24968-99-8

Basic information

• Product Name: 2-Propenoic acid, 3-phenyl-, ethenyl ester, homopolymer
• Synonyms: 2-Propenoic acid, 3-phenyl-, ethenyl ester, homopolymer;3-Phenyl-2-propenoic acid, ethenyl ester homopolymer
• CAS NO: 24968-99-8
• Molecular Formula: (C11H10O2)x
• Molecular Weight: 0
• Mol File: 24968-99-8.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propenoic acid, 3-phenyl-, ethenyl ester, homopolymer(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-phenyl-, ethenyl ester, homopolymer(24968-99-8)
• EPA Substance Registry System: 2-Propenoic acid, 3-phenyl-, ethenyl ester, homopolymer(24968-99-8)

Safety Data

• Hazardous Substances Data: 24968-99-8(Hazardous Substances Data)

Upstream product

• 140-10-3 (E)-3-phenylacrylic acid 
• 108-05-4 vinyl acetate 
• 621-82-9 Cinnamic acid 
• 2768-02-7 (vinyl)trimethoxylsilane 

Downstream Products

• 212707-61-4 (2E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylprop-2-enamide 
• 1454308-49-6 vinyl 3-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate 

Relevant articles and documents

Multi-gram preparation of cinnamoyl tryptamines as skin whitening agents through a chemo-enzymatic flow process

A 2-step flow-based chemo-enzymatic synthesis of selected cinnamoyl tryptamines as potential cosmetic ingredients has been developed. A first reaction catalyzed by immobilized Pd(OAc)2 gave the acyl donors employed as starting material in the s

Palladium(II) acetate as catalyst in transvinylation reactions of hydroxycinnamic acid and its derivatives

The study on application of palladium(II) acetate as catalyst in transvinylation reactions of hydroxycinnamic acids has been done. This study was intended to assess the capability of palladium(II) acetate as a safer replacement for mercuric(II) catalysts

Chemo-enzymatic synthesis of vinyl and L-ascorbyl phenolates and their inhibitory effects on advanced glycation end products

This study successfully established the feasibility of a two-step chemo-enzymatic synthesis of L-ascorbyl phenolates. Intermediate vinyl phenolates were first chemically produced and then underwent trans-esterification with L-ascorbic acid in the presence of Novozyme 435 (Candida Antarctica lipase B) as a catalyst. Twenty vinyl phenolates and 11 ascorbyl phenolates were subjected to in vitro bioassays to investigate their inhibitory activity against advanced glycation end products (AGEs). Among them, vinyl 4-hydroxycinnamate (17VP), vinyl 4-hydroxy-3-methoxycinnamate (18VP), vinyl 4-hydroxy-3,5-dimethoxycinnamate (20VP), ascorbyl 4-hydroxy-3-methoxycinnamate (18AP) and ascorbyl 3,4-dimethoxycinnamate (19AP) showed 2–10 times stronger inhibitory activities than positive control (aminoguanidine and its precursors). These results indicated that chemo-enzymatically synthesized compounds have AGE inhibitory effect and thus are effective in either preventing or retarding glycation protein formation.