130163-39-2

Basic information

• Product Name: Methyl-6-O-trityl-2,3,4-tri-O-benzoyl-α-D-galactopyranoside
• Synonyms: Methyl-6-O-trityl-2,3,4-tri-O-benzoyl-α-D-galactopyranoside;Methyl 2,3,4-tri-O-benzoyl-6-O-trityl-a-D-galactopyranoside;Methyl 6-O-(triphenylmethyl)-alpha-D-galactopyranoside tribenzoate
• CAS NO: 130163-39-2
• Molecular Formula: C₄₇H₄₀O₉
• Molecular Weight: 748.824
• Product Categories: Carbohydrates
• Mol File: 130163-39-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl-6-O-trityl-2,3,4-tri-O-benzoyl-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-6-O-trityl-2,3,4-tri-O-benzoyl-α-D-galactopyranoside(130163-39-2)
• EPA Substance Registry System: Methyl-6-O-trityl-2,3,4-tri-O-benzoyl-α-D-galactopyranoside(130163-39-2)

Safety Data

• Hazardous Substances Data: 130163-39-2(Hazardous Substances Data)

Upstream product

• 76-83-5 trityl chloride 
• 98-88-4 benzoyl chloride 
• 3396-99-4 methyl α-D-galactopyranoside 
• 18311-26-7 methyl 6-O-triphenylmethyl-α-D-galactopyranoside 

Downstream Products

• 130163-40-5 methyl 2,3,4-tri-O-benzoyl-α-D-galactopyranoside 6-(sodium sulphate) 

Relevant articles and documents

Visible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glycoamino Acids

An approach for efficient synthesis of C-glycosyl amino acids is described. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylations using both armed and disarmed pentose and hexose derivatives.