13673-76-2

Basic information

• Product Name: O¹,O²,O³,O⁴-tetrabenzoyl-O⁶-(tetra-O-benzoyl-α-D-galactopyranosyl)-ξ-D-glucopyranose
• CAS NO: 13673-76-2
• Molecular Weight: 1175.17
• Mol File: 13673-76-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: O¹,O²,O³,O⁴-tetrabenzoyl-O⁶-(tetra-O-benzoyl-α-D-galactopyranosyl)-ξ-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: O¹,O²,O³,O⁴-tetrabenzoyl-O⁶-(tetra-O-benzoyl-α-D-galactopyranosyl)-ξ-D-glucopyranose(13673-76-2)
• EPA Substance Registry System: O¹,O²,O³,O⁴-tetrabenzoyl-O⁶-(tetra-O-benzoyl-α-D-galactopyranosyl)-ξ-D-glucopyranose(13673-76-2)

Safety Data

• Hazardous Substances Data: 13673-76-2(Hazardous Substances Data)

Upstream product

• 536-11-8 D-melibiose 
• 98-88-4 benzoyl chloride 

Downstream Products

• 773145-62-3 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate 
• 851078-70-1 C₆₁H₄₉BrO₁₇ 

Relevant articles and documents

Synthesis and hemolytic activity of some hederagenin diglycosides

Glycosylation of hederagenin with the trichloroacetimidate derivatives of six commercial disaccharides (D-cellobiose, D-lactose, D-maltose, D-melibiose, D-gentiobiose, D-isomaltose) was performed giving the protected saponins in high yields. Deprotection

Synthesis of 12- O-Mono- and Diglycosyl-oxystearates, a New Class of Agonists for the C-type Lectin Receptor Mincle

Fifteen glycosyl-oxystearates were synthesized by Crich's 4,6-benzylidene and K?ening-Knorr strategies. Assessment of structure-activity relationships using macrophage-inducible C-type lectin (Mincle) receptor cells expressing nuclear factor of activated