http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2046114-A5
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f3898631ea6344e6839114c1a7ca7514 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-32 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-32 |
| filingDate | 1970-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1971-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1971-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | FR-2046114-A5 |
| titleOfInvention | Benzimidazole derivs anthelmintic, antifung - al bactericidal, aericidal, insecticidal, nema |
| abstract | Benzimidazole derivs; anthelmintic, antifungal, bactericidal, acaricidal, insecticidal, nematocidal. Cpds. of formula (I): (where R is 1-4 substituents chosen from halo, alkyl, aryl, alkoxy, alkylthio, CN, NO2; R1 is H, alkyl, alkenyl, aryl, aralkyl, trihalomethylthio, ethylthio or vinylthio in which at least 2 of the H atoms are replaced by halogen, -CZ-Y-R4 (III) A1 is alkyl, alkenyl, aralkyl, aralkenyl, cycloalkyl, cycloalkyl-alkyl, aryl, heteroaryl, heteroaralkyl (these gps. are opt. substd. by halo, alkoxy, NO2, CN) dialkylamino or nitrogen heterocyclic joined by the N atom (the heterocyclic opt. contains an oxygen or a second nitrogen, and has an alkyl and/or cycloalkyl residue contg. 1-12 atoms of C; A2 is H or lower alkyl or A1 and A2 together are opt. unsatd. divalent hydrocarbyl, a heterocarbon gp. contg. an S, O or N atom. these groups opt. contain an alkyl and/or cycloalkyl gp. contg. 1-12C atoms; Y and Z are O or S; R4 is alkyl, alkenyl, aralkyl, aralkenyl, phenyl, naphthyl, cycloalkyl, cycloalkylalkyl, furyl, thienyl, pyridyl, thiazolyl, oxazolyl, isothiazolyl, isoxazolyl, thiadiazolyl (all opt. substd. by halo, alkyl, phenyl, alkoxy, alkylthio, cyano, nitro or dialkylamino); R2 is H, alkyl, aryl (e.g. phenyl, naphthyl), heteroaryl, these gps. opt. substd. by halo, alkyl, phenyl, alkoxy, alkylthio, cyano, nitro; R3 is alkyl, alkenyl, aralkyl, aralkenyl, cycloalkyl, cycloalkyl-alkyl, phenyl, naphthyl, furyl, thienyl, pyridyl, thiazolyl, oxazolyl, isothiazolyl, isoxazolyl or thiadiazolyl (all opt. substd. by one or more halo, alkyl, phenyl, alkoxy, alkylthio, CN, NO2, dialkylamino) or an N-contg. heterocyclic joined via the N-atom (the heterocyclic may contain an oxygen or a second nitrogen atom and has an alkyl and/or cycloalkyl residue contg. 1-12 C atoms); when R2 = H or unsatd. alkyl, R3 must be a heteroaryl as above or one of the other gps. which carries a substituent nitrogen except when R1 is a Group II in which A1 is a residue carrying an N-substituent or A1 and A2 together form a divalent heterocarbon gp.). |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6930121-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6720349-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9310101-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6916836-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6906091-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016063293-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3978075-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6653335-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5475005-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6984654-B2 |
| priorityDate | 1970-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 37.