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2-Deoxy-3,5-di-O-benzoylribofuranose, a modified sugar derivative, has garnered attention in various research fields due to its unique chemical properties and versatile applications. One significant area of study involves its utilization as a building block in the synthesis of nucleoside analogs, particularly in the development of antiviral and anticancer agents. The compound serves as a precursor for the synthesis of nucleoside analogs by introducing functional groups onto the ribose moiety, altering their pharmacokinetic and pharmacodynamic properties. Additionally, 2-Deoxy-3,5-di-O-benzoylribofuranose has been employed in carbohydrate chemistry research to investigate glycosylation reactions and enzymatic transformations. Its structural features, such as the deoxyribose backbone and benzoyl substituents, enable precise manipulation and control over glycosidic bond formation and cleavage processes. Furthermore, this compound has been utilized in the synthesis of carbohydrate-based materials and as a molecular probe for studying carbohydrate-protein interactions. Overall, 2-Deoxy-3,5-di-O-benzoylribofuranose serves as a valuable tool in organic synthesis, carbohydrate chemistry, and drug discovery research, facilitating the exploration of new chemical entities and bioactive compounds.
Ordering Information
Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Deoxy-3,5-di-O-benzoylribofuranose, 100 mg | sc-391817 | 100 mg | $300.00 |