http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2261615-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 |
filingDate | 1997-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76c0e22fd61c0beef1a1ff9d7ee2a948 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1de1d62ae5ee3e29e20518028490b83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c70246e8d81eeb8c019c2e94d74d7584 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4552b0207e1e027dc6e4179b4346b1bb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06816ca43df3db56f2a7d2e2f4157c8b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a704ea2b371a76ac39100b02af866026 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39a4d6aa5d0db29b07698d9a94598564 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8a1fd1e291fb6b077dff0ce40adabf0 |
publicationDate | 1998-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CA-2261615-A1 |
titleOfInvention | Substituted 3-phenyl pyrazoles |
abstract | Compounds having the formula (I) and their salts are useful as herbicides. In the formula {R1 = C1-C4-alkyl, halogenated C1-C4-alkyl, R2 = CN, C1-C4-alkyl, halogenated C1-C4-alkyl, C1-C4-alkoxy, halogenated C1-C4-alkoxy, C1-C4-alkylthio, halogenated C1-C4-alkylthio, C1-C4-alkylsulphinyl, halogenated C1-C4-alkylsulphinyl, C1-C4-alkylsulphonyl, halogenated C1-C4-alkylsulphonyl; R3 = H, CN, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl; R4 = H, halogen; R5 = CN, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl, C1-C4-alkoxy, halogenated C1-C4-alkoxy; R6, R7 = C1-C6-alkyl, halogenated C1-C6-alkyl, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, halogenated C1-C4-alkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-C1-C4-alkyl, amino-C1-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, halogenated C1-C4-alkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkinylthio-C1-C4-alkyl, C1-C4-alkylsulphinil-C1-C4-alkyl, halogenated C1-C4-alkylsulphinyl-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphonyl-C1-C4-alkyl, halogenated C1-C4-alkylsulphonyl-C1-C4-alkyl, C3-C4-alkenylsulphonyl-C1-C4-alkyl, C3-C4-alkinylsulphonyl-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, halogenated C3-C6-alkenyl, C3-C6-alkinyl, cyano-C3-C6-alkinyl, halogenated cyano-C3-C6-alkinyl, (C1-C4-alkyl)carbonyl, (halogenated C1-C4-alkyl)carbonyl, (C1-C4-alkoxy)carbonyl, H2N-CO, (C1-C4-alkyl)NH-CO; (C1-C4-alkyl)2N-CO, (C1-C4-alkoxy- C1-C4-alkyl)carbonyl, C1-C4-alkyl-SO2-, halogenated C1-C4-alkyl-SO2-, (C1-C4-alkyl)carbonyl- C1-C4-alkyl, (halogenated C1-C4-alkyl)-carbonyl- C1-C4-alkyl, (C3-C8-cycloalkyl)carbonyl- C1-C4-alkyl, (C1-C4-alkoxy)imino- C1-C4-alkyl, (C3-C4-alkenyloxy)imino- C1-C4-alkyl, hydroxycarbonyl- C1-C4-alkyl, optionally substituted (C1-C4-alkoxy)carbonyl- C1-C4-alkyl, (halogenated C1-C4-alkoxy)-carbonyl- C1-C4-alkyl, (C1-C4-alkylthio)carbonyl- C1-C4-alkyl, H2NCO- C1-C4-alkyl, (C1-C4-alkylamino)carbonyl- C1-C4-alkyl, di(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, optionally substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl- C1-C4-alkyl, phenyl, phenyl- C1-C4-alkyl, 3- to 7-membered heterocyclyl or heterocyclyl- C1-C4-alkyl, whereas all cycloalkyl or heterocyclyl rings may contain CO or Cs; X stands for a bond, -CC-, *-CH2-CH(R8)- or *-CH=C(R8)-(asterisk = bond with the phenyl ring; R8 = H, CN, NO2, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl); and Y = O, S} |
priorityDate | 1996-08-01-04:00^^<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: 405.