879281-40-0

Upstream product

• 18509-03-0 sodium trans-cinnamate 
• 106-89-8 epichlorohydrin 
• 140-10-3 (E)-3-phenylacrylic acid 
• 63073-96-1 potassium cinnamate 
• 556-52-5 oxiranyl-methanol 
• 103-26-4 Methyl cinnamate 

Downstream Products

• 60456-23-7 (S)-oxiranemethanol 
• 1258600-23-5 (E)-3-(cinnamoyloxy)-2-hydroxypropyl 3-(3,4-dihydroxyphenyl)acrylate 
• 1258600-20-2 (E)-3-(cinnamoyloxy)-2-hydroxypropyl 3-(3,4-dimethoxyphenyl)acrylate 
• 1258600-21-3 (E)-2-(cinnamoyloxy)-3-hydroxypropyl 3-(3,4-dimethoxyphenyl)acrylate 

Relevant academic research and scientific papers

METHOD FOR PRODUCING GLYCIDYL ESTER

PROBLEM TO BE SOLVED: To provide a production method which makes it possible to obtain glycidyl ester with high yields from the ester exchange reaction between ester and glycidol with a convenient catalyst in a mild reaction condition. SOLUTION: Glycidyl ester is produced by the ester exchange reaction between ester and glycidol in the presence of a polystyrene-carrying quaternary ammonium salt. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Derivatives of Propane Diyl Dicinnamate

The present invention provides a method for treating a cancer in a subject involving administering to the subject a compound of formula (II) or (II′): wherein R1, R2, R3, R4, R5, R6 and Rs

PHOTOREACTIVE POLYSACCHARIDE, PHOTOCROSSLINKED POLYSACCHARIDE PRODUCT AND METHOD OF MAKING SAME AND MEDICAL MATERIALS MADE FROM THE CROSSLINKED POLYSACCHARIDE

A photoreactive polysaccharide which comprises a polysaccharide bound to a glycidyl ester via a covalent bond, a photocrosslinked-polysaccharide prepared by using the photoreactive polysaccharide, and medical products comprising the photocrosslinked-polys

Novel synthesis and enzymatic resolution of (±)-2,3-epoxy propyl esters

A novel method of synthesizing glycidyl esters (±) -2,3-epoxy propyl esters has been developed involving reaction of epichlorohydrin with sodium salt of carboxylic acids in the presence of 15-crown-5 as catalyst with excellent yields. Enzymatic resolution of these glycidyl esters by lipasePS- C has been achieved with remarkable substrate selectivity.

Irreversible inactivation of papain and cathepsin B by epoxidic substrate analogues

Epoxidic substrate analogues related to allylamine (4a-4e) and allyl alcohol (5a-5f) were synthesized and tested as models of cysteine-protease inhibitors.They proved to be irreversible inhibitors of papain and cathepsin B with pseudo-first-order inactiva