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2-(4-Methoxybenzylidene)imino-2-deoxy-D-glucopyranose, a derivative of D-glucopyranose, holds significance in glycobiology research due to its potential applications in carbohydrate chemistry and chemical biology. The compound features an imine group and a methoxybenzylidene moiety attached to a glucopyranose scaffold, offering versatility in synthetic strategies for the generation of glycosides and glycoconjugates. One of its notable research applications is its utilization as a glycosyl donor in glycosylation reactions, where the imine functionality acts as a reactive site for glycosidic bond formation. Researchers have employed this compound in the synthesis of complex oligosaccharides and glycoconjugates, contributing to the development of carbohydrate-based probes, sensors, and biomaterials. Additionally, its potential as a glycosylation reagent has been explored in the preparation of glycosylated molecules for studies investigating carbohydrate-protein interactions, cellular recognition processes, and bioconjugation strategies. Furthermore, the compound′s structural features enable precise control over glycosylation reactions, facilitating the synthesis of structurally-defined carbohydrates for various research applications in glycobiology, chemical biology, and biotechnology.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-(4-Methoxybenzylidene)imino-2-deoxy-D-glucopyranose, 2.5 g | sc-208927 | 2.5 g | $326.00 |