http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6016986-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_43000a5cfa837b51a2a690856b95ada2 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-88 |
| filingDate | 1983-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4cb4e37b52b808b803eafbd16fd70ae0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc6d996a0f4f4364d618ff3fd9f39ab3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a375aec6ab68532b9b46aed275812cf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_adbb1821a7da78a87083ee6f4a105043 |
| publicationDate | 1985-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S6016986-A |
| titleOfInvention | Benzothiadiazine compound and herbicide |
| abstract | NEW MATERIAL:1-[ 4-( 2,4-Dichlorobenzoyl )-1,3-dimethylpyrazol-5-yl-oxycarbonyl]-3-isopropyl-1H-2,1,3-benzothiadiazin-4-(3H)-one-2,2-dioxide shown by the formula. n USE: A herbicide. n PREPARATION: For example, 3-isopropyl-1H-2,1,3-benzothiadiazine-4-(3H)-one-2,2- dioxide is reacted with phosgene or trichloromethyl chloroformate in the presence of a base such as triethylamine, etc. (preferably ≥ equimolar amount based on raw material), to synthesize carbamoyl chloride firstly. It is then reacted with 1,3-dimethyl-4-(2,4-dichlorobenzoyl)-5-hydroxypyrazole in the presence of a base. n COPYRIGHT: (C)1985,JPO&Japio |
| priorityDate | 1983-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 28.