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3-Acetyl-1,2-O-isopropylidene-6-O-trityl-α-D-galactofuranose plays a significant role in carbohydrate chemistry research, particularly in the synthesis of complex glycoconjugates and oligosaccharides. Its structural features, including the acetyl, isopropylidene, and trityl groups, make it a valuable precursor for the construction of diverse carbohydrate derivatives. In research, this compound is utilized for glycosylation reactions, where the isopropylidene group serves as a protecting group, enabling selective functionalization of hydroxyl groups. Additionally, the trityl group provides stability during synthetic transformations, facilitating the introduction of α-D-galactofuranose moieties into oligosaccharide chains. This compound is instrumental in the study of glycan biosynthesis pathways and carbohydrate-protein interactions. Furthermore, it enables the synthesis of glycoconjugates for investigating molecular recognition events and developing carbohydrate-based materials with potential applications in various fields, including biomaterials, biotechnology, and glycobiology. Overall, 3-Acetyl-1,2-O-isopropylidene-6-O-trityl-α-D-galactofuranose serves as a versatile building block for the synthesis of complex carbohydrates, contributing to advancements in carbohydrate chemistry and glycobiology research.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Acetyl-1,2-O-isopropylidene-6-O-trityl-α-D-galactofuranose, 10 mg | sc-209514 | 10 mg | $360.00 |