| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cea139ad438b9ce7d33159d45b154c6b |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C327-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-185
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-14 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08H3-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-185
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-10 |
| filingDate |
1976-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
1977-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b328a9f09eb94ff4256cb1b167d4c99e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_338b9dfbb409ea6141aa765176bad02d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72fdb64b0b8f9a0c69c7561a8d06e2cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06a1735bc47d48435ae11e72843f1104
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8abb3250d1dec382e8618d1a564a755f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3511ef202e49144270d4844796992b9e |
| publicationDate |
1977-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-4062841-A |
| titleOfInvention |
Heterocyclic fatty acid amides |
| abstract |
Acetylthio amides and esters were prepared by the free radical addition of thiolacetic acid to the terminal and nonterminal double bonds of N-substituted fatty amides and fatty esters. The free radical additions of the thiolacetic acid to the unsaturated compounds were initiated by irradiation using cobalt-60. The process using irradiation with cobalt-60 was also used to bring about the addition of bromotrichloromethane to N-substituted fatty amides and fatty esters to produce halogen-containing amides and esters. These new sulfur or halogen-containing compounds were found to have antimicrobial activity and to possess properties making them useful as antimicrobial agents. |
| priorityDate |
1976-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |