http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H07126263-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e43b4ca6b41ce9f54c9a895d474c81a |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-58 |
| filingDate | 1993-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25aabea5a31934c7f3d96f42634b88f6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62fc0aeb510e1032db52605f97be4b21 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5a9b87fe5c42d5cf089944e81bc9374 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b93e49b5a5669431fe4b6186e68fafdc |
| publicationDate | 1995-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H07126263-A |
| titleOfInvention | Chromanate and its manufacturing method |
| abstract | (57) [Summary] (Modified) [Structure] The dihydrochromanate represented by the general formula (2) is oxidized with sulfur in a mixed solvent of xylene and N, N-diethylaniline to give the general formula. A method for producing a chromanic acid ester represented by (3) and the compound of the general formula (3) thus obtained. [In the formula, R 2 represents a C 1 -C 4 alkyl group including an ethyl group. However, R 2 as a chromanic acid ester of the compound itself represents a C 1 -C 8 alkyl group excluding an ethyl group.] [Effect] A dihydrochromanic acid ester as a synthetic intermediate for a benzoylhydrazine insecticide is easy. In addition, it can be obtained in high yield. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0773216-A1 |
| priorityDate | 1993-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 61.