6129-66-4

Basic information

• Product Name: 4-hydroxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
• CAS NO: 6129-66-4
• Molecular Weight: 440.404
• Mol File: 6129-66-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-hydroxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(6129-66-4)
• EPA Substance Registry System: 4-hydroxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(6129-66-4)

Safety Data

• Hazardous Substances Data: 6129-66-4(Hazardous Substances Data)

Upstream product

• 123-31-9 hydroquinone 
• 3947-62-4 2,3,4,6-tetraacetylglucose 
• 604-69-3 β-D-glucose pentaacetate 
• 78942-86-6 2,3,4,6-tetra-O-acetyl-1-O-trifluoroacetyl-α-D-glucopyranose 

Downstream Products

• 14698-56-7 4-acetoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 497-76-7 arbutin 

Relevant articles and documents

Preparation method of glucoside and derivatives thereof

The invention discloses a preparation method of glucoside and derivatives thereof. According to the method, all hydroxyl groups on a sugar molecule structure are acetylated, a ligand containing phenolic hydroxyl groups is prepared at the same time, then boron trifluoride-diethyl ether is used as a catalyst, the two substances are condensed to obtain tetraacetylated glucoside, and finally acetyl protecting groups are removed to obtain the required glucoside. The method can selectively catalyze hemiacetal hydroxyl of monosaccharide to react with hydroxyl to obtain glucoside, and the product is single. The method is simple in production operation and low in equipment requirement, can be used for synthesizing glucoside and derivatives thereof with similar structures, is green and environment-friendly, and can be used for large-scale production.

Synthesis and G-quadruplex binding study of a novel full visible absorbing perylene diimide dye

A novel perylene diimide dye containing glucopyranosyl groups in 1- and 7-positions of the perylene ring has been synthesized and characterized to obtain highly efficient and stable photosensitized material in photodynamic therapy. Solvatochromic studies

Glycosides. Part 1. New Synthesis of 1,2-trans O-Aryl Glycosides, via Tributyltin Phenoxides

A new method of glycosidation of phenols has been studied.The reaction of tributyltin phenoxides 2 with 1,2,3,4,6-penta-O-acetyl-D-hexopyranosides 3, 7 and 9, in the presence of tin tetrachloride is described.Glycosides 4, 8 and 10 have been isolated in g