| Patent Number |
Title Of Patent |
Date Issued |
| RE39607 |
Herbicidal sulphonylamino(thio) carbonyl compounds |
May 1, 2007 |
| The invention relates to novel sulphonylamino(thio) carbonyl compounds of the formula (I), ##STR00001## in which A represents a single bond, oxygen, sulphur or the group N--R, in which R represents hydrogen, alkyl, alkenyl, alkinyl or cycloalkyl, Q represents oxygen or sulphur, R.sup |
| RE32677 |
Polyamines, a process for the production of polyamines and their use in the production of polyur |
May 24, 1988 |
| The invention relates to a simplified, economic process for the production of polyamines by the alkaline hydrolysis of compounds containing terminal aromatic and/or aliphatic isocyanate groups (including modified isocyanates or NCO-prepolymers and semi-prepolymers with NCO-contents of |
| RE29224 |
Polyurethane urea elastomers based on polycarbonate macrodiols |
May 17, 1977 |
| Polyurethane urea elastomers with novel dissolution behavior and which are synthesized from polycarbonate macrodiols, diisocyanates and diamines and which can be prepared and dissolved in aqueous solvents.These elastomers have the advantage of being less of a physiological hazard, more r |
| 6686478 |
Thienylsulphonylamino(thio)carbonyl compounds |
February 3, 2004 |
| The invention relates to novel thienylsulphonylamino(thio)carbonyl compounds of the formula (I), ##STR1##in which Q represents oxygen or sulphur, R.sup.1 represents cyano, halogen or in each case optionally cyano-, halogen- or C.sub.1 -C.sub.4 -alkoxy-substituted alkyl, alkenyl, al |
| 6677277 |
Substituted sulphonyl amino(thio)carbonyl compounds and their use as herbicides |
January 13, 2004 |
| The invention relates to novel sulfonylamino(thio)carbonyl compounds of the formula (I), ##STR1##in which n represents the numbers 0, 1 or 2, A represents a single bond, or oxygen or sulfur, or the grouping N--R, in which R represents hydrogen, alkyl, alkenyl, alkinyl or cycloalkyl |
| 6566536 |
Thienylsulphonylamino(thio)carbonyl compounds |
May 20, 2003 |
| The invention relates to novel thienylsulphonylamino(thio)carbonyl compounds of the formula (I), ##STR1##in which Q represents oxygen or sulphur, R.sup.1 represents cyano, halogen or in each case optionally cyano-, halogen- or C.sub.1 -C.sub.4 -alkoxy-substituted alkyl, alkenyl, al |
| 6525211 |
Herbicidal sulphonylamino(thio)carbonyl compounds |
February 25, 2003 |
| The invention relates to novel sulphonylamino(thio)carbonyl compounds of the formula (I), ##STR1##in which A represents a single bond, oxygen, sulphur or the group N--R, in which R represents hydrogen, alkyl, alkenyl, alkinyl or cycloalkyl, Q represents oxygen or sulphur, R.sup. |
| 6403535 |
Substituted thiazol(in) ylideneamino sulfonylamino (thio)carbonyl-triazolinones |
June 11, 2002 |
| The invention relates to novel substituted thiazol(in)ylidenaminosulphonyl-amino(thio)carbonyl-triazolinones of the formula (I) ##STR1##in whichQ represents oxygen or sulphur,R.sup.1 represents hydrogen, amino, alkylideneamino or represents an in each case optionally substituted radi |
| 6383988 |
Thienysulfonylamino (thio) carbonyl compounds |
May 7, 2002 |
| The invention relates to novel thienylsulphonylamino(thio)carbonyl compounds of the formula (I), ##STR1##in whichQ represents oxygen or sulphur,R.sup.1 represents cyano, halogen or in each case optionally cyano-, halogen- or C.sub.1 -C.sub.4 -alkoxy-substituted alkyl, alkenyl, alkinyl, |
| 6251831 |
Herbicidal sulphonylamino(thio)carbonyl compounds |
June 26, 2001 |
| The invention relates to novel sulphonylamino(thio)carbonyl compounds of the formula (I), ##STR1##in whichA represents a single bond, oxygen, sulphur or the group N--R, in which R represents hydrogen, alkyl, alkenyl, alkinyl or cycloalkyl,Q represents oxygen or sulphur,R.sup.1 represents |
| 6210523 |
Compositions useful as binders for the production of composite materials |
April 3, 2001 |
| Compositions made up of an aromatic polyisocyanate and a polyester having an average molecular weight of from about 600 to about 5000, obtainable by self-condensation of ricinoleic acid, optionally with co-utilization of a C.sub.2 -C.sub.20 starter polyol and optional additives. These |
| 6200934 |
Substituted arylsulphonylamino(thio)carbonyl-triazolin(thi)ones as herbicides |
March 13, 2001 |
| The invention relates to novel substituted arylsulphonylamino(thio)carbonyl-triazolin(thi)ones of the formula (I) ##STR1##useful as herbicides. |
| 6200931 |
5,6-dihydro-(1,4,2)-Dioxazin-substituted (hetero) aryl-(oxy-, imino-, alkyl-)-sulphonylamino(thi |
March 13, 2001 |
| The invention relates to novel substituted sulphonylamino(thio)carbonyl compounds of the formula (I) ##STR1##in whichA represents a single bond, represents oxygen, imino (NH), alkanediyl (alkylene) or alkylimino (N-alkyl),J represents a (hetero)aryl grouping selected from the series phen |
| 6153761 |
Sulphonylaminocarbonyltriazolinones having halogenoalkylthio substituents |
November 28, 2000 |
| The invention relates to novel sulphonylaminocarbonyltriazolinones of the formula (I), ##STR1## in which R.sup.1 represents hydrogen, hydroxyl, amino, alkylideneamino or a respectively optionally substituted radical from the group consisting of alkyl, alkenyl, alkinyl, alkylamino |
| 6121204 |
Herbicidal or fungicidal sulphonylaminocarbonyltriazolinones with halogenated alk(en)oxy substit |
September 19, 2000 |
| The invention relates to novel sulphonylaminocarbonyltriazolinones having halogenoalkoxy substituents of the formula (I) ##STR1## in which R.sup.1 represents hydrogen, hydroxyl, amino, alkylideneamino or a respectively optionally substituted radical from the group consisting of a |
| 6054528 |
Aqueous coating adhesive and sealant compositions containing oxadiazolinones and polyamines |
April 25, 2000 |
| The present invention relates to aqueous compositions containinga) bis(1,3,4-oxadiazolin-5-ones) corresponding to formula (I) ##STR1## wherein R represents a single bond or a divalent aliphatic, araliphatic or aromatic radical having 1 to 18 carbon atoms andb) organic polyamines or polya |
| 6042133 |
Index shifter for bicycle transmissions |
March 28, 2000 |
| An index shifter for a bicycle transmission, which index shifter is mounted on a part of a bicycle and has a casing, a locking element with notches which is connected to a rotary hand grip, and a winding drum for actuating a cable pull. The casing has a ring-shaped recess disposed therei |
| 6001776 |
Herbicidal sulphonylamino(thio)carbonyl triazolin(thi)ones with heterocyclyl(alk)oxy substituent |
December 14, 1999 |
| The novel title compounds of the formula (I) ##STR1## in which Q.sup.1 represents oxygen or sulphur,Q.sup.2 represents oxygen or sulphur,R.sup.1 represents hydrogen, hydroxyl, amino or alkylideneamino or represents an in each case optionally substituted radical from the series consis |
| 5998538 |
Solvent-free, two-component polyurethane adhesive systems |
December 7, 1999 |
| The present invention relates to solvent-free two-component polyurethane adhesive systems with high initial strengths and low levels of migration derived from a select reactants comprising a hydroxyl polyester and an isocyanate containing prepolymer. |
| 5994273 |
Herbicidal or fungicidal sulphonylaminocarbonyltriazolinones with halogenated alk(en)ylthio subs |
November 30, 1999 |
| The invention relates to novel sulphonylaminocarbonyltriazolinones of the formula (I), ##STR1## in which R.sup.1 represents hydrogen, hydroxyl, amino, alkylideneamino or a respectively optionally substituted radical from the group consisting of alkyl, alkenyl, alkinyl, alkylamino |
| 5972844 |
Sulphonyl amino (thio) carbonyl-1,2,4-triazolin (thi) one derivatives and the use thereof as her |
October 26, 1999 |
| The invention relates to sulphonylamino(thio)carbonyl-triazolin(ethi)ones of the general formula (I) ##STR1## in which Q.sup.1 represents oxygen or sulphur,Q.sup.2 represents oxygen or sulphur,R.sup.1 represents hydrogen, hydroxyl, amino, alkylideneamino or a respectively optionally |
| 5917083 |
Process for the manufacture of allophanates having isocyanate groups |
June 29, 1999 |
| The present invention relates to a process for preparing an isocyanate group-containing allophanate corresponding to formula (I) ##STR1## wherein R represents the residue obtained by removing the isocyanate groups from a (cyclo)aliphatic or araliphatic diisocyanate,Y represents the r |
| 5892054 |
Process for the preparation of alkoxytriazolinones |
April 6, 1999 |
| Alkoxytriazolinones of the formula (I), ##STR1## in which R.sup.1 and R.sup.2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl,(which can be used as intermediates for the preparation of |
| 5869681 |
Herbicidal sulphonylaminocarbonyltriazolinones having substituents bonded via oxygen of the form |
February 9, 1999 |
| Herbicidal sulphonylaminocarbonyltriazolinones having substituents bonded via oxygen of the formula ##STR1## in which R.sup.1 represents hydrogen, amino, or an optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aralkyl, aryl, alkylamino, cycloalkylamino or dialkylamino r |
| 5861358 |
Substituted sulphonylaminocarbonyltriazolinones and their use as herbicides |
January 19, 1999 |
| The invention relates to novel substituted sulphonylaminocabonyltriazolinones of the formula (I), in which Q represents oxygen, sulphur or the grouping --N(R.sup.4)--, R.sup.3 represents aryl or arylalkyl which are in each case substituted at least twice, with one of the substituents |
| 5846383 |
Process for producing structurally resistant paper |
December 8, 1998 |
| Process for the production of structurally strong papers (or paper-like materials) which have a terminable strength by treatment of paper in the pulp or of finished paper in the surface with 0.0001 to 50% by weight, preferably 0.01-25% by weight (based on the pulp), of a mixture of i |
| 5834579 |
Tertiary amines having carbonate and urethane groups |
November 10, 1998 |
| Tertiary amines having carbonate and urethane groups and optionally hydroxyl groups are produced by reacting a) a polyhydric alcohol and b) a primary-tertiary diamine with c) a carbonic acid derivative selected from the group consisting of optionally cyclic carbonates, urea, phosgene and |
| 5750629 |
Uretdione diisocyanates and a process for their production |
May 12, 1998 |
| The present invention relates to a process for preparing pure bis(isocyanatoalkyl)monouretdiones corresponding to formula (I) ##STR1## wherein R represents identical or different, linear or branched alkyl groups having 4 to 9 carbon atoms,by oligomerizing at least a portion of the is |
| 5738197 |
Freewheel hub for bicycles |
April 14, 1998 |
| A freewheel hub for bicycles to provide propulsion by means of a plurality of sprockets when a derailleur is used. A sprocket or gear carrier transmits the rotational forces introduced to the sprockets mounted on the sprocket carrier by means of a drive sleeve, a ratchet and a pawl carri |
| 5710303 |
Process for the preparation of alkoxytriazolinones |
January 20, 1998 |
| Alkoxytriazolinones of the formula (I), ##STR1## are obtained in good yields and in high purity by reacting iminocarbonic diesters (II) with carbazinic esters (III) ##STR2## at -20.degree. C. to +120.degree. C. (1st step) and subjecting the semicarbazide derivatives (IV) form |
| 5710233 |
Polyurethane elastomers with reduced gas permeability |
January 20, 1998 |
| Polyurethane elastomers with reduced gas permeability are prepared by reaction of:a) diisocyanates,b) compounds with a molecular weight of 500 to 10,000 having at least two hydrogen atoms that are reactive towards isocyanates,c) compounds with a molecular weight of 61 to 499 having at least |
| 5705672 |
Tertiary amines having carbonate and urethane groups |
January 6, 1998 |
| Tertiary amines having carbonate and urethane groups and optionally hydroxyl groups are produced by reacting a) a polyhydric alcohol and b) a primary-tertiary diamine with c) a carbonic acid derivative selected from the group consisting of optionally cyclic carbonates, urea, phosgene and |
| 5705594 |
Polyamine crosslinking agent formulation and its preparation |
January 6, 1998 |
| Liquid polyamine crosslinking agent formulations based on trimerized toluylene 2,4- and/or 2,6-diisocyanate, with formation of an isocyanurate structure and hydrolysis of the isocyanate groups to amine groups, are described. The novel crosslinking agent formulations have a content of 40 |
| 5703260 |
Process for the preparation of alkoxytriazolinones |
December 30, 1997 |
| Alkoxytriazolinones of the general formula (I), ##STR1## in which R.sup.1 represents hydrogen, or represents in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, andR.sup.2 represents in each case optionally substituted alkyl, a |
| 5672713 |
Herbicidal and fungicidal substituted triazolinones |
September 30, 1997 |
| Herbicidal and fungicidal substituted triazolinones of the formula ##STR1## in which R.sup.1 represents hydrogen, alkyl, alkenyl, alkinyl, halogenoalkyl, halogenoalkenyl, halogenoalkinyl, alkoxyalkyl, cycloalkyl or cycloalkylalkyl, or represents tetrahydrofuranyl or tetrahydrofur |
| 5654438 |
Sulphonylaminocarbonyltriazolinones |
August 5, 1997 |
| The invention relates to new sulphonylaminocarbonyltriazolinones of the formula (I) ##STR1## in which Q represents oxygen, sulphur or one of the following groups ##STR2## (in which the radicals R.sup.1, R.sup.2, R.sup.3 and R.sup.4 have the meanings given in the description) |
| 5652372 |
Substituted 5-alkoxy-1,2,4-triazol-3-(THI) ones |
July 29, 1997 |
| Herbicidal 5-alkoxy-1,2,4-triazol-3-(thi)ones of the gerneral formula ##STR1## (in which the radicals R.sup.1, R.sup.2, R.sup.3, X and Y have the meanings given in the description),processes for their preparation, and their use as herbicides, and also new intermediates of the formula |
| 5631380 |
Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen |
May 20, 1997 |
| Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen, of the formula ##STR1## in which R.sup.1 represents hydrogen or an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl and aralkyl,R.s |
| 5625073 |
Herbicidal substituted triazolinones |
April 29, 1997 |
| Intermediates for herbicides, the intermediates having the formula ##STR1## in which R is i-propyl, n-butyl, i-buty, s-butyl or cyclopropyl. |
| 5621065 |
Polycarbonate diols, their preparation and use as starting products for polyurethane plastics |
April 15, 1997 |
| This invention relates to novel polycarbonates having hydroxyl end groups and an average molecular weight of 500 to 12,000, as determined by measuring the OH number, and being based on dimer diols containing either 36 or 44 carbon atoms. These novel polycarbonates are particularly su |
| 5612408 |
Polyurethane-based thickeners for aqueous compositions |
March 18, 1997 |
| The present invention relates to a process for the preparation of polyurethanes suitable for use as thickeners for aqueous compositions by reacting at an NCO/OH equivalent ratio of 0.9:1 to 1.2:1a) a polyether component having an OH number of 10 to 30 mg KOH/g and obtained by the alkoxyl |
| 5606070 |
Process for the preparation of alkoxytriazolinones |
February 25, 1997 |
| Alkoxytriazolinones of the general formula (I), ##STR1## in which R.sup.1 and R.sup.2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl,(which can be used as intermediates for the prepara |
| 5599945 |
Process for the preparation of alkoxytriazolinones |
February 4, 1997 |
| Alkoxytriazolinones of the formula (I), ##STR1## in which R.sup.1 and R.sup.2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl,(which can be used as intermediates for the preparation of |
| 5597939 |
Herbicidal sulphonylaminocarbonyltriazolinones having substituents bonded via oxygen of the form |
January 28, 1997 |
| R.sup.2 represents an optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aralkyl or aryl radical, andR.sup.3 represents an optionally substituted alkyl, aralkyl, aryl or heteroaryl radical,and salts thereof, with the exception of the compounds:2-(2-methoxycarbonyl-phen |
| 5594148 |
Process for the preparation of alkoxytriazolinones |
January 14, 1997 |
| Alkoxytriazolinones of the general formula (I), ##STR1## in which R.sup.1 and R.sup.2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl,(which can be used as intermediates for the prepara |
| 5594147 |
Process for the preparation of alkoxytriazolinones |
January 14, 1997 |
| Alkoxytriazolinones of the general formula (I), ##STR1## in which R.sup.1 represents hydrogen, or represents in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, andR.sup.2 represents in each case optionally substituted alkyl, a |
| 5594087 |
Polyurethane thickeners and their use for thickening aqueous systems |
January 14, 1997 |
| Water soluble or water dispersible polyurethane, which are suitable as thickeners for aqueous systems and prepared from a selected alcohol component a) based on a hydrophilic/hydrophobic mixture of alcohols and an isocyanate component b), and to their use for thickening aqueous systems. |
| 5554761 |
Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen |
September 10, 1996 |
| Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen, of the formula ##STR1## in which R.sup.1 represents hydrogen or an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl and aralkyl,R.s |
| 5552369 |
Sulphonylaminocarbonyltriazolinones |
September 3, 1996 |
| The invention relates to new sulphonylaminocarbonyltriazolinones of the formula (I) ##STR1## in which Q represents oxygen, sulphur or one of the following groups ##STR2## (in which the radicals R.sup.1, R.sup.2, R.sup.3 and R.sup.4 have the meanings given in the description) |
| 5541337 |
Substituted 5-alkoxy-1,2,4-triazol-3-(thi)ones |
July 30, 1996 |
| Herbicidal 5-alkoxy-1,2,4-triazol-3-(thi)ones of the gerneral formula ##STR1## (in which the radicals R.sup.1, R.sup.2, R.sup.3, X and Y have the meanings given in the description), processes for their preparation, and their use as herbicides, and also new intermediates of the formul |
