191332-82-8

Basic information

• Product Name: methyl 6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside
• Synonyms: methyl 6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside
• CAS NO: 191332-82-8
• Molecular Weight: 466.531
• Mol File: 191332-82-8.mol

Chemical Properties

• CAS DataBase Reference: methyl 6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside(191332-82-8)
• EPA Substance Registry System: methyl 6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside(191332-82-8)

Safety Data

• Hazardous Substances Data: 191332-82-8(Hazardous Substances Data)

Upstream product

• 191332-83-9 methyl 2,3,4-tri-O-benzyloxycarbonyl-6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 

Downstream Products

• 1304043-53-5 methyl 6-deoxy-6-(diethylphospate)-2,3,4-tri-O-benzyl-α-D-mannopyranozide 
• 1304043-35-3 6-(methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-manno-pyranozide) boronic acid 
• 122588-56-1 (2S,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-2-methoxy-6-vinyl-tetrahydro-pyran 
• 40653-15-4 methyl 2,3,4-tri-O-benzyl-α-D-manno-hexodialdo-1,5-pyranoside 
• 191332-86-2 methyl 4-O-benzoyl-2,3,6-tri-O-benzyloxycarbonyl-α-D-mannopyranoside 
• 191332-85-1 methyl 2,3,6-tri-O-benzyloxycarbonyl-α-D-mannopyranoside 
• 191332-84-0 methyl 2,3,4-tri-O-benzyloxycarbonyl-α-D-mannopyranoside 
• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 791820-19-4 methyl 2,3,4-tri-O-benzyl-6-monomethoxytrityl-α-D-mannopyranoside 
• 191332-83-9 methyl 2,3,4-tri-O-benzyloxycarbonyl-6-O-(4-methoxyphenyldiphenylmethyl)-α-D-mannopyranoside 

Relevant articles and documents

Selective Removal of Benzyl Carbonate Used as a Protecting Group in Carbohydrate Chemistry

It has been demonstrated that benzyl carbonate protecting group is orthogonal with tert-butyldimethylsilyl and (4-methoxy)trityl ethers. Moreover, benzyl carbonates can be selectively cleaved using aminolysis conditions.

NOVEL MANNOPYRANOSIDE DERIVATIVES WITH ANTICANCER ACTIVITY

The present invention relates to mannopyranoside-derived compounds and to the use thereof as medicaments, in particular in the treatment of cancer diseases, and also to the method for preparing same and to pharmaceutical compositions comprising such compo

Chain elongation of primary alcohols of carbohydrates

The chain elongation of primary alcohol of saccharides (α-d-ribose, α-d-glucose, α-d-mannose) and a disaccharide (α-d-melibiose) has been achieved via a Mitsunobu reaction using bis(2,2,2-trifluoroethyl) malonate as nucleophile.

The benzyloxycarbonyl group: An alternative protective group in the mannose series

A procedure for the O-benzyloxycarbonylation at positions 2-4 in the mannose series is described. Starting from methyl 6-O-(4-methoxy)trityl-α-D-mannopyranoside, methyl 2,3,4-tri-O-benzyloxycarbonyl-6-O-(4-methoxy)trityl-α-D- mannopyranoside was obtained.