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?? ??:
9050-06-0
???:
??(?? CINNAMATE)
???(??):
??(??CINNAMATE);??(??CINNAMATE)(POLY(VINYLCINNAMATE));??(???????)
???:
POLY(VINYL CINNAMATE)
???(??):
PVCi;POLY(VINYL CINNAMATE);VINYL CINNAMATE POLYMER;vinyl cinnamate homopolymer;POLY(VINYL CINNAMATE) ISO 9001:2015 REACH;Ethenol,homopolymer,3-phenyl-2-propenoate;Vinylalcohol,cinnamoylchloridereactionproduct;Poly(vinyl cinnamate) average Mn 40,000, powder;POLY(VINYL CINNAMATE), AVERAGE MW CA. 20 0,000 (GPC)
CBNumber:
CB8414982
???:
C11H12O3
??? ??:
192.21118
MOL ??:
9050-06-0.mol
MSDS ??:
SDS

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Room Temperature
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InChI
1S/C9H8O2.C2H4O/c10-9(11)7-6-8-4-2-1-3-5-8;1-2-3/h1-7H,(H,10,11);2-3H,1H2/b7-6+;
InChIKey
HCCVHWNULIPQNY-UHDJGPCESA-N
SMILES
C=COC(=O)\C=C\c1ccccc1
EPA
Ethenol, homopolymer, 3-phenyl-2-propenoate (9050-06-0)

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WGK ?? 3
TSCA TSCA listed
???? ??? 11 - Combustible Solids
???? ?? KE-29064

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white to light yellow powder

Synthesis

Poly(vinyl cinnamates) (PVCi) can be prepared by esterification of the hydroxyl group in polyvinyl alcohol (PVA) and the carboxyl group in p-chlorocinnamic acid. All grafting modification was carried out in a four-necked flask equipped with a mechanical stirrer, con denser, and nitrogen inlet. PVA was dissolved in DMSO (5 wt% solution) at 80℃, certain amounts of cinnamic acid was added in PVA solution, the reaction mixture was stirred at 35℃ for 24 h with the catalysis of DCC and DMAP. At the end of the reaction, the product was precipitated twice in ethanol to completely remove the solvent. Then the product was purified by removing the unreacted cinnamic acid in extractor with ethanol and then dried under vacuum at 30℃ for 24 h. The modified PVCi was completely insoluble in water in which PVA had been freely soluble before graft modification. The DS was controlled by adjusting the molar ratio of cinnamic acid to the hydroxyl groups.
Synthesis of Poly(vinyl cinnamates) by esterifying of PVA with p-chloro cinnamate
[1] HAIYAN DU. The synthesis of poly(vinyl cinnamates) and its self-assembled structure[J]. Polymer Engineering and Science, 2013, 25 1: 1154-1160. DOI:10.1002/PEN.23370.

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