162426-81-5

Basic information

• Product Name: 2-O-acetyl-1,4:3,6-dianhydro-5-O-benzyl-D-glucitol
• Synonyms: 2-O-acetyl-1,4:3,6-dianhydro-5-O-benzyl-D-glucitol
• CAS NO: 162426-81-5
• Molecular Weight: 278.305
• Mol File: 162426-81-5.mol

Chemical Properties

• CAS DataBase Reference: 2-O-acetyl-1,4:3,6-dianhydro-5-O-benzyl-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-acetyl-1,4:3,6-dianhydro-5-O-benzyl-D-glucitol(162426-81-5)
• EPA Substance Registry System: 2-O-acetyl-1,4:3,6-dianhydro-5-O-benzyl-D-glucitol(162426-81-5)

Safety Data

• Hazardous Substances Data: 162426-81-5(Hazardous Substances Data)

Upstream product

• 652-67-5 Isosorbide 
• 100-39-0 benzyl bromide 
• 13042-39-2 isosorbide 2-acetate 

Downstream Products

• 72631-67-5 (1R,4S,5R,8R)-8-benzyloxy-2,6-dioxabicyclo<3.3.0>octan-4-ol 
• 853016-81-6 N-benzyl-N-[(3R,3aR,6R,6aS)-6-(benzyloxy)hexahydrofuro[3,2-b]furan-3-yl]amine 
• 853016-84-9 N-benzyl-N-[(3R,3aR,6R,6aS)-6-(benzyloxy)hexahydrofuro[3,2-b]furan-3-yl]-N-methylamine 
• 153062-03-4 (1R,4S,5R,8R)-8-benzyloxy-4-toluenesulfonyloxy-2,6-dioxabicyclo<3.3.0>octane 

Relevant articles and documents

The synthesis and applications of asymmetric phase-transfer catalysts derived from isomannide and isosorbide

We report herein the synthesis of various derivatives of isomannide and isosorbide. Alkylation on N-(diphenylmethylene)glycine tert-butyl ester show the new catalysts to be effective phase-transfer catalysts with moderately good enantioselectivity. The ef

Selective alkylations of 1,4:3,6-dianhydro-D-glucitol (isosorbide)

Each of the two hydroxyl groups of isosorbide can be alkylated selectively, either by direct alkylation with benzyl chloride or allyl bromide according to the reaction conditions, or by a three-step procedure involving selective monoacetylation, alkylation with four different reagents, and finally deacetylation.Monobutyl and monomethyl derivatives from isosorbide are also described.