http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3910945-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_56666880a5e2b7703e98a4f9b2d9daf6 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-94 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-94 |
| filingDate | 1973-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1975-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0950e5d0b817db4206f0511e79e336d2 |
| publicationDate | 1975-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-3910945-A |
| titleOfInvention | 2-(2-Methyl-5-nitro-1-imidazolyl)ethyl-N-arylalkyldithiocarbamates |
| abstract | 2-(2-Methyl-5-nitro-1-imidazolyl)ethyl esters of Narylalkyldithiocarbamates of the formula wherein n is an integer from 1 to 7, R1 is hydrogen or lower alkyl, and R2 is hetero or carbomonocyclicaryl. These compounds are anti-microbial agents. The compounds are prepared in 2 steps. The reaction of the appropriate amine with carbon disulfide in aqueous base forms the dithiocarbamate salt and the final products are formed by the reaction of this salt with 1-(2chloroethyl)-2-methyl-5-nitroimidazole. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4160827-A |
| priorityDate | 1972-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 98.