http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6150303-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 |
| filingDate | 1998-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2000-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | 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_4552b0207e1e027dc6e4179b4346b1bb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c70246e8d81eeb8c019c2e94d74d7584 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76c0e22fd61c0beef1a1ff9d7ee2a948 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95c19a681112f1501cf34507922c8d1a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39a4d6aa5d0db29b07698d9a94598564 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1de1d62ae5ee3e29e20518028490b83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8a1fd1e291fb6b077dff0ce40adabf0 |
| publicationDate | 2000-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-6150303-A |
| titleOfInvention | Substituted 3-phenylisoxazolines |
| abstract | PCT No. PCT/EP98/04489 Sec. 371 Date Jan. 21, 2000 Sec. 102(e) Date Jan. 21, 2000 PCT Filed Jul. 20, 1998 PCT Pub. No. WO99/05130 PCT Pub. Date Feb. 4, 1999Substituted 3-phenylisoxazolines I, and their salts and enol ethers, are described as herbicides where X=-O-, -S-, -N(R9)-; R1=CN, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylsulfonyl; R2=H or unsubstituted or substituted C1-C6-alkyl, (C1-C6-alkyl)carbonyl, C1-C6-alkylsulfonyl, C2-C6-alkenyl, (C2-C6-alkenyl)carbonyl, C2-C6-alkynyl, (C2-C6-alkynyl)carbonyl; R3=H, halogen; R4=CN, halogen, C1-C3-haloalkyl; R5=H, CN, halogen, C1-C3-haloalkyl; R6=H, CN, halogen, C1-C3-haloalkyl or unsubstituted or substituted C1-C6-alkoxy; R7=CN, halogen; R8 in position alpha , R7 in this case being in position beta , or in position beta , R7 in this case being in position alpha , is 1) H, OH, SH, CN, NO2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-haloalkylthio, C1-C6-alkylthio-(C1-C6-alkyl)carbonyl, (C1-C6-alkyl)iminooxycarbonyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxyamino-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkylamino-C1-C6-alkyl, 2) unsubstituted or substituted C1-C6-alkoxy, C1-C6-alkylthio, C3-C6-cycloalkoxy, C3-C6-cycloalkylthio, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkynyloxy, C2-C6-alkynylthio, (C1-C6-alkyl)carbonyloxy, (C1-C6-alkyl)carbonylthio, (C1-C6-alkoxy)carboxyloxy, (C2-C6-alkenyl)carbonyloxy, (C2-C6-alkenyl)carbonylthio, (C2-C6-alkynyl)carbonyloxy, (C2-C6-alkynyl)carbonylthio, C1-C6-alkylsulfonyloxy or C1-C6-alkylsulfonyl, 3) 29 further radicals; R9=H, C1-C6-alkyl, C3-C6-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl, (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, (C3-C6-alkenyloxy)carbonyl-C1-C6-alkyl, unsubstituted or substituted phenyl or phenyl-C1-C6-alkyl. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103596936-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9585392-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104797564-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104812739-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103596936-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008027059-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104797564-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019122393-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104812739-A |
| priorityDate | 1997-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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