147556-28-3

Basic information

• Product Name: 1,2,3,4,5-penta-O-benzyl-aldehydo-L-glucose
• Synonyms: 1,2,3,4,5-penta-O-benzyl-aldehydo-L-glucose
• CAS NO: 147556-28-3
• Molecular Weight: 630.781
• Mol File: 147556-28-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,2,3,4,5-penta-O-benzyl-aldehydo-L-glucose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,5-penta-O-benzyl-aldehydo-L-glucose(147556-28-3)
• EPA Substance Registry System: 1,2,3,4,5-penta-O-benzyl-aldehydo-L-glucose(147556-28-3)

Safety Data

• Hazardous Substances Data: 147556-28-3(Hazardous Substances Data)

Upstream product

• 96192-07-3 2,3,5-tri-O-benzyl-L-arabinofuranose 
• 258343-41-8 6-O-trityl-D-gulitol 
• 258270-19-8 6-O-trityl-D-gulono-1,4-lactone 
• 6322-07-2 D-gulono-1,4-lactone 
• 100-39-0 benzyl bromide 
• 147648-80-4 2,3,4,5,6-Penta-O-benzyl-L-glucitol 
• 115704-95-5 2,3,4,5,6-penta-O-benzyl-D-glucose diethyl dithioacetal 
• 100-44-7 benzyl chloride 
• 258270-21-2 1,2,3,4,5-penta-O-benzyl-6-O-trityl-D-gulitol 

Downstream Products

• 121682-94-8 2,3,4,5,6-penta-O-benzyl-D-gluconic acid 
• 121709-48-6 1,3-dibenzyloxy-5-benzyloxymethyl-4-<(2R,3S,4R,5R)-2,3,4,5,6-pentabenzyloxy-1-hexanonyl> benzene 
• 121683-00-9 5-benzyloxymethyl-1,3-dimethoxy-4-<(2R,3S,4R,5R)-2,3,4,5,6-penta-benzyloxy-1-hexanonyl> benzene 
• 121682-95-9 methyl 2,3,4,5,6-penta-O-benzyl-D-gluconate 
• 121682-98-2 1,3-dibenzyloxy-5-benzyloxymethyl-4-<(1RS,2R,3S,4R,5R)-1-hydroxy-2,3,4,5,6-pentabenzyloxyhexyl> benzene 
• 121682-96-0 5-benzyloxy-1,3-dimethoxy-4-<(1RS,2R,3S,4R,5R)-1-hydroxy-2,3,4,5,6-pentabenzyloxyhexyl> benzene 

Relevant articles and documents

Synthesis of L-glucose from D-gulono-1,4-lactone

An efficient method for the synthesis of L-glucose from D-gulono-1,4-lactone via 1,2,3,4,5-penta-O-benzyl/acetyl/benzoyl-D-gulitol is described in 34-53% overall yield. Copyright (C) 1999 Elsevier Science Ltd.

Synthesis of L-glucose derivatives from D-glucose and L-arabinose

L-Glucose derivatives are prepared by two different routes.The first involves a modification of the previously reported multi-step approach by Shiozaki, starting from a D-glucurono-1,5-lactone derivative, resulting in the isolation of 2,3,4,6-tetra-O-benz