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Methyl 2-acetamido-2-deoxy-4,6-O-benzylidene-O-β-D-glucopyranoside is a key compound in carbohydrate chemistry and glycobiology research. Its mechanism of action centers around its role as a glycosyl donor in synthetic glycosylation reactions. Specifically, it serves as an essential building block for the synthesis of complex oligosaccharides through glycosylation processes. The benzylidene group acts as a protecting group, enhancing the regioselectivity and stereoselectivity of glycosylation reactions, thereby facilitating the formation of glycosidic bonds with high efficiency and specificity. Researchers have extensively utilized this compound in synthetic strategies aimed at accessing structurally diverse glycoconjugates and oligosaccharides. By employing this molecule as a glycosyl donor, scientists can create complex carbohydrate structures for various research applications. These applications span diverse fields, including glycobiology, chemical biology, materials science, and drug discovery. Furthermore, its role as a key intermediate in carbohydrate synthesis has paved the way for advancements in glycan array technology, carbohydrate-based vaccine development, and the study of carbohydrate-protein interactions. Overall, methyl 2-acetamido-2-deoxy-4,6-O-benzylidene-O-β-D-glucopyranoside stands as a crucial tool in carbohydrate research, enabling the synthesis of complex glycan structures for a wide range of scientific investigations.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Methyl 2-acetamido-2-deoxy-4,6-O-benzlydene-O-β-D-glucopryanoside, 50 mg | sc-218732 | 50 mg | $300.00 |