Methyl 6-Deoxy-2-O-methyl-3-O-benzyl-α-D-galactopyranoside (CAS 110594-91-7)

Methyl 6-Deoxy-2-O-methyl-3-O-benzyl-α-D-galactopyranoside is a synthetic compound widely employed in carbohydrate chemistry research for its pivotal role in the synthesis of complex oligosaccharides and glycoconjugates. Its chemical structure, characterized by a deoxy sugar moiety, a methyl group at the second position, and a benzyl ether at the third position, offers unique reactivity and selectivity in glycosylation reactions. Researchers utilize this compound to explore various synthetic strategies for constructing structurally diverse carbohydrate molecules with precise control over regiochemistry and stereochemistry. Additionally, methyl 6-Deoxy-2-O-methyl-3-O-benzyl-α-D-galactopyranoside serves as a valuable tool in elucidating the mechanisms of glycosylation reactions, including the role of protecting groups in controlling glycosidic bond formation and the stereochemical outcomes of glycosylation reactions. Furthermore, this compound finds applications in biochemical and biophysical studies, such as the development of glycoconjugates for investigating carbohydrate-protein interactions or the synthesis of carbohydrate-based materials for biomaterials research. Its versatility and utility in carbohydrate chemistry research contribute to advancing our understanding of carbohydrate biochemistry and the development of novel carbohydrate-based materials and methodologies.