http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1361213-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e938e28337fbaa9944d781f3ccf86b5e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C381-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C381-00 |
| filingDate | 1971-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1974-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1361213-A |
| titleOfInvention | Substituted ueas |
| abstract | 1361213 Substituted ureas CHEVRON RESEARCH CO 9 Nov 1971 [9 Nov 1970] 52082/71 Heading C2C Compounds of Formula I (A) where R is phenyl optionally substituted with F, Cl, Br, NO 2 , C 1-4 alkyl or C 1-4 alkoxy; R<SP>1</SP>, R<SP>2</SP> are H or C 1-4 alkyl; and R<SP>3</SP> is C 1-14 hydrocarbyl optionally substituted with F, Cl, Br, NO 2 , or C 1-4 alkoxy, may be prepared by reacting compounds of Formula II (B) with HSR<SP>3</SP> in an inert solvent, e.g. benzene, where R<SP>4</SP>, R<SP>5</SP> are alkyl, haloalkyl, cycloalkyl or halocycloalkyl and R<SP>5</SP> may also be H, or R<SP>4</SP> and R<SP>5</SP> together form C 3-5 alkylene. R<SP>3</SP> may be alkyl, cycloalkyl, aryl, alkaryl or aralkyl. Compounds II may be prepared by reacting a urea (R-NR<SP>1</SP>-CO-NH-R<SP>2</SP>) with an acylamidosulphenyl chloride (ClS-NR<SP>4</SP>-CO-R<SP>5</SP>) preferably in methylene chloride with pyridine as acid acceptor. Compounds I are herbicides. |
| priorityDate | 1970-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 21.