161907-34-2

Basic information

• Product Name: Methyl 3,5,6-tri-O-benzyl-α-D-mannofuranoside
• CAS NO: 161907-34-2
• Molecular Weight: 464.558
• Mol File: 161907-34-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Methyl 3,5,6-tri-O-benzyl-α-D-mannofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 3,5,6-tri-O-benzyl-α-D-mannofuranoside(161907-34-2)
• EPA Substance Registry System: Methyl 3,5,6-tri-O-benzyl-α-D-mannofuranoside(161907-34-2)

Safety Data

• Hazardous Substances Data: 161907-34-2(Hazardous Substances Data)

Upstream product

• 53928-30-6 1,2-O-isopropylidene-3,5,6-tri-O-benzyl-α-D-glucofuranoside 
• 35958-64-6 3,5,6-Tri-O-benzyl-α,β-D-glucofuranose 
• 67-56-1 methanol 
• 161835-09-2 1,2-anhydro-3,5,6-tri-O-benzyl-β-D-mannofuranose 

Relevant articles and documents

Synthesis and glycosidic reaction of 1,2-anhydromanno-, lyxo-, gluco-, and xylofuranose perbenzyl ethers

Stereospecific synthesis of 1,2-anhydromanno-, lyxo-, gluco-, and xylofuranose perbenzyl ethers was successfully achieved via intramolecular SN2 reaction of the corresponding C-1 alkoxide with C-2 bearing tosyloxy group. The key intermediates, furanose 2-sulfonates, were prepared from the corresponding 1,2-diols and tosyl chloride under phase transfer conditions in good yields. Condensation of the anhydro sugars with 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose or N-benzyloxycarbonyl L-serine methyl ester in the absence of catalyst gave 1,2-trans-linked glycofuranosides in high yield.