http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5452074-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f6e33603375c486b0ab3505830af9e8 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 |
| filingDate | 1977-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9082ca54ae9359a81b2be6721a82dc69 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_592035482fc97be221b36afc5816735e |
| publicationDate | 1979-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S5452074-A |
| titleOfInvention | Isoxazole derivative |
| abstract | NEW MATERIAL:Isoxazole derivative I (R 1 is H, halogen; R 2 is H, 1-4C alkyl, aryl; X is O, S, sulfonyl; Y is H, 1-3C alkyl, 3-5C alkenyl, 1-3C alkoxy, 1-3C alkylthio, 1-3C alkylsulfinyl, carboxyl, 2-4C alkoxycarbonyl, -R 3 COR 4 ; R 3 is 1-3C alkylene, R 4 is OH, etc.; n is 1-3). n EXAMPLE: 3-(2,4-Dinitrophenoxy)-5-methyl-isoxazole. n USE: Herbicide. n PROCESS: The compound IV which is one of the objective compound I, is prepared e.g. by reacting 3-hydroxyisoxazole metal salt II (M 1 is metal) with a halide III (Hal is halogen) pref. in an inert solvent such as dimethylformamide, at room temperature to 150°C n COPYRIGHT: (C)1979,JPO&Japio |
| priorityDate | 1977-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 23.