2-Methyl-4,5-(3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyrano)-Δ2-oxazoline (CAS 35954-65-5)

2-Methyl-4,5-(3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyrano)-Δ2-oxazoline is a versatile compound with significant applications in carbohydrate chemistry and glycobiology research. Its chemical structure consists of an oxazoline ring attached to a modified glucopyranose unit, with acetyl groups providing protection to specific hydroxyl groups. This compound has been extensively utilized as a glycosyl donor in oligosaccharide synthesis and glycosylation reactions due to its ability to act as a glycosylating agent in the presence of suitable activators or catalysts. Additionally, 2-Methyl-4,5-(3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyrano)-Δ2-oxazoline serves as a valuable building block for the preparation of complex carbohydrates and glycoconjugates, including glycopeptides, glycolipids, and glycoproteins. Its unique reactivity and stability make it an indispensable tool for studying glycan biosynthesis, carbohydrate recognition, and carbohydrate-mediated biological processes. Furthermore, this compound facilitates the synthesis of structurally diverse carbohydrate derivatives for investigating carbohydrate-protein interactions and developing carbohydrate-based materials. Its utility extends to various research areas, including chemical biology, glycotechnology, biomaterials science, and drug discovery, where precise control over glycan structure and function is essential for elucidating biological mechanisms and developing innovative solutions.