117371-67-2

Basic information

• Product Name: Methyl 2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside
• Synonyms: Methyl 2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside
• CAS NO: 117371-67-2
• Molecular Weight: 358.434
• Mol File: 117371-67-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Methyl 2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside(117371-67-2)
• EPA Substance Registry System: Methyl 2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside(117371-67-2)

Safety Data

• Hazardous Substances Data: 117371-67-2(Hazardous Substances Data)

Upstream product

• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 138665-01-7 Methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-ribo-hexopyranoside 
• 128537-01-9 Methyl 4-O-acetyl-2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside 
• 76375-66-1 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 100-44-7 benzyl chloride 
• 65530-28-1 methyl 4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 

Downstream Products

• 128537-13-3 methyl 2,6-di-O-benzyl-4,5-didehydro-3,4-dideoxy-α-D-glucopyranoside 
• 128537-08-6 Methyl 2,6-di-O-benzyl-3-deoxy-4-O-(methylsulfonyl)-α-D-xylo-hexopyranoside 
• 128537-03-1 (2R,3R,5R,6S)-5-Benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-ol 
• 128537-07-5 Methyl 4-O-benzoyl-2,6-di-O-benzyl-3-deoxy-α-D-xylo-hexopyranoside 
• 128537-09-7 Methyl 4-azido-2,6-di-O-benzyl-3,4-dideoxy-α-D-ribo-hexopyranoside 

Relevant articles and documents

Regioselectivity of Reductive Cleavage of Methyl 4,6-O-Benzylidene-3-deoxyhexopyranosides Containing Fluorine at the 2- or 3-Position with LiAlH4-AlCl3

Reductive ring-opening reactions of the 4,6-O-benzylidene derivatives of methyl 3-deoxy-β-D-arabino-, 3-deoxy-α-D-ribo-, and 2-O-benzyl-3-deoxy-α-D-ribo-hexopyranosides with LiAlH4 and AlCl3 in the molar ratio of 4:4 gave the 4- and 6-O-benzyl derivatives

Syntheses of specifically deoxygenated methyl α-isomaltotriosides

Specifically deoxygenated methyl α-isomaltotriosides were synthesized by the silver perchlorate-mediated condensation of a protected α-isomaltosyl chloride with suitably blocked derivatives of methyl α-D-glucopyranoside deoxygenated respectively at positi