http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1031909-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c72d118f5664072de841f9c5c34b9d99
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-0025
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G8-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G8-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G8-28
filingDate 1963-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1966-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1031909-A
titleOfInvention Modified novolac resins
abstract Soluble fusible reaction products result from the reaction of (1) a novolac of recurring structural units <FORM:1031909/C3/1> where A is an aromatic hydrocarbon nucleus, R is alkylidene ortho to the OH of both A nuclei to which it is attached, R1 is an alkyl or aromatic hydrocarbon radical para to the OH, and n is 0 or 1; with (2) a diisocyanate; (1) may be obtained by standard novolac procedures from a p-alkyl or p-aryl phenol when n is 1, or from a p-halophenol, followed by replacement of Ha by H when n is 0, and an aldehyde, e.g. formaldehyde, acetaldehyde, butyraldehyde or benzaldehyde. Reaction may be effected in an inert solvent over a wide temperature range. The products may be used in coatings and impregnants for paper, textiles and leather; in paints, varnishes, adhesives and rubber; as moulding compounds with fillers, e.g. wood flour, cotton flock or glass fibres; and when thermoset as binders for sand asbestos, silicon carbide or paper. Specified diisocyanates are toluene-, naphthalene-, 4,4-diphenylmethane-, and C2- 4-alkylene-diisocyanates. The product of the examples is soluble in methylene chloride.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4029846-A
priorityDate 1962-11-30-04:00^^<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: 27.