http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02290882-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5d4ada69388e0a1b68daaf536597c732
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0889
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G77-388
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-388
filingDate 1990-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37a92992ba5413e486a1572f7806fcea
publicationDate 1990-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02290882-A
titleOfInvention Production of acylaminoorganosilicone compound
abstract PURPOSE: To obtain the title compd. useful as a polar silicone-containing additive for paint without generating phase separation by successively reacting a specific hydroxysilicon compd. with a base, cyclic silylamine and an acyl halide in a non-aq. solvent. n CONSTITUTION: At first, in a non-aq. solvent, a hydroxysilicon compd. having an OH group bonded to Si and characterized in that all of the remaining of Si valency is satisfied by an org. group or an O-atom bonded to Si is reacted to form a silanolate anion which is, in turn, reacted with a cyclic aminosilicone compd. in a non-aq. solvent to obtain a siloxyalkylamide. Finally, this compd. is reacted with an acyl halide in the non-aq. solvent to obtain the objective compd. containing an acylamino substd. hydrocarbon bonded to Si. n COPYRIGHT: (C)1990,JPO
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010530873-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014167123-A
priorityDate 1989-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 23.