http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3962305-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e899199238cd97bdebfa84869ece733b |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-2458 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-24 |
| filingDate | 1975-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1976-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89532be9dd94ec5a68554cb18f248160 |
| publicationDate | 1976-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-3962305-A |
| titleOfInvention | Acylformanidine thiocarbamates |
| abstract | A composition of matter is described herein which has insecticidal and miticidal activity and methods of use. The composition may be defined by the following generic formula: CH3 N=CH-N ANGLE R3 wherein R1 and R2 are independently methyl or halogen; R3 is selected from the following groups: XR5 PARALLEL -C-R4, -C-R4, -SO2R4, -S-R4, -P ANGLE PARALLEL PARALLEL PARALLEL O S O R6 R4 is selected from the group consisting of: alkyl, alkenyl, haloalkyl, haloalkenyl, cycloalkyl, cycloalkylalkyl, alkoxy, alkylthio, alkylamido, arylamido, alkoxyalkyl, alkylthioalkyl, alkylamidoalkyl, arylamidoalkyl, ketoalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkylthiocarbonyl, alkylthiocarbonylalkyl, alkylamidocarbonyl, alkylamidocarbonylalkyl, arylamidocarbonylalkyl, hydroxyalkyl, N-alkylcarbamoylalkyl, N-arylcarbamoylalkyl, cyanoalkyl, thiocyanoalkyl, isothiocyanoalkyl, cyanatoalkyl, phenyl, furyl, thienyl, pyridyl with or without substituents, wherein said substituents can be selected from halogen, alkyl, haloalkyl, alkoxy, carbamyl, nitro, carboxylic acids and their esters, haloalkylcarbamyl, phenylalkyl; phenylhaloalkyl; phenylalkenyl; substituted phenylalkenyl wherein said substituents can be selected from halogen, alkyl, alkoxy; halophenoxy; phenylalkoxy, phenylalkylcarboxyalkyl; phenylcycloalkyl; halophenylalkenoxy; bicycloalkyl; with the priviso that when R4 is alkoxycarbonyl, alkylthiocarbonyl or alkylamidocarbonyl R3 can only be -C-R4. PARALLEL O X = oxygen or sulfur. R5 and R6 are independently alkyl, haloalkyl, aryl, alkoxy, aryloxy, alkylthio, arylthio, alkylamido and arylamido. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4263288-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0002826-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4425361-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4528392-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4946983-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0054898-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4154825-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4207334-A |
| priorityDate | 1974-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 104.