http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103193729-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7610cef0de1410bf21e1e54706e208a |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-16 |
| filingDate | 2013-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efb150cd1f511431d2e883f1c0fb6634 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4d9e7a573dd8e3294cf84eb5e20fe96 |
| publicationDate | 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103193729-B |
| titleOfInvention | Preparation method of (2-hydrocarbon sulfenyl thiazoline-5-yl) methanol and carboxylic ester thereof |
| abstract | The invention provides a preparation method of (2-hydrocarbon sulfenyl thiazoline-5-yl) methanol and carboxylic ester of (2-hydrocarbon sulfenyl thiazoline-5-yl) methanol. Corresponding (2-hydrocarbon sulfenyl thiazoline-5-yl) methyl carboxyate is obtained by reacting N-allyl amino sulfo-formic ether with free radical of peroxy-carboxylic anhydride, and (2-hydrocarbon sulfenyl thiazoline-5-yl) methanol can be further prepared by hydrolyzing (2-hydrocarbon sulfenyl thiazoline-5-yl) methyl carboxylate. The preparation method has simple and easily assessable raw materials and is convenient to operate; and an obtained compound can be used as raw materials for preparing medicines and agriculture chemicals with antimicrobial activity. |
| priorityDate | 2013-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 102.