http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3652599-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c902faf6ae746c51fc8010672fc22894 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F8-30 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F8-30 |
filingDate | 1970-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1972-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49859c8391d98e46e50903738386d20e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84d575871fb09314cb29b7a822d6549e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6703ef13c14a517a8de41201b2788139 |
publicationDate | 1972-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-3652599-A |
titleOfInvention | Novel azidosulfonylcarbanilates |
abstract | AZIDOSULFONYLCARBANILATES ARE DISCLOSED WHICH ARE DERIVED FROM ALIPHATIC ALCOHOLS IN WHICH THE HYDROGEN ATOM IN ONE OR MORE OF THE HYDROXYL GROUPS IS REPLACED BY AN AZIDOSULFONYLPHENYLCARBAMOYL GROUP. THE COMPOUNDS HAVE THE FORMULA: (((R)Y,(N3-O2S-)X-PHENYL)-NH-COO)M-A-(OH)N WHEREIN A IS THE RESIDUE OF AN ALIPHATIC ALCHOL HAVING (N+M) HYDROXYL GROUPS AND A MOLECULAR WEIGH OF LESS THAN 300, N IS AN INTEGER FROM 0 TO 5, M IS AN NTEGER FROM 1 TO 6, PROVIDED THAT THE SUM OF N+M IS NOT GREATER THAN 6, R IS LOWE-ALKYL OR HALOGEN, X IS AN INTEGER FROM 1 TO 2, Y IS AN INTEGER FROM 0 TO 2, PROVIDED THAT THE SUM OF X+Y IS NOT GREATER THAN 3, AND THE SO2N3 GROUP IS IN ANY OF POSITIONS 3,4, OR 5, ONE OF SAID POSITIONS BEING UNSUBSTITUTED. THE ABOVE COMPOUNDS ARE PREPARED BY REACTING THE STARTING ALIPHATIC ALCOHOL WITH THE APPROPRIATE PROPORTION OF THE APPROPRIATELY SUBSTITUTED ISOCYANATOBENZENESULFONYL CHLORIDE AND REACTING THE INTERMEDIATE CHOROSULFONYLCARBANILAT WITH SODIUM AZIDE. THE ABOVE COMPOUNDS ARE USEFUL AS CROSSLINKERS IN A WIDE VARIETY OF POLYMER SYSTEMS CONTAINING C-H BONDS, AND ARE ACTIVATED EITHER PHOTOLYTICALLY OR THERMALLY. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102374081-B1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016146151-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20220014149-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3844787-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016146597-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009242831-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10385016-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4031068-A |
priorityDate | 1970-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 101.