1,3,4,6-Tetra-O-acetyl-2-amino-2-desoxy-β-D-glucopyranose hydrochloride (CAS 10034-20-5)

1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-β-D-glucopyranose hydrochloride, a derivative of amino sugar, has garnered significant attention in scientific research due to its versatile applications and intriguing chemical properties. One notable area of investigation lies in its role as a building block for the synthesis of complex carbohydrates and glycoconjugates. Researchers utilize this compound as a key intermediate in the preparation of various glycosylation reactions, enabling the creation of structurally diverse carbohydrates with tailored properties. Moreover, its selective acetylation pattern facilitates precise control over glycosidic linkages, allowing for the synthesis of glycoconjugates with defined stereochemistry and regioselectivity. Additionally, 1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-β-D-glucopyranose hydrochloride serves as a valuable tool in the study of carbohydrate-protein interactions and glycosylation processes. By incorporating this compound into glycan substrates, researchers can investigate the molecular recognition events underlying biological phenomena such as cell-cell interactions, host-pathogen recognition, and immune responses. Furthermore, its hydrochloride salt form enhances solubility and facilitates purification processes, making it suitable for various synthetic and analytical applications in glycobiology research. Ongoing efforts continue to explore the diverse roles and potential applications of this compound in carbohydrate chemistry and glycobiology, further advancing our understanding of complex biological processes and facilitating the development of novel research tools, biological targets, and diagnostics.