http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106922679-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D241-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-60 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-46 |
| filingDate | 2017-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-106922679-B |
| titleOfInvention | The formamide of azophenlyene 1 transforms application of the compound 15 1 in Sclerotinia sclerotiorum is suppressed |
| abstract | A kind of application of the formamide of azophenlyene 1 transformation compound 15 1 in Sclerotinia sclerotiorum is suppressed, the formamide of azophenlyene 1 transformation compound 15 1 is using the formamide of azophenlyene 1 as parent, is obtained through structure of modification, its structural formula is as follows.The present invention determines the inhibitory action of the formamide of azophenlyene 1 transformation 15 1 pairs of Sclerotinia sclerotiorums of compound using growth rate method simultaneously, as a result shows：15 1 pairs of Sclerotinia sclerotiorums of the transformation compound have that preferable inhibition is good, and the inhibition is better than its formamide of parental phenazine 1, shows that the transformation compound 15 1 can be as the lead compound of prevention and control sclerotinia sclerotiorum novel pesticide. |
| priorityDate | 2017-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 63.