29586-98-9

Basic information

• Product Name: 3-O-acetyl-1,2,5,6-di-isopropylidene-α-D-glucofuranose
• Synonyms: 3-O-acetyl-1,2,5,6-di-isopropylidene-α-D-glucofuranose
• CAS NO: 29586-98-9
• Molecular Weight: 302.324
• Mol File: 29586-98-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-O-acetyl-1,2,5,6-di-isopropylidene-α-D-glucofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-acetyl-1,2,5,6-di-isopropylidene-α-D-glucofuranose(29586-98-9)
• EPA Substance Registry System: 3-O-acetyl-1,2,5,6-di-isopropylidene-α-D-glucofuranose(29586-98-9)

Safety Data

• Hazardous Substances Data: 29586-98-9(Hazardous Substances Data)

Upstream product

• 14686-88-5 3-O-acetyl-1,2:5,6-di-O-isopropylidene-α-D-erythro-hex-3-enofuranose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-D-glucofuranoside 
• 79-20-9 acetic acid methyl ester 

Downstream Products

• 20689-03-6 1-((3aR,4S,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-ethane-1,2-diol 
• 582-52-5 1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose 
• 79-20-9 acetic acid methyl ester 
• 582-52-5 diacetone glucose 

Relevant articles and documents

A Novel Electrochemical Method of Acetylation of Alcohols by Methyl Acetate

A new electrochemical method of acetylation, using methyl acetate at room temperature, was developed.The current efficiency in all the reactions with primary alcohols exceeded 100 percent, ranging from 126 to 166 percent indicating that this method of acetylation is advantageous for the preparation of acetates from the viewpoint of energy economy.Keywords--acetic acid methyl ester; acetylation; alcoholysis; electrochemical reduction; transesterification; alcoholate anion