134039-09-1

Basic information

• Product Name: methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside
• Synonyms: methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside
• CAS NO: 134039-09-1
• Molecular Weight: 404.46
• Mol File: 134039-09-1.mol

Chemical Properties

• CAS DataBase Reference: methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside(134039-09-1)
• EPA Substance Registry System: methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside(134039-09-1)

Safety Data

• Hazardous Substances Data: 134039-09-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 134039-06-8 methyl 2,6-di-O-benzyl-4-deoxy-α-L-threo-hex-4-enopyranoside 
• 216577-87-6 methyl 4-O-acetyl-2,6-di-O-benzyl-5-C-methoxy-β-D-xylo-hexopyranosyl-3-ulose 
• 216577-81-0 methyl 4-O-acetyl-2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 102854-30-8 methyl 2,6-di-O-benzyl-3,4-O-isopropylidene-β-D-galactopyranoside 
• 14897-47-3 methyl 3,4-di-O-isopropylidene-β-D-galactopyranoside 

Downstream Products

• 143520-31-4 methyl 3,4-di-O-acetyl-2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside 
• 143520-39-2 2-Benzyloxy-1-((2R,3R,4R,5S)-4-benzyloxy-3,5-dihydroxy-tetrahydro-furan-2-yl)-ethanone 
• 143520-47-2 2-Benzyloxy-1-((2R,3R,4R,5R)-4-benzyloxy-3,5-dihydroxy-tetrahydro-furan-2-yl)-ethanone 
• 216577-81-0 methyl 4-O-acetyl-2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside 
• 497162-84-2 (2R,3R,4R,5R,6R)-3,5-Bis-benzyloxy-2-benzyloxymethyl-2,6-dimethoxy-tetrahydro-pyran-4-ol 
• 188779-01-3 2,6-di-O-benzyl-L-arabino-aldohexos-5-ulose 
• 216577-78-5 methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-gulopyranoside 
• 216577-87-6 methyl 4-O-acetyl-2,6-di-O-benzyl-5-C-methoxy-β-D-xylo-hexopyranosyl-3-ulose 
• 216577-86-5 methyl 4-O-acetyl-3-O-benzoyl-2,6-di-O-benzyl-5-C-methoxy-β-D-gulopyranoside 
• 216577-83-2 methyl 4-O-acetyl-2,6-di-O-benzyl-5-C-methoxy-3-O-trifluoromethanesulfonyl-β-D-galactopyranoside 
• 1044736-05-1 C₂₃H₃₀O₇ 
• 143520-43-8 Acetic acid (2R,3R,4R,5R,6R)-4,5-diacetoxy-2-benzyloxymethyl-2,6-dimethoxy-tetrahydro-pyran-3-yl ester 
• 143520-42-7 methyl 6-O-benzyl-5-C-methoxy-β-D-galactopyranoside 
• 259751-64-9 methyl 2,6-di-O-benzyl-3,4-O-isopropylidene-5-C-methoxy-β-D-talopyranoside 

Relevant articles and documents

A simple stereospecific route to 5-C-alkoxy-D-galactopyranosides and to L-arabino-hexos-5-uloses

5-C-alkoxy-β-D-galactopyranosides, which are easily convertible into L-arabino-hexos-5-uloses, can be prepared from β-D-galactopyranoside via peroxyacid oxidation in an alcoholic solvent of intermediate 4-deoxy-α-L-threo-hex-4-enopyranosides.

A new method for the synthesis of carba-sugar enones (gabosines) using a mercury(II)-mediated opening of 4,5-cyclopropanated pyranosides as the key-step

The stereoselective transformation of the cyclopropyl derivative 2, stereoselectively obtained with the Simmons-Smith reaction of methyl 2,6-di-O-benzyl-α-l-threo-hex-4-enopyranoside (1), into gabosines and deoxy-carbahexoses is described. The treatment o

Preparation of L-lyxo-hexos-5-ulose through C-3 epimerization of bis-glycopyranosides of L-arabino-hexos-5-ulose 1

The unreported title compound and its 2,6-di-O-benzyl derivative have been prepared from methyl β-D-galactopyranoside through a sequence involving the bisglycoside methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside 8, the precursor of L-arabino-hexo

A new route to D-xylo-hexo-5-ulose and some of its selectively protected derivatives from D-galactose(

A new approach to D-xylo-hexos-5-ulose, a useful synthetic intermediate, is described, starting from methyl β-D-galactopyranoside and involving as the key step an epoxidation/methanolysis of 3-O-protected methyl 2,6-di-O-benzyl-4-deoxy-α-L-threo-hex-4-eno

NEW SYNTHETIC PATHWAYS TO 5-C-ALKOXYPYRANOSIDES AND TO HEXOS-5-ULOSE DERIVATIVES

Several new 5-C-alkoxy-D-galactopyranosides have been obtained by oxidation of 4-deoxy-α-L-threo-hex-4-enopyranosides (easily available from β-D-galactopyranosides) with MCPBA in alcoholic solvents.They have been converted into the so far unreported L-ara