| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_28a869d6fc950d50f6df03f549ca3afa |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-06 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06 |
| filingDate |
1970-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
1973-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0dfa7fb15bf6642858de6571dd5651a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_59fdc7eb00f831e52698230b0cd61c12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91ab68ce7c01b215e123f906fd906838
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a982ed79d50074f59af9a49812e15f01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1e6c285125b5d7179a87cf8bab876fc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04a105d2e10feae705f8722d88db2605
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_809f0a70046ff14338a9142935dbbacb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a999f17f9bfced79c6f1be8e2b4d7571
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84b53bc538af32c6e2b2a0a0a3a9b97e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe5185b1b70b44f44a3cace49ac36a13 |
| publicationDate |
1973-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-3721667-A |
| titleOfInvention |
Novel antibacterial compounds and a process for the preparation of the same |
| abstract |
There are described new chemical compounds, or more specifically 1-(5-nitrofuryl)-2-(2-cyclohexeno-azolyl)-ethylene of the following formula: WHEREIN X is a member selected from the group consisting of oxygen and sulfur. AND A METHOD FOR THE PREPARATION OF THE SAME, AS WELL AS COMPOSITIONS CONTAINING THE SAME. These new compounds represent superior antibacterial properties and a low mammalian toxicity, and are not subjected to inactivation in medium. The method for the preparation thereof comprises: reacting a compound selected from the group consisting of 2-methylcyclohexeno-oxazole and 2-methyl-cyclohexeno-thiazole with a compound selected from the group consisting of 5-nitrofurfural and the diacetate thereof. |
| priorityDate |
1969-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |