Product Information
- 2-Propenoic acid, 3-[4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)phenyl]-
- 3-[4-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)phenyl]-2-propenoic acid
- 4-(b-D-Glucopyranosyloxy)cinnamic acid
- 4-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)cinnamic acid
- 4-O-b-D-Glucopyranosyl-p-coumaricacid
- 4-O-β-<span class="text-smallcaps">D</span>-Glucopyranosyl cinnamate
- 4-O-β-<span class="text-smallcaps">D</span>-Glucopyranosyl-p-coumaric acid
- Cinnamic acid, p-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-
- Cinnamicacid, p-(b-D-glucopyranosyloxy)- (6CI,8CI)
- Glucopyranoside, p-(2-carboxyvinyl)phenyl, b-D- (8CI)
- See more synonyms
- Glucopyranoside, p-(2-carboxyvinyl)phenyl, β-<span class="text-smallcaps">D</span>-
- Glucosido-p-coumaric acid
- p-(Glucosyloxy)cinnamic acid
- p-Coumaric acid 4-O-β-<span class="text-smallcaps">D</span>-glucopyranoside
- p-Coumaric acid glucoside
- p-Coumaric acid β-glucoside
- p-Coumaric acid4-O-b-D-glucopyranoside
- p-Coumaricacid b-glucoside
- trans-p-Coumaricacid-4-O-b-D-glucopyranoside
Coumaric acid 4-O-glucoside is a compound that is found in plants and can be extracted from flaxseed. It has been shown to have antioxidative activity, especially in the prevention of oxidation of fatty acids. Coumaric acid 4-O-glucoside has also been shown to inhibit the synthesis of n-3 fatty acids and secoisolariciresinol, as well as to regulate the biosynthesis of these lipids. The efficient method for preparing this compound is by hydrolysis of coumaroyl ester linkages using hydrochloric acid in methanol. Coumaric acid 4-O-glucoside was synthesized by reacting methyl acetoacetate with sodium hydroxide and hydrochloric acid in methanol at a temperature range of 0°C to 25°C. This reaction was followed by purification using phase liquid chromatography.
Chemical properties
Technical inquiry about: 3D-MC71595 Coumaric acid 4-O-glucoside
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