Methyl 2,3-Dibenzoyl-4,6-O-benzylidene-β-D-galactopyranoside (CAS 53598-03-1)

Methyl 2,3-dibenzoyl-4,6-O-benzylidene-β-D-galactopyranoside is a compound frequently employed in carbohydrate chemistry research due to its utility in glycosylation reactions and the synthesis of complex carbohydrate derivatives. Its benzoyl and benzylidene functionalities serve as protecting groups for the hydroxyl groups on the sugar scaffold, facilitating selective deprotection under mild conditions. This compound is commonly utilized as a glycosyl donor or acceptor substrate in chemical or enzymatic glycosylation processes, allowing for the efficient assembly of diverse glycan structures. Researchers utilize it to investigate glycosylation mechanisms, develop novel glycosylation methodologies, and explore carbohydrate-protein interactions. By leveraging its reactivity and stability properties, scientists can synthesize tailored glycan molecules with precise regio- and stereochemistry, enabling studies on carbohydrate recognition events, cell signaling pathways, and host-pathogen interactions. Additionally, methyl 2,3-dibenzoyl-4,6-O-benzylidene-β-D-galactopyranoside contributes to the synthesis of carbohydrate-based probes, glycan microarrays, and synthetic oligosaccharide libraries, facilitating investigations into carbohydrate biology, glycobiology, and glycoscience research. Overall, this compound serves as a valuable tool for advancing our understanding of carbohydrate structure-function relationships and their roles in various biological processes.