http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1208227-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d7dfd84f9157ae12c41e319ec325338d |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-00 |
| filingDate | 1983-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1986-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77ee7d196fc005d9a20f1765c6a2becf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b33ab9c9bd44d8d4c1e3a4e6433a5ba7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78849aa3e8b9dde90ac2b8e301af1142 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d002c2ea95f975173697c49cbd4b027 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_958e7a91fe419f14e336072e59a960d8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73314b48f4aa644f942d170cc802349e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90c4256b46864efb65cc2d247a76770e |
| publicationDate | 1986-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-1208227-A |
| titleOfInvention | Tetrazole derivatives |
| abstract | ABSTRACT OF THE DISCLOSURE: Triidoallyl- or iodopropargyl-substituted tetrazole compounds are provided which are prepared by reacting substituted tetrazole compound with reactive derivatives of corresponding triidoallyl alcohol or iodopropargyl alcohol or by iodinating propargyltetrazole compounds, as well as antibacterial and antifungal compositions for medicinal, agricultural and industrial fields which contain as active ingredient said tetrazole compounds. The tetrazole compounds have the following general structure wherein X represents a group of -C?CI or a group of when X is a group of -C?CI, R represents an alkyl group, a benzyl group, a phenyl group or a phenyl group substituted by one or more groups selected from the class consisting of alkoxy, halo, trifluoromethyl, cyano, hydroxy, alkyl, carbamoyl, nitro, mono-alkylamino, di-alkylamino and carboxy, provided that R cannot be a 3-chloro-2-nitrophenyl group; and when X is a group of , R represents an alkyl group having two or more carbon atoms, a benzyl group or a phenyl group substituted by one or more groups selected from the class consisting of alkoxy, halo, trifluoromethyl, cyano, hydroxy, alkyl, carbamoyl, nitro, mono-alkylamino, di-alkyl-amino and carboxy, provided that R cannot be a 3-chloro-2-nitrophenyl group. |
| priorityDate | 1982-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 147.