Methyl 3-Acetylamino-4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-ribo-hexopyranoside (CAS 57865-92-6)

Methyl 3-Acetylamino-4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-ribo-hexopyranoside is a synthetic compound widely utilized in carbohydrate chemistry research for its utility in glycosylation reactions and the synthesis of complex oligosaccharides. Its unique structure, featuring acetyl and benzoyl groups, along with a bromine atom and a deoxy sugar moiety, enables precise control over glycosidic bond formation and regioselectivity. Researchers leverage its chemical properties to explore diverse synthetic strategies for constructing carbohydrate-based molecules with specific biological activities or structural motifs. Additionally, this compound serves as a valuable tool in studying the enzymatic and chemical mechanisms underlying glycosylation reactions, shedding light on the stereochemical outcomes and kinetics of glycosidic bond formation. Furthermore, methyl 3-Acetylamino-4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-ribo-hexopyranoside finds applications in the preparation of carbohydrate derivatives for various research purposes, including the development of glycoconjugates, carbohydrate-based materials, and molecular probes for studying carbohydrate-protein interactions. Its versatility and importance in carbohydrate chemistry research contribute to advancing our understanding of carbohydrate biochemistry and the development of novel carbohydrate-based materials and methodologies.