109526-95-6

Basic information

• Product Name: methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside
• Synonyms: methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside
• CAS NO: 109526-95-6
• Molecular Weight: 268.31
• Mol File: 109526-95-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside(109526-95-6)
• EPA Substance Registry System: methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside(109526-95-6)

Safety Data

• Hazardous Substances Data: 109526-95-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 100-44-7 benzyl chloride 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 86447-92-9 methyl 4-O-benzyl-6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 

Downstream Products

• 148431-61-2 methyl 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 151803-47-3 methyl 4-O-benzyl-6-deoxy-3-O-methyl-α-D-mannopyranoside 
• 73889-45-9 methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hexopyranoside 
• 21317-50-0 methyl 2,3,6-trideoxy-α-D-erythro-hexopyranoside 
• 144993-44-2 methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside 
• 151803-49-5 methyl 3,4-di-O-benzyl-6-deoxy-2-O-<(methylthio)thiocarbonyl>-α-D-mannopyranoside 
• 151803-48-4 methyl 4-O-benzyl-6-deoxy-3-O-methyl-2-O-<(methylthio)thiocarbonyl>-α-D-mannopyranoside 
• 151803-51-9 methyl 3,4-di-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 151803-50-8 methyl 4-O-benzyl-2,6-dideoxy-3-O-methyl-α-D-arabino-hexopyranoside 
• 152174-28-2 1,3-di-O-acetyl-2,4-di-O-benzyl-α-D-rhamnopyranose 

Relevant articles and documents

Synthesis of a Trisaccharide Repeating Unit of the O-Antigen from Burkholderia multivorans and Its Oligomers

Burkholderia multivorans is a Gram-negative bacterium, and an important opportunistic human pathogen that can cause fatal infections. Its O-antigens are useful templates for the development of carbohydrate-based vaccines. A highly convergent and efficient

Synthesis of the Methyl α-D-Glycosides of Amicetose, Perosamine and Janose

New methods for the synthesis of tri- and di-deoxy sugar, namely methyl α-D-amicetoside, methyl α-D-perosaminoside and methyl α-D-janoside are described.The readily available methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside has been used as chiral