http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0034431-A2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D521-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-65 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00 |
filingDate | 1981-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_801c15ec2185a8d7b951575900eb8b62 |
publicationDate | 1981-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-0034431-A2 |
titleOfInvention | 2-Isocyanatosulfonylbenzoic acid esters and preparation thereof |
abstract | 2-Isocyanatosulfonylbenzoic acid esters of the general formulan n wherein R is selected from various hydrocarbyl and substituted hydrocarbyl groups; R 2 is H, Cl, Br, F, C 1 -C 3 alkyl, -NO 2 , -OCH 3 , -SCH 3 , CF 3 , SO 2 CH 3 , N(CH 3 ) 2 , CN, or 4-N=C=O; and R 3 is H, Cl, Br or CH 3 with the proviso that when R is other than C 3 -C 10 alkynyl, then R 2 must be 4-NCO. are novel intermediates for the preparation of herbicidal ureas. The isocyanates may be prepared e.g. by reacting a corresponding 2-sulfamoylbenzoate ester of general formulan wherein R 2 ' is NH 2 or R 2 as defined above, with a hydrocarbyl isocyanate and phosgene in the presence of a catalytic amount of a tertiary amine base and an inert solvent. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9606826-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4659366-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-1047166-C |
priorityDate | 1980-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 245.