http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1460356-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_af99df08b153738cd418446a75d09bfc |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-5537 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-572 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-553 |
| filingDate | 1974-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1977-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1460356-A |
| titleOfInvention | Process for preparing cyclicdicarboximidosubstituted phos phonithioates |
| abstract | 1460356 Preparing cyclic dicarboximidophosphonothioates DOW CHEMICAL CO 8 April 1974 [9 April 1973] 15483/74 Heading C2P A compound of the formula wherein R is phthalimido, monomethylphthalimido, 4 - cyclohexene - 1,2 - dicarboximido or monomethyl - 4 - cyclohexene - 1,2 - dicarboximido is obtained by reacting (alkoxy) 2 P(S)Cl wherein each alkoxy is C 1 -C 4 alkoxy with a salt of the formula where Me is Na or K and R<SP>1</SP> is H or CH 3 at 0-100 C. in the presence of an inert tertiary alcohol and of a catalytic amount of 1,4-diazabicyclo-(2,2,2)-octane. A co-solvent may also be employed in addition to the tertiary alcohol, specified co-solvents being hexane, heptane, benzene, xylene, cyclohexane, petroleum ethers, CCl 4 , CHCl 3 and CH 2 Cl 2 . The preferred tertiary alcohol is tert.-butyl alcohol. The products have pesticidal and bactericidal properties and may be used in admixture with a carrier therefor. |
| priorityDate | 1973-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 35.