92516-62-6

Basic information

• Product Name: methyl 6-azido-2,3,4-tri-O-benzoyl-6-deoxy-β-D-galactopyranoside
• Synonyms: methyl 6-azido-2,3,4-tri-O-benzoyl-6-deoxy-β-D-galactopyranoside
• CAS NO: 92516-62-6
• Molecular Weight: 531.522
• Mol File: 92516-62-6.mol

Chemical Properties

• CAS DataBase Reference: methyl 6-azido-2,3,4-tri-O-benzoyl-6-deoxy-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 6-azido-2,3,4-tri-O-benzoyl-6-deoxy-β-D-galactopyranoside(92516-62-6)
• EPA Substance Registry System: methyl 6-azido-2,3,4-tri-O-benzoyl-6-deoxy-β-D-galactopyranoside(92516-62-6)

Safety Data

• Hazardous Substances Data: 92516-62-6(Hazardous Substances Data)

Upstream product

• 92516-63-7 methyl 2,3,4-tri-O-benzoyl-6-O-p-toluenesulfonyl-β-D-galactopyranoside 
• 10257-28-0 D-Galactose 
• 98-59-9 p-toluenesulfonyl chloride 
• 356060-83-8 methyl 2,3,4-tri-O-benzoyl-6-triisopropylsilyl-β-D-galactopyranoside 
• 1824-94-8 methyl beta-D-galactopyranoside 
• 53182-61-9 methyl 2,3,4-tri-O-benzoyl-β-D-galactopyranoside 

Downstream Products

• 3396-99-4 methyl α-D-galactopyranoside 
• 1824-94-8 methyl beta-D-galactopyranoside 

Relevant articles and documents

Discovery of novel aminosaccharide-based sulfonamide derivatives as potential carbonic anhydrase II inhibitors

In this paper, a new class of novel sulfonamides incorporating aminosaccharide tails were designed and synthesized based on the sugar-tail approach. Then, all the novel compounds were evaluated for their inhibitory activities against three carbonic anhydr

A mild and efficient approach for the regioselective silyl-mediated protection-deprotection of C-4 hydroxyl group on carbohydrates

A regioselective route is reported, which makes the free 4-OH group of hexopyranoses and derivatives easily and rapidly available. This protocol shows high efficiency on intermediates, such as 1a, which contain a TIPS protective group at C-6 and necessarily a benzoyl group at C-4. Treatment of 1a with TBAF cleaves the TIPS protecting group and gives rise to an intramolecular migration of the benzoyl group at C-4 to the less crowded C-6 position.

Dioxolanylium Ions Derived from Carbohydrates. IX. Rearrangement between Dioxolanylium and Dioxanylium Ions

The formation of 4,6-acetoxonium and benzoxonium ion derivatives of methyl gluco-, manno-, galacto- and idopyranosides from the 6-azido-6-deoxy compounds on treatment with nitrosonium ion is described and the formation and rearrangement of the 3,5-benzoxonium ion derived from methyl α-d-xylofuranoside discussed.