| Patent Number |
Title Of Patent |
Date Issued |
| 5712304 |
Carboxylic acid amide benzothiophenecarboxamide s-oxides |
January 27, 1998 |
| New benzothiophenecarboxamide S-oxides of the formula (I) ##STR1## in which R.sup.1 represents optionally substituted alkyl, or represents alkenyl or alkinyl, or represents in each case optionally substituted cycloalkyl or cycloalkylalkyl, or represents in each case optionally su |
| 5622546 |
Mould-resistant emulsion paints |
April 22, 1997 |
| The application relates to emulsion paints which are protected against fungal infestation by the use of N-alkyl-benzothiophene-2-carboxamide S,S-dioxides. |
| 5502069 |
1-thiocarbamoyl-5-hydroxy-pyrazoles as microbicides |
March 26, 1996 |
| 1-Thiocarbamoyl-5-hydroxy-pyrazoles have a microbicidal action and are therefore suitable for use for the preservation of materials. Since, in contrast to other microbicides, they are ecologically acceptable and do not discolour plastics, paints and paint films, they are particularly |
| 5385926 |
Microbicidal active compound combinations |
January 31, 1995 |
| New synergistic microbicidal active compound combinations, and the use thereof, comprising an azole fungicide, such as hexaconazole, and an iodopropargyl derivative, such as IPBC, if appropriate with the addition of other active compounds. |
| 5354777 |
Cyanoalkene derivatives, process for their preparation, and their use as microbicide for the pro |
October 11, 1994 |
| New cyanoalkene derivatives of the formula (I) ##STR1## are described, in which R and R.sup.1 have the meaning given in the description, and a process for their preparation.The new cyanoalkene derivatives are used for combating microorganisms for the protection of industrial material |
| 5332765 |
Microbicidal agents |
July 26, 1994 |
| There were described microbicidal agents for the protection of aqueous functional fluids which contain, as active substances, a combination of at least one iodopropargyl derivative and benzyl alcohol mono(poly)hemiformal. |
| 5292744 |
1-[pyri(mi)dyl-(2)]-5-hydroxy-pyrazole microbicides |
March 8, 1994 |
| The invention relates to the use of certain 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characterized by formula (I) given in the description, as microbicides for the protection of industrial materials, and to certain novel 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characte |
| 5200421 |
Microbicidal active compound combinations |
April 6, 1993 |
| New synergistic microbicidal active compound combinations, and the use thereof, comprising an azole fungicide, such as tebuconazole, and an iodopropargyl derivative, such as IPBC, if appropriate with the addition of other active compounds. |
| 5177090 |
Microbicidal agents |
January 5, 1993 |
| The invention relates to the use of 2,5-substituted 1,3,4-thiadiazoles of the formula ##STR1## in which R.sup.1 stands for straight-chain or branched halogenoalkyl,R.sup.2 stands for straight-chain or branched alkyl andn stands for the numbers 1 or 2,as microbicides for protecting indust |
| 5175176 |
1-[pyri(mi)dyl-(2)]-hydroxy-pyrazole microbicides |
December 29, 1992 |
| The invention relates to the use of certain 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characterized by formula (I) given in the description, as microbicides for the protection of industrial materials, and to certain novel 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characte |
| 5175169 |
Halogenovinyl-azole derivatives |
December 29, 1992 |
| New halogenovinyl-azole derivatives of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted cycloalkyl or optionally substituted aryl, or represents optionally substituted heteroaryl,R.sup.2 represents h |
| 5147443 |
Microbicidal agents |
September 15, 1992 |
| The invention relates to the use of 2,5-substituted 1,3,4-thiadiazoles of the formula ##STR1## in which R.sup.1 stands for straight-chain or branched halogenoalkyl,R.sup.2 stands for straight-chain or branched alkyl andn stands for the numbers 1 or 2,as microbicides for protecting indust |
| 5118702 |
Fungicidal and microbicidal substituted 1-aminomethyl-3-aryl-4-cyano-pyrroles |
June 2, 1992 |
| Fungicidal and microbicidal substituted 1-aminomethyl-3-aryl-4-cyano-pyrroles of the formula ##STR1## in which Ar represents optionally substituted phenyl,R.sup.1 represents optionally substituted alkyl, alkenyl, alkynyl or cycloalkyl or in each case optionally substituted aralkyl or |
| 5081140 |
Halogenovinyl-azole derivatives |
January 14, 1992 |
| New halogenovinyl-azole derivatives of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted cycloalkyl or optionally substituted aryl, or represents optionally substituted heteroaryl,R.sup.2 represents h |
| 5075326 |
Pesticidal 4-halogeno-5-nitrothiazoles |
December 24, 1991 |
| Fungicidal 4-halogeno-5-nitrothiazoles of the formula ##STR1## in which Hal represents halogen,A represents O, S, SO, SO.sub.2 or N--R.sup.1, whereinR and R.sup.1 each independently is hydrogen or an organic radical, or together withN form a heterocyclic ring,with the exception that R is |
| 5071865 |
Pesticidal 2-acylamino-4-halogeno-5-nitrothiazoles |
December 10, 1991 |
| Pesticidal 2-acylamino-4-halogeno-5-nitrothiazoles of the formula ##STR1## in which Hal represents halogen,x represents an integer 0 or 1,A represents O, S or N--R.sup.2, whereR.sup.2 represents hydrogen, alkyl, alkenyl, halogenoalkyl, cyanoalkyl or alkoxycarbonylalkyl, or represents cyc |
| 4966974 |
2-phenylsulphinyl-nitro-pyridines, and their use as fungicides |
October 30, 1990 |
| The invention relates to 2-phenylsulphinyl-nitro-pyridines of the formula ##STR1## in which R.sub.1 denotes hydrogen, alkyl or halogen andR.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 independently of one another represent hydrogen, halogen, alkyl, haloalkyl, alkyoxy, haloalkoxy, cyano, |
| 4962102 |
Pesticidal 4-halogeno-5-nitrothiazoles |
October 9, 1990 |
| Fungicidal 4-halogeno-5-nitrothiazoles of the formula ##STR1## in which Hal represents halogen,A represents O, S, SO, SO.sub.2 or N-R.sup.1, whereinR and R.sup.1 each independently is hydrogen or an organic radical, or together withN form a heterocyclic ring,with the exception that R is |
| 4879310 |
New cyanohydrin iodopropargyl ethers, process for their preparation and their use as microbicide |
November 7, 1989 |
| The invention relates to new cyanonhydrin iodopropargyl ethers of the formula ##STR1## in which R denotes C.sub.1 -C.sub.10 -alkyl, C.sub.2 -C.sub.10 -alkenyl, C.sub.5-C.sub.8 -cycloalkyl or -cycloalkenyl, which can be optionally substituted by C.sub.1 -C.sub.4 -alkyl or halogen, |
| 4855318 |
Iodopropargyl ethers useful as antimicrobial agents |
August 8, 1989 |
| Iodopropargyl ethers of the formula ##STR1## wherein A represents oxygen or a methylene group,R.sup.1 denotes hydrogen or lower alkyl,R.sup.2 and R.sup.3 are identical or different and represent hydrogen, lower alkyl, alkenyl or unsubstituted or halogen-substituted phenyl, or R.sup.2 |
| 4806540 |
1-heteroaryl-4-aryl-pyrazole microbicides |
February 21, 1989 |
| Novel microbicidally active 1-heteroaryl-4-arylpyrazole derivatives of the formulae (I) and/or (1A) ##STR1## in which R represents hydrogen or alkyl,R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, a radical --S(O).sub.p -alkyl which |
| 4798905 |
Sulphenylated carbamic acid esters, a process for their preparation and their use |
January 17, 1989 |
| The new sulphenylated carbamic acid esters of the formula ##STR1## in which R.sup.1 to R.sup.3 are identical or different and denote hydrogen, halogen, nitro, cyano, alkyl, alkoxy, alkylmercapto, trihalogenomethyl, trihalogenomethoxy or trihalogenomethylmercapto,R.sup.4 represents an |
| 4778511 |
Fluorine-containing N-sulphenylated indazoles for use as bactericides and fungicides |
October 18, 1988 |
| Novel fluorine-containing N-sulfenylated indazoles are prepared by reacting the corresponding indazoles with sulfenyl halides in the presence of a solvent and/or diluent and in the presence of an acid-binder. The novel fluorine-containing N-sulfenylated indazoles are useful in the protec |
| 4772608 |
1-heteroaryl-4-aryl-pyrazole microbicides |
September 20, 1988 |
| Novel microbicidally active 1-heteroaryl-4-aryl-pyrazole derivatives of the formulae (I) and/or (1A) ##STR1## in which R represents hydrogen or alkyl,R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, a radical--S(O).sub.p -alkyl which |
| 4767444 |
Herbicidal and microbiocidal 2-trifluoromethyl-benzimidazoles |
August 30, 1988 |
| The present invention relates to new 2-trifluoromethyl-benzimidazoles of the general formula (I) ##STR1## in which R.sup.1 represents halogenoalkyl,R.sup.2 represents optionally substituted alkyl orR.sup.1 and R.sup.2 together represent optionally substituted alkylene,R.sup.3 represents |
| 4764433 |
Agent for the protection of materials |
August 16, 1988 |
| An agent for the protection of material containing an N-sulphenylated benzenesulphonamide of the formula ##STR1## wherein R.sup.1, and R.sup.2 and R.sup.3 independently of one another represent hydrogen, halogen, nitro, alkyl or halogenoalkyl andR.sup.4 denotes an unsubstituted or su |
| 4719227 |
Iodopropargyl cyclic ethers useful as Microbicidal agents |
January 12, 1988 |
| Iodopropargyl ethers of the formula ##STR1## wherein A represents oxygen or a methylene group,R.sup.1 denotes hydrogen or lower alkyl,R.sup.2 and R.sup.3 are identical or different and represent hydrogen, lower alkyl, alkenyl or unsubstituted or halogen-substituted phenyl, or R.sup.2 |
| 4698357 |
2,4-dichloro-5-nitro-thiazole |
October 6, 1987 |
| The compound 2,4-dichloro-5-nitro-thiazole of the formula ##STR1## is microbicidally active. |
| 4686236 |
3-(3-iodopropargyloxy)-propionitrile, a process for its preparation and its use |
August 11, 1987 |
| 3-(3-iodopropargyloxy)-propionitrile of the formulais prepared by iodination of propargyloxypropionitrile. The 3-(3-iodopropargyloxy)-propionitrile is used as an active compound in microbicidal agents. |
| 4663327 |
1-heteroaryl-4-aryl-pyrazolin-5-ones |
May 5, 1987 |
| Microbicidally active novel 1-heteroaryl-4-aryl-pyrazolin-5-ones of the formula ##STR1## in which R represents hydrogen or alkyl,R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted phenoxy, a radical --S(O).sub |
| 4661632 |
Halogenopropargylformamide pesticides |
April 28, 1987 |
| Halogenopropargylformamides of the formula ##STR1## in which R is hydrogen, alkyl, halogenoalkyl, cycloalkyl, halogenoalkyl, cycloalkyl, alkenyl, alkinyl, halogenoalkinyl, optionally substituted aralkyl and optionally substituted aryl, andHal is halogen.which possess fungicidal and b |
| 4647687 |
Halogenated sulphides, process for their preparation and their use in microbicidal agents |
March 3, 1987 |
| The new halogenated sulphides of the formula ##STR1## in which R.sup.1 to R.sup.8 are identical or different and denote hydrogen or halogen, at least one of the radicals R.sup.1 to R.sup.8 representing halogen,and whereinR.sup.1 and R.sup.2, and/or R.sup.3 and R.sup.4 can optionally |
| 4645776 |
N-(dichlorofluoromethylthio)-3,4-dimethylmaleimide and its use as a fungicide |
February 24, 1987 |
| The new compound N-(dichlorofluoromethylthio)-3,4-dimethylmaleimide can be prepared by reacting 3,4-dimethylmaleimide with dichlorofluoromethanesulphenyl chloride in the presence of an acid-binding agent. N-(dichlorofluoromethylthio)-3,4-dimethylmaleimide is an active compound in mic |
| 4644000 |
Microbicidal agents containing 2-(1H-pyrazol-1-yl)-4-(3H)-quinazolinones |
February 17, 1987 |
| 2-(1H-pyrazol-1-yl)-4-(3H)-quinazolinones of the formula ##STR1## in which R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are identical or different and denote hydrogen, halogen, alkyl, alkoxy, hydroxyl or amino andR.sup.5 represents hydrogen or a cation,are active compounds in microbicidal agent |
| 4599427 |
Microbicidal azolylmethylamines |
July 8, 1986 |
| The new azolylmethylamines can be prepared by reaction of amines and azoles with formaldehyde. They can be used in microbicidal agents. |
| 4575517 |
Microbicidal agent for preserving industrial materials |
March 11, 1986 |
| Cyclopropylmethyl(ene) ethers have an outstanding action in microbicidal agents for preserving industrial materials from damage or destruction by microorganisms. |
| 4562208 |
N-Sulphenylated ureas, microbicidal agents containing these compounds and their use |
December 31, 1985 |
| The new N-sulphenylated ureas can be prepared by reaction of the corresponding N-substituted carbamic acid-fluorides and a primary or secondary amine in the presence of a diluent and an acid-binding agent. They have microbicidal properties and can be used in particular for the protec |
| 4547517 |
Microbicidal N-sulphenylated hydantoins |
October 15, 1985 |
| The new hydantoins of the formula ##STR1## in which R.sup.1 denotes an optionally substituted alkyl, alkenyl, cycloalkyl or aralkyl radical andR.sup.2 and R.sup.3 are identical or different and denote hydrogen, alkyl or alkenyl or are linked to form a cycloalkyl radical,can be prepar |
| 4545994 |
Trihaloallyl thiocyanates, a process for their preparation and their use in microbicidal agents |
October 8, 1985 |
| New trihaloallyl thiocyanates of the formula ##STR1## in which X and Y are identical or different and denote chlorine, bromine or iodine, can be prepared by reacting trihaloallyl compounds ##STR2## in which X and Y are identical or different and denote chlorine, bromine or io |
| 4532259 |
Bis[(fluoro- and chloro-methylthio)formamides], a process for their preparation and their use |
July 30, 1985 |
| The new bis[(fluoro- and chloro-methylthio)formamides] of the formula ##STR1## in which A.sup.1 and A.sup.2 are identical or different and represent the radical ##STR2## or the radical ##STR3## wherein R.sup.1 denotes an optionally halogenated lower alkyl or alkoxy r |
| 4521412 |
Pesticidal iodopropargylammonium salts |
June 4, 1985 |
| The present invention relates to iodopropargyl-ammonium salts of the formula (I) ##STR1## in which R, R.sup.1, R.sup.2 and X.sup..phi. have the meanings given in the description.They are obtained, for example, by reacting tertiary amines with an iodopropargyl halide. In a second |
| 4513003 |
Process for protecting wood using N-(dichlorofluoromethylthio)-3,6-endomethylene-.DELTA..sup.4 |
April 23, 1985 |
| The novel N-(dichlorofluoromethylthio)-3,6-endomethylene-.DELTA..sup.4 -tetrahydrophthalimides can be prepared from 3,6-endomethylene-.DELTA..sup.4 -tetrahydrophthalimide with dichlorofluoromethanesulphenyl chloride in the presence of an acid-binding agent in solution. They can be us |
| 4457930 |
Todopropargylsulphamides, microbicidal compositions and use |
July 3, 1984 |
| 3-Iodopropargyl-sulphamides of the formula ##STR1## in which R represents hydrogen, alkyl, optionally substituted cycloalkyl, optionally substituted phenylalkyl, optionally substituted heterocyclylalkyl or optionally substituted phenyl, andR.sup.1 and R.sup.2 are identical or differe |
| 4455309 |
Halomethyl-thioamino-benzamides, a process for their preparation and their use |
June 19, 1984 |
| New halo-methyl-thioamino-benzamides of the formula ##STR1## wherein X.sup.1 represents optionally substituted alkylene, arylene or alkarylene, it being possible for the alkylene and/or arylene and/or alkarylene groups to be linked via oxo, thio, carboxo, carboxamido or sulphoxo |
| 4427698 |
Use of N,N-dimethyl-N'-p-tolyl-N'-dichlorofluoromethylthio-sulphamide for combating fungi which |
January 24, 1984 |
| N,N-dimethyl-N'-p-tolyl-N'-dichlorofluoromethylthio-sulphamide and its use as an anti-fungal agent especially in preventing fungi damage to wood. |
| 4402980 |
Sulphonic acid cycloalkylamides and their use as microbicides |
September 6, 1983 |
| A N-sulphenylated sulphonic acid cyclohexylamide of the formula ##STR1## wherein R.sup.1 denotes lower alkyl, chloroalkyl or dialkylamino,R.sup.2 denotes a cycloalkyl radical which is optionally substituted by lower alkyl andX.sup.1, X.sup.2 and X.sup.3 are identical or different and rep |
| 4395274 |
Microbicidal agent and its use |
July 26, 1983 |
| Synergistic combinations of active compounds consisting of benzimidazolyl-alkyl-carbonates and (2,2'-dihydroxy-5,5'-dichlor)-diphenyl-methane or 2-hydroxy-diphenyl have a strong activity against micro-organisms. The combination can be employed e.g. for protecting industrial materials |
| 4344962 |
Sulphenylated acylurethanes and their use as fungicides |
August 17, 1982 |
| A sulphenylated acylurethane of the formula ##STR1## wherein R.sup.1 denotes hydrogen, halogen, nitro, alkyl, alkoxy or halogenomethyl,R.sup.2 denotes alkyl, alkenyl, alkinyl, cycloalkyl or aralkyl andX.sup.1, X.sup.2 and X.sup.3 are identical or different and denote halogen; a proce |
| 4228065 |
Microbiocidal organopolysiloxane molding compositions |
October 14, 1980 |
| An organopolysiloxane composition having a microbiocidal action comprising an .alpha.,.omega.-dihydroxypolydiorganosiloxane and a benzimidazolyl-alkyl-carbamate of the formula ##STR1## wherein R.sup.1 is an alkyl radical with 1 to 4 carbon atoms, optionally substituted by the rad |
| 4198428 |
Aryl-thiocarboxylic acid thiocyanomethyl esters |
April 15, 1980 |
| An aryl-thiocarboxylic acid thiocyanomethyl ester of the formula ##STR1## wherein R.sup.1 represents an optionally substituted aryl radical; a process for preparing the same, a pesticidal composition comprising such aryl-thiocarboxylic acid thiocyanomethyl ester and the use of such |
