73108-30-2

Basic information

• Product Name: benzyl 2,6-di-O-benzyl-β-D-galactopyranoside
• Synonyms: benzyl 2,6-di-O-benzyl-β-D-galactopyranoside
• CAS NO: 73108-30-2
• Molecular Weight: 450.532
• Mol File: 73108-30-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: benzyl 2,6-di-O-benzyl-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2,6-di-O-benzyl-β-D-galactopyranoside(73108-30-2)
• EPA Substance Registry System: benzyl 2,6-di-O-benzyl-β-D-galactopyranoside(73108-30-2)

Safety Data

• Hazardous Substances Data: 73108-30-2(Hazardous Substances Data)

Upstream product

• 73108-28-8 benzyl 2,6-O-benzyl-3,4-di-O-isopropylidene-β-D-galactopyranoside 
• 4304-12-5 benzyl β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 14897-51-9 Benzyl 3,4-O-isopropylidene-β-D-galactopyranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 115216-32-5 benzyl-2,6-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-azido-2-desoxy-β-D-galactopyranosyl)-β-D-galactopyranosid 
• 62420-56-8 benzyl 2,6-di-O-benzyl-endo-3,4-O-benzylidene-β-D-galactopyranoside 
• 96520-15-9 benzyl O--(2-3)-2,6-di-O-benzyl-β-D-galactopyranoside 
• 96520-16-0 benzyl O--(2-3)-2,6-di-O-benzyl-β-D-galactopyranoside 
• 73960-72-2 methyl-2,3-didehydro-4,7,8,9-tetra-O-acetyl-N-acetylneuraminate 
• 113473-47-5 C₄₆H₅₃NO₁₇ 
• 57783-81-0 Benzyl 2,3,6-tri-O-benzyl-β-D-galactopyranoside 
• 74801-02-8 benzyl 2,6-di-O-benzyl-3-O-trityl-β-D-galactopyranoside 
• 76637-92-8 benzyl 3-O-benzoyl-2,6-di-O-benzyl-β-D-galactopyranoside 
• 102854-36-4 benzyl 2,6-di-O-benzyl-3-O-β-D-galactopyranosyl-β-D-galactopyranoside 
• 102854-34-2 benzyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside 
• 584-30-5 3-O-β-galactopyranosyl-D-galactose 
• 96520-18-2 benzyl O--(2-3)-4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside 

Relevant articles and documents

Regioselective removal of the anomeric O-benzyl from differentially protected carbohydrates

A mild, regioselective deprotection of the anomeric O-benzyl from multi-functionally protected carbohydrates via catalytic transfer hydrogenation is described. The protocol is tolerant of O-benzyl and O-benzylidene protections at non-anomeric positions, g

ENTWICKLUNG EINES SYNTHESEBLOCKS DER 3-O-β-D-GALACTOPYRANOSYL-D-GALACTOPYRANOSE

In the presence of trimethylsilyl triflate, 1,2,3,4,6-penta-O-acetyl-β-D-galactopyranose reacted with benzyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside to give benzyl 2,6-di-O-benzyl-3-O-β-D-galactopyranosyl-β-D-galactopyranoside further converted i

A Mild Procedure for the Regiospecific Benzylation and Allylation of Polyhydroxy-compounds via their Stannylene Derivatives in Non-polar Solvents

The reactions of benzyl and allylbromides on the stannylene derivatives of polyhydroxy-compounds, which normally proceed only at insignificant speed in refluxing benzene solution, are greatly accelerated in the presence of quaternary ammonium halides.Thes