http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001506581-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-24 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 |
| filingDate | 1997-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2001-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2001506581-A |
| titleOfInvention | 1-sulfonyl-3-phenylpyrazole |
| abstract | (57) Abstract: 1-sulfonyl-3-phenylpyrazole of formula I, and salts thereof. (Wherein R 1 ＣC 1 -C 4 alkyl, C 1 -C 4 haloalkyl, R 2 ＣC 1 -C 4 alkyl, C 1 -C 4 haloalkyl, R 3 ＨH, CN, halogen, C 1 -C 4 4 alkyl, R 4 = H, halogen, R 5 = H, CN, NO 2 , halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy , X = chemical bond, unsubstituted or substituted methylene, ethylene, propane-1,3-diyl, ethane-1,2-diyl chain, oxamethylene bonded to a phenyl ring via a hetero atom, thiamethylene chain R 6 = H, NO 2, CN, halogen, SO 2 - halogen, -O-Y-R 8 - , - O-CO-Y-R 8, -N (Y-R 8) (Z-R 9), - N (Y-R 8) -SO 2 -Z-R 9, -N (SO 2 -Y-R 8) (SO 2 -Z-R 9) -N (Y-R 8) -CO -Z-R 9, -N (Y-R 8) (O-Z-R 9), - S-Y-R 8 -, - SO-Z-R 8, —SO 2 —Y—R 8 , —SO 2 —O—Y—R 8 , —SO 2 —N (Y—R 8 ) (Z—R 9 ), —CO—Y—R 8 , and —C (= NOR 10) -Y-R 8, -C (= NOR 10) -O-Y-R 8, -CO-O-Y-R 8, -CO-S-Y-R 8, -CO-N (Y -R 8) (Z-R 9 ), - CO-N (Y-R 8) (O-Z-R 9), - PO (O-Y-R 8) 2, R 7 = H or R 5, + XR 6 or XR 6 + R 7 together with the carbon atom of the phenyl ring to which they are attached form a fused unsubstituted or substituted carbocyclic ring having 1 to 3 heteroatoms, a 5- or 6-membered heterocyclic ring, May have one, two CO, CS, SO 2 in the ring, Y and Z = chemical Binding ,, carboxyl, unsubstituted or substituted methylene refers to ethylene chain, R 8 and R 9 = H, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 - C 6 alkynyl, C 2 -C 6 haloalkynyl, -CH (R 11) (R 12), - C (R 11) (R 12) -NO 2, -C (R 11) (R 12) -CN, -C (R 11) (R 12 ) - halogen, -C (R 11) (R 12) -OR 13, -C (R 11) (R 12) -N (R 13) R 14, -C (R 11) (R 12) -N ( R 13) -OR 14, -C (R 11) (R 12) -SR 13, -C (R 11) (R 12) -SO-R 13, -C (R 11) (R 12) -SO 2 -R 13, -C (R 11) (R 12) -SO 2 -OR 13, -C (R 11) (R 12) -SO 2 -N (R 13) R 14 , -C (R 11 ) (R 12 ) -CO-R 13, -C (R 11) ( R 12) -C (= NOR 15) -R 13, -C (R 11) (R 12) -CO-OR 13, -C (R 11) (R 12) - CO-SR 13, -C (R 11) (R 12) -CO-N (R 13) R 14, -C (R 11) (R 12) -CO-N (R 13) OR 14, -C ( R 11 ) (R 12 ) -PO- (OR 13 ) 2 , unsubstituted or substituted C 3 -C 8 cycloalkyl optionally having CO or CS in the ring, or having CO or CS in the ring A 3- to 7-membered heterocyclic group, R 10 = H, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2- C 6 alkynyl, C 2 -C 6 haloalkynyl, C 3 -C 8 cycloalkyl, phenyl, phenyl -C 1 -C 4 alkyl, R 11 and R 12 = H, C 1 -C 4 alkyl, C 1 -C Four Alkoxy-C 1 -C 4 alkyl, C 1 -C 4 alkylthio-C 1 -C 4 alkyl, (C 1 -C 4 alkoxy) carbonyl-C 1 -C 4 alkyl, or unsubstituted or substituted phenyl-C 1- C 4 alkyl, R 13 and R 14 = hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkynyl, unsubstituted or substituted C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl -C 1 -C 4 alkyl, phenyl, phenyl -C 1 -C 4 alkyl, 3- to 7-membered Heterocyclic group or heterocyclyl-C 1 -C 4 alkyl (cycloalkyl and heterocyclic group may each have CO or CS in the ring), R 15 ＨH, C 1 -C 6 alkyl, C 1- C 6 haloalkyl, C 2 -C 6 Al Cycloalkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkynyl, C 3 -C 8 cycloalkyl, phenyl, phenyl -C 1 -C 4 alkyl. ) Uses: as herbicides, for drying / falling plants. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020080534-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021215480-A1 |
| priorityDate | 1996-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 435.