http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PT-76848-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_70ec63d39d6704bacc5c7068c93ded43 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D- http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N- http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F13-00 |
filingDate | 1983-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1983-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | PT-76848-A |
titleOfInvention | Process for preparing anti-coagulants of the 4-hydroxycoumarin type and rodenticidal compositions comprising such anti-coagulants |
abstract | Cpds. of formula (I) having blood anticoagulant properties are new. In (I) Z is halogen; n is 0-2; R4 is (1) phenylene attached directly or indirectly to the tetralin ring and having in the p-posn. an electron-withdrawing atom or gp. whose rotational vol. does not exceed that of a Ph gp. and forming with the phenylene a polarisable structure; or (2) 4-pyridinyl, p-(4-pyridinyl)phenyl or p-(4-pyridinyloxy)phenyl; or (3) phenylene attached directly to the tetralin ring and p-substd. by substd. furanyl or thiophenyl attached directly or through O and/or CH2, the furanyl or thiophenyl having an electron-withdrawing atom or gp. as substituent in a posn. to form with the furanyl or thiophenyl gp. a polymerisable structure, the atom or gp. having a rotational vol. that does not exceed that of a Ph gp. Cpds. (I) are blood anticoagulants and some cpds. are more active than Bradifacoum and Difenacoum; and so they are esp. effective as rodenticides. |
priorityDate | 1983-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 20.