JPS603389B

NEW MATERIAL:An imidazole-allantoin addition product shown by the formulaI {R1 is H, beta-cyanoethyl, beta-[3,5-diamino-S-triazinyl-(1)]-ethyl; R2 is CH3, C2H5, C6H5; R3 is H or CH3}. EXAMPLE:2-Phenylimidazole-allantoin addition product shown by the formula II. USE:A one-pack type curing agent for e...

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Hauptverfasser: SAWA NATSUO, SAEKI TOKUICHI
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creator SAWA NATSUO
SAEKI TOKUICHI
description NEW MATERIAL:An imidazole-allantoin addition product shown by the formulaI {R1 is H, beta-cyanoethyl, beta-[3,5-diamino-S-triazinyl-(1)]-ethyl; R2 is CH3, C2H5, C6H5; R3 is H or CH3}. EXAMPLE:2-Phenylimidazole-allantoin addition product shown by the formula II. USE:A one-pack type curing agent for epoxy resin. Improving extermely pot life of epoxy resin at room temperature, starting curing reaction quickly by heating at 90-150 deg.C. PROCESS:An imidazole compound shown by the formula III is reacted with an equimolar or less allantoin in a solvent, preferably water under normal pressure at 100 deg.C for 1 hour, to give a compound shown by the formulaI.
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USE:A one-pack type curing agent for epoxy resin. Improving extermely pot life of epoxy resin at room temperature, starting curing reaction quickly by heating at 90-150 deg.C. PROCESS:An imidazole compound shown by the formula III is reacted with an equimolar or less allantoin in a solvent, preferably water under normal pressure at 100 deg.C for 1 hour, to give a compound shown by the formulaI.</description><language>eng</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; HETEROCYCLIC COMPOUNDS ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>1985</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19850128&amp;DB=EPODOC&amp;CC=JP&amp;NR=S603389B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25544,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19850128&amp;DB=EPODOC&amp;CC=JP&amp;NR=S603389B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SAWA NATSUO</creatorcontrib><creatorcontrib>SAEKI TOKUICHI</creatorcontrib><title>JPS603389B</title><description>NEW MATERIAL:An imidazole-allantoin addition product shown by the formulaI {R1 is H, beta-cyanoethyl, beta-[3,5-diamino-S-triazinyl-(1)]-ethyl; R2 is CH3, C2H5, C6H5; R3 is H or CH3}. EXAMPLE:2-Phenylimidazole-allantoin addition product shown by the formula II. USE:A one-pack type curing agent for epoxy resin. Improving extermely pot life of epoxy resin at room temperature, starting curing reaction quickly by heating at 90-150 deg.C. 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EXAMPLE:2-Phenylimidazole-allantoin addition product shown by the formula II. USE:A one-pack type curing agent for epoxy resin. Improving extermely pot life of epoxy resin at room temperature, starting curing reaction quickly by heating at 90-150 deg.C. PROCESS:An imidazole compound shown by the formula III is reacted with an equimolar or less allantoin in a solvent, preferably water under normal pressure at 100 deg.C for 1 hour, to give a compound shown by the formulaI.</abstract><oa>free_for_read</oa></addata></record>
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subjects CHEMISTRY
COMPOSITIONS BASED THEREON
HETEROCYCLIC COMPOUNDS
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
title JPS603389B
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