N-Allylcarbamat-Verbindungen und deren Verwendung, insbesondere in strahlungshaertenden Beschichtungen
DE 102009058297 A1 UPAB: 20110624 NOVELTY - N-allyl carbamate compound (I), is new. DETAILED DESCRIPTION - N-allyl carbamate compound of formula (R2-C(R3)=C(R4)-CH2-N-C(=O)-O-)cR1) (I), is new. R1 = optionally branched, cyclic, optionally substituted aliphatic hydrocarbon and heterocyclic residue, w...
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Zusammenfassung: | DE 102009058297 A1 UPAB: 20110624 NOVELTY - N-allyl carbamate compound (I), is new. DETAILED DESCRIPTION - N-allyl carbamate compound of formula (R2-C(R3)=C(R4)-CH2-N-C(=O)-O-)cR1) (I), is new. R1 = optionally branched, cyclic, optionally substituted aliphatic hydrocarbon and heterocyclic residue, where R1 has ethylenically unsaturated bond (Q); R2, R3, R4 = H or hydrocarbon; and c = greater than or equal to 1. . INDEPENDENT CLAIMS are also included for: (1) a composition for use in radiation curable coating, comprising (I); (2) a coating composition comprising (I) or the composition; and (3) a UV-radically curable coating composition comprising (I) as an aliphatic reactive diluent, where R1 is derived from hydrocarbon unit with 2-5 carbon atoms and/or a triallyl triazine compound, optionally in tautomeric form. USE - (I) is useful as a part of the coating composition, preferably UV-radically curable coating composition. ADVANTAGE - (I): improves chemical resistance, consistency, transparency, and mechanical resistance, without affecting the weathering stability or surface luster of the coating composition; ensures a high compatibility with binder systems; comprises UV-curable double bonds connected with less steric hindrance, via flexible bonds, thus it is highly reactive; can be easily prepared. |
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