http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2751317-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-52 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-52 |
| filingDate | 1977-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4db6e16b6b9e6ab1e6f7292b07358fef http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7346747eeb3ce2a749c24cc81c2828b3 |
| publicationDate | 1978-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-2751317-A1 |
| titleOfInvention | PHENYLFORMAMIDINE DERIVATIVES AND THEIR SALTS, PROCESS FOR THEIR MANUFACTURING AND THEIR USE IN VICTORY CONTROL |
| abstract | Phenyl-formamidine derivs. of formula (I) are new:- (where R1 is Me or Et; one of R2 and R3 is H and the other is Me). (I) are broad-spectrum pesticides, esp. insecticides and acaricides. They are also active against nematodes, viruses, bacteria and plant-pathogenic fungi. (I) are esp. active against plant-pathogenic biting insects (e.g. Spodoptera littoralis, Heliothis virescers, Leptinotarsa decemlineata and Myzus persical), and also have high activity against flies and mosquito larvae. (I) are pref. used in combination with synergists, e.g. piperonyl butoxide. (I) are more stable in solns. and slurries than the analogues of DT1542715. In an example, N,N-dimethyl-N'-(2,3-dimethyl-4-chlorophenyl)-formamidine was prepd. by reacting 2,3-dimethyl-aniline with DMF dimethyl-acetal then chlorinating. |
| priorityDate | 1976-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 87.