http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10500673-A
Outgoing Links
Predicate | Object |
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classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-65031 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N53-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6503 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N53-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 |
filingDate | 1995-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1998-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H10500673-A |
titleOfInvention | Substituted 3-phenylpyrazole |
abstract | (57) [Summary] Formula I Wherein R 1 is H, CN, NO 2 , halogen, alkyl, alkenyl, alkynyl, alkyl halide, alkenyl halide, alkynyl halide, cyanoalkyl, alkyl-OR 6 , alkyl-O-CO- R 6 , alkenyl-OR 6 alkynyl-OR 6 , alkyl-SR 6 , alkenyl-SR 6 , alkynyl-SR 6 , alkyl-SO-R 6 , alkenyl-SO-R 6 , alkynyl -SO-R 6, alkyl -SO 2 -R 6, alkenyl -SO 2 -R 6, alkynyl -SO 2 -R 6, -O-R 6, -S-R 6, -SO-R 6, —SO 2 —R 6 , —SO 2 —Cl, —SO 2 —O—R 6 , —SO 2 —N (R 7 , R 8 ), —N (R 7 , R 8 ), NH—CO—O -R 6, -O-CONH-R7 , -NH-CONH-R13, -O -CS-N (C1-C4-alkyl) 2, -OCS-NH2, -A-CO-O-R6, -AP (O) (OR6) 2, -O- (C1-C4-alkyl)- CO-OR6, - (alkyl) -O- (alkyl) -C (H / alkyl / phenyl / benzyl) = N-O-alkyl, isoxazolidinyl carbonyl, etc; R 2 is CN, CF 3 R 3 is H, C 1 -C 4 -alkyl, C 1 -C 4 -halogenated alkyl; R 4 is C 1 -C 4 -alkyl, C 1 -C 4 -halogenated alkyl R 5 is H, NO 2 , halogen, —COOR 29 or a substituted or unsubstituted aminocarbonyl; Z is —O—, —S—, —SO—, —SO 2 —; Bond, methylene, ethylene, 1,3-propylene, 1,4-butylene, It is Ren or 1,4-butadienylene; R 6, R 29 is H, C 1 ~C 8 - alkyl, C 1 -C 8 - alkyl halide, C 3 -C 6 - alkenyl, substituted or unsubstituted C 3 -C 7 - cycloalkyl or C 5 -C 7 - cycloalkyl, C 3 -C 6 - alkenyl halide, cyano -C 1 -C 8 - alkyl, C 3 -C 6 - alkynyl, C 1 -C 4 - alkoxy -C 1 -C 4 - alkyl, 2-tetrahydrofuryl -C 1 -C 8 - alkyl, 3-oxetanyl, 3-thietanyl, carboxyl -C 1 -C 6 - alkyl, C 1 -C 8 - alkoxycarbonyl - C 1 -C 6 - alkyl, C 1 -C 4 - alkoxy -C 1 -C 4 - alkoxycarbonyl -C 1 -C 6 - alkyl, cyclopropylmethyl, (1-methylthio) methyl, C 3 ~ C 9 - (alpha-alkyl-alkylidene) iminoxy -C 1 -C 6 - alkyl, C 1 -C 4 - alkylcarbonyl, alkoxy -, halogenated alkoxy -, alkenyloxy -, halogenated alkenyloxy - or aryl alkoxyiminoalkyl , substituted or unsubstituted phenyl, phenyl -C 1 -C 6 - alkyl, phenyl -C 2 -C 6 - alkenyl, phenyl -C 3 -C 6 - alkynyl, phenoxy -C 1 -C 6 - alkyl, heteroaryl, R 7 , R 8 , R 13 are H. Heteroaryl-C 1 -C 6 -alkyl, heteroaryl-C 3 -C 6 -alkenyl, heteroaryl-C 3 -C 6 -alkynyl or heteroaryloxy; , C 1 ~C 8 - alkyl, C 1 ~C 8 - alkyl halide, C 2 ~C 8 - alkenyl, C 2 -C 8 Alkynyl, C 1 -C 4 - alkoxy -C 1 -C 4 - alkyl, C 1 -C 4 - alkylthio -C 1 -C 4 - alkyl, cyano -C 1 -C 8 - alkyl, carboxyl -C 1 -C 4 - alkyl, C 1 -C 4 - alkoxycarbonyl -C 1 -C 4 - alkyl, C 1 -C 4 - alkylsulfonyl -C 1 -C 4 - alkyl, C 3 -C 8 - cycloalkyl, C 1 ~ C 6 - alkoxy, C 3 ~C 6 - cycloalkoxycarbonyl -C 1 -C 4 - alkyl, C 1 ~C 4 - alkoxy -C 1 -C 4 - alkoxycarbonyl -C 1 -C 4 - alkyl, C 1 -C 4 - alkylcarbonyl, C 1 -C 4 - alkyl halides carbonyl, tetrahydrofuran-2-onyl, substituted or unsubstituted phenyl, phenyl -C 1 -C 4 - alkyl, heteroaryl or het Roariru -C 1 -C 4 - alkyl, or R 7 and R 8 together, a substituted or unsubstituted tetramethylene, substituted 3-phenylpyrazole represented by a pentamethylene or ethyleneoxyethylene chain] And the agriculturally usable salts of I are used as herbicides. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9743667-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004536806-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9198433-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010523570-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8822521-B2 |
priorityDate | 1994-05-20-04:00^^<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: 341.