http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-20003987-A3

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filingDate 1999-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76c0e22fd61c0beef1a1ff9d7ee2a948
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publicationDate 2001-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-20003987-A3
titleOfInvention Substituted (4-bromopyrazol-3-yl) benzazoles
abstract Substituted (4-bromopyrazol-3-yl) benzazoles general -------nof formula I wherein R1 = H, C1-C4-alkyl, C1-C4-haloalkyl; R2 =nCN, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, CrC 4 -nhaloalkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkylthio, CrnC4-alkylsulfinyl, C1-C4-haloalkylsulfinyl, CrC4-nalkylsulfonyl, C 1 -C 4 -haloalkylsulfonyl; R4 = H, halogen;nR 5 = H, CN, halogen, C 1 -C 4 -alkyl, C 1 -C 4 haloalkyl, CrC 4 -nalkoxy or C1-C4-haloalkoxy; Z = -N = C (CR 6) -O- or -nN = C (XR 6) -S-, attached to and through nitrogen, oxygen or sulfur, wherenX = chemical bond, oxygen, sulfur, -S (O) -, -SO 2 -, -NH-, or -nN (R 7) and R 6 and R 7 have specific meanings. Their waynproduction and intermediates for their production and their salts.nThe compounds are used as herbicides, for examplendesiccation / defoliation of plants.
priorityDate 1999-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 401.