.3 H.sub.7 691 CH.sub.3 4-Pyridimidyl H 692 CH.sub.3 4-Pyridimidyl CH.sub.3 693 CH.sub.3 4-Pyridimidyl C.sub.2 H.sub.5 694 CH.sub.3 4-Pyridimidyl n-C.sub.3 H.sub.7 695 CH.sub.3 4-Pyridimidyl i-C.sub.3 H.sub.7 696 CH.sub.3 5-Pyridimidyl H 697 CH.sub.3 5-Pyridimidyl CH.sub.3 698 CH.sub.3 5-Pyridimidyl C.sub.2 H.sub.5 699 CH.sub.3 5-Pyridimidyl n-C.sub.3 H.sub.7 700 CH.sub.3 5-Pyridimidyl i-C.sub.3 H.sub.7 701 CH.sub.3 1,3,5-Triazinyl H 702 CH.sub.3 1,3,5-Triazinyl CH.sub.3 703CH.sub.3 1,3,5-Triazinyl C.sub.2 H.sub.5 704 CH.sub.3 1,3,5-Triazinyl n-C.sub.3 H.sub.7 705 CH.sub.3 1,3,5-Triazinyl i-C.sub.3 H.sub.7 706 CH.sub.3 2-Furyl H 707 CH.sub.3 2-Furyl CH.sub.3 708 CH.sub.3 2-Furyl C.sub.2 H.sub.5 709 CH.sub.3 2-Furyln-C.sub.3 H.sub.7 710 CH.sub.3 2-Furyl i-C.sub.3 H.sub.7 711 CH.sub.3 3-Furyl H 712 CH.sub.3 3-Furyl CH.sub.3 713 CH.sub.3 3-Furyl C.sub.2 H.sub.5 714 CH.sub.3 3-Furyl n-C.sub.3 H.sub.7 715 CH.sub.3 3-Furyl i-C.sub.3 H.sub.7 716 CH.sub.3 2-ThienylH 717 CH.sub.3 2-Thienyl CH.sub.3 718 CH.sub.3 2-Thienyl C.sub.2 H.sub.5 719 CH.sub.3 2-Thienyl n-C.sub.3 H.sub.7 720 CH.sub.3 2-Thienyl i-C.sub.3 H.sub.7 721 CH.sub.3 3-Thienyl H 722 CH.sub.3 3-Thienyl CH.sub.3 723 CH.sub.3 3-Thienyl C.sub.2H.sub.5 724 CH.sub.3 3-Thienyl n-C.sub.3 H.sub.7 725 CH.sub.3 3-Thienyl i-C.sub.3 H.sub.7 726 CH.sub.3 2-Oxazolyl H 727 CH.sub.3 2-Oxazolyl CH.sub.3 728 CH.sub.3 2-Oxazolyl C.sub.2 H.sub.5 729 CH.sub.3 2-Oxazolyl n-C.sub.3 H.sub.7 730 CH.sub.32-Oxazolyl i-C.sub.3 H.sub.7 731 CH.sub.3 4-Oxazolyl H 732 CH.sub.3 4-Oxazolyl CH.sub.3 733 CH.sub.3 4-Oxazolyl C.sub.2 H.sub.5 774 CH.sub.3 4-Oxazolyl n-C.sub.3 H.sub.7 735 CH.sub.3 4-Oxazolyl i-C.sub.3 H.sub.7 736 CH.sub.3 2-Thiazolyl H 737CH.sub.3 2-Thiazolyl CH.sub.3 738 CH.sub.3 2-Thiazolyl C.sub.2 H.sub.5 739 CH.sub.3 2-Thiazolyl n-C.sub.3 H.sub.7 740 CH.sub.3 2-Thiazolyl i-C.sub.3 H.sub.7 741 CH.sub.3 4-Thiazolyl H 742 CH.sub.3 4-Thiazolyl CH.sub.3 743 CH.sub.3 4-ThiazolylC.sub.2 H.sub.5 744 CH.sub.3 4-Thiazolyl n-C.sub.3 H.sub.7 745 CH.sub.3 4-Thiazolyl i-C.sub.3 H.sub.7 746 CH.sub.3 3-Isoxazolyl H 747 CH.sub.3 3-Isoxazolyl CH.sub.3 748 CH.sub.3 3-Isoxazolyl C.sub.2 H.sub.5 749 CH.sub.3 3-Isoxazolyl n-C.sub.3H.sub.7 750 CH.sub.3 3-Isoxazolyl i-C.sub.3 H.sub.7 751 CH.sub.3 5-Isoxazolyl H 752 CH.sub.3 5-Isoxazolyl CH.sub.3 753 CH.sub.3 5-Isoxazolyl C.sub.2 H.sub.5 754 CH.sub.3 5-Isoxazolyl n-C.sub.3 H.sub.7 755 CH.sub.3 5-Isoxazolyl i-C.sub.3 H.sub.7 756 CH.sub.3 2-Imidazolyl H 757 CH.sub.3 2-Imidazolyl CH.sub.3 758 CH.sub.3 2-Imidazolyl C.sub.2 H.sub.5 759 CH.sub.3 2-Imidazolyl n-C.sub.3 H.sub.7 760 CH.sub.3 2-Imidazolyl i-C.sub.3 H.sub.7 761 CH.sub.3 3-Pyrazolyl H 762 CH.sub.3 3-PyrazolylCH.sub.3 763 CH.sub.3 3-Pyrazolyl C.sub.2 H.sub.5 764 CH.sub.3 3-Pyrazolyl n-C.sub.3 H.sub.7 765 CH.sub.3 3-Pyrazolyl i-C.sub.3 H.sub.7 766 CH.sub.3 4-Pyrazolyl H 767 CH.sub.3 4-Pyrazolyl CH.sub.3 768 CH.sub.3 4-Pyrazolyl C.sub.2 H.sub.5 769CH.sub.3 4-Pyrazolyl n-C.sub.3 H.sub.7 770 CH.sub.3 4-Pyrazolyl i-C.sub.3 H.sub.7 771 OCH.sub.3 H H 772 OCH.sub.3 H CH.sub.3 773 OCH.sub.3 H C.sub.2 H.sub.5 774 OCH.sub.3 H n-C.sub.3 H.sub.7 775 OCH.sub.3 H i-C.sub.3 H.sub.7 776 OCH.sub.3 OH H 777 OCH.sub.3 OH CH.sub.3 778 OCH.sub.3 OH C.sub.2 H.sub.5 779 OCH.sub.3 OH n-C.sub.3 H.sub.7 780 OCH.sub.3 OH i-C.sub.3 H.sub.7 781 OCH.sub.3 Cl n-C.sub.4 H.sub.9 782 OCH.sub.3 Cl CH.sub.3 783 OCH.sub.3 Cl C.sub.2 H.sub.5 784 OCH.sub.3 Cln-C.sub.3 H.sub.7 785 OCH.sub.3 Cl i-C.sub.3 H.sub.7 786 OCH.sub.3 OCH.sub.3 H 787 OCH.sub.3 OCH.sub.3 CH.sub.3 788 OCH.sub.3 OCH.sub.3 C.sub.2 H.sub.5 789 OCH.sub.3 OCH.sub.3 n-C.sub.3 H.sub.7 790 OCH.sub.3 OCH.sub.3 i-C.sub.3 H.sub.7 791OCH.sub.3 SCH.sub.3 H

702 OCH.sub.3 SCH.sub.3 CH.sub.3 793 OCH.sub.3 SCH.sub.3 C.sub.2 H.sub.5 794 OCH.sub.3 SCH.sub.3 n-C.sub.3 H.sub.7 795 OCH.sub.3 SCH.sub.3 i-C.sub.3 H.sub.7 796 OCH.sub.3 CH.sub.3 H 797 OCH.sub.3 CH.sub.3 CH.sub.3 798 OCH.sub.3 CH.sub.3C.sub.2 H.sub.5 790 OCH.sub.3 CH.sub.3 n-C.sub.3 H.sub.7 800 OCH.sub.3 CH.sub.3 i-C.sub.3 H.sub.7 801 OCH.sub.3 Cyclopropyl H 802 OCH.sub.3 Cyclopropyl CH.sub.3 803 OCH.sub.3 Cyclopropyl C.sub.2 H.sub.5 804 OCH.sub.3 Cyclopropyl n-C.sub.3 H.sub.7 805 OCH.sub.3 Cyclopropyl i-C.sub.3 H.sub.7 806 OCH.sub.3 2-Pyridyl H 807 OCH.sub.3 2-Pyridyl CH.sub.3 808 OCH.sub.3 2-Pyridyl C.sub.2 H.sub.5 809 OCH.sub.3 2-Pyridyl n-C.sub.3 H.sub.7 810 OCH.sub.3 2-Pyridyl i-C.sub.3 H.sub.7 811 OCH.sub.33-Pyridyl H 812 OCH.sub.3 3-Pyridyl CH.sub.3 813 OCH.sub.3 3-Pyridyl C.sub.2 H.sub.5 814 OCH.sub.3 3-Pyridyl n-C.sub.3 H.sub.7 815 OCH.sub.3 3-Pyridyl i-C.sub.3 H.sub.7 816 OCH.sub.3 4-Pyridyl H 817 OCH.sub.3 4-Pyridyl CH.sub.3 818 OCH.sub.34-Pyridyl C.sub.2 H.sub.5 819 OCH.sub.3 4-Pyridyl n-C.sub.3 H.sub.7 820 OCH.sub.3 4-Pyrimidyl i-C.sub.3 H.sub.7 821 OCH.sub.3 2-Pyrimidyl H 822 OCH.sub.3 2-Pyrimidyl CH.sub.3 823 OCH.sub.3 2-Pyrimidyl C.sub.2 H.sub.5 824 OCH.sub.3 2-Pyrimidyln-C.sub.3 H.sub.7 825 OCH.sub.3 2-Pyrimidyl i-C.sub.3 H.sub.7 826 OCH.sub.3 4-Pyrimidyl H 827 OCH.sub.3 4-Pyrimidyl CH.sub.3 828 OCH.sub.3 4-Pyrimidyl C.sub.2 H.sub.5 829 OCH.sub.3 4-Pyrimidyl n-C.sub.3 H.sub.7 830 OCH.sub.3 4-Pyrimidyl i-C.sub.3H.sub.7 831 OCH.sub.3 5-Pyrimidyl H 832 OCH.sub.3 5-Pyrimidyl CH.sub.3 833 OCH.sub.3 5-Pyrimidyl C.sub.2 H.sub.5 834 OCH.sub.3 5-Pyrimidyl n-C.sub.3 H.sub.7 835 OCH.sub.3 5-Pyrimidyl i-C.sub.3 H.sub.7 836 OCH.sub.3 1,3,5-Triazinyl H 837 OCH.sub.31,3,5-Triazinyl CH.sub.3 838 OCH.sub.3 1,3,5-Triazinyl C.sub.2 H.sub.5 839 OCH.sub.3 1,3,5-Triazinyl n-C.sub.3 H.sub.7 840 OCH.sub.3 1,3,5-Triazinyl i-C.sub.3 H.sub.7 841 OCH.sub.3 2-Furyl H 842 OCH.sub.3 2-Furyl CH.sub.3 843 OCH.sub.3 2-FurylC.sub.2 H.sub.5 844 OCH.sub.3 2-Furyl n-C.sub.3 H.sub.7 845 OCH.sub.3 2-Furyl i-C.sub.3 H.sub.7 846 OCH.sub.3 3-Furyl H 847 OCH.sub.3 3-Furyl CH.sub.3 848 OCH.sub.3 3-Furyl C.sub.2 H.sub.5 849 OCH.sub.3 3-Furyl n-C.sub.3 H.sub.7 850 OCH.sub.33-Furyl i-C.sub.3 H.sub.7 851 OCH.sub.3 2-Thienyl H 852 OCH.sub.3 2-Thienyl CH.sub.3 853 OCH.sub.3 2-Thienyl C.sub.2 H.sub.5 854 OCH.sub.3 2-Thienyl n-C.sub.3 H.sub.7 855 OCH.sub.3 2-Thienyl i-C.sub.3 H.sub.7 856 OCH.sub.3 3-Thienyl H 857OCH.sub.3 3-Thienyl CH.sub.3 858 OCH.sub.3 3-Thienyl C.sub.2 H.sub.5 859 OCH.sub.3 3-Thienyl n-C.sub.3 H.sub.7 860 OCH.sub.3 3-Thienyl i-C.sub.3 H.sub.7 861 OCH.sub.3 2-Oxazolyl H 862 OCH.sub.3 2-Oxazolyl CH.sub.3 863 OCH.sub.3 2-Oxazolyl C.sub.2H.sub.5 864 OCH.sub.3 2-Oxazolyl n-C.sub.3 H.sub.7 865 OCH.sub.3 2-Oxazolyl i-C.sub.3 H.sub.7 866 OCH.sub.3 4-Oxazolyl H 867 OCH.sub.3 4-Oxazolyl CH.sub.3 868 OCH.sub.3 4-Oxazolyl C.sub.2 H.sub.5 869 OCH.sub.3 4-Oxazolyl n-C.sub.3 H.sub.7 870OCH.sub.3 4-Oxazolyl i-C.sub.3 H.sub.7 871 OCH.sub.3 2-Thiazolyl H 872 OCH.sub.3 2-Thiazolyl CH.sub.3 873 OCH.sub.3 2-Thiazolyl C.sub.2 H.sub.5 874 OCH.sub.3 2-Thiazolyl n-C.sub.3 H.sub.7 875 OCH.sub.3 2-Thiazolyl i-C.sub.3 H.sub.7 876 OCH.sub.34-Thiazolyl H 877 OCH.sub.3 4-Thiazolyl CH.sub.3 878 OCH.sub.3 4-Thiazolyl C.sub.2 H.sub.5 879 OCH.sub.3 4-Thiazolyl n-C.sub.3 H.sub.7 880 OCH.sub.3 4-Thiazolyl i-C.sub.3 H.sub.7 881 OCH.sub.3 3-Isoxazolyl H 882 OCH.sub.3 3-Isoxazolyl CH.sub.3 883OCH.sub.3 3-Isoxazolyl C.sub.2 H.sub.5 884 OCH.sub.3 3-Isoxayolyl n-C.sub.3 H.sub.7 885 OCH.sub.3 3-Isoxazolyl i-C.sub.3 H.sub.7 886 OCH.sub.3 5-Isoxazolyl H 887 OCH.sub.3 5-Isoxazolyl CH.sub.3 888 OCH.sub.3 5-Isoxazolyl C.sub.2 H.sub.5 889OCH.sub.3 5-Isoxazolyl n-C.sub.3 H.sub.7 890 OCH.sub.3 5-Isoxazolyl i-C.sub.3 H.sub.7 891 OCH.sub.3 2-Imidazolyl H 892 OCH.sub.3 2-Imidazolyl CH.sub.3 893 OCH.sub.3 2-Imidazolyl C.sub.2 H.sub.5 894 OCH.sub.3 2-Imidazolyl n-C.sub.3 H.sub.7 895OCH.sub.3 2-Imidazolyl i-C.sub.3 H.sub.7 896 OCH.sub.3 3-Pyrazolyl H 897 OCH.sub.3 3-Pyrazolyl CH.sub.3 898 OCH.sub.3 3-Pyrazolyl C.sub.2 H.sub.5 899 OCH.sub.3 3-Pyrazolyl n-C.sub.3 H.sub.7 900 OCH.sub.3 3-Pyrazolyl i-C.sub.3 H.sub.7 901 OCH.sub.34-Pyrazolyl H 902 OCH.sub.3 4-Pyrazolyl CH.sub.3 903 OCH.sub.3 4-Pyrazolyl C.sub.2 H.sub.5 904 OCH.sub.3 4-Pyrazolyl n-C.sub.3 H.sub.7 905 OCH.sub.3 4-Pyrazolyl i-C.sub.3 H.sub.7 906 OH H H 907 OH H CH.sub.3 908 OH H C.sub.2 H.sub.5 909 OH Hn-C.sub.3 H.sub.7 910 OH H i-C.sub.3 H.sub.7 911 OH OH H 912 OH OH CH.sub.3 913 OH OH C.sub.2 H.sub.5 914 OH OH n-C.sub.3 H.sub.7 915 OH OH i-C.sub.3 H.sub.7 916 OH Cl n-C.sub.4 H.sub.9 917 OH Cl CH.sub.3 918 OH Cl C.sub.2 H.sub.5 919 OH Cln-C.sub.3 H.sub.7 920 OH Cl i-C.sub.3 H.sub.7 921 OH OCH.sub.3 H 922 OH OCH.sub.3 CH.sub.3 923 OH OCH.sub.3 C.sub.2 H.sub.5 924 OH OCH.sub.3 n-C.sub.3 H.sub.7 925 OH OCH.sub.3 i-C.sub.3 H.sub.7 926 OH SCH.sub.3 H 927 OH SCH.sub.3 CH.sub.3 928 OHSCH.sub.3 C.sub.2 H.sub.5 929 OH SCH.sub.3 n-C.sub.3 H.sub.7 930 OH SCH.sub.3 i-C.sub.3 H.sub.7 931 OH CH.sub.3 H 932 OH CH.sub.3 CH.sub.3 933 OH CH.sub.3 C.sub.2 H.sub.5 934 OH CH.sub.3 n-C.sub.3 H.sub.7 935 OH CH.sub.3 i-C.sub.3 H.sub.7 936 OHCyclopropyl H 937 OH Cyclopropyl CH.sub.3 938 OH Cyclopropyl C.sub.2 H.sub.5 939 OH Cyclopropyl n-C.sub.3 H.sub.7 940 OH Cyclopropyl i-C.sub.3 H.sub.7 941 OH 2-Pyridyl H 942 OH 2-Pyridyl CH.sub.3 943 OH 2-Pyridyl C.sub.2 H.sub.5 944 OH 2-Pyridyln-C.sub.3 H.sub.7 945 OH 2-Pyridyl i-C.sub.3 H.sub.7 946 OH 3-Pyridyl H 947 OH 3-Pyridyl CH.sub.3 948 OH 3-Pyridyl C.sub.2 H.sub.5 949 OH 3-Pyridyl n-C.sub.3 H.sub.7 950 OH 3-Pyridyl i-C.sub.3 H.sub.7 951 OH 4-Pyridyl H 952 OH 4-Pyridyl CH.sub.3 953 OH 4-Pyridyl C.sub.2 H.sub.5 954 OH 4-Pyridyl n-C.sub.3 H.sub.7 955 OH 4-Pyridyl i-C.sub.3 H.sub.7 956 OH 2-Pyrimidyl H 957 OH 2-Pyrimidyl CH.sub.3 958 OH 2-Pyrimidyl C.sub.2 H.sub.5 959 OH 2-Pyrimidyl n-C.sub.3 H.sub.7 960 OH 2-Pyrimidyli-C.sub.3 H.sub.7 961 OH 4-Pyrimidyl H 962 OH 4-Pyrimidyl CH.sub.3 963 OH 4-Pyrimidyl C.sub.2 H.sub.5 964 OH 4-Pyrimidyl n-C.sub.3 H.sub.7 965 OH 4-Pyrimidyl i-C.sub.3 H.sub.7 966 OH 5-Pyrimidyl H 967 OH 5-Pyrimidyl CH.sub.3 968 OH 5-PyrimidylC.sub.2 H.sub.5 969 OH 5-Pyrimidyl n-C.sub.3 H.sub.7 970 OH 5-Pyrimidyl i-C.sub.3 H.sub.7 971 OH 1,3,5-Triazinyl H 972 OH 1,3,5-Triazinyl CH.sub.3 973 OH 1,3,5-Triazinyl C.sub.2 H.sub.5 974 OH 1,3,5-Triazinyl n-C.sub.3 H.sub.7 975 OH1,3,5-Triazinyl i-C.sub.3 H.sub.7 976 OH 2-Furyl H 977 OH 2-Furyl CH.sub.3 978 OH 2-Furyl C.sub.2 H.sub.5 979 OH 2-Furyl n-C.sub.3 H.sub.7 980 OH 2-Furyl i-C.sub.3 H.sub.7 981 OH 3-Furyl H 982 OH 3-Furyl CH.sub.3 983 OH 3-Furyl C.sub.2 H.sub.5 984 OH 3-Furyl n-C.sub.3 H.sub.7 985 OH 3-Furyl i-C.sub.3 H.sub.7 986 OH 2-Thienyl H 987 OH 2-Thienyl CH.sub.3 988 OH 2-Thienyl C.sub.2 H.sub.5 989 OH 2-Thienyl n-C.sub.3 H.sub.7 990 OH 2-Thienyl i-C.sub.3 H.sub.7 991 OH 3-Thienyl H 992 OH3-Thienyl CH.sub.3 993 OH 3-Thienyl C.sub.2 H.sub.5 994 OH 3-Thienyl n-C.sub.3 H.sub.7 995 OH 3-Thienyl i-C.sub.3 H.sub.7 996 OH 2-Oxazolyl H 997 OH 2-Oxazolyl CH.sub.3 998 OH 2-Oxazolyl C.sub.2 H.sub.5 999 OH 2-Oxazolyl n-C.sub.3 H.sub.7 1000 OH2-Oxazolyl i-C.sub.3 H.sub.7 1001 OH 4-Oxazolyl H 1002 OH 4-Oxazolyl CH.sub.3 1003 OH 4-Oxazolyl C.sub.2 H.sub.5 1004 OH 4-Oxazolyl n-C.sub.3 H.sub.7 1005 OH 2-Thiazolyl i-C.sub.3 H.sub.7 1006 OH 2-Thiazolyl H 1007 OH 2-Thiazolyl CH.sub.3 1008 OH2-Thiazolyl C.sub.2 H.sub.5 1009 OH 2-Thiazolyl n-C.sub.3 H.sub.7 1010 OH 2-Thiazolyl i-C.sub.3 H.sub.7 1011 OH 4-Thiazolyl H 1012 OH 4-Thiazolyl CH.sub.3 1013 OH 4-Thiazolyl C.sub.2 H.sub.5 1014 OH 4-Isoxazolyl n-C.sub.3 H.sub.7 1015 OH4-Isoxazolyl i-C.sub.3 H.sub.7 1016 OH 3-Isoxazolyl H 1017 OH 3-Isoxazolyl CH.sub.3 1018 OH 3-Isoxazolyl C.sub.2 H.sub.5 1019 OH 3-Isoxazolyl n-C.sub.3 H.sub.7 1020 OH 3-Isoxazolyl i-C.sub.3 H.sub.7 1021 OH 5-Isoxazolyl H 1022 OH 5-IsoxazolylCH.sub.3 1023 OH 5-Isoxazolyl C.sub.2 H.sub.5 1024 OH 5-Isoxazolyl n-C.sub.3 H.sub.7 1025 OH 5-Isoxazolyl i-C.sub.3 H.sub.7 1026 OH 2-Imidazolyl H 1027 OH 2-Imidazolyl CH.sub.3 1028 OH 2-Imidazolyl C.sub.2 H.sub.5 1029 OH 2-Imidazolyl n-C.sub.3H.sub.7 1030 OH 2-Imidazolyl i-C.sub.3 H.sub.7 1031 OH 3-Pyrazolyl H 1032 OH 3-Pyrazolyl CH.sub.3 1033 OH 3-Pyrazolyl C.sub.2 H.sub.5 1034 OH 3-Pyrazolyl n-C.sub.3 H.sub.7 1035 OH 3-Pyrazolyl i-C.sub.3 H.sub.7 1036 OH 4-Pyrazolyl H 1037 OH4-Pyrazolyl CH.sub.3 1038 OH 4-Pyrazolyl C.sub.2 H.sub.5 1039 OH 4-Pyyazolyl n-C.sub.3 H.sub.7 1040 OH 4-Pyrazolyl i-C.sub.3 H.sub.7 1041 H H H 1042 H H CH.sub.3

1043 H H C.sub.2 H.sub.5 1044 H H n-C.sub.3 H.sub.7 1045 H H i-C.sub.3 H.sub.7 1046 H OH H 1047 H OH CH.sub.3 1048 H OH C.sub.2 H.sub.5 1049 H OH n-C.sub.3 H.sub.7 1050 H OH i-C.sub.3 H.sub.7 1051 H Cl n-C.sub.4 H.sub.9 1052 H ClCH.sub.3 1053 H Cl C.sub.2 H.sub.5 1054 H Cl n-C.sub.3 H.sub.7 1055 H Cl i-C.sub.3 H.sub.7 1056 H OCH.sub.3 H 1057 H OCH.sub.3 CH.sub.3 1058 H OCH.sub.3 C.sub.2 H.sub.5 1059 H OCH.sub.3 n-C.sub.3 H.sub.7 1060 H OCH.sub.3 i-C.sub.3 H.sub.7 1061 HCH.sub.3 H 1062 H CH.sub.3 CH.sub.3 1063 H CH.sub.3 C.sub.2 H.sub.5 1064 H CH.sub.3 n-C.sub.3 H.sub.7 1065 H CH.sub.3 i-C.sub.3 H.sub.7 1066 H Cyclopropyl H 1067 H Cyclopropyl CH.sub.3 1068 H Cyclopropyl C.sub.2 H.sub.5 1069 H Cyclopropyln-C.sub.3 H.sub.7 1070 H Cyclopropyl i-C.sub.3 H.sub.7 1071 Cl H H 1072 Cl H CH.sub.3 1073 Cl H C.sub.2 H.sub.5 1074 Cl H n-C.sub.3 H.sub.7 1075 Cl H i-C.sub.3 H.sub.7 1076 Cl OH H 1077 Cl OH CH.sub.3 1078 Cl OH C.sub.2 H.sub.5 1079 Cl OHn-C.sub.3 H.sub.7 1080 Cl OH i-C.sub.3 H.sub.7 1081 Cl Cl n-C.sub.4 H.sub.9 1082 Cl Cl CH.sub.3 1083 Cl Cl C.sub.2 H.sub.5 1084 Cl Cl n-C.sub.3 H.sub.7 1085 Cl Cl i-C.sub.3 H.sub.7 1086 Cl OCH.sub.3 H 1087 Cl OCH.sub.3 CH.sub.3 1088 Cl OCH.sub.3C.sub.2 H.sub.5 1089 Cl OCH.sub.3 n-C.sub.3 H.sub.7 1090 Cl OCH.sub.3 i-C.sub.3 H.sub.7 1091 Cl CH.sub.3 H 1092 Cl CH.sub.3 CH.sub.3 1093 Cl CH.sub.3 C.sub.2 H.sub.5 1094 Cl CH.sub.3 n-C.sub.3 H.sub.7 1095 Cl CH.sub.3 i-C.sub.3 H.sub.7 1096 ClCyclopropyl H 1097 Cl Cyclopropyl CH.sub.3 1098 Cl Cyclopropyl C.sub.2 H.sub.5 1099 Cl Cyclopropyl n-C.sub.3 H.sub.7 1109 Cl Cyclopropyl i-C.sub.3 H.sub.7 1101 SCH.sub.3 H H 1102 SCH.sub.3 H CH.sub.3 1103 SCH.sub.3 H C.sub.2 H.sub.5 1104SCH.sub.3 H n-C.sub.3 H.sub.7 1105 SCH.sub.3 H i-C.sub.3 H.sub.7 1106 SCH.sub.3 OH H 1107 SCH.sub.3 OH CH.sub.3 1108 SCH.sub.3 OH C.sub.2 H.sub.5 1109 SCH.sub.3 OH n-C.sub.3 H.sub.7 1110 SCH.sub.3 OH i-C.sub.3 H.sub.7 1111 SCH.sub.3 CH.sub.3 H 1112 SCH.sub.3 CH.sub.3 CH.sub.3 1113 SCH.sub.3 CH.sub.3 C.sub.2 H.sub.5 1114 SCH.sub.3 CH.sub.3 n-C.sub.3 H.sub.7 1115 SCH.sub.3 CH.sub.3 i-C.sub.3 H.sub.7 1116 SCH.sub.3 SCH.sub.3 H 1117 SCH.sub.3 SCH.sub.3 CH.sub.3 1118 SCH.sub.3 SCH.sub.3C.sub.2 H.sub.5 1119 SCH.sub.3 SCH.sub.3 n-C.sub.3 H.sub.7 1120 SCH.sub.3 SCH.sub.3 i-C.sub.3 H.sub.7 1121 SCH.sub.3 Cyclopropyl H 1122 SCH.sub.3 Cyclopropyl CH.sub.3 1123 SCH.sub.3 Cyclopropyl C.sub.2 H.sub.5 1124 SCH.sub.3 Cyclopropyl n-C.sub.3H.sub.7 1125 SCH.sub.3 Cyclopropyl i-C.sub.3 H.sub.7 1126 Cyclo- H H propyl 1127 Cyclo- H CH.sub.3 propyl 1128 Cyclo- H C.sub.2 H.sub.5 propyl 1129 Cyclo- H n-C.sub.3 H.sub.7 propyl 1130 Cyclo- H i-C.sub.3 H.sub.7 propyl 1131 Cyclo- OH H propyl 1132 Cyclo- OH CH.sub.3 propyl 1133 Cyclo- OH C.sub.2 H.sub.5 propyl 1134 Cyclo- OH n-C.sub.3 H.sub.7 propyl 1135 Cyclo- OH i-C.sub.3 H.sub.7 propyl 1136 Cyclo- Cl n-C.sub.4 H.sub.9 propyl 1137 Cyclo- Cl CH.sub.3 propyl 1138 Cyclo- ClC.sub.2 H.sub.5 propyl 1139 Cyclo- Cl n-C.sub.3 H.sub.7 propyl 1140 Cyclo- Cl i-C.sub.3 H.sub.7 propyl 1141 Cyclo- OCH.sub.3 H propyl 1142 Cyclo- OCH.sub.3 CH.sub.3 propyl 1143 Cyclo- OCH.sub.3 C.sub.2 H.sub.5 propyl 1144 Cyclo- OCH.sub.3n-C.sub.3 H.sub.7 propyl 1145 Cyclo- OCH.sub.3 i-C.sub.3 H.sub.7 propyl 1146 Cyclo- SCH.sub.3 H propyl 1147 Cyclo- SCH.sub.3 CH.sub.3 propyl 1148 Cyclo- SCH.sub.3 C.sub.2 H.sub.5 propyl 1149 Cyclo- SCH.sub.3 n-C.sub.3 H.sub.7 propyl 1150Cyclo- SCH.sub.3 i-C.sub.3 H.sub.7 propyl 1151 Cyclo- CH.sub.3 H propyl 1152 Cyclo- CH.sub.3 CH.sub.3 propyl 1153 Cyclo- CH.sub.3 C.sub.2 H.sub.5 propyl 1154 Cyclo- CH.sub.3 n-C.sub.3 H.sub.7 propyl 1155 Cyclo- CH.sub.3 i-C.sub.3 H.sub.7 propyl 1156 CH.sub.3 2-F--C.sub.6 H.sub.4 CH.sub.3 1157 CH.sub.3 2-F--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1158 CH.sub.3 2-F--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1159 CH.sub.3 2-F--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1160 CH.sub.3 2-F--C.sub.6 H.sub.4n-C.sub.4 H.sub.9 1161 CH.sub.3 2-F--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1162 CH.sub.3 2-F--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1163 CH.sub.3 2-F--C.sub.6 H.sub.4 Prop-1-en-3-yl 1164 CH.sub.3 2-F--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1165CH.sub.3 2-F--C.sub.6 H.sub.4 Propyn-3-yl 1166 CH.sub.3 2-F--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1167 CH.sub.3 3-F--C.sub.6 H.sub.4 H 1168 CH.sub.3 3-F--C.sub.6 H.sub.4 CH.sub.3 1169 CH.sub.3 3-F--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1170 CH.sub.33-F--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1171 CH.sub.3 3-F--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1172 CH.sub.3 3-F--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1173 CH.sub.3 3-F--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1174 CH.sub.3 3-F--C.sub.6 H.sub.4 n-C.sub.6H.sub.13 1175 CH.sub.3 3-F--C.sub.6 H.sub.4 Prop-1-en-3-yl 1176 CH.sub.3 3-F--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1177 CH.sub.3 3-F--C.sub.6 H.sub.4 Propyn-3-yl 1178 CH.sub.3 3-F--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1179 CH.sub.34-F--C.sub.6 H.sub.4 H 1180 CH.sub.3 4-F--C.sub.6 H.sub.4 CH.sub.3 1181 CH.sub.3 4-F--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1182 CH.sub.3 4-F--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1183 CH.sub.3 4-F--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1184 CH.sub.34-F--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1185 CH.sub.3 4-F--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1186 CH.sub.3 4-F--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1187 CH.sub.3 4-F--C.sub.6 H.sub.4 Prop-1-en-3-yl 1188 CH.sub.3 4-F--C.sub.6 H.sub.4(E)-1-Chloroprop-1-en-3-yl 1189 CH.sub.3 4-F--C.sub.6 H.sub.4 Propyn-3-yl 1190 CH.sub.3 4-F--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1191 CH.sub.3 2-Cl--C.sub.6 H.sub.4 H 1192 CH.sub.3 2-Cl--C.sub.6 H.sub.4 CH.sub.3 1193 CH.sub.3 2-Cl--C.sub.6H.sub.4 C.sub.2 H.sub.5 1194 CH.sub.3 2-Cl--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1195 CH.sub.3 2-Cl--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1196 CH.sub.3 2-Cl--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1197 CH.sub.3 2-Cl--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1198CH.sub.3 2-Cl--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1199 CH.sub.3 2-Cl--C.sub.6 H.sub.4 Prop-1-en-3-yl 1200 CH.sub.3 2-Cl--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1201 CH.sub.3 2-Cl--C.sub.6 H.sub.4 Propyn-3-yl 1202 CH.sub.3 2-Cl--C.sub.6 H.sub.43-Methyl-but-2-en-1-yl 1203 CH.sub.3 3-Cl--C.sub.6 H.sub.4 H 1204 CH.sub.3 3-Cl--C.sub.6 H.sub.4 CH.sub.3 1205 CH.sub.3 3-Cl--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1206 CH.sub.3 3-Cl--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1207 CH.sub.3 3-Cl--C.sub.6 H.sub.4i-C.sub.3 H.sub.7 1208 CH.sub.3 3-Cl--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1209 CH.sub.3 3-Cl--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1210 CH.sub.3 3-Cl--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1211 CH.sub.3 3-Cl--C.sub.6 H.sub.4 Prop-1-en-3-yl 1212 CH.sub.33-Cl--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1213 CH.sub.3 3-Cl--C.sub.6 H.sub.4 Propyn-3-yl 1214 CH.sub.3 3-Cl--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1215 CH.sub.3 4-Cl--C.sub.6 H.sub.4 H 1216 CH.sub.3 4-Cl--C.sub.6 H.sub.4 CH.sub.3 1217CH.sub.3 4-Cl--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1218 CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1219 CH.sub.3 4-Cl--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1220 CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1221 CH.sub.3 4-Cl--C.sub.6 H.sub.4t-C.sub.4 H.sub.9 1222 CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1223 CH.sub.3 4-Cl--C.sub.6 H.sub.4 Prop-1-en-3-yl 1224 CH.sub.3 4-Cl--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1225 CH.sub.3 4-Cl--C.sub.6 H.sub.4 Propyn-3-yl 1226 CH.sub.34-Cl--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1227 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 H 1228 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 CH.sub.3 1229 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1230 CH.sub.3 2,3-Cl.sub.2 --C.sub.6H.sub.3 n-C.sub.3 H.sub.7 1231 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1232 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1233 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1234 CH.sub.3 2,3-Cl.sub.2--C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1235 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1236 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1237 CH.sub.3 2,3-Cl.sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1238 CH.sub.32,3-Cl.sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1239 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 H 1240 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 CH.sub.3 1241 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1242 CH.sub.3 2,4-Cl.sub.2--C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1243 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1244 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1245 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1246 CH.sub.32,4-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1247 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1248 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1249 CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1250CH.sub.3 2,4-Cl.sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1251 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 H 1252 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 CH.sub.3 1253 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1254 CH.sub.32,5-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1255 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1256 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1257 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1258CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1259 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1260 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1261 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1262 CH.sub.3 2,5-Cl.sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1263 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 H

1264 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 CH.sub.3 1265 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1266 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1267 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1268 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1269 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1270 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1271 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1272 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1273 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1274 CH.sub.3 2,6-Cl.sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1275 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 H 1276CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 CH.sub.3 1277 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1278 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1279 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1280 CH.sub.33,4-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1281 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1282 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1283 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1284 CH.sub.33,4-Cl.sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1285 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1286 CH.sub.3 3,4-Cl.sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1287 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 H 1288 CH.sub.33,5-Cl.sub.2 --C.sub.6 H.sub.3 CH.sub.3 1289 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1290 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1291 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1292 CH.sub.33,5-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1293 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1294 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1295 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1296 CH.sub.33,5-Cl.sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1297 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1298 CH.sub.3 3,5-Cl.sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1299 CH.sub.3 2-Br--C.sub.6 H.sub.4 H 1300 CH.sub.3 2-Br--C.sub.6H.sub.4 CH.sub.3 1301 CH.sub.3 2-Br--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1302 CH.sub.3 2-Br--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1303 CH.sub.3 2-Br--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1304 CH.sub.3 2-Br--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1305 CH.sub.32-Br--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1306 CH.sub.3 2-Br--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1307 CH.sub.3 2-Br--C.sub.6 H.sub.4 Prop-1-en-3-yl 1308 CH.sub.3 2-Br--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1309 CH.sub.3 2-Br--C.sub.6 H.sub.4Propyn-3-yl 1310 CH.sub.3 2-Br--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1311 CH.sub.3 3-Br--C.sub.6 H.sub.4 H 1312 CH.sub.3 3-Br--C.sub.6 H.sub.4 CH.sub.3 1313 CH.sub.3 3-Br--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1314 CH.sub.3 3-Br--C.sub.6 H.sub.4n-C.sub.3 H.sub.7 1315 CH.sub.3 3-Br--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1316 CH.sub.3 3-Br--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1317 CH.sub.3 3-Br--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1318 CH.sub.3 3-Br--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1319 CH.sub.33-Br--C.sub.6 H.sub.4 Prop-1-en-3-yl 1320 CH.sub.3 3-Br--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1321 CH.sub.3 3-Br--C.sub.6 H.sub.4 Propyn-3-yl 1322 CH.sub.3 3-Br--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1323 CH.sub.3 4-Br--C.sub.6 H.sub.4 H 1324CH.sub.3 4-Br--C.sub.6 H.sub.4 CH.sub.3 1325 CH.sub.3 4-Br--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1326 CH.sub.3 4-Br--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1327 CH.sub.3 4-Br--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1328 CH.sub.3 4-Br--C.sub.6 H.sub.4 n-C.sub.4H.sub.9 1329 CH.sub.3 4-Br--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1330 CH.sub.3 4-Br--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1331 CH.sub.3 4-Br--C.sub.6 H.sub.4 Prop-1-en-3-yl 1332 CH.sub.3 4-Br--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1333 CH.sub.34-Br--C.sub.6 H.sub.4 Propyn-3-yl 1334 CH.sub.3 4-Br--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1335 CH.sub.3 2-I--C.sub.6 H.sub.4 H 1336 CH.sub.3 2-I--C.sub.6 H.sub.4 CH.sub.3 1337 CH.sub.3 2-I--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1338 CH.sub.32-I--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1339 CH.sub.3 2-I--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1340 CH.sub.3 2-I--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1341 CH.sub.3 2-I--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1342 CH.sub.3 2-I--C.sub.6 H.sub.4 n-C.sub.6H.sub.13 1343 CH.sub.3 2-I--C.sub.6 H.sub.4 Prop-1-en-3-yl 1344 CH.sub.3 2-I--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1345 CH.sub.3 2-I--C.sub.6 H.sub.4 Propyn-3-yl 1346 CH.sub.3 2-I--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1347 CH.sub.33-I--C.sub.6 H.sub.4 H 1348 CH.sub.3 3-I--C.sub.6 H.sub.4 CH.sub.3 1349 CH.sub.3 3-I--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1350 CH.sub.3 3-I--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1351 CH.sub.3 3-I--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1352 CH.sub.33-I--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1353 CH.sub.3 3-I--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1354 CH.sub.3 3-I--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1355 CH.sub.3 3-I--C.sub.6 H.sub.4 Prop-1-en-3-yl 1356 CH.sub.3 3-I--C.sub.6 H.sub.4(E)-1-Chloroprop-1-en-3-yl 1357 CH.sub.3 3-I--C.sub.6 H.sub.4 Propyn-3-yl 1358 CH.sub.3 3-I--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1359 CH.sub.3 4-I--C.sub.6 H.sub.4 H 1360 CH.sub.3 4-I--C.sub.6 H.sub.4 CH.sub.3 1361 CH.sub.3 4-I--C.sub.6 H.sub.4C.sub.2 H.sub.5 1362 CH.sub.3 4-I--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1363 CH.sub.3 4-I--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1364 CH.sub.3 4-I--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1365 CH.sub.3 4-I--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1366 CH.sub.34-I--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1367 CH.sub.3 4-I--C.sub.6 H.sub.4 Prop-1-en-3-yl 1368 CH.sub.3 4-I--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1369 CH.sub.3 4-I--C.sub.6 H.sub.4 Propyn-3-yl 1370 CH.sub.3 4-I--C.sub.6 H.sub.43-Methyl-but-2-en-1-yl 1371 CH.sub.3 2-CN--C.sub.6 H.sub.4 H 1372 CH.sub.3 2-CN--C.sub.6 H.sub.4 CH.sub.3 1373 CH.sub.3 2-CN--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1374 CH.sub.3 2-CN--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1375 CH.sub.3 2-CN--C.sub.6 H.sub.4i-C.sub.3 H.sub.7 1376 CH.sub.3 2-CN--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1377 CH.sub.3 2-CN--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1378 CH.sub.3 2-CN--C.sub.6 H.sub.4 n-C.sub.6H.sub.13 1379 CH.sub.3 2-CN--C.sub.6 H.sub.4 Prop-1-en-3-yl 1380 CH.sub.32-CN--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1381 CH.sub.3 2-CN--C.sub.6 H.sub.4 Propyn-3-yl 1382 CH.sub.3 2-CN--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1383 CH.sub.3 3-CN--C.sub.6 H.sub.4 H 1384 CH.sub.3 3-CN--C.sub.6 H.sub.4 CH.sub.3 1385CH.sub.3 3-CN--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1386 CH.sub.3 3-CN--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1387 CH.sub.3 3-CN--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1388 CH.sub.3 3-CN--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1389 CH.sub.3 3-CN--C.sub.6 H.sub.4t-C.sub.4 H.sub.9 1390 CH.sub.3 3-CN--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1391 CH.sub.3 3-CN--C.sub.6 H.sub.4 Prop-1-en-3-yl 1392 CH.sub.3 3-CN--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1393 CH.sub.3 3-CN--C.sub.6 H.sub.4 Propyn-3-yl 1394 CH.sub.33-CN--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1395 CH.sub.3 4-CN--C.sub.6 H.sub.4 H 1396 CH.sub.3 4-CN--C.sub.6 H.sub.4 CH.sub.3 1397 CH.sub.3 4-CN--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1398 CH.sub.3 4-CN--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1399 CH.sub.34-CN--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1400 CH.sub.3 4-CN--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1401 CH.sub.3 4-CN--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1402 CH.sub.3 4-CN--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1403 CH.sub.3 4-CN--C.sub.6 H.sub.4Prop-1-en-3-yl 1404 CH.sub.3 4-CN--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1405 CH.sub.3 4-CN--C.sub.6 H.sub.4 Propyn-3-yl 1406 CH.sub.3 4-CN--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1407 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 H 1408 CH.sub.34-NO.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1409 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1410 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1411 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1412 CH.sub.3 4-NO.sub.2--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1413 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1414 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1415 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1416 CH.sub.3 4-NO.sub.2--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1417 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1418 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1419 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 H 1420 CH.sub.3 3-NO.sub.2 --C.sub.6H.sub.4 CH.sub.3 1421 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1422 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1423 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1424 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.4H.sub.9 1425 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1426 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1427 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1428 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4(E)-1-Chloroprop-1-en-3-yl 1429 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1430 CH.sub.3 3-NO.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1431 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 H 1432 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1433CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1434 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1435 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1436 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1437 CH.sub.34-NO.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1438 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1439 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1440 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1441 CH.sub.34-NO.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1442 CH.sub.3 4-NO.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1443 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 H 1444 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1445 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4C.sub.2 H.sub.5 1446 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1447 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1448 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1449 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4t-C.sub.4 H.sub.9 1450 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1451 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1452 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1453 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4Propyn-3-yl 1454 CH.sub.3 2-CH.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1455 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 H 1456 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1457 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1458 CH.sub.33-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1459 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1460 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1461 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1462 CH.sub.33-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1463 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1464 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1465 CH.sub.3 3-CH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1466 CH.sub.33-CH.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1467 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 H 1468 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1469 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1470 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4n-C.sub.3 H.sub.7 1471 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1472 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1473 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1474 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4n-C.sub.6 H.sub.13 1475 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1476 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1477 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1478 CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.43-Methyl-but-2-en-1-yl 1479 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 H 1480 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 CH.sub.3 1481 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1482 CH.sub.3 2,3-(CH.sub.3).sub.2--C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1483 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1484 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1485 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1486 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1487 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1488 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1489 CH.sub.32,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1490 CH.sub.3 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1491 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 H 1492 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 CH.sub.3 1493CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1494 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1495 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1496 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6H.sub.3 n-C.sub.4 H.sub.9 1497 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1498 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1499 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1500 CH.sub.32,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1501 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1502 CH.sub.3 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1503 CH.sub.3 2,5-(CH.sub.3).sub.2--C.sub.6 H.sub.3 H 1504 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 CH.sub.3 1505 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1506 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1507 CH.sub.32,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1508 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1509 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1510 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3n-C.sub.6 H.sub.13

1511 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1512 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1513 CH.sub.3 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1514 CH.sub.32,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1515 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 H 1516 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 CH.sub.3 1517 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1518 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1519 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1520 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1521 CH.sub.3 2,6-(CH.sub.3).sub.2--C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1522 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1523 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1524 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1525 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1526 CH.sub.3 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1527 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 H 1528 CH.sub.33,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 CH.sub.3 1529 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1530 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1531 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 i-C.sub.3H.sub.7 1532 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1533 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 t-C.sub.4 H.sub.9 1534 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1535 CH.sub.33,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1536 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1537 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1538 CH.sub.3 3,4-(CH.sub.3).sub.2 --C.sub.6H.sub.3 3-Methyl-but-2-en-1-yl 1539 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 H 1540 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 CH.sub.3 1541 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 C.sub.2 H.sub.5 1542 CH.sub.33,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.3 H.sub.7 1543 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 i-C.sub.3 H.sub.7 1544 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.4 H.sub.9 1545 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3t-C.sub.4 H.sub.9 1546 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 n-C.sub.6 H.sub.13 1547 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Prop-1-en-3-yl 1548 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 (E)-1-Chloroprop-1-en-3-yl 1549CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 Propyn-3-yl 1550 CH.sub.3 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 3-Methyl-but-2-en-1-yl 1551 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 H 1552 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 CH.sub.3 1553 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1554 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1555 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1556 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4n-C.sub.6 H.sub.13 1557 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1558 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1559 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 Propyn-3-yl 1560 CH.sub.3 2-C.sub.2H.sub.5 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1561 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 H 1562 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 CH.sub.3 1563 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1564 CH.sub.3 3-C.sub.2H.sub.5 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1565 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1566 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1567 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1568 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1569 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1570 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1571 CH.sub.3 3-C.sub.2 H.sub.5--C.sub.6 H.sub.4 Propyn-3-yl 1572 CH.sub.3 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1573 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 H 1574 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 CH.sub.3 1575 CH.sub.3 4-C.sub.2 H.sub.5--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1576 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1577 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1578 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1579CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1580 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1581 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1582 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1583 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 Propyn-3-yl 1584 CH.sub.3 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1585 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 H 1586 CH.sub.3 2-i-C.sub.3 H.sub.7--C.sub.6 H.sub.4 CH.sub.3 1587 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1588 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1589 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1590 CH.sub.32-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1591 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1592 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1593 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4Prop-1-en-3-yl 1594 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1595 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 Propyn-3-yl 1596 CH.sub.3 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1597 CH.sub.33-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 H 1598 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 CH.sub.3 1599 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1600 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1601CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1602 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1603 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1604 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6H.sub.4 n-C.sub.6 H.sub.13 1605 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1606 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1607 CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 Propyn-3-yl 1608CH.sub.3 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1609 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 H 1610 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 CH.sub.3 1611 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 C.sub.2H.sub.5 1612 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1613 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1614 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1615 CH.sub.3 4-i-C.sub.3H.sub.7 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1616 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1617 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1618 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1610 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 Propyn-3-yl 1620 CH.sub.3 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1621 CH.sub.3 2-OH--C.sub.6 H.sub.4 H 1622 CH.sub.3 2-OH--C.sub.6 H.sub.4 CH.sub.3 1623 CH.sub.3 2-OH--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1624 CH.sub.3 2-OH--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1625 CH.sub.3 2-OH--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1626 CH.sub.3 2-OH--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1627 CH.sub.3 2-OH--C.sub.6 H.sub.4t-C.sub.4 H.sub.9 1628 CH.sub.3 2-OH--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1629 CH.sub.3 2-OH--C.sub.6 H.sub.4 Prop-1-en-3-yl 1630 CH.sub.3 2-OH--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1631 CH.sub.3 2-OH--C.sub.6 H.sub.4 Propyn-3-yl 1632 CH.sub.32-OH--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1633 CH.sub.3 3-OH--C.sub.6 H.sub.4 H 1634 CH.sub.3 3-OH--C.sub.6 H.sub.4 CH.sub.3 1635 CH.sub.3 3-OH--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1636 CH.sub.3 3-OH--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1637 CH.sub.33-OH--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1638 CH.sub.3 3-OH--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1639 CH.sub.3 3-OH--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1640 CH.sub.3 3-OH--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1641 CH.sub.3 3-OH--C.sub.6 H.sub.4Prop-1-en-3-yl 1642 CH.sub.3 3-OH--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1643 CH.sub.3 3-OH--C.sub.6 H.sub.4 Propyn-3-yl 1644 CH.sub.3 3-OH--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1645 CH.sub.3 4-OH--C.sub.6 H.sub.4 H 1646 CH.sub.34-OH--C.sub.6 H.sub.4 CH.sub.3 1647 CH.sub.3 4-OH--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1648 CH.sub.3 4-OH--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1649 CH.sub.3 4-OH--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1650 CH.sub.3 4-OH--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1651CH.sub.3 4-OH--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1652 CH.sub.3 4-OH--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1653 CH.sub.3 4-OH--C.sub.6 H.sub.4 Prop-1-en-3-yl 1654 CH.sub.3 4-OH--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1655 CH.sub.3 4-OH--C.sub.6H.sub.4 Propyn-3-yl 1656 CH.sub.3 4-OH--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1657 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 H 1658 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1659 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1660CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1661 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1662 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1663 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1664CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1665 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1666 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1667 CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1668CH.sub.3 2-OCH.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1669 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 H 1670 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1671 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1672 CH.sub.3 3-OCH.sub.3--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1673 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1674 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1675 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1676 CH.sub.3 3-OCH.sub.3--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1677 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1678 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1679 CH.sub.3 3-OCH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1680 CH.sub.3 3-OCH.sub.3--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1681 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 H 1682 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1683 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1684 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4n-C.sub.3 H.sub.7 1685 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1686 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1687 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1688 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4n-C.sub.6 H.sub.13 1689 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1690 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1691 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1692 CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.43-Methyl-but-2-en-1-yl 1693 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 H 1694 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 CH.sub.3 1695 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1696 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6H.sub.4 n-C.sub.3 H.sub.7 1697 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1698 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1699 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1700 CH.sub.32-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1701 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1702 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1703 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4Propyn-3-yl 1704 CH.sub.3 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1705 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 H 1706 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 CH.sub.3 1707 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4C.sub.2 H.sub.5 1708 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1709 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1710 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1711 CH.sub.3 3-OC.sub.2H.sub.5 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1712 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1713 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1714 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1715 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 Propyn-3-yl 1716 CH.sub.3 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1717 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 H 1718 CH.sub.3 4-OC.sub.2 H.sub.5--C.sub.6 H.sub.4 CH.sub.3 1719 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1720 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1721 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1722 CH.sub.34-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1723 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1724 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1725 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4Prop-1-en-3-yl 1726 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1727 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 Propyn-3-yl 1728 CH.sub.3 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1729 CH.sub.32-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 H 1730 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 CH.sub.3 1731 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1732 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1733 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1734 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1735 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1736 CH.sub.3 2-O-(i-C.sub.3H.sub.7)--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1737 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 Prop-1-en-3-yl

1738 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1739 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 Propyn-3-yl 1740 CH.sub.3 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1741 CH.sub.33-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 H 1742 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 CH.sub.3 1743 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1744 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1745 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1746 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1747 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1748 CH.sub.3 3-O-(i-C.sub.3H.sub.7)--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1749 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 Prop-1-en-3-yl 1750 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1751 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6H.sub.4 Propyn-3-yl 1752 CH.sub.3 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1753 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 H 1754 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 CH.sub.3 1753 CH.sub.3 4-O-(i-C.sub.3H.sub.7)--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1756 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1757 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1758 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4n-C.sub.4 H.sub.9 1759 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1760 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1761 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 Prop-1-en-3-yl 1762 CH.sub.34-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1763 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 Propyn-3-yl 1764 CH.sub.3 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1765 CH.sub.3 2-O-(t-C.sub.4H.sub.9)--C.sub.6 H.sub.4 H 1766 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 CH.sub.3 1767 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1768 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1769 CH.sub.32-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1770 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1771 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1772 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6H.sub.4 n-C.sub.6 H.sub.13 1773 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 Prop-1-en-3-yl 1774 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1775 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 Propyn-3-yl 1776 CH.sub.3 2-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1777 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 H 1778 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 CH.sub.3 1779 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6H.sub.4 C.sub.2 H.sub.5 1780 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1781 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1782 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1783CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1784 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1785 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 Prop-1-en-3-yl 1786 CH.sub.3 3-O-(t-C.sub.4H.sub.9)--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1787 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 Propyn-3-yl 1788 CH.sub.3 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1789 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6H.sub.4 H 1790 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 CH.sub.3 1791 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1792 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1793 CH.sub.3 4-O-(t-C.sub.4H.sub.9)--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1794 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1795 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1796 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4n-C.sub.6 H.sub.13 1797 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 Prop-1-en-3-yl 1798 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1799 CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 Propyn-3-yl 1800CH.sub.3 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1801 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 H 1802 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1803 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1804 CH.sub.32-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1805 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1806 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1807 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1808 CH.sub.32-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1809 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1810 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1811 CH.sub.3 2-CF.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1812 CH.sub.32-CF.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1813 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 H 1814 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1815 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1816 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4n-C.sub.3 H.sub.7 1817 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1818 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1819 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1820 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4n-C.sub.6 H.sub.13 1821 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1822 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1823 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1824 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.43-Methyl-but-2-en-1-yl 1825 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 H 1826 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1827 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1828 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1829CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1830 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1831 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1832 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1833CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1834 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1835 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1836 CH.sub.3 4-CF.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1837CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 H 1838 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1839 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1840 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1841 CH.sub.3 2-NH.sub.2 --C.sub.6H.sub.4 i-C.sub.3 H.sub.7 1842 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1843 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1844 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1845 CH.sub.3 2-NH.sub.2 --C.sub.6H.sub.4 Prop-1-en-3-yl 1846 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1847 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1848 CH.sub.3 2-NH.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1849 CH.sub.3 3-NH.sub.2 --C.sub.6H.sub.4 H 1850 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1851 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1852 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1853 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1854CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1855 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1856 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1857 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1858 CH.sub.33-NH.sub.2 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1859 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1860 CH.sub.3 3-NH.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1861 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 H 1862 CH.sub.3 4-NH.sub.2--C.sub.6 H.sub.4 CH.sub.3 1863 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1864 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1865 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1866 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4n-C.sub.4 H.sub.9 1867 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1868 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1869 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1870 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4(E)-1-Chloroprop-1-en-3-yl 1871 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1872 CH.sub.3 4-NH.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1873 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 H 1874 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1875 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1876 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1877 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1878 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1879CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1880 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1881 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1882 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1883 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1884 CH.sub.3 2-NMe.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1885 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 H 1886 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1887 CH.sub.3 3-NMe.sub.2--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1888 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1889 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1890 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1891 CH.sub.3 3-NMe.sub.2--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1892 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1893 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1894 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1895 CH.sub.33-NMe.sub.2 --C.sub.6 H.sub.4 Propyn-3-yl 1896 CH.sub.3 3-NMe.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1897 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 H 1898 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 CH.sub.3 1899 CH.sub.3 4-NMe.sub.2 --C.sub.6H.sub.4 C.sub.2 H.sub.5 1900 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1901 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1902 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1903 CH.sub.3 4-NMe.sub.2 --C.sub.6H.sub.4 t-C.sub.4 H.sub.9 1904 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1905 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1906 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1907 CH.sub.3 4-NMe.sub.2--C.sub.6 H.sub.4 Propyn-3-yl 1908 CH.sub.3 4-NMe.sub.2 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1909 CH.sub.3 2-Aminothiocarbo- H nyl-C.sub.6 H.sub.4 1910 CH.sub.3 2-Aminothiocarbo- CH.sub.3 nyl-C.sub.6 H.sub.4 1911 CH.sub.3 2-Aminothiocarbo-C.sub.2 H.sub.5 nyl-C.sub.6 H.sub.4 1912 CH.sub.3 2-Aminothiocarbo- n-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 1913 CH.sub.3 2-Aminothiocarbo- i-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 1914 CH.sub.3 2-Aminothiocarbo- n-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 1915 CH.sub.3 2-Aminothiocarbo- t-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 1916 CH.sub.3 2-Aminothiocarbo- n-C.sub.6 H1.sub.3 nyl-C.sub.6 H.sub.4 1917 CH.sub.3 2-Aminothiocarbo- Prop-1-en-3-yl nyl-C.sub.6 H.sub.4 1918 CH.sub.3 2-Aminothiocarbo-(E)-1-Chloroprop-1-en-3-yl nyl-C.sub.6 H.sub.4 1919 CH.sub.3 2-Aminothiocarbo- Propyn-3-yl nyl-C.sub.6 H.sub.4 1920 CH.sub.3 3-Aminothiocarbo- 3-Methyl-but-2-en-yl nyl-C.sub.6 H.sub.4 1921 CH.sub.3 3-Aminothiocarbo- H nyl-C.sub.6 H.sub.4 1922CH.sub.3 3-Aminothiocarbo- CH.sub.3 nyl-C.sub.6 H.sub.4 1923 CH.sub.3 3-Aminothiocarbo- C.sub.2 H.sub.5 nyl-C.sub.6 H.sub.4 1924 CH.sub.3 3-Aminothiocarbo- n-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 1925 CH.sub.3 3-Aminothiocarbo- i-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 1926 CH.sub.3 3-Aminothiocarbo- n-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 1927 CH.sub.3 3-Aminothiocarbo- t-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 1928 CH.sub.3 3-Aminothiocarbo- n-C.sub.6 H.sub.13 nyl-C.sub.6 H.sub.4 1929 CH.sub.33-Aminothiocarbo- Prop-1-en-3-yl nyl-C.sub.6 H.sub.4 1930 CH.sub.3 3-Aminothiocarbo- (E)-1-Chloroprop-1-en-3-yl nyl-C.sub.6 H.sub.4 1931 CH.sub.3 3-Aminothiocarbo- Propyn-3-yl nyl-C.sub.6 H.sub.4 1932 CH.sub.3 3-Aminothiocarbo-3-Methyl-but-2-en-1-yl nyl-C.sub.6 H.sub.4 1933 CH.sub.3 4-Aminothiocarbo- H nyl-C.sub.6 H.sub.4 1934 CH.sub.3 4-Aminothiocarbo- CH.sub.3 nyl-C.sub.6 H.sub.4 1935 CH.sub.3 4-Aminothiocarbo- C.sub.2 H.sub.5 nyl-C.sub.6 H.sub.4 1936 CH.sub.34-Aminothiocarbo- n-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 1937 CH.sub.3 4-Aminothiocarbo- i-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 1938 CH.sub.3 4-Aminothiocarbo- n-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 1939 CH.sub.3 4-Aminothiocarbo- t-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 1940 CH.sub.3 4-Aminothiocarbo- n-C.sub.6 H.sub.13

nyl-C.sub.6 H.sub.4 1941 CH.sub.3 4-Aminothiocarbo- Prop-1-en-3-yl nyl-C.sub.6 H.sub.4 1942 CH.sub.3 4-Aminothiocarbo- (E)-1-Chloroprop-1-en-3-yl nyl-C.sub.6 H.sub.4 1943 CH.sub.3 4-Aminothiocarbo- Propyn-3-yl nyl-C.sub.6 H.sub.4 1944CH.sub.3 4-Aminothiocarbo- 3-Methyl-but-2-en-1-yl nyl-C.sub.6 H.sub.4 1945 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 H 1946 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1947 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1948 CH.sub.32-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1949 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1950 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1951 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1952 CH.sub.32-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1953 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1954 CH.sub.3 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1955 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1956CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1957 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1958 CH.sub.3 2-OCF.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1959 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 H 1960 CH.sub.33-OCF.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1961 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1962 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1963 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1964 CH.sub.3 3-OCF.sub.3--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1965 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1966 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1967 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1968 CH.sub.3 3-OCF.sub.3--C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1969 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1970 CH.sub.3 3-OCF.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1971 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 H 1972 CH.sub.3 4-OCF.sub.3 --C.sub.6H.sub.4 CH.sub.3 1973 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1974 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1975 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1976 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4n-C.sub.4 H.sub.9 1977 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1978 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1979 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1980 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4(E)-1-Chloroprop-1-en-3-yl 1981 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1982 CH.sub.3 4-OCF.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1983 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 H 1984 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1985 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 1986 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1987 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 1988 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 1989CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 1990 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 1991 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 1992 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 1993 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 1994 CH.sub.3 2-SCH.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 1995 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 H 1996 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 1997 CH.sub.3 3-SCH.sub.3--C.sub.6 H.sub.4 C.sub.2 H.sub.5 1998 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 1999 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 2000 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 2001 CH.sub.3 3-SCH.sub.3--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 2002 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 2003 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 2004 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 2005 CH.sub.33-SCH.sub.3 --C.sub.6 H.sub.4 Propyn-3-yl 2006 CH.sub.3 3-SCH.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 2007 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 H 2008 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 2009 CH.sub.3 4-SCH.sub.3 --C.sub.6H.sub.4 C.sub.2 H.sub.5 2010 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 2011 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 2012 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 2013 CH.sub.3 4-SCH.sub.3 --C.sub.6H.sub.4 t-C.sub.4 H.sub.9 2014 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 2015 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 Prop-1-en-3-yl 2016 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 (E)-1-Chloroprop-1-en-3-yl 2017 CH.sub.3 4-SCH.sub.3--C.sub.6 H.sub.4 Propyn-3-yl 2018 CH.sub.3 4-SCH.sub.3 --C.sub.6 H.sub.4 3-Methyl-but-2-en-1-yl 2019 CH.sub.3 2-Methyl- H sulfonyl-C.sub.6 H.sub.4 2020 CH.sub.3 2-Methyl- CH.sub.3 sulfonyl-C.sub.6 H.sub.4 2021 CH.sub.3 2-Methyl- C.sub.2 H.sub.5 sulfonyl-C.sub.6 H.sub.4 2022 CH.sub.3 2-Methyl- n-C.sub.3 H.sub.7 sulfonyl-C.sub.6 H.sub.4 2023 CH.sub.3 2-Methyl- i-C.sub.3 H.sub.7 sulfonyl-C.sub.6 H.sub.4 2024 CH.sub.3 2-Methyl- n-C.sub.4 H.sub.9 sulfonyl-C.sub.6 H.sub.4 1025 CH.sub.32-Methyl- t-C.sub.4 H.sub.9 sulfonyl-C.sub.6 H.sub.4 2026 CH.sub.3 2-Methyl- n-C.sub.6 H.sub.13 sulfonyl-C.sub.6 H.sub.4 2027 CH.sub.3 2-Methyl- Prop-1-en-3-yl sulfonyl-C.sub.6 H.sub.4 2028 CH.sub.3 2-Methyl- (E)-1-Chloroprop-1-en-3-yl sulfonyl-C.sub.6 H.sub.4 2029 CH.sub.3 2-Methyl- Propyn-3-yl sulfonyl-C.sub.6 H.sub.4 2030 CH.sub.3 2-Methyl- 3-Methyl-but-2-en-1-yl sulfonyl-C.sub.6 H.sub.4 2031 CH.sub.3 3-Methyl- H sulfonyl-C.sub.6 H.sub.4 2032 CH.sub.3 3-Methyl- CH.sub.3 sulfonyl-C.sub.6 H.sub.4 2033 CH.sub.3 3-Methyl- C.sub.2 H.sub.5 sulfonyl-C.sub.6 H.sub.4 2034 CH.sub.3 3-Methyl- n-C.sub.3 H.sub.7 sulfonyl-C.sub.6 H.sub.4 2035 CH.sub.3 3-Methyl- i-C.sub.3 H.sub.7 sulfonyl-C.sub.6 H.sub.4 2036 CH.sub.3 3-Methyl-n-C.sub.4 H.sub.9 sulfonyl-C.sub.6 H.sub.4 2037 CH.sub.3 3-Methyl- t-C.sub.4 H.sub.9 sulfonyl-C.sub.6 H.sub.4 2038 CH.sub.3 3-Methyl- n-C.sub.6 H.sub.13 sulfonyl-C.sub.6 H.sub.4 2039 CH.sub.3 3-Methyl- Prop-1-en-3-yl sulfonyl-C.sub.6 H.sub.4 2040CH.sub.3 3-Methyl- (E)-1-Chloroprop-1-en-3-yl sulfonyl-C.sub.6 H.sub.4 2041 CH.sub.3 3-Methyl- Propyn-3-yl sulfonyl-C.sub.6 H.sub.4 2042 CH.sub.3 3-Methyl- 3-Methyl-but-2-en-1-yl sulfonyl-C.sub.6 H.sub.4 2043 CH.sub.3 4-Methyl- H sulfonyl-C.sub.6H.sub.4 2044 CH.sub.3 4-Methyl- CH.sub.3 sulfonyl-C.sub.6 H.sub.4 2045 CH.sub.3 4-Methyl- C.sub.2 H.sub.5 sulfonyl-C.sub.6 H.sub.4 2046 CH.sub.3 4-Methyl- n-C.sub.3 H.sub.7 sulfonyl-C.sub.6 H.sub.4 2047 CH.sub.3 4-Methyl- i-C.sub.3 H.sub.7 sulfonyl-C.sub.6 H.sub.4 2048 CH.sub.3 4-Methyl- n-C.sub.4 H.sub.9 sulfonyl-C.sub.6 H.sub.4 2049 CH.sub.3 4-Methyl- t-C.sub.4 H.sub.9 sulfonyl-C.sub.6 H.sub.4 2050 CH.sub.3 4-Methyl- n-C.sub.6 H.sub.13 sulfonyl-C.sub.6 H.sub.4 2051 CH.sub.34-Methyl- Prop-1-en-3-yl sulfonyl-C.sub.6 H.sub.4 2052 CH.sub.3 4-Methyl- (E)-1-Chloroprop-1-en-3-yl sulfonyl-C.sub.6 H.sub.4 2053 CH.sub.3 4-Methyl- Propyn-3-yl sulfonyl-C.sub.6 H.sub.4 2054 CH.sub.3 4-Methyl- 3-Methyl-but-2-en-1-yl sulfonyl-C.sub.6 H.sub.4 2055 CH.sub.3 2-Methoxycarbo- H nyl-C.sub.6 H.sub.4 2056 CH.sub.3 2-Methoxycarbo- CH.sub.3 nyl-C.sub.6 H.sub.4 2057 CH.sub.3 2-Methoxycarbo- C.sub.2 H.sub.5 nyl-C.sub.6 H.sub.4 2058 CH.sub.3 2-Methoxycarbo- n-C.sub.3H.sub.7 nyl-C.sub.6 H.sub.4 2059 CH.sub.3 2-Methoxycarbo- i-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 2060 CH.sub.3 2-Methoxycarbo- n-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 2061 CH.sub.3 2-Methoxycarbo- t-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 2062 CH.sub.32-Methoxycarbo- n-C.sub.6 H.sub.13 nyl-C.sub.6 H.sub.4 2063 CH.sub.3 2-Methoxycarbo- Prop-1-en-3-yl nyl-C.sub.6 H.sub.4 2064 CH.sub.3 2-Methoxycarbo- (E)-1-Chloroprop-1-en-3-yl nyl-C.sub.6 H.sub.4 2065 CH.sub.3 2-Methoxycarbo- Propyn-3-yl nyl-C.sub.6 H.sub.4 2066 CH.sub.3 2-Methoxycarbo- 3-Methyl-but-2-en-1-yl nyl-C.sub.6 H.sub.4 2067 CH.sub.3 3-Methoxycarbo- H nyl-C.sub.6 H.sub.4 2068 CH.sub.3 3-Methoxycarbo- CH.sub.3 nyl-C.sub.6 H.sub.4 2069 CH.sub.3 3-Methoxycarbo- C.sub.2H.sub.5 nyl-C.sub.6 H.sub.4 2070 CH.sub.3 3-Methoxycarbo- n-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 2071 CH.sub.3 3-Methoxycarbo- i-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 2072 CH.sub.3 3-Methoxycarbo- n-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 2073 CH.sub.33-Methoxycarbo- t-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 2074 CH.sub.3 3-Methoxycarbo- n-C.sub.6 H.sub.13 nyl-C.sub.6 H.sub.4 2075 CH.sub.3 3-Methoxycarbo- Prop-1-en-3-yl nyl-C.sub.6 H.sub.4 2076 CH.sub.3 3-Methoxycarbo- (E)-1-Chloroprop-1-en-3-yl nyl-C.sub.6 H.sub.4 2077 CH.sub.3 3-Methoxycarbo- Propyn-3-yl nyl-C.sub.6 H.sub.4 2078 CH.sub.3 3-Methoxycarbo- 3-Methyl-but-2-en-1-yl nyl-C.sub.6 H.sub.4 2079 CH.sub.3 4-Methoxycarbo- H nyl-C.sub.6 H.sub.4 2080 CH.sub.3 4-Methoxycarbo- CH.sub.3 nyl-C.sub.6 H.sub.4 2081 CH.sub.3 4-Methoxycarbo- C.sub.2 H.sub.5 nyl-C.sub.6 H.sub.4 2082 CH.sub.3 4-Methoxycarbo- n-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 2083 CH.sub.3 4-Methoxycarbo- i-C.sub.3 H.sub.7 nyl-C.sub.6 H.sub.4 2084 CH.sub.34-Methoxycarbo- n-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 2085 CH.sub.3 4-Methoxycarbo- t-C.sub.4 H.sub.9 nyl-C.sub.6 H.sub.4 2086 CH.sub.3 4-Methoxycarbo- n-C.sub.6 H.sub.13 nyl-C.sub.6 H.sub.4 2087 CH.sub.3 4-Methoxycarbo- Prop-1-en-3-yl nyl-C.sub.6H.sub.4 2088 CH.sub.3 4-Methoxycarbo- (E)-1-Chloroprop-1-en-3-yl nyl-C.sub.6 H.sub.4 2089 CH.sub.3 4-Methoxycarbo- Propyn-3-yl nyl-C.sub.6 H.sub.4 2090 CH.sub.3 4-Methoxycarbo- 3-Methyl-but-2-en-1-yl nyl-C.sub.6 H.sub.4 2091 CH.sub.3 2-Ethoxy- H carbonyl-C.sub.6 H.sub.4 2092 CH.sub.3 2-Ethoxy- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2093 CH.sub.3 2-Ethoxy- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2094 CH.sub.3 2-Ethoxy- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2095 CH.sub.3 2-Ethoxy-i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2096 CH.sub.3 2-Ethoxy- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2097 CH.sub.3 2-Ethoxy- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2098 CH.sub.3 2-Ethoxy- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2099 CH.sub.3 2-Ethoxy- Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2100 CH.sub.3 2-Ethoxy- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2101 CH.sub.3 2-Ethoxy- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2102 CH.sub.3 2-Ethoxy- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4

2103 CH.sub.3 3-Ethoxy- H carbonyl-C.sub.6 H.sub.4 2104 CH.sub.3 3-Ethoxy- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2105 CH.sub.3 3-Ethoxy- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2106 CH.sub.3 3-Ethoxy- n-C.sub.3 H.sub.7 carbonyl-C.sub.6H.sub.4 2107 CH.sub.3 3-Ethoxy- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2108 CH.sub.3 3-Ethoxy- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2109 CH.sub.3 3-Ethoxy- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2110 CH.sub.3 3-Ethoxy- n-C.sub.6H.sub.13 carbonyl-C.sub.6 H.sub.4 2111 CH.sub.3 3-Ethoxy- Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2112 CH.sub.3 3-Ethoxy- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2113 CH.sub.3 3-Ethoxy- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2114CH.sub.3 3-Ethoxy- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2115 CH.sub.3 4-Ethoxy- H carbonyl-C.sub.6 H.sub.4 2116 CH.sub.3 4-Ethoxy- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2117 CH.sub.3 4-Ethoxy- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2118CH.sub.3 4-Ethoxy- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2119 CH.sub.3 4-Ethoxy- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2120 CH.sub.3 4-Ethoxy- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2121 CH.sub.3 4-Ethoxy- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2122 CH.sub.3 4-Ethoxy- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2123 CH.sub.3 4-Ethoxy- Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2124 CH.sub.3 4-Ethoxy- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2125 CH.sub.34-Ethoxy- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2126 CH.sub.3 4-Ethoxy- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2127 CH.sub.3 2-Amino- H carbonyl-C.sub.6 H.sub.4 2128 CH.sub.3 2-Amino- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2129 CH.sub.32-Amino- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2130 CH.sub.3 2-Amino- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2131 CH.sub.3 2-Amino- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2132 CH.sub.3 2-Amino- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2133 CH.sub.3 2-Amino- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2134 CH.sub.3 2-Amino- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2135 CH.sub.3 2-Amino- Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2136 CH.sub.3 2-Amino- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2137 CH.sub.3 2-Amino- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2138 CH.sub.3 2-Amino- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2139 CH.sub.3 3-Amino- H carbonyl-C.sub.6 H.sub.4 2140 CH.sub.3 3-Amino- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2141 CH.sub.3 3-Amino- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2142 CH.sub.3 3-Amino- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2143 CH.sub.3 3-Amino- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2144 CH.sub.3 3-Amino-n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2145 CH.sub.3 3-Amino- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2146 CH.sub.3 3-Amino- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2147 CH.sub.3 3-Amino- Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2148CH.sub.3 3-Amino- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2149 CH.sub.3 3-Amino- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2150 CH.sub.3 4-Amino- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2151 CH.sub.3 4-Amino- H carbonyl-C.sub.6H.sub.4 2152 CH.sub.3 4-Amino- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2153 CH.sub.3 4-Amino- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2154 CH.sub.3 4-Amino- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2155 CH.sub.3 4-Amino- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2156 CH.sub.3 4-Amino- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2157 CH.sub.3 4-Amino- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2158 CH.sub.3 4-Amino- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2159 CH.sub.3 4-Amino-Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2160 CH.sub.3 4-Amino- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2161 CH.sub.3 4-Amino- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2162 CH.sub.3 4-Amino- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2163 CH.sub.3 2-(N-Methylamino- H carbonyl)-C.sub.6 H.sub.4 2164 CH.sub.3 2-(N-Methylamino- CH.sub.3 carbonyl)-C.sub.6 H.sub.4 2165 CH.sub.3 2-(N-Methylamino- C.sub.2 H.sub.5 carbonyl)-C.sub.6 H.sub.4 2166 CH.sub.3 2-(N-Methylamino- n-C.sub.3H.sub.7 carbonyl)-C.sub.6 H.sub.4 2167 CH.sub.3 2-(N-Methylamino- i-C.sub.3 H.sub.7 carbonyl)-C.sub.6 H.sub.4 2168 CH.sub.3 2-(N-Methylamino- n-C.sub.4 H.sub.9 carbonyl)-C.sub.6 H.sub.4 2169 CH.sub.3 2-(N-Methylamino- t-C.sub.4 H.sub.9 carbonyl)-C.sub.6 H.sub.4 2170 CH.sub.3 2-(N-Methylamino- n-C.sub.6 H.sub.13 carbonyl)-C.sub.6 H.sub.4 2171 CH.sub.3 2-(N-Methylamino- Prop-1-en-3-yl carbonyl)-C.sub.6 H.sub.4 2172 CH.sub.3 2-(N-Methylamino- (E)-1-Chloroprop-1-en-3-yl carbonyl)-C.sub.6 H.sub.4 2173 CH.sub.3 2-(N-Methylamino- Propyn-3-yl carbonyl)-C.sub.6 H.sub.4 2174 CH.sub.3 2-(N-Methylamino- 3-Methyl-but-2-en-1-yl carbonyl)-C.sub.6 H.sub.4 2175 CH.sub.3 3-(N-Methylamino- H carbonyl)-C.sub.6 H.sub.4 2176CH.sub.3 3-(N-Methylamino- CH.sub.3 carbonyl)-C.sub.6 H.sub.4 2177 CH.sub.3 3-(N-Methylamino- C.sub.2 H.sub.5 carbonyl)-C.sub.6 H.sub.4 2178 CH.sub.3 3-(N-Methylamino- n-C.sub.3 H.sub.7 carbonyl)-C.sub.6 H.sub.4 2179 CH.sub.3 3-(N-Methylamino-i-C.sub.3 H.sub.7 carbonyl)-C.sub.6 H.sub.4 2180 CH.sub.3 3-(N-Methylamino- n-C.sub.4 H.sub.9 carbonyl)-C.sub.6 H.sub.4 2181 CH.sub.3 3-(N-Methylamino- t-C.sub.4 H.sub.9 carbonyl)-C.sub.6 H.sub.4 2182 CH.sub.3 3-(N-Methylamino- n-C.sub.6 H.sub.13 carbonyl)-C.sub.6 H.sub.4 2183 CH.sub.3 3-(N-Methylamino- Prop-1-en-3-yl carbonyl)-C.sub.6 H.sub.4 2184 CH.sub.3 3-(N-Methylamino- (E)-1-Chloroprop-1-en-3-yl carbonyl)-C.sub.6 H.sub.4 2185 CH.sub.3 3-(N-Methylamino- Propyn-3-yl carbonyl)-C.sub.6H.sub.4 2186 CH.sub.3 3-(N-Methylamino- 3-Methyl-but-2-en-1-yl carbonyl)-C.sub.6 H.sub.4 2187 CH.sub.3 4-(N-Methylamino- H carbonyl)-C.sub.6 H.sub.4 2188 CH.sub.3 4-(N-Methylamino- CH.sub.3 carbonyl)-C.sub.6 H.sub.4 2189 CH.sub.3 4-(N-Methylamino-C.sub.2 H.sub.5 carbonyl)-C.sub.6 H.sub.4 2190 CH.sub.3 4-(N-Methylamino- n-C.sub.3 H.sub.7 carbonyl)-C.sub.6 H.sub.4 2191 CH.sub.3 4-(N-Methylamino- i-C.sub.3 H.sub.7 carbonyl)-C.sub.6 H.sub.4 2192 CH.sub.3 4-(N-Methylamino- n-C.sub.4 H.sub.9 carbonyl)-C.sub.6 H.sub.4 2193 CH.sub.3 4-(N-Methylamino- t-C.sub.4 H.sub.9 carbonyl)-C.sub.6 H.sub.4 2194 CH.sub.3 4-(N-Methylamino- n-C.sub.6 H.sub.13 carbonyl)-C.sub.6 H.sub.4 2195 CH.sub.3 4-(N-Methylamino- Prop-1-en-3-yl carbonyl)-C.sub.6H.sub.4 2196 CH.sub.3 4-(N-Methylamino- (E)-1-Chloroprop-1-en-3-yl carbonyl)-C.sub.6 H.sub.4 2197 CH.sub.3 4-(N-Methylamino- Propyn-3-yl carbonyl)-C.sub.6 H.sub.4 2198 CH.sub.3 4-(N-Methylamino- 3-Methyl-but-2-en-1-yl carbonyl)-C.sub.6 H.sub.4 2199 CH.sub.3 2-Dimethylamino- H carbonyl-C.sub.6 H.sub.4 2200 CH.sub.3 2-Dimethylamino- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2201 CH.sub.3 2-Dimethylamino- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2202 CH.sub.3 2-Dimethylamino- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2203 CH.sub.3 2-Dimethylamino- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2204 CH.sub.3 2-Dimethylamino- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2205 CH.sub.3 2-Dimethylamino- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2206 CH.sub.3 2-Dimethylamino- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2207 CH.sub.3 2-Dimethylamino- Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2208 CH.sub.3 2-Dimethylamino- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2209 CH.sub.32-Dimethylamino- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2210 CH.sub.3 2-Dimethylamino- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2211 CH.sub.3 3-Dimethylamino- H carbonyl-C.sub.6 H.sub.4 2212 CH.sub.3 3-Dimethylamino- CH.sub.3 carbonyl-C.sub.6H.sub.4 2213 CH.sub.3 3-Dimethylamino- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2214 CH.sub.3 3-Dimethylamino- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2215 CH.sub.3 3-Dimethylamino- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2216 CH.sub.33-Dimethylamino- n-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2217 CH.sub.3 3-Dimethylamino- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2218 CH.sub.3 3-Dimethylamino- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2219 CH.sub.3 3-Dimethylamino-Prop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2220 CH.sub.3 3-Dimethylamino- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2221 CH.sub.3 3-Dimethylamino- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2222 CH.sub.3 3-Dimethylamino- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4 2223 CH.sub.3 4-Dimethylamino- H carbonyl-C.sub.6 H.sub.4 2224 CH.sub.3 4-Dimethylamino- CH.sub.3 carbonyl-C.sub.6 H.sub.4 2223 CH.sub.3 4-Dimethylamino- C.sub.2 H.sub.5 carbonyl-C.sub.6 H.sub.4 2226 CH.sub.34-Dimethylamino- n-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2227 CH.sub.3 4-Dimethylamino- i-C.sub.3 H.sub.7 carbonyl-C.sub.6 H.sub.4 2228 CH.sub.3 4-Dimethylamino- n-C.sub.4 H.sub.9

carbonyl-C.sub.6 H.sub.4 2229 CH.sub.3 4-Dimethylamino- t-C.sub.4 H.sub.9 carbonyl-C.sub.6 H.sub.4 2230 CH.sub.3 4-Dimethylamino- n-C.sub.6 H.sub.13 carbonyl-C.sub.6 H.sub.4 2231 CH.sub.3 4-Dimethylamino- Prop-1-en-3-yl carbonyl-C.sub.6H.sub.4 2232 CH.sub.3 4-Dimethylamino- (E)-1-Chloroprop-1-en-3-yl carbonyl-C.sub.6 H.sub.4 2233 CH.sub.3 4-Dimethylamino- Propyn-3-yl carbonyl-C.sub.6 H.sub.4 2234 CH.sub.3 4-Dimethylamino- 3-Methyl-but-2-en-1-yl carbonyl-C.sub.6 H.sub.4

The compounds I are suitable as fungicides.

The compounds I are distinguished by an outstanding activity against a broad spectrum of phytopathogenic fungi, in particular from the class of the Ascomycetes and Basidiomycetes. They are systemically active in some cases and can be employed asfoliar and soil fungicides.

They are of particular importance for the control of a multiplicity of fungi on various crop plants such as wheat, rye, barley, oats, rice, corn, grass, cotton, soybean, coffee, sugar cane, grapes, fruit and decorative plants and vegetable plantssuch as cucumbers, beans and cucurbits, and on the seeds of these plants.

They are specifically suitable for the control of the following plant diseases: Erysiphe graminis (powdery mildew) in cereals, Erysiphe cichoracearum and Sphaerotheca fuliginea on cucurbits, Podasphaera leucotricha on apples, Uncinula necator onvines, Puccinia species on cereals, Rhizoctonia species on cotton and lawns, Ustilago species on cereals and sugar cane, Venturia inaequalis (scab) on apples, Helminthosporium species on cereals, Septoria nodorum on wheat, Botrytis cinerea (gray mold) onstrawberries, vines, Cercospora arachidicola on groundnuts, Pseudocercosporella herpotrichoides on wheat, barley, Pyricularia oryzae on rice, Phytophthora infestans on potatoes and tomatoes, .[.Fusa7-rium [sic].]. .Iadd.Fusarium .Iaddend.andVerticillium species on various plants, Plasmopara viticola on vines, Alternaria species on vegetables and fruit.

The compounds I are applied by treating the fungi or the plants, seeds, materials or the soil to be protected from fungal attack with a fungicidally effective amount of the active compounds. They are applied before or after the infection of thematerials, plants or seeds by the fungi.

They can be converted into the customary formulations, such as solutions, emulsions, suspensions, dusts, powders, pastes and granules. The application form depends on the particular intended use; it should in any case guarantee a fine anduniform dispersion of the .[.ortho-substituted benzyl ester of a cyclopropanecarboxylic acid [sic].]. .Iadd.phenylacetic acid derivative.Iaddend.. The formulationd are prepared in a known manner, eg. by extending the active compound with solventsand/or carriers, if desired using emulsifiers and dispersants, it also being possible to use other organic solvents as auxiliary solvents when water is used as a diluent. Suitable auxiliary substances for this purpose are essentially: solvents such asaromatics (eg. xylene), chlorinated aromatics (eg. chlorobenzenes), paraffins (eg. petroleum fractions), alcohols (eg. methanol, butanol), ketones (eg. cyclohexanone), amines (eg. ethanolamine, dimethylformamide) and water; carriers such as groundnatural minerals (eg. kaolins, clays, talc, chalk) and ground synthetic minerals (eg. highly disperse silicic acid, silicates); emulsifiers such as nonionic and anionic emulsifers (eg. polyoxyethylene fatty alcohol ethers, alkylsulfonates andarylsulfonates) and dispersants such as lignin-sulfite waste liquors and methylcellulose.

The fungicidal compositions in general contain from 0.1 to 95, preferably from 0.5 to 90, % by weight of active compound.

Depending on the type of effect desired, the application rates are from 0.01 to 2.0 kg of active compound per ha.

In seed treatment, active compound amounts of from 0.001 to 0.1 g, preferably from 0.01 to 0.05 g, per kilogram of seed are in general needed.

The compositions according to the invention can also be present in the application form as fungicides together with other active compounds, .[.the [sic].]. eg. with herbicides, insecticides, growth regulators, fungicides or alternatively withfertilizers.

On mixing with fungicides, in many cases an increase in the fungicidal spectrum of action is obtained here.

The following list of fungicides with which the compounds according to the invention can be applied together is intended to illustrate the combination possibilities, but not restrict them: sulfur, dithiocarbamates and their derivatives, such asferric dimethyldithiocarbamate, zinc dimethyldithiocarbamate, zinc ethylenebisdithiocarbamate, manganese ethylenebisdithiocarbamate, manganese zinc ethylenediamine bisdithiocarbamate, tetramethylthiuram .[.disulfides [sic].]. .Iadd.disulfide.Iaddend.,ammonia complex of zinc (N,N-ethylenebisdithiocarbamate), ammonia complex of zinc (N,N'-propylenebisdithiocarbamate), zinc (N,N'-propylenebisdithiocarbamate), N,N'-polypropylenebis(thiocarbamoyl) disulfide; nitro derivatives, such asdinitro(1-methylheptyl)phenyl crotonate, 2-sec-butyl-4,6-dinitrophenyl 3,3-dimethylacrylate, 2-sec-butyl-4,6-dinitrophenyl isopropylcarbonate, diisopropyl 5-nitroisophthalate; heterocyclic substances, such as 2-heptadecyl-2-imidazoline acetate,2,4-dichloro-6(o-chloroanilino)-s-triazine, O,O-diethyl phthalimidophosphonothioate, 5-amino-1-[bis(dimethylamino)-phosphinyl]-3-phenyl-1,2,4-triazole, 2,3-dicyano-1,4-dithioanthraquinone, 2-thio-1,3-dithiolo[4,5-b] quinoxaline, methyl1-(butylcarbamoyl)-2-benzimidazole carbamate, 2-methoxycarbonylaminobenzimidazole, 2-(fur-2-yl) benzimidazole, 2-(thiazol-4-yl)benzimidazole, N-(1,1, 2,2-tetrachloroethylthio)tetrahydrophthalamide, N-trichloromethylthiotetrahydrophthalimide,N-trichloromethylthiophthalimide; N-dichlorofluoromethylthio-N',N'-dimethyl-N-phenylsulfamide, 5-ethoxy-3-trichloromethyl-1,2,3-thiadiazole, 2-thiocyanatomethylthiobenzothiazole, 1,4-dichloro-2,5-dimethoxybenzene,4-(2-chlorophenylhydrazono)-3-methyl-5-isoxazolone, .[.pyridine-2-thio-1-oxide [sic].]. .Iadd.2-thiopyridine-1-oxide.Iaddend., 8-hydroxyquinoline or its copper salt, 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiin,2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiin-4,4-dioxide, 2-methyl-5,6-dihydro-4H-pyran-3-carboxanilide, 2-methylfuran-3-carboxanilide, 2,5-dimethylfuran-3-carboxanilide, 2,4,5-trimethylfuran-3-carboxanilide,N-cyclohexyl-2,5-dimethylfuran-3-carboxamide, N-cyclohexyl-N-methoxy-2,5-dimethylfuran-3-carboxamide, 2-methylbenzanilide, 2-iodobenzanilide, N-formyl-N-morpholine-2,2,2-trichloroethyl acetal, piperazine-1,4-diylbis(1-(2,2,2-trichloroethyl)formamide,1-(3,4-dichloroanilino)-1-formylamino-2,2,2-trichloroethane, 2,6-dimethyl-N-tridecylmorpholine or its salts, 2,6-dimethyl-N-cyclododecylmorpholine or its salts, N-[3-(p-tert-butylphenyl)-2-methylpropyl]-cis-2,6-dimethylmorpholine,N-[3-(p-tert-butylphenyl)-2-methylpropyl]piperidine, 1-[2-(2,4-dichlorophenyl)-4-ethyl-1,3-dioxolan-2-ylethyl]-1H-1,2,4-triazol , 1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-yl-ethyl]-1H-1,2,4-tri azole,N-(n-propyl)-N-(2,4,6-trichlorophenoxyethyl)-N'-imidazolylurea, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazole-1-yl)-2-butanone, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazole-1-yl)-2-butanol, .alpha.-(2-chlorophenyl-5-pyrimidinemethanol,5-butyl-2-dimethylamino-4-hydroxy-6-methylpyrimidine, bis(p-chlorophenyl)-3-pyrimidinemethanol, 1,2-bis(3-ethoxycarbonyl-2-thioureido)benzene, 1,2-bis(3-methoxycarbonyl-2-thioureido)benzene, and also various fungicides, such as dodecylguanidine acetate,3-[3-(3,5-dimethyl-2-oxycyclohexyl)-2-hydroxyethyl]glutarimide, hexachlorobenzene, DL-methyl-N-(2,6-dimethylphenyl)-N-2-furoyl alaninate, DL-N-(2,6-dimethylphenyl)-N-(2'-methoxyacetyl)alanine methyl ester,N-(2,6-dimethylphenyl)-N-chloroacetyl-D,L-2-aminobutyrolactone, DL-N-(2,6-dimethylphenyl)-N-(phenylacetyl)alanine methyl ester, 5-methyl-5-vinyl-3-(3,5-dichlorophenyl)-2,4-dioxo-1,3-oxazolidine,.[.3-[3,5-dichlorophenyl(5-methyl-5-methoxymethyl]-1,3-oxazolidine-2,4-dio ne [sic].]. .Iadd. 3-[3,5-dichlorophenyl-(5-methyl-5-methoxymethyl]-1,3-oxazolidine-2,4-dione .Iaddend., 3-(3,5-dichlorophenyl)-1-isopropylcarbamoylhydantoin,N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide, .[.2-cyano-[N-(ethylaminocarbonyl)-2-methoximino]acetamide [sic].]. .Iadd.2-cyano-[N-ethylaminocarbonyl-2-methoximino]acetamide.Iaddend.,1-[2-(2,4-dichlorophenyl)pentyl]-1H-1,2,4-triazole, 2,4-difluoro-.alpha.-(1H-1,2,4-triazolyl-1-methyl)benzhydryl alcohol, N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-3-chlor o-2-aminopyridine,1-((bis(4-fluorophenyl)methylsilyl)methyl)-1H-1,2,4-triazole.

The compounds of the formula I are additionally suitable for controlling pests from the class of insects, arachnids and nematodes effectively. They can be employed as pesticides in plant protection and in the hygiene, stored products protectionand veterinary sectors.

The harmful insects include from the order of the butterflies (Lepidoptera), argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneruafumiferana, Choristonerua occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus ligonosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleriamellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygmaexigua, Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Memestra brassicae, Orgyia pseudotsugata, Ostrinianubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phtorimaea operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena scarbra, Plutella xylostella, Pseudoplusia includens, Rhyacionia frustrana,Scrobipalpula absoluta, Sitotroga cerealella, Spargnothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix viridana, Trichoplusia ni, Zeiraphera canadensis.

From the order of the beetles (Coleoptera), for example, Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitalis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Atomaria linearis, Blastophagus piniperda,Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Ceuthorrhynchus assimilis, Ceuthorrynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Diabroticalongicornis, Diabrotica 1-punctata, Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus brasiliensis, Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsadecemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae, Ortiorrhynchus sulcatus, Otiorrhynchus ovatus, Phaedon cochleariae, Phyllotretachrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus, Sitophilus granaria.

From the order of the dipterous insects (Diptera), for example, Aedes aegypti, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Contarinia sorghicola,Cordylobia anthropophaga, Culex pipiens, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Fannia canicularis, Gasterophilus intestinalis, Glossina morsitans, Haematobia irritans, Haplodiplosis equestris, Hylemyia platura, Hypoderma lineata, Liriomyzasativae, Liriomyza trifolii, Lucilia caprina [sic], Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mayetiola destructor, Musca domestica, Muscina stabulans, Oestrus ovis, Oscinella frit, Pegomya hysocyami, Phorbia antiqua, Phorbia brassicae,Phorbia coarctata, Rhagoletis cerasi, Rhagoletis pomonella, Tabanus bovinus, Tipula oleracea, Tipula paludosa.

From the order of the thrips (Thysanoptera), for example, Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirothrips citri, Thrips oryzae, Thrips palmi, Thrips tabaci.

From the order of the hymenopterous insects (Hymenoptera), for example, Althalia rosae, Atta cephalotes, Atta sexdens, Atta texana, Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharonis, Solenopsis geminata, Solenopsis invicta.

From the order of the bed bugs (Heteroptera), for example, Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lyguslineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis, Thyanta perditor.

From the order of the plant-sucking insects (Homoptera), for example, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis pomi, Aphis sambuci, Brachycaudus cardui, Brevicornye brassicae, Cerosipha gossypii, Dreyfusianordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Empoasca fabae, Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Metopolophium dirhodum, Myzodes persicae, Myzus cerasi, Nilaparvata lugens,Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Trialeurodes vaporariorum, Viteusvitifolli.

From the order of the termites (Isoptera), for example, Calotermes flavicollis, Leucotermes flavipes, Reticulitermes lucifugus, Termes natalensis.

From the order of the orthopterous insects (Orthoptera), for example, Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum,Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Periplaneta americana, Schistocerca americana, Schistocerca peregrina, Stauronotus maroccanus, Tachycines asynamorus.

From the class of the Arachnoidea, for example spiders (Acarina) such as Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annalatus, Boophilus decoloratus, Boophilus microplus, Brevipalpus phoenicis, Bryobia praetiosa,Dermacentor silvarum, Eotetranychus carpini, Eriophyes sheldoni, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus moubata, Otobius megnini, Paratetranychus pilosus, Dermanyssus gallinae, Phyllocoptruta oleivora, Polyphagotarsonemuslatus, Psoroptes ovis, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius, Tetranychus urticae.

From the class of the nematodes, for example, root gall nematodes, eg. Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, cyst-forming nematodes, eg. Globodera rostochiensis, Heterodera avenae, Heterodera glycines, Heteroderaschachtii, Heterodera trifolii, stem and leaf eelworms, eg. Belonolaimus longicaudatus, Ditylenchus destructor, Ditylenchus dipsaci, Heliocotylenchus multicinctus, Longidorus elongatus, Radopholus similis, Rotylenchus robustus, Trichodorus primitivus,Tylenchorhynchus claytoni, Tylenchorhynchus dubius, Pratylenchus neglectus, Pratylenchus penetrans, Pratylenchus curvitatus, Pratylenchus goodeyi.

The active compounds can be applied as such or in the form of their formulations or the application forms prepared therefrom, eg. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions,pastes, dusts, scattering compositions or granules by spraying, atomizing dusting, scattering or pouring. The application forms depend entirely on the purposes of use; they should in any case as far as possible guarantee the finest dispersion of theactive compounds according to the invention.

The active compound concentrations in the ready-for-application preparations can be varied within quite substantial ranges.

In general, they are from 0.0001 to 10%, preferably from 0.01 to 1%.

The active compounds can also be used with great success in ultra-low volume processes (ULV), where it is possible to apply formulations containing more than 95% by weight of active compound or even the active compound without additives.

The application rate of active compound for controlling pests under outdoor conditions is from 0.1 to 2.0, preferably from 0.2 to 1.0 kg/ha.

For the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions, mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, and also coal tar oils and oils of vegetable or animal origin,aliphatic, cyclic and aromatic hydrocarbons, eg. benzene, toluene, xylene, paraffin, tertrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol,cyclohexanone, chlorobenzene, isophorone, strongly polar solvents, eg. dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and water are suitable.

Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (oil dispersions) by addition of water. For the preparation of emulsions, pastes or oil dispersions, the substances can be homogenized in water assuch or dissolved in an oil or solvent, by means of wetting agents, tackifiers, dispersants or emulsifiers. However, concentrates consisting of active substance, wetting agent, tackifier, dispersant or emulsifier and possible solvent or oil can also beprepared, which are suitable for dilution with water.

Suitable surface-active substances are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkylsulfates,alkylsulfonates, fatty alcohol sulfates and fatty acids and their alkali metal and alkaline earth metal salts, salts of sulfated fatty alcohol glycol ether, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde,condensation products of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ether, tributylphenyl polyglycol ether,alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ether, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin-sulfite wasteliquors and methylcellulose.

Powders, scattering compositions and dusts can be prepared by mixing or joint grinding of the active substances with a solid carrier.

The formulations in general contain from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound. The active compounds are employed here in a purity of from 90% to 100% , preferably 95% to 100% (according to NMRspectrum).

Examples of formulations are:

I. 5 parts by weight of a compound according to the invention are intimately mixed with 95 parts by weight of finely divided kaolin. A dust which contains 5% by weight of the active compound is obtained in this way.

II. 30 parts by weight of a compound according to the invention are intimately mixed with a mixture of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed on the surface of this silica gel. Apreparation of the active compound having good adhesion is obtained in this way (active compound content 23% by weight).

III. 10 parts by weight of a compound according to the invention are dissolved in a mixture which consists of 90 parts by weight of xylene, 6 parts by weight of the addition product of 8 to 10 mol of ethylene oxide to 1 mol of oleic acidN-monoethanolamide, 2 parts by weight of calcium salt of dodecylbenzenesulfonic acid and 2 parts by weight of the addition product of 40 mol of ethylene oxide to 1 mol of castor oil (active compound content 9% by weight). IV. 20 parts by weight of acompound according to the invention are dissolved in a mixture which consists of 60 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 5 parts by weight of the addition product of 7 mol of ethylene oxide to 1 mol of isooctylphenol and 5parts by weight of the addition product of 40 mol of ethylene oxide to 1 mol of castor oil (active compound content 16% by weight). V. 80 parts by weight of a compound according to the invention are well mixed with 3 parts by weight of the sodium saltof diisobutylnaphthalene-alpha-sulfonic acid, 10 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 7 parts by weight of powdered silica gel and the mixture is ground in a hammer mill (active compound content 80%by weight). VI. 90 parts by weight of a compound according to the invention are mixed with 10 parts by weight of N-methyl-.alpha.-pyrrolidone and a solution is obtained which is suitable for application in the form of very small drops (active compoundcontent 90% by weight). VII. 20 parts by weight of a compound .[.No. 11.]. according to the invention are dissolved in a mixture which consists of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of theaddition product of 7 mol of ethylene oxide to 1 mol of isooctylphenol and 10 parts by weight of the addition product of 40 mol of ethylene oxide to 1 mol of castor oil. By pouring the solution into and finely dispersing it in 100,000 parts by weight ofwater, an aqueous dispersion is obtained which contains 0.02% by weight of the active compound. VIII. 20 parts by weight of a compound according to the invention are well mixed with 3 parts by weight of the sodium salt ofdiisobutylnaphthalene-.alpha.-sulfonic acid, 17 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 60 parts by weight of powdered silica gel and the mixture is ground in a hammer mill. By finely dispersing themixture in 20,000 parts by weight of water, a spray liquor is obtained which contains 0.1% by weight of the active compound.

Granules, eg. coated, impregnated and homogeneous granules, can be produced by binding the active compounds to solid carriers. Solid carriers are eg. mineral earths, such as silica gel, silicic acids, .[.silica gels [sic].]. silicates, talc,kaolin, attapulgite, limestone, lime chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate and magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as eg. ammonium sulfate, ammonium phosphate, ammoniumnitrate, ureas and vegetable products, such as grain meal, tree bark, wood and nut shell meal, cellulose powder and other solid carrier.

Oils of various types, herbicides, fungicides, other pesticides and bactericides can be added to the active compounds, if appropriate even only immediately before application (tank mix). These agents can be admixed to the compositions accordingto the invention in the weight ratio 1:10-10:1.

SYNTHESIS EXAMPLES

The procedures presented in the synthesis examples below were utilized with appropriate modification of the starting compounds to obtain further compounds I. The compounds thus obtained are shown in the following tables with physical data.

Example 1

Preparation of methyl (E,E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-acetyl)iminooxymethyl]phenylacetate

21 g (0.21 mol) of diacetyl monoxime are added under protective gas and with slight cooling at room temperature to 6.4 g (0.21 mol) of sodium hydride (80%) in 150 ml of dry dimethylformamide and the mixture is stirred for 30 min at roomtemperature. A solution of 60 g (0.21 mol) of methyl 2-methoxyimino-2-(2'bromomethyl)phenylacetate in 360 ml of dimethylformamide is then added dropwise and the mixture is stirred at room temperature for 16 h. After addition of 10% strength hydrochloricacid, it is extracted with methyl tert-butyl ether. The combined organic phases are washed with water, dried over Na.sub.2 SO.sub.4 and concentrated. The residue is suspended in a little cold methanol. After filtering off with suction, 38 g (59%) ofthe title compound are obtained as light brown crystals having a melting point of 69-71.degree. C.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.87(s,3H); 2.30(s,3H); 3.85(s,3H); 4.05(s,3H); 5.15(s,2H); 7.17-7.48(m,4H) ppm.

Example 2

Preparation of methyl (E,E,E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'"-ethoxyiminoethyl)) iminooxymethyl]phenylacetate

0.96 g (9.8 mmol) of O-ethylhydroxylamine hydrochloride and 0.6 g of dry molecular sieve beads (3 A) are added to a solution of 2.5 g (8.2 mmol) of methyl (E,E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-acetyl) iminooxymethyl]phenylacetate in 60 ml ofwarm methanol after cooling to room temperature and the mixture is allowed to stand at room temperature for 5 days. After filtering off the molecular sieve, the solution is concentrated, the residue is partitioned between methyl tert-butyl ether andwater, and the organic phase is washed with water, dried over Na.sub.2 SO.sub.4 and concentrated. After triturating the residue with n-hexane and filtering off with suction, 1.8 g (63%) of the title compound are obtained as pale yellow crystals having amelting point of 69-72.degree. C.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.27(t,3H); 1.96(s,3H); 1.99(s,3H); 3.84(s,3H); 4.04(s,3H); 4.17(q,2H); 5.06(s,2H); 7.17-7.49 (m,4H) ppm

Example 3

Preparation of (E,E,E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'"-ethoxyiminoethyl))iminooxymethyl] phenylacetic acid monomethylamide

0.90 g (2.60 mmol) of methyl (E,E,E)-2-methoxyimino-2-[2'-(1"-methyl,1"-ethoxyiminoethyl)) iminooxymethyl]-phenylacetate is dissolved in 50 ml of tetrahydrofuran, treated with 2.0 g of 40% strength aqueous monomethylamine solution and stirred atroom temperature for 16 h. The mixture is then treated with water and extracted with methyl tert-butyl ether, and the organic phase is washed with water, dried over Na.sub.2 SO.sub.4 and concentrated on a rotary evaporator. As a residue, 0.80 g (89%) ofthe title compound remains as a pale yellow oil.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.28(t,3H); 1.97(s,3H); 1.99(s,3H); 2.90(d,3H); 3.96(s,3H); 4.18(g,2H); 5.07(s,2H); 6.74(br, 1H); 7.17-7.48(m,4H) ppm.

Example 4

Preparation of 4-hydroxyimino-2,2-dimethylpentan-3-one

A solution of 40 g of hydrogen chloride in 156 g of diethyl ether is added dropwise at room temperature to 96 g (0.84 mol) of 2,2-dimethyl-3-pentanone in 960 g of toluene. After cooling to -10.degree. C., a solution of 95g of n-butyl nitrite in470 g of diethyl ether is added dropwise. The mixture is stirred at from -10.degree. C. to 0.degree. C. for 4 hours and then allowed to come to room temperature. After a total of 16 h, the reaction mixture is washed three times with 1 l of ice-watereach time and then extracted twice with 1 l of 1M sodium hydroxide solution each time. The alkaline phase is separated off and neutralized with 20% strength sulfuric acid. The crude product is filtered off with suction and, after drying, recrystallizedfrom n-hexane. 66 g (55%) of the title compound are obtained as a pale yellow powder of melting point 107-110.degree. C.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.29(s,9H); 1.99(s,3H); 8.30(s, 1H) ppm

Example 5

Preparation of methyl (E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'",1'"-dimethylethylcarbonyl)) iminooxymethyl]phenylacetate

25 g (0.17 mol) of 4-hydroxyimino-2,2-dimethylpentan-3-one are added in portions under protective gas to 6.4 g (0.21 mol) of sodium hydride (80%) in 150 ml of dry dimethylformamide, the reaction mixture warming to 50.degree. C. Stirring iscontinued for 30 min, then a solution of 50 g (0.17 mol) of methyl 2-methoxyimino-2-(2'-bromomethyl)phenylacetate in 300 ml of dimethylformamide is added dropwise and the mixture is stirred at room temperature for 16 h. After addition of 10% strengthhydrochloric acid, it is extracted with methyl tert-butyl ether. The combined organic phases are washed with water, dried over .[.Na.sub.2 SO.sub.2 [sic].]. .Iadd.Na.sub.2 SO.sub.4 .Iaddend.and concentrated. The black oily residue is purified bycolumn chromatography on silica gel (methyl tert-butyl ether/n-hexane) and the .[.tube [sic].]. .Iadd.crude .Iaddend.product thus obtained is suspended in ice-cold methanol. After filtering off with suction, 24 g (41%) of the title compound areobtained as an almost colorless powder of melting point 58-62.degree. C.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.19(s,9H); 1.90(s,3H); 3.83(s,3H); 4.04(s,3H); 5.11(s,2H); 7.18-7.45(m,4H) ppm.

Example 6

Preparation of methyl (E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'"-(6""-(4'""-chlorophenyl) hexyloxyimino), 2'",2'"-dimethylpropyl)) iminooxymethyl]phenylacetate

5.9 g (26 mmol) of O-6-(4'-chlorophenyl) hexylhydroxylamine, 3.6 g of dry molecular sieze beads (3 A) and 1.6 g (8.6 mmol) of p-toluenesulfonic acid hydrate are added to a solution of 3.0 g (8.6 mmol) of methyl(E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'", 1'"-dimethylethylcarbonyl))iminooxymethyl]phenylacetate in 60 ml of warm methanol after cooling to room temperature and the mixture is refluxed for 3 h. After filtering off the molecular sieve, the solutionis concentrated, the residue is partitioned between methyl tert-butyl ether and water, and the organic phase is washed with water, dried over Na.sub.2 SO.sub.4 and concentrated. After column chromatography on silica gel (hexane/methyl tert-butyl ether),3.8 g (79%) of the title compound are obtained as a pale yellow oil.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.09(s,9H); 1.26-1.42(m,4H); 1.52-1.67(m,4H); 1.90(s,3H); 2.57(t,2H); 3.84(s,3H): 3.99 (t,2H); 4.03(s,3H); 5.02(s,2H); 7.07-7.47(m,8H) ppm.

Example 7

Preparation of (E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'"-(6""-(4'""-chlorophenyl) hexyloxyimino), 2'", 2'"-dimethylpropyl)) iminooxymethyl]phenylacetic acid monomethylamide

2.8 g (5.0 mmol) of methyl (E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'"-(6""-(4'""-chlorophenyl) hexyloxyimino), 2'", 2'"-dimethylpropyl)iminooxymethyl] phenylacetate are dissolved in 10 ml of tetrahydrofuran, treated with 3.9 g of 40% strengthaqueous monomethylamine solution and stirred at room temperature for 16 h. The mixture is then treated with water and extracted with methyl tert-butyl ether, and the organic phase is washed with water, dried over Na.sub.2 SO.sub.4 and concentrated on arotary evaporator. As a residue, 2.3 g (82%) of the title compound remain as a colorless oil.

.sup.1 H-NMR (CDCl.sub.3):.delta.=1.08(s,9H); 1.26-1.41(m,4H); 1.53-1.67(m,4H); 1.89(s,3H); 2.56(t,2H); 2.87(d,3H); 3.93 (s,3H); 3.99(t,2H); 5.02(s,2H); 6.74(s,broad,1H); 7.05-7.45 (m,8H) ppm.

Example 8

Preparation of (E)-2-methoxyimino-2-[2'-(1"-methyl, 1"(1'"-methoxyimino, 1'"paramethoxyphenyl)methyl)iminooxymethyl] phenylacetic acid monomethylthioamide (Cpd. II.01, Table II)

1.9 g (4.5 mmol) of (E)-2-methoxyimino-2-[2'-(1"-methyl, 1"(1'"-methoxyimino, 1'"paramethoxyphenyl) methyl)iminooxymethyl]phenylacetic acid monomethylamide are dissolved in 80 ml of xylene, treated with 1.8 g (4.5 mmol) of Lawesson's reagent andstirred at 100.degree. C. for 45 min.

The reaction solution is concentrated and the residue is purified by column chromatography.

1.5 g (75%) of the title compound are isolated as an isomer mixture in the form of a yellowish oil.

IR [cm.sup.-1 ] Film: 834, 977, 1027, 1065, 1175, 1251, 1358, 1512, 1608, 2936, 3330

Example 9

Isomerization of .[.(E)-2-methoxyimono-2-[2'-(1"-methyl, 1"-(1'"-(Z/E)methoxyimino [sic].]. .Iadd.(E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1"'-(Z/E)methoxyimino.Iaddend., 1'"-phenyl)methyl)-(E)-iminooxymethyl]phenylacetic acid monomethylamide to(E)-2-methoxyimino-2-[2'-(1"-methyl, 1"-(1'"-(E)-methoxyimino, .[.[sic].]. , 1'"-phenyl)methyl]-(E)-iminooxymethyl]phenylacetic acid monomethylamide:

5 g of E,E,E/E,Z,E isomer mixture (30:70) are dissolved in 50 ml of methanol, treated with 15 ml of methanol saturated with HCl and allowed to stand at room temperature for 18 hours. The reaction solution is added to ice-water and extracted withdichloromethane, and the extract is dried over Na.sub.2 SO.sub.4. After concentrating on the rotary evaporator, 5 g of an oil (E,E,E:E,Z,E, approx. 65:35) are obtained. The desired (E,E,E)-isomer crystallizes on addition of methanol (2.1 g=42%) in theform of a colorless solid.

M.p. (E,E,E-isomer): 134-136.degree. C.

Note: The filtrate can be isomerized again using methanol HCl.

TABLE I ##STR24## No. R.sub.m.sup.2 R.sup.3 R.sup.4 R.sup.5 Data I.01 H CH.sub.3 CH.sub.3 H m.p.: 135-138.degree. C. I.02 H CH.sub.3 CH.sub.3 CH.sub.3 m.p.: 78-82.degree. C. I.03 H CH.sub.3 CH.sub.3 C.sub.2 H.sub.5 oil. IR (Film): 3350, 2975, 2937, 1669, 1526, 1366, 1092, 1039, 980, 920, 899 I.04 H CH.sub.3 CH.sub.3 i-C.sub.3 H.sub.7 oil; .sup.1 H-NMR(CDCl.sub.3)I; .delta.= 1.26(d, 6H) 1.95(s, 3H); 2.0(s, 3H); 2.91(d, 3H); 3.96(s, 3H); 4.37(q, 1H); 5.06(s, 2H). 6.72(s,br, 1H); 7.17-7.59(m, 4H)ppm I.05 H CH.sub.3 CH.sub.3 n-C.sub.4 H.sub.9 m.p.: 89-93 C I.06 H CH.sub.3 CH.sub.3 i-C.sub.4 H.sub.9 oil; .sup.1 H-NMR((CDCl.sub.3): .delta.= 1.29(s, 9H); 1.94(s, 3H); 2.00(s, 3H); 2.99(d, 3H); 3.96(s, 3H); 5.06(s, 2H); 6.79(s, br, 1H); 7.17-747(m, 4H)ppm I.07 H CH.sub.3 CH.sub.3 n-C.sub.6 H.sub.13 m.p.: 83-85.degree. C. I.08 H CH.sub.3 CH.sub.3 CH.sub.2 CN m.p.: 92-96.degree. C. I.09 H CH.sub.3 CH.sub.3 CH.sub.2 CH.sub.2 CN m.p.: 92-96.degree. C. I.10 H CH.sub.3 CH.sub.3 3-Methyl- m.p.: 86-88.degree. C. but-2-en-1-yl I.11 H CH.sub.3 CH.sub.3 4-Cl--C.sub.6 H.sub.4 --CH.sub.2 m.p.: 152-154.degree. C. I.12 H CH.sub.3 CH.sub.3 2-Naphthryl-CH.sub.2 oil; .sup.1 H-NMR(CDCl.sub.3): .delta.= 1.98(s, 3H); 2.02(s, 3H); 2.87(d, 3H); 3.92(s, 3H); 5.06(s, 2H); 5.33(s, 2H); 6.79(s br, 1H); 7.17-7.88(m, 11H)ppm I.13 H CH.sub.3 CH3 6-(4'-Chloro- oil. .sup.1 H-NMR(CDCl.sub.3): .delta.= phenyl)hex-1-yl 1.27-1.70(m, 8H); 1.95(s, 3H); 1.98(s, 3H); 2.58(t-2H); 2.90(d, 3H); 3.95(s, 3H); 4.19(t, 2H); 5.06(s, 2H); 6.71(s, br, 3H); 7.08-7.46(m, 8H)ppm I.14 H CH.sub.3 CH.sub.3 3-CF.sub.3 --C.sub.6 H.sub.4 m.p.: 119-124.degree. C. I.15 H CH.sub.3 CH.sub.3 4-CF.sub.3.6-Cl-py-m.p.: 129-132.degree. C. rid-2-yl I.16 H CH.sub.3 CH.sub.3 4-CF.sub.3 -pyrid-2-yl m.p.: 144-147.degree. C. I.17 H CH.sub.3 CH.sub.3 (E)-1-Chloropro- m.p.: 96-98.degree. C. pen-3-yl I.18 H CH.sub.3 CH.sub.3 (E)-4-(4'- oil; .sup.1 H-NMR(CLCl.sub.3): Chlorophenyl)- 1.97(s, 6H); but-2-en-1-yl 2.90(d, 3H); 3.36(d, 2H); 3.96(s, 3H); 4.60(d, 2H); 5.06(s, 2H). 5.65-5.92(m, 2M); 7.68(s, br, 1H), 7.09-7.48(m, 8H)ppm I.19 H CH.sub.3 CH.sub.3 Propyn-3-yl m.p.: 106-109.degree.C. I.20 H CH.sub.3 CH.sub.3 2-Hydroxy- JR: 884, 929, 980, prop-1-yl 1036, 1092, 1366, 1529, 1665, 2937, 3370 I.21 H CH.sub.3 CH.sub.3 6-Hydroxy-2-me- 217-270.degree. C. thyl-pyrimi- din-4-ylmethyl I.22 H CH.sub.3 CH.sub.3 6-Hydroxy-2-iso- 219-221.degree. C. propyl-pyrimi- din-4-yhmethyl I.23 H CH.sub.3 CH.sub.3 6-Hydroxy-2-cy- 220-224.degree. C. clopropyl-pyn- midin-4-ylmethyl I.24 H CH.sub.3 CH.sub.3 5-(2'-Furan)- 57-61.degree. C. pent-1-yl I.25 H CH.sub.3 CH.sub.35-(2'-N-Methyl- 40-44.degree. C. pyrrol)-pent-1- yl I.26 H CH.sub.3 CH.sub.3 2-(4'-Chloro- 110-120.degree. C. phenyl)-oxazol- 4-ylmethyl I.27 H CH.sub.3 CH.sub.3 3-Trifluoro- 104-107.degree. C. methylpyrid-2-yl I.28 H CH.sub.3 CH.sub.35-Trifluoro- 126-130.degree. C. methylpyrid-2-yl I.29 H CH.sub.3 CH.sub.3 6-(2'-Thio- 694, 893, 980, 1037, phen)-hex-1-yl 1092, 1365, 1525, 1673, 2935, 3340, 3400 I.30 H CH.sub.3 t-C.sub.4 H.sub.9 H oil; .sup.1 H-NMR(CDCl.sub.3): .delta.= 1.10(s, 9H); 1.95(s, 3H); 2.88(d, 3H); 3.95(s, 3H); 5.05(s, 2H); 6.76(s, br, 1H); 7.17-7.47(m, 4H); 8.04(s, 1H)pm I.31 H CH.sub.3 t-C.sub.4 H.sub.9 CH.sub.3 oil, IR (Film): 3360, 2963, 2936, 1671, 1525, 1364, 1090, 1041, 979, 887 I.32 HCH.sub.3 t-C.sub.4 H.sub.9 C.sub.2 H.sub.5 oil; IR (Film): 3350, 2969, 2935, 1669, 1524, 1364, 1093, 1041, 978, 917, 883 I.33 H CH.sub.3 t-C.sub.4 H.sub.9 i-C.sub.3 H.sub.7 m,p.: 95-99.degree. C. I.34 H CH.sub.3 t-C.sub.4 H.sub.9 n-C.sub.4H.sub.9 oil; IR (Film): 3360, 2938, 2935, 2872, 1671, 1525, 1364, 1092, 1037, 979, 922 I.35 H CH.sub.3 t-C.sub.4 H.sub.9 i-C.sub.4 H.sub.9 m.p.: 89-92.degree. C. I.36 H CH.sub.3 t-C.sub.4 H.sub.9 n-C.sub.6 H.sub.13 oil; IR (Film). 3360,2956, 2933, 2870, 1675, 1525, 1364, 1093, 1039, 979, 918 I.37 H CH.sub.3 t-C.sub.4 H.sub.9 (E)-1-Chloro- oil: IR (Film): propen-3-yl 3319, 2966, 2935, 1673, 1526, 1365, 1091, 1037, 980, 918, 881 I.38 H CH.sub.3 t-C.sub.4 H.sub.9Propyn-3-yl oil; IR (Film): 3303, 2967, 2935, 1672, 1525, 1365, 1094, 1037, 1005, 979, 918 I.39 H CH.sub.3 t-C.sub.4 H.sub.9 3-Methyl- oil; IR (Film): but-2-en-1-yl 3360, 2968, 2935, 1675, 1525, 1364, 1093, 1038, 979, 919, 880 I.40 HCH.sub.3 t-C.sub.4 H.sub.9 2-Naphthyl-CH.sub.2 oil; IR (Film): 3361, 2966, 2935, 1675, 1523, 1364, 1037, 1002, 979, 929, 752 I.41 H CH.sub.3 t-C.sub.4 H.sub.9 4-Cl--C.sub.6 H.sub.4 --CH.sub.2 oil; IR (Film): 3360, 2970, 2945, 1677, 1525, 1492, 1365, 1090, 1038, 1014, 983, 919, 881 I.42 H CH.sub.3 t-C.sub.4 H.sub.9 (E)-4-(4'- oil; IR (Film): Chlorophenyl) 3360, 2967, 1676, but-2-en-1-yl 1525, 1491,

1365, 1093, 1037, 1015, 979, 919 I.43 H CH.sub.3 t-C.sub.4 H.sub.0 6(4'-Chloro- oil; IR (Film): phenyl)bex-1-yl 3360, 2934, 1679, 1524, 1492, 1364, 1092, 1038, 1015, 979 I.44 H CH.sub.3 i-C.sub.4 H.sub.9 3-CF.sub.3 --C.sub.6 H.sub.4oil; IR (Film): 3360, 2975, 1675, 1450, 1331, 1165, 1126, 1092, 1038, 980, 940, 926 I.45 H CH.sub.3 C.sub.6 H.sub.5 H m.p.: 165-167.degree. C. I.46 H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 m.p.: 134-136.degree. C. I.47 H CH.sub.3 C.sub.6 H.sub.5C.sub.2 H.sub.5 oil; IR (Film): 3340, 2938, 1674, 1526, 1445, 1091, 1037, 979. 925, 767, 694 I.48 H CH.sub.3 C.sub.6 H.sub.5 i-C.sub.3 H.sub.7 m.p.: 77-80.degree. C. I.49 H CH.sub.3 C.sub.4 H.sub.5 n-C.sub.4 H.sub.9 oil: IR (Film): 3340,2958, 2936, 1675, 1525, 1445, 1092, 1070, 1036, 979, 694 I.50 H CH.sub.3 C.sub.6 H.sub.5 4-Cl--C.sub.6 H.sub.4 --CH.sub.3 oil: IR (Film): 3340, 2937, 1675, 1522, 1492, 1445, 1091, 1036, 1012, 979, 918 I.51 H CH.sub.3 C.sub.6 H.sub.53-CF.sub.3 --C.sub.6 H.sub.4 oil; IR (Film): 3340, 2930, 1675, 1449, 1328, 1169, 1126, 1062, 1038, 979, 944, 697 I.52 H CH.sub.3 C.sub.6 H.sub.5 6-(4'-Chloro- oil; IR (Films): phenyl)hex-1-yl 3340, 2935, 2858, 1679, 1524, 1492, 1445, 1091, 1037, 1015, 939 I.53 H CH.sub.3 C.sub.6 H.sub.5 (E)-4-(4' oil; IR (Film): Chlorophenyl) 3347 2937, 1675, but-2-en-1-yl 1525, 1491, 1444, 1092, 1036, 1015, 978, 918 I.54 H C.sub.6 H.sub.5 C.sub.6 H.sub.5 CH.sub.3 m.p.; 60-65.degree. C. I.55 HC.sub.6 H.sub.5 C.sub.6 H.sub.5 C.sub.2 H.sub.5 m.p.: 45-48.degree. C. I.56 H C.sub.6 H.sub.5 C.sub.6 H.sub.5 nC.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 693, 766, 980, 1037, 1064, 1445, 1526, 1676, 2937, 2965, 3330, 3410 I.57 H C.sub.6H.sub.5 C.sub.6 H.sub.5 i-C.sub.3 H.sub.7 m.p.: 53-58.degree. C. I.58 H C.sub.6 H.sub.5 C.sub.6 H.sub.5 n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) 693, 766, 978, 1015, 1036, 1445, 1525, 1677, 2936, 2958, 3340, 3420 I.59 H C.sub.6 H.sub.5C.sub.6 H.sub.5 i-C.sub.4 H.sub.9 m.p. 45-50.degree. C. I.60 H C.sub.6 H.sub.5 C.sub.6 H.sub.5 n-C.sub.6 H.sub.13 oil, IR [cm.sup.-1 ](Film) 693, 766, 979, 1014, 1037, 1445, 1525, 1678, 2934, 2954, 3330, 3410 I.61 H C.sub.6 H.sub.5 C.sub.6H.sub.5 3-Methyl- oil, IR [cm.sup.-1 ](Film) but-2-en-1-yl 693, 766, 921, 979, 1037, 1445, 1493, 1526, 1675, 2937, 3330, 3410 I.62 H CH.sub.3 CH.sub.3 4-Phenyl- oil, IR [cm.sup.-1 ](Film) but-1-yl 700, 748, 894, 923, 979, 1037, 1365, 1524,1673, 2938, 3340, 3410 I.63 H CH.sub.3 CH.sub.3 4-Phenoxy- oil, IR [cm.sup.-1 ](Film) but-1-yl 755, 891, 980, 1037, 1245, 1498, 1525, 1600, 1674, 2939, 3350, 3410 I.64 H CH.sub.3 CH.sub.3 2-(2'-Fluoro- oil, IR [cm.sup.-1 ](Film) phenoxy)eth-1-yl 749, 889, 924, 979, 1037. 1260, 1366, 1517, 1524, 1673, 2937, 3349, 3410 I.65 H CH.sub.3 CH.sub.3 3-(2'-Fluoro- oil, IR [cm.sup.-1 ](Film) phenoxy)-prop-1- 749, 979, 1037, yl 124, 1260, 1280, 1366, 1517, 1524, 1675, 2930, 3340, 3420 I.66 H CH.sub.3 CH.sub.3 E-4-(2'-Fluoro- oil, IR [cm.sup.-1 ](Film) phenoxy)-but-1- 749, 891, 980, 1037, yl 1235, 1259, 1366, 1507, 1524, 1675, 2930, 3340, 3420 I.67 H CH.sub.3 CH.sub.3 6-(4'-Chloro- m.p.: 58-62.degree. C. phenoxy)-hex-1- yl I.68 H CH.sub.3 CH.sub.3 2-(4'-Chloro- oil, IR [cm.sup.-1 ](Film) phenoxy)-prop-1- 885, 979, 1007, 1037, yl 1091, 1241, 1366, 1490, 1525, 1674, 2930, 3310, 3420 I.69 H CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 --C.sub.2 H.sub.4 --O--C.sub.2 H.sub.4 -- oil, IR [cm.sup.-1 ](Film) 893, 920, 979, 1038, 1092, 1124, 1365, 1524, 1674, 2937, 3350, 3420 I.70 H CH.sub.3 CH.sub.3 E-4-(3'-Methoxy- oil, IR [cm.sup.-1 ](Film) phenyl)-but-3- 890, 978, 1038, 1156, m-1-yl 1365,1525, 1579, 1598, 1675, 2937, 3320, 3390 I.71 H CH.sub.3 CH, E-4-(4'-Fluoro- m.p., 77-81.degree. C. phenyl)-but-3- en-1-yl I.72 H CH.sub.3 CH.sub.3 (3-Bromoisox- oil, IR [cm.sup.-1 ](Film) azol-5-yl)- 769, 889, 904, 951, methyl 988, 1001, 1035, 1359, 1526, 1677, 3420 I.73 H CH.sub.3 CR13 (3-CF.sub.3 -isoxazol- IR [cm.sup.-1 ](KBr) 5-yl)-methyyl 769, 893, 987, 999, 1034, 1150, 1192, 1221, 1674, 3430 I.74 H CH.sub.3 CH.sub.3 (3-iso-Propylis- oil, IR [cm.sup.-1 ](Film) oxazol-yl)- 883, 900, 980, 1000, methyl 1036, 1366, 1525, 1673, 2937, 2968, 3340 I.75 H CH.sub.3 CH.sub.3 (3-Cyclopropyl oil, IR [cm.sup.-1 ](Film) isoxazol-5-yl)- 883, 907, 980, 1000, methyl 1036, 1366, 1434, 1526, 1608, 1673, 2930, 3340 I.76 H CH.sub.3 CH.sub.3 (3-iso-Propyl- oil, IR [cm.sup.-1 ](Film) 1,2,4-Oxadazol- 882, 979, 1019, 1037, 5-yl)-methyl 1091, 1366, 1525, 1674, 2938,

2972, 3340 I.77 H CH.sub.3 CH.sub.3 ##STR25## m.p.: 160-165.degree. C. I.78 H CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 m.p.: 121-325.degree. C. I.79 H CH.sub.3 4-OCH.sub.3 C.sub.6 H.sub.4 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 922, 979, 1036, 1091, 1176, 1252, 1512, 1608, 1675, 2937, 3340 I.80 H CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 979, 1037, 1067, 1176. 1252, 1512, 1608, 1676, 2936, 2965, 3350 I.81 H CH.sub.34-OCH.sub.3 --C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 977, 1037, 1122, 1174, 1252, 1512, 1605, 1676, 2937, 2974, 3340 I.82 H CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) 835, 978,1035, 1176, 1252, 1512, 1608, 1675, 2936, 2958, 3340 I.83 H CH.sub.3 4-OCH.sub.3 --C.sub.6 H.sub.4 t-C.sub.6 H.sub.9 oil, IR [cm.sup.-1 ](Film) 958, 979, 1036, 1174, 1191, 1253, 1364, 1513, 1609, 1678, 2930, 2970, 3420 I.84 H CH.sub.3C.sub.6 H.sub.5 ##STR26## m.p.: 120-124.degree. C. I.85 H CH.sub.3 C.sub.6 H.sub.5 3-Fluorobenzyl oil, IR [cm.sup.-1 ](Film) 695, 919, 979, 1002, 1036, 1447, 1488, 1525, 1591, 1676, 2920, 3330, 3410 I.86 H CH.sub.3 C.sub.6 H.sub.53-Bromobenzyl oil, IR [cm.sup.-1 ](Film) 696, 776, 979, 1002, 1036, 1069, 1092, 1445, 1524, 1676, 2920, 3330, 3401 I.87 H CH.sub.3 C.sub.6 H.sub.5 3-CF.sub.3 -Benzyl oil, IR [cm.sup.-1 ](Film) 979, 1003, 1036, 1074, 1125, 1166, 1231,1333, 1525, 1676, 2920, 3330 I.88 H CH.sub.3 C.sub.6 H.sub.5 4-Chlorophenyl m.p, 58-62.degree. C. I.89 H CH.sub.3 C.sub.6 H.sub.5 3,4-Dichloro- oil, IR [cm.sup.-1 ](Film) benzyl 693, 880, 919, 979, 1002, 1035, 1445, 1471, 1525, 1676, 2930,3340, 3423 I.90 H CH.sub.3 CH.sub.3 2-Methoxy- oil, IR [cm.sup.-1 ](Film) eth-1-yl 891, 919, 980, 1038, 1093, 1127, 1366, 1525, 1673, 2870, 2937, 3350 I.91 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 CH.sub.3 oil, IR [cm.sup.-1 ](Film) 875, 894, 979, 1012, 1037, 1991, 1491, 1525, 1674, 2890, 2938, 3340 I.92 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 924, 979, 1012, 1037, 1991, 1491, 1326, 1673, 2938, 2976, 3340 I.93 H CH.sub.3 4-Cl--C.sub.6 H.sub.4n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 979, 1012, 1038, 1067, 1192, 1491, 1525, 1675, 2937, 2967, 3340 I.94 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 977, 1016, 1038, 1091, 1121, 1370, 1490, 1525, 1675, 2931, 2975, 3340 I.95 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) 979, 1012, 1037, 1070, 1091, 1491, 1525, 1674, 2936, 2959, 3330 I.96 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 m.p.: 67-71.degree. C. I.97 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 oil, IR [cm.sup.-1 ](Film) 979, 1011, 1038, 1091, 1491, 1525, 1675, 2872, 2934, 2954, 3330 I.98 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 3-Methyl- oil, IR [cm.sup.-1 ](Film) but-2-en-1-yl 833, 878, 979, 1038, 1091, 1447, 1491, 1525, 1675, 2937, 3330 I.99 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 Propargyl m.p.: 109-114.degree. C. I.100 H CH.sub.3 4-F--C.sub.6 H.sub.4 CH.sub.3 m.p.: 130-132.degree. C. I.101 H CH.sub.34-F--C.sub.6 H.sub.4 C.sub.2 H.sub.5 m.p.: 105-110.degree. C. I.102 H CH.sub.3 4-F--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 840, 979, 1038, 1223, 1508, 1523, 1605, 1673, 2937, 2967, 3360 I.103 H CH.sub.3 4-F--C.sub.6H.sub.4 i-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 840, 978, 1038, 1122, 1158, 1224, 1509, 1525, 1675, 2930, 2975, 3340 I.104 H CH.sub.3 4-F--C.sub.6 H.sub.4 i-C.sub.4 H.sub.9 m.p.: 95-100.degree. C. I.105 H CH.sub.3 4-F--C.sub.6 H.sub.4n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) 840, 979, 1013, 1037, 1224, 1509, 1524, 1675, 2936, 2959, 3340 I.106 H CH.sub.3 4-F--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 oil, IR [cm.sup.-1 ](Film) 840, 979, 1011, 1038, 1225, 1509, 1524, 1605,1676, 2935, 3340 I.107 H CH.sub.3 4-F--C.sub.6 H.sub.4 3-Methyl- oil, IR [cm.sup.-1 ](Film) but-2-en-1-yl 841, 980, 3038, 1159, 1224, 1509, 1525, 1605, 1675, 2938, 3350 I.108 H CH.sub.3 4-F--C.sub.6 H.sub.4 Propargyl oil, IR [cm.sup.-1](Film) 841, 875, 980, 1005, 1035, 1222, 1509, 1525, 1602, 1674, 2110, 2930, 3250, 3340 I.109 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 3-iso-Propyl- oil, IR [cm.sup.-1 ](Film) 1,2,4-oxadiazol- 874, 980, 1011, 1038, 5-yl)-methyl 1092, 1491, 1523, 1588, 1676, 2940, 2973, 3350 I.110 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 Thiazol-4-yl- m.p.: 46-48.degree. C. methyl I.111 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 (3-iso-Propyl- oil, IR [cm.sup.-1 ](Film) isoxazol- 981, 909 1013,

1036, 5-yl)-methyl 1092, 491, 1526, 1675, 2938, 2968, 3340 I.112 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 (3-Bromo-isoxazol- m.p.: 46-49.degree. C. 5-yl)methyl I.113 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 (3-CF.sub.3 -isoxazol- oil, IR [cm.sup.-1](Film) 5-yl)-methyl 970, 980, 999, 1013, 1036, 1992 1155, 1190, 1491, 1671, 2940, 3340 I.114 H CH.sub.3 3-Cl--C.sub.6 H.sub.5 CH.sub.3 mp.: 117-120.degree. C. I.115 H CH.sub.3 C.sub.2 H.sub.5 CH.sub.3 m.p.: 74-77.degree. C. I.116 H CH.sub.3C.sub.2 H.sub.5 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 768, 926, 960, 975, 1021, 1041, 1053, 1654, 1671, 2970, 3296 I.117 H CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 CH.sub.3 oil, IR [cm.sup.-1 ](Film) 989, 1006, 1037, 1992, 1447, 1461, 1528, 1669, 2939, 3349 I.118 H CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 923, 954, 989, 1037, 1991, 1447, 1528, 1669, 2938, 2976, 3340 I.119 H CH.sub.3 4-CH.sub.3 --C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 911, 979, 1039, 1067, 1992, 1458, 1525, 1673, 2936, 2965, 3340 I.120 H CH.sub.3 3-Cl--C.sub.6 H.sub.4 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 924, 979, 1012, 1037, 1991, 1411, 1525, 1673, 2937, 2976, 3350 I.121 H CH.sub.3 3-Cl--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 917, 980, 1038, 1067, 1193, 1411, 1525, 1673, 2937, 2966, 3340 I.122 H CH.sub.3 3-Cl--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 979, 1038, 1993, 1121, 1370, 1412, 1526, 1673, 2937, 2975, 3340 I.123 H CH.sub.3 3-Cl--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) 882, 979, 1037, 1071, 1992, 1412, 1525, 1674, 2936, 2959, 3350 I.124 H CH.sub.3 3-Cl--C.sub.6 H.sub.43-Chloro- oil, IR [cm.sup.-1 ](Film) prop-2-en-1-yl 789, 880, 932, 980, 1006, 1037, 1992, 1412, 1525, 1675, 2930, 3420 I.125 H CH.sub.3 3-Cl--C.sub.6 H.sub.4 Propargyl oil, IR [cm.sup.-1 ](Film) 695, 885, 927, 981, 1006, 1033, 1992, 1412,1525, 1674, 2110, 2931, 3290 I.126 H CH.sub.3 2-Cl--C.sub.6 H.sub.4 CH.sub.3 m.p.: 160-162.degree. C. I.127 H CH.sub.3 2-Cl--C.sub.6 H.sub.4 C.sub.2 H.sub.5 m.p.: 125-127.degree. C. I.128 H CH.sub.3 2-Cl--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 m.p.: 102-103.degree. C. I.129 H CH.sub.3 3-CH.sub.3 -isox- CH.sub.3 oil, IR [cm.sup.-1 ](Film) azol-5-yl 3345, 2940, 1675, 1526, 1446, 1412, 1068, 1038, 979, 959, 897 I.130 H CH.sub.3 3-CH.sub.3 -isox- C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) azol-5-yl 3340, 2939, 1675, 1526, 1446, 1412, 1091, 1037, 980, 957, 921 I.131 H CH.sub.3 3-CH.sub.3 -isox- n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) azol-5-yl 3350, 2938, 1675, 1526, 1447, 1412, 1068, 1037, 1011, 980, 960 I.132 HCH.sub.3 3-CH.sub.3 -isox- 1-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) azol-5-yl 3345, 2977, 2938, 1675, 1527, 1412, 1371, 1119, 1037, 982, 949 I.133 H CH.sub.3 3-CH.sub.3 -isox- n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) azol-5-yl 3343,2959, 2937, 1676, 1526, 1447, 1412, 1071, 1036, 980, 951 I.134 H CH.sub.3 3-CH.sub.3 -isol- n-C.sub.6 H.sub.13 oil, IR [cm.sup.-1 ](Film) azol-5-yl 3340, 2935, 1676, 1526, 1447, 1412, 1092, 1037, 1016, 980, 951 I.135 H CH.sub.3 3-CH.sub.3-isox- Prop-1-en-3-yl oil, IR [cm.sup.-1 ](Film) azol-5-yl 3345, 2935, 1675, 1527, 1446, 1413, 1092, 036, 1014, 981, 942, 919 I.136 H CH.sub.3 3-CH.sub.3 -isox- (E)-1-Chloro- oil, IR [cm.sup.-1 ](Film) azol-5-yl prop-1-en-3-yl 3340, 2938, 1674, 1527, 1446, 1412, 1092, 1036, 1014, 981, 949 I.137 Cl CH.sub.3 CH.sub.3 CH.sub.3 m.p.: 120-122.degree. C. I.138 Cl CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 m.p.: 190-192.degree. C. I.139 Cl CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 1039, 1444, 1528, 1676, 2038, 3350 I.140 H SCH.sub.3 CH.sub.3 CH.sub.3 oil, IR [cm.sup.-1 ](Film) 3340, 1671, 1526, 1094, 1074, 1039, 1014, 980, 957, 877 I.141 H SCH.sub.3 CH.sub.3 C.sub.2 H.sub.5 oil, IR [cm.sup.-1](Film) 3335, 2936, 1672, 1526, 1442, 1411, 1365, 1092, 1039, 981, 884 I.142 H SCH.sub.3 CH.sub.3 n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 3340, 2965, 2936, 1672, 1526, 1365, 1094, 1064, 1037, 981, 960 I.143 H SCH.sub.7 CH.sub.3i-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 3340, 2958, 2935, 2871, 1672, 1526, 1436, 1365, 1093, 1037, 980 I.144 H SCH.sub.3 CH.sub.3 n-C.sub.6 H.sub.13 oil, IR [cm.sup.-1 ](Film) 3340, 2934, 2933, 28712, 1672, 1526, 115 1436, 1365, I(93. 1037, 980 I.145 H SCH.sub.3 CH.sub.3 Prop-1-en-3-yl oil, IR [cm.sup.-1 ](Film) 3340, 2935, 1672, 1526, 1412, 1094, 1036, 980, 959, 923, 871 I.146 H SCH.sub.3 CH.sub.3 3-CF.sub.3 C.sub.6 H.sub.4 --CH.sub.2 oil, IR [cm.sup.-1 ](Film) 3340, 2930,

1673, 1528, 1330, 1165, 1125, 1098, 1074, 1038, 982 I.147 H CH.sub.3 3-Pyridyl CH.sub.3 oil, IR [cm.sup.-1 ](Film) 3340, 2939, 1672, 1526, 1412, 1071, 1038, 1005, 979, 896, 873

TABLE II ##STR27## No. R.sub.m.sup.2 R.sup.3 R.sup.4 R.sup.5 Data II.01 H CH.sub.3 p-OCH.sub.3 -- CH.sub.3 oil, IR [cm.sup.-1 ](Film) C.sub.6 H.sub.4 834, 977, 1027, 1065, 1175, 1251, 1358, 1512, 1175, 1608, 2936, 3330 II.02 H CH.sub.3p-OCH.sub.3 -- n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) C.sub.6 H.sub.4 977, 1027, 1066, 1176, 1251, 1358, 1512, 1607, 2935, 2964, 3340 II.03 H CH.sub.3 p-OCH.sub.3 -- n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) C.sub.6 H.sub.4 834. 975,1027, 1175, 1252, 1359, 1512, 1607, 2934, 2957, 3340 II.04 H CH.sub.3 C.sub.6 H.sub.5 3-Fluror- m.p. 142-150.degree. C. benzyl II.05 H CH.sub.3 C.sub.6 H.sub.5 3-CF.sub.3 -- oil, IR [cm.sup.-1 ](Film) benzyl 701, 1027, 1073, 1100, 1125, 1166, 1201, 1329, 1361, 1519, 2320, 3340 II.06 H CH.sub.3 C.sub.6 H.sub.5 3,4- oil, IR [cm.sup.-1 ](Film) Dichloro- 694, 769, 877, 893, benzyl 975, 1028, 1357, 1471, 1519, 2935, 3340 II.07 H CH.sub.3 C.sub.6 H.sub.5 4-Chloro- m.p. 55-60.degree. C. phenyl II.08 H CH.sub.3 C.sub.6 H.sub.5 3-Bromo- oil, IR [cm.sup.-1 ](Film) benzyl 696, 773, 876, 893, 975, 1028, 1064, 1358, 1519, 2935, 3350 II.09 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 i-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 942, 974, 1027,1091, 1121, 1358, 1369, 1490, 1518, 2920, 2975, 3350 II.10 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.4 H.sub.9 oil, IR [cm.sup.-1 ](Film) 830, 976, 1027, 1091, 1358, 1490, 1518, 2934, 2958, 3350 II.11 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 t-C.sub.4H.sub.9 oil, IR [cm.sup.-1 ](Film) 894, 973, 1030, 1089, 1188, 1311, 1490, 1519, 2934, 2977, 3350 II.12 H CH.sub.3 4-Cl--C.sub.6 H.sub.4 n-C.sub.6 H.sub.13 oil, IR [cm.sup.-1 ](Film) 830, 977, 1027, 1091, 1357, 1490, 1518, 2871, 2932, 2954, 3350 II.13 H CH.sub.3 4-F--C.sub.6 H.sub.4 C.sub.2 H.sub.5 oil, IR [cm.sup.-1 ](Film) 841, 976, 1027, 1058, 1225, 1358, 1509, 2936, 2970, 3360 II.14 H CH.sub.3 4-F--C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 oil, IR [cm.sup.-1 ](Film) 840, 978, 1027, 1065 1225, 1359, 1508, 1604, 2936, 2966, 3360 II.15 H CH.sub.3 4-F--C.sub.6 H.sub.4 t-C.sub.4 H.sub.9 m.p 113-119.degree. C.

Examples of the action against harmful fungi:

It was possible to show the fungicidal action of the compounds of the general formula I by the following tests:

The active compounds were prepared as a 20% strength emulsion in a mixture of 70% by weight of cyclohexanone, 20% by weight of Nekanil.RTM. LN (Lutensol.RTM. AP6, wetting agent having emulsifying and dispersent action based on ethoxylatedalkylphenols) and 10% by weight of Emulphor.RTM. .[.{character pullout}.]. EL (Emulan.RTM. EL, emulsifier based on ethoxylated fatty alcohols) and correspondingly diluted to the desired concentration with water.

.[.1. [sic].]. Erysiphe graminis var. tritici

Leaves of wheat seedlings (Kanzler variety) were first treated with the aqueous preparation of the active compounds (containing 250 ppm). After about 24 h, the plants were dusted with spores of powdery mildew of wheat (Erysiphe graminis var. tritici). The plants treated in this way were then incubated for 7 days at 20-22.degree. C. and a relative atmospheric humidity of 75-80%. The extent of fungal development was then determined.

In this test, the plants treated with the compounds according to the invention showed an attack of 5% or less, the plants treated with a known active compound (compound No. 195, Table 3, EP-A 463 488) showed 25% attack and the untreated plantsshowed 70% attack.

In a corresponding test (wheat seedlings of the Kanzler variety, application rate 250 ppm), the plants were first infected and incubated and then treated with the active compounds. In this test, the plants treated with the compounds according tothe invention showed an attack of 5% or less and the untreated plants showed 60% attack.

Examples of the action against animal pests:

It was possible to show the insecticidal action of the compounds of the general formula I by the following tests:

The active compounds were prepared a) as a 0.1% strength solution in acetone or b) as a 10% strength emulsion in a mixture of 70% by weight of cyclohexanol, 20% by weight of Nekanil.RTM. LN (Lutensol.RTM. AP6, wetting agent having emulsifyingand dispersant action based on ethoxylatd alkylphenols) and 10% by weight of Emulphor.RTM. EL (Emuluan.RTM. EL, emulsifier based on ethoxylated fatty alcohols)

and correspondingly diluted to the desired concentration with acetone in the case of a) or with water in the case of b).

After termination of the tests, in each case the lowest concentration was determined at which the compounds still caused an 80-100% inhibition or mortality in comparison to untreated control tests (action threshold or minimum concentration).

Aphis fabae (black fly), contact action

Heavily infested dwarf beans (Vicia faba) were treated with the aqueous active compound preparation. The mortality rate was determined after 24 h.

In this test, the compounds I.68, I.69, I.70, I.71, I.81, I.86, I.94, I.97, I.103, I,105, I.106, II.12 and II.13 according to the invention showed action thresholds of 400 ppm or less.

Nephotettix cincticeps (green rice leaf hopper), contact action

Circular filters were treated with the aqueous active compound preparation and then occupied by 5 adult leaf hoppers. The mortality was assessed after 24 h.

In this test, the compounds I.02, I.04, I.10, I.17, I.24, I.29, I.46, I.47, I.48, I.52, I.55, I.74, I.75, I.78, I.79 and I.92 according to the invention showed action thresholds of 0.4 mg or less.

Prodenia litura (Egyptian cotton leaf worm), contact action

Filters treated with the aqueous active compound preparation were occupied by 5 caterpillars. The first assessment is carried out after 4 h. If at least one caterpillar is still living, a feed mixture is added. The mortality was determinedafter 24 h.

In this test, the compounds I.04, I.17, I.78, I.79, I.91, I.92, I.94, I.101, I.102, I.103 and I.108 according to the invention showed action thresholds of 0.4 mg or less.

Tetranychus telarius (common red spider mite), contact action

Potted dwarf beans having the second successive pair of leaves were treated with aqueous active compound preparation. After 24 h, the plants were infected using heavily infested pieces of leaf. The attack was determined after 12 days in thegreenhouse.

In this test, the compounds I.37, I.91, I.92, I.93, I.97, I.101, I.102, I.104, I.105, I.106, I.108, II.13, II.14 and II.15 showed action thresholds of 400 ppm or less.

* * * * *
 
 
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