http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-498861-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0ff16e899ce32685c9600075c1cc21 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G59-10 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-10 |
filingDate | 1968-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e185d3c797668b9f7af5cbfd92e857f2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e1093636dd959aa78270a16d7564afa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e88abfd13823b9c62a122a78dc10d667 |
publicationDate | 1970-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CH-498861-A |
titleOfInvention | Process for the preparation of adducts containing epoxy groups from polyepoxy compounds and N-heterocyclic compounds |
abstract | 'Advanced' adducts contng. epoxy grps., made by heating together (i) an N-heterocyclic cpd. where Z = divalent residue, free from N atoms, giving an opt. subst. 5- or 6-membered ring, and (ii) a polyepoxy cpd. (II) pref. contng. an average of 2-3 epoxy grps., using 1 equiv. (pref. 0.02-0.5, esp. 0.06-0.3 equiv.) NH in (I) per 1 equiv. epoxy grp. in (II). Examples of specific cpds. (II) are diglycidyl ethers of biphenols, e.g. diglycidyl ether of 2,2-bis(p-hydroxyphenyl)propane; cycloaliphatic polyepoxy cpds. Cpds. (I) may be e.g. hydantoin derivs:- such as 5,5-dimethylhydantoin or 5-isopropylhydantoin. Cured products have excellent electrical properties, esp. resistance to tracking. |
priorityDate | 1968-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 260.