http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-276322-B6
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1d73b30001e07f53675a946996c96393 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-74 |
filingDate | 1989-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67e41302a19a5366d614594f2fdd531a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f6fc66db7217d2f8c2f46dab25f73a67 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebdc15ed23a65d72faec897bceb45fb1 |
publicationDate | 1992-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CS-276322-B6 |
titleOfInvention | 2- / 2,6-DimetylanilĂnokarhoxymetyltio / benzothiazol |
abstract | The previously unknown 2- [2,6-dimethylanilinoocarhoxymethylthio] benzothiazole was prepared. The synthesis of said compound is carried out by reacting the potassium salt of 2-mercaptobenzothiazole with N-chloroacetyl-2,6-dimethylaniline in a mixture of water, dimethyl sulfoxide and ethanol at reflux. The compound is antihelmintically active against the model helminth of Nippostron gylus brasiliensis. |
priorityDate | 1989-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.