http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1124646-A

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-14
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C271-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C269-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C265-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C263-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-06
filingDate 1965-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65031d0839ae877c3a95c8d2adfc1c76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14f70bce007b6017df95382cd0c9daf8
publicationDate 1968-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1124646-A
titleOfInvention Organic mono and polyisocyanates
abstract The invention comprises compounds of the formula <FORM:1124646/C2/1> where R4, R5 and R6, which may be the same or different, represent alkyl radicals which may be interrupted by ether oxygen atoms, aryl radicals, cycloalkyl radicals or aralkyl radicals, at least one of which radicals is substituted by an isocyanate group, which radicals may be further substituted by other groups. The compounds are prepared by reacting an amine of the formula <FORM:1124646/C2/2> or the hydrochloride or carbamate thereof, in which R1, R2 and R3, which may be the same or different, represent alkyl radicals which may be interrupted by ether oxygen atoms, aryl radicals, cycloalkyl radicals or aralkyl radicals, at least one of which radicals is substituted by a primary amino group, which radicals may be further substituted by other groups, with phosgene. Specified substituents include chlorine and bromine and thioether, nitrile, sulpho, sulphonic acid ester, carboxylic acid ester, alkoxy, phenoxy, sulphene and further carbamate groups. Phosgenation is effected by known methods, e.g. the cold phase-hot phase process. A reaction solvent may be used. The amino urethane reactants may be prepared by reduction of the corresponding nitro-, cyano- or carbamoyl-urethanes.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-8810250-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0298636-A1
priorityDate 1964-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 41.