38916-91-5

Basic information

• Product Name: (+)-Erythro-guaiacylglycerol
• Synonyms: (+)-Erythro-guaiacylglycerol;(1R,2S)-rel-1-(4-Hydroxy-3-methoxyphenyl)-1,2,3-propanetriol
• CAS NO: 38916-91-5
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 214.21500
• Mol File: 38916-91-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (+)-Erythro-guaiacylglycerol(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-Erythro-guaiacylglycerol(38916-91-5)
• EPA Substance Registry System: (+)-Erythro-guaiacylglycerol(38916-91-5)

Safety Data

• Hazardous Substances Data: 38916-91-5(Hazardous Substances Data)

Usage

Uses

erythro-Guaiacylglycerol is a component of Viticis Fructus (Vitex rotundifolia) with analgesic effects.

Upstream product

• 1370004-83-3 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)guaiacylglycerol 
• 14065-26-0 (1RS,2SR)-1,2,3-triacetoxy-1-(4-acetoxy-3-methoxy-phenyl)-propane 
• 93722-55-5 (2RS,3SR)-2,3-diacetoxy-3-(4-acetoxy-3-methoxy-phenyl)-propionic acid methyl ester 
• 7213-02-7 D-threo-guaiacylglycerol 7-O-β-D-glucopyranoside 
• 2309-07-1 Methyl ferulate 
• 93728-44-0 (1RS,2RS)-1-(4-benzyloxy-3-methoxy-phenyl)-propane-1,2,3-triol 
• 60525-32-8 ethyl 3-[4-(benzyloxy)-3-methoxyphenyl]-3-oxopropanoate 
• 7572-99-8 α-(Acetoxy-benzylvanilloylessigsaeure-aethylester 
• 93722-55-5 (2RS,3RS)-2,3-diacetoxy-3-(4-acetoxy-3-methoxy-phenyl)-propionic acid methyl ester 
• 14070-76-9 1-(4-hydroxy-3-methoxy)-phenyl-2-[4-(1,2,3- trihydroxypropyl)-2-methoxy]-phenoxy-1, 3-propandiol 

Downstream Products

• 4756-11-0 (1RS,2SR)-1-(3,4-dimethoxy-phenyl)-propane-1,2,3-triol 
• 4899-74-5 2-propanone,1-hydroxy-3-(4-hydroxy-3-methoxyphenyl)- 

Relevant articles and documents

New CuCl2-induced glucoside esters and other constituents from Portucala oleracea

Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl2. A new sugar ester (3) and two known compounds (4 and 5) were also isolated. Their structures were established by spectroscopic means. The antioxidative activities of stress metabolites and the related isolates were evaluated by DPPH assay. The results showed that new stress-driven adducts of monolignans and monoterpenes with a glucose bridge exhibited much stronger antioxidative activities than other compounds.