Cyanuric acid triallyl ester

Beilstein Handbook Reference) Activator OC Ai3-26448 BRN 0235560 Cyanuric acid, tri-2-propenyi ester Cyanuric acid triallyl ester EINECS 202-936-7 NSC 4804 Perkalink 300 Perkalink 300-50D Rhenofit TAC TAG Triallyl cyanurate Tripropargyl cyanurate 2,4,6-Tri(allyloxy)-s-triazine 2,4,6-Triallyloxy-1,3,5-triazine 1,3,5-Triazine, 2,4,6-tris(2-propenyloxy)- s-Triazine, 2,4,6-tris(allyloxy)- 2,4,6-Triprop-2-ynyloxy-s-triazine ... 

It many ways the alkyl cyanurates behave as typical esters. They are hydrolyzed to cyanuric acid and the appropriate alcohol, and readily undergo transesterification reactions. Cyanurates react with ammonia to form melamine under severe conditions <59HC(l3)l, p.i7). The reaction with amines usually gives mixed products, but triallyl cyanurates react to form the monosubstituted products in excellent yields (Scheme 35) (75S182.75S184). 

Trichlorophenoxyacetic acid Triallyl cyanurate Trimethylacetamidomethyl A-Methylanilinium trifluoroacetate A-a-p-Tosyl-L-arginine methyl ester hydrochloride tetrakis(acetoxymercuri)methane... 

For this reason, only di- and triallyl monomers have achieved commercial significance, and then only the esters. Since the cross-linked polymer occurring in this polymerization involves the side chains containing ester groups, they are also sometimes referred to industrially as polyesters. The di- and triallyl ester monomers are produced by the reaction of allyl alcohol with acids, acid anhydrides, or acid chlorides. Examples of monomers are diallyl phthalate (1) from phthallic anhydride, and triallyl cyanurate (II) from trichloro-5-triazine ... 

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