Benzyl 2,3,4-Tri-O-benzyl-D-glucuronate Acetate (CAS 4550-93-0)

Benzyl 2,3,4-Tri-O-benzyl-D-glucuronate Acetate is a synthetically modified carbohydrate derivative extensively used in the realms of organic synthesis and carbohydrate chemistry research. This compound features a D-glucuronate sugar moiety, which is a key component in mimicking the structural attributes of naturally occurring polysaccharides. The benzyl groups attached to the 2, 3, and 4 hydroxyl positions of the glucuronate act as protective groups, crucial for preventing unwanted side reactions during chemical synthesis, thereby facilitating selective modifications at other sites within the molecule. The acetate group at the carboxylic acid end enhances the molecule′s solubility in organic solvents, thereby increasing its utility in various synthetic applications. Researchers utilize Benzyl 2,3,4-Tri-O-benzyl-D-glucuronate Acetate primarily to investigate the stereochemical outcomes in glycosylation reactions, where understanding the orientation and reactivity of sugar molecules is essential. Such studies are vital for constructing complex oligosaccharides with precise configurations, which are important for exploring fundamental biochemical pathways and the synthesis of high-purity compounds for material science applications. Through these investigations, significant insights into the mechanics of carbohydrate assembly and disassembly are gained, contributing to advancements in synthetic organic chemistry.