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2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl ethylxanthate is a vital compound in carbohydrate chemistry research due to its role as a glycosyl donor in glycosylation reactions. Its mechanism of action involves facilitating the transfer of the β-D-glucopyranosyl moiety to acceptor molecules under mild reaction conditions. This compound enables the synthesis of complex oligosaccharides and glycoconjugates, contributing to the study of carbohydrate-protein interactions, cell recognition processes, and host-pathogen interactions. Researchers utilize it to create diverse glycan structures, explore the role of carbohydrates in biological systems, and develop glycan-based probes and vaccines. Additionally, its ethylxanthate functionality provides increased reactivity and selectivity in glycosylation reactions, making it a valuable tool for carbohydrate synthesis. The compound′s versatility and efficiency in glycosylation chemistry have led to its widespread application in glycobiology research, where it aids in elucidating the complex roles of carbohydrates in various biological processes and advancing our understanding of carbohydrate-mediated phenomena.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate, 1 g | sc-213975 | 1 g | $360.00 |