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Benzyl 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranoside, commonly utilized in carbohydrate chemistry research, acts as a glycosylation agent, facilitating the synthesis of complex carbohydrates. Its mechanism of action involves its ability to serve as a glycosyl donor, participating in glycosylation reactions to form glycosidic bonds between sugar moieties. This compound is particularly valuable in the synthesis of oligosaccharides and glycoconjugates due to its high reactivity and compatibility with various glycosyl acceptors. Researchers exploit its chemical properties to construct structurally diverse carbohydrate derivatives, mimicking natural glycan structures for studying carbohydrate-protein interactions and delucidating glycan biosynthesis pathways. Additionally, Benzyl 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranoside finds application in the preparation of glycosylated biomolecules for bioconjugation strategies, enabling the attachment of carbohydrates to proteins, peptides, or nanoparticles for various biomedical and biotechnological applications. Its versatility and synthetic accessibility make it a valuable tool in the field of glycobiology, advancing our understanding of carbohydrate-mediated biological processes and facilitating the development of novel glycotherapeutics and biomaterials.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Benzyl 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranoside, 1 g | sc-221310 | 1 g | $320.00 |