Acetyl 6-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-2,3,4-tri-O-acetyl-D-mannopyrannose (CAS 123809-60-9)

Acetyl 6-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-2,3,4-tri-O-acetyl-D-mannopyrannose, a derivative of mannose, plays a pivotal role in carbohydrate chemistry research due to its unique chemical structure and reactivity. This compound serves as a versatile building block for synthesizing complex oligosaccharides and glycoconjugates, contributing significantly to the advancement of glycobiology and glycochemistry. One of its primary research applications lies in the synthesis of oligosaccharides with defined structures, allowing scientists to investigate the structure-function relationships of carbohydrates and their interactions with proteins, lectins, and pathogens. By selectively modifying the hydroxyl groups of mannose residues with acetyl groups, researchers can precisely control the chemical properties and biological activities of the resulting glycoconjugates. Moreover, Acetyl 6-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-2,3,4-tri-O-acetyl-D-mannopyrannose has been employed in the preparation of carbohydrate-based materials, such as glycosylated polymers and nanoparticles, for applications in drug delivery, diagnostics, and biomaterials engineering. Its use in chemical synthesis and material science underscores its significance as a fundamental tool for probing carbohydrate-mediated biological processes and developing innovative glycoengineering strategies. Overall, this compound plays a crucial role in expanding our understanding of carbohydrate biology and exploiting carbohydrates′ unique properties for various research and technological applications.