http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001506641-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-04 |
| filingDate | 1997-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2001-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2001506641-A |
| titleOfInvention | Substituted pyrazol-3-ylbenzoazole |
| abstract | (57) [Summary] A substituted pyrazol-3-ylbenzoazole represented by the formula and a salt thereof: [R 1 = hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl; R 2 = cyano, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 4 haloalkoxy, C 1 -C 4 alkylthio, C 1 -C 4 haloalkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 haloalkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 1 -C 4 haloalkylsulfonyl R 3 = hydrogen, cyano, nitro, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl: R 4 = hydrogen, halogen; R 5 = hydrogen, halogen, cyano, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy or C 1 -C 4 haloalkoxy; Z = nitrogen, -N = C (XR 6) that binds to α via an oxygen or sulfur -O- or -N = C (XR 6) -S-; X = reduction Bond, oxygen, sulfur, -S (O) -, - SO 2 -, - NH- or -N (R 7) -; R 6, R 7 = C 1 ~C 6 alkyl, C 1 -C 6 haloalkyl, cyano -C 1 -C 4 alkyl, hydroxy -C 1 -C 4 alkyl, C 3 -C 6 alkenyl, cyano -C 3 -C 6 alkenyl, C 3 -C 6 haloalkenyl, C 3 -C 6 alkynyl, cyano -C 3 -C 6 alkynyl, C 3 -C 6 haloalkynyl, C 1 -C 4 alkoxy -C 1 -C 4 alkyl, C 1 -C 4 haloalkoxy -C 1 -C 4 alkyl, C 3 -C 4 alkenyloxy -C 1 -C 4 alkyl, C 3 -C 4 alkynyloxy -C 1 -C 4 alkyl, C 3 -C 8 cycloalkyloxy -C 1 -C 4 alkyl, amino -C 1 -C 4 alkyl, C 1 -C 4 alkylamino -C 1 -C 4 alkyl, di (C 1 -C 4 alkyl) A Roh -C 1 -C 4 alkyl, C 1 -C 4 alkylthio -C 1 -C 4 alkyl, C 1 -C 4 haloalkylthio -C 1 -C 4 alkyl, C 3 -C 4 alkenylthio -C 1 -C 4 alkyl, C 3 -C 4 alkynylthio -C 1 -C 4 alkyl, C 1 -C 4 alkylsulfinyl -C 1 -C 4 alkyl, C 1 -C 4 haloalkylsulfinyl -C 1 -C 4 alkyl, C 3 -C 4 alkenylsulfinyl -C 1 -C 4 alkyl, C 3 -C 4 alkynylsulfinyl -C 1 -C 4 alkyl, C 1 -C 4 alkylsulfonyl -C 1 -C 4 alkyl, C 1 -C 4 haloalkylsulfonyl -C 1 -C 4 alkyl, C 3 -C 4 alkenylsulfonyl -C 1 -C 4 alkyl, C 3 -C 4 alkynylsulfonyl -C 1 -C 4 alkyl, hydroxycarbonyl -C 1 -C 4 alkyl, cyano Further (C 1 -C 4 alkoxy) may have a carbonyl group (C 1 -C 4 alkoxy) carbonyl -C 1 -C 4 alkyl, (C 1 ~C 4 alkylthio) carbonyl -C 1 -C 4 alkyl , aminocarbonyl -C 1 -C 4 alkyl, C 1 -C 4 alkylaminocarbonyl -C 1 -C 4 alkyl, di (C 1 -C 4 alkyl) aminocarbonyl -C 1 -C 4 alkyl, di (C 1 -C 4 alkyl) phosphonyl -C 1 -C 4 alkyl, (C 1 -C 4 alkoxy) imino -C 1 -C 4 alkyl, (C 3 -C 4 alkenyloxy) imino -C 1 -C 4 alkyl, or 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 heterocyclyl or heterocyclyl -C 1 -C 4 alkyl Represents One cycloalkyl and heterocyclyl ring may have a carbonyl or thiocarbonyl ring member; X is a chemical bond, oxygen, sulfur, -NH- or -N (R 7) - when referring to is, R 6 Represents (C 1 -C 4 alkyl) carbonyl, (C 1 -C 4 haloalkyl) carbonyl, (C 1 -C 4 alkoxy) carbonyl, C 1 -C 4 alkylsulfonyl or C 1 -C 4 haloalkylsulfonyl. Good; when X represents a chemical bond, R 6 is further hydrogen, cyano, mercapto, amino, halogen, —CH 2 —CH (halogen) —R 8 , —CH ＝ CH—R 8 or —CH ＝ C (halogen) -R 8 {R 8 = hydroxycarbonyl, (C 1 -C 4 alkoxy) carbonyl, (C 1 -C 4 alkylthio) carbonyl, aminocarbonyl, C 1 -C 4 alkylamino Cal Sulfonyl, di (C 1 -C 4 alkyl) aminocarbonyl or di (C 1 -C 4 alkyl) may represent a phosphonyl; or R 6 + R 7 = may have a substituent 1,3-propylene , Tetramethylene, pentamethylene or ethyleneoxyethylene chains] Uses: for herbicides, plant drying and / or defoliants. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005511758-A |
| priorityDate | 1996-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 449.