Benzyl 2,3,4,6-Tetra-O-acetyl-β-D-Glucopyranoside (CAS 10343-13-2)

Benzyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside, assigned CAS number 10343-13-2, is extensively utilized in carbohydrate chemistry for its crucial role in glycosylation studies. This compound is a benzyl glycoside where the glucose moiety is protected by acetyl groups at the 2, 3, 4, and 6 positions, making it a versatile intermediate for synthesizing complex glycosides. The presence of the benzyl and acetyl groups serves to protect the sugar from undesired chemical reactions during synthesis, allowing for selective deprotection and controlled glycosidic linkage formation. This specific structure is particularly valuable in the study of carbohydrate-protein interactions, as it can be used to mimic natural glycosidic bonds found in biological systems. Researchers employ this compound to explore the mechanisms of glycosyltransferases, enzymes that catalyze the transfer of sugar moieties to other molecules, which is fundamental in understanding biomolecular recognition and signaling. Moreover, its use in synthetic chemistry provides insights into the development of new methodologies for assembling carbohydrates that could be applied to produce materials with specific biological activities. The research applications of Benzyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside are solely focused on advancing scientific knowledge in synthetic and analytical chemistry, contributing significantly to the field.