http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001518110-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 |
| filingDate | 1998-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2001-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2001518110-A |
| titleOfInvention | Pyrazole derivatives as herbicides |
| abstract | (57) [Summary] Formula I (Where W is R 11 is hydrogen, fluorine, chlorine, bromine or methyl; R 12 is hydrogen, halogen, methyl, halomethyl, nitro, amino, hydroxy, OHC—, HOC (O) —, cyano, C 1 —. C 1 alkoxycarbonyl or halomethoxy, X 1 is O, S, R 20 N— or R 25 ON =, and R 13 is hydroxy, C 1 -C 6 alkoxy, C 3 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy, C 1 -C 6 haloalkoxy, C 3 -C 6 haloalkenyloxy, C 1 -C 6 alkoxy -C 1 -C 6 alkyl, C 3 -C 6 alkenyloxy -C 1 -C 6 alkyl, C 3 -C 6 alkynyloxy -C 1 -C 6 alkyl, C 1 -C 6 alkoxy -C 1 -C 6 alkoxy -C 1 -C 6 alkyl, B 1 -C 1 -C 6 alkoxy, R 21 (R 22) N, C 1 -C 6 Alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 2 -C 6 haloalkyl, C 3 -C 6 haloalkenyl, C 3 -C 6 cycloalkyl, C 3 -C 6 halocycloalkyl, B 1 -C 1 -C 6 alkyl, OHC-, C 1 -C 6 alkylcarbonyl, C 1 -C 6 alkylcarbonyloxy, C 1 -C 6 haloalkylcarbonyl, C 2 -C 6 alkenylcarbonyl, C 1 -C 6 alkoxy carbonyl, C 1 -C 6 alkyl -S (O) 2 -, C 1 -C 6 haloalkyl -S (O) 2 -, ( C 1 -C 6 alkyl) 2 N-N = CH-, B 1 -CH = N -, ( CH 3) 2 N-CH = N -, (C 1 -C 5 hydroxyalkyl) -CH 2 -, (B 1 -C 1 -C 5 hydroxyalkyl) -CH 2 - , (B 1 -C 1 -C 5 haloalkyl) -CH 2 -, (hydroxy -C 1 -C 5 alkyl) -O- or (B 1 -C 1 -C 5 hydroxyalkyl) -O-, and or , X 1 and R 13 together are a = N—Y— group, where Y is attached to a ring nitrogen atom, and R 20 , R 21 , R 25 , B 1 and y The pyrazole N-oxides, the pesticidally acceptable salts and the stereoisomers of the compounds of the formula I have good selective herbicidal properties before and after germination. . The preparation of these compounds and their use as herbicidally active ingredients is described. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017528486-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020143112-A |
| priorityDate | 1997-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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