Methyl 2,3,6-Tri-O-benzoyl-α-D-galactopyranoside (CAS 3601-36-3)

Methyl 2,3,6-Tri-O-benzoyl-α-D-galactopyranoside is a compound widely utilized in carbohydrate chemistry research for its role as a versatile building block in the synthesis of complex carbohydrates and glycoconjugates. Its mechanism of action lies in its ability to serve as a protected form of α-D-galactopyranoside, facilitating the synthesis of structurally diverse galactose-containing compounds. Researchers employ this compound as a starting material for the preparation of glycosides, glycopeptides, and glycolipids with tailored structures, enabling investigations into the structure-function relationships of glycans and their interactions with biological molecules. Additionally, Methyl 2,3,6-Tri-O-benzoyl-α-D-galactopyranoside serves as a precursor for the synthesis of glycosyl donors and acceptors, which are essential for enzymatic and chemical glycosylation reactions. Its application extends to the synthesis of carbohydrate-based probes and inhibitors for studying carbohydrate-processing enzymes and carbohydrate-binding proteins involved in various physiological and pathological processes. Furthermore, this compound finds utility in the development of glycan microarrays and glycoproteomic strategies for high-throughput screening of carbohydrate-protein interactions. Overall, Methyl 2,3,6-Tri-O-benzoyl-α-D-galactopyranoside serves as a valuable tool in carbohydrate synthesis and glycobiology research, enabling the exploration of carbohydrate-mediated biological phenomena.