http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104557749-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-04 |
| filingDate | 2014-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2017-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2017-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104557749-B |
| titleOfInvention | 3-phenyl-5-(4-trifluoromethylanilino)-4H-1,2,4-triazole and its synthesis process and application |
| abstract | The present invention relates to triazole compounds, specifically 3-phenyl-5-(4-trifluoromethylanilino)-4H-1,2,4-triazole and its synthesis process and application, including the following steps : 1) take benzoyl chloride as raw material to generate benzoyl isothiocyanate through reaction with potassium thiocyanate; 2) react it with p-trifluoromethylaniline to produce intermediate 1-benzoyl-3-( 4-trifluoromethylphenyl) thiourea; 3) react the intermediate with hydrazine hydrate to produce target product 3-phenyl-5-(4-trifluoromethylanilino)-4H-1,2,4 ‑Triazole, the beneficial effect of the present invention is: the new compound of the present invention is under the concentration of 200ppm of the target compound, measured by spraying method, 24 hours control malt effect 60%, 48 hours control effect 70%, has further development as insecticidal agent potential. |
| priorityDate | 2014-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 17.