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Methyl 2,3,4-tri-O-acetyl-β-D-glucuronic acid methyl ester plays a pivotal role in carbohydrate chemistry research, particularly in the synthesis of complex glycosides and glycoconjugates. Its chemical structure, featuring three acetyl groups on the glucuronic acid moiety, offers unique opportunities for selective functionalization and subsequent glycosylation reactions. This compound serves as a versatile building block for the preparation of various carbohydrate derivatives, enabling the construction of complex glycan structures with tailored functionalities. Researchers have utilized methyl 2,3,4-tri-O-acetyl-β-D-glucuronic acid methyl ester in the synthesis of glycosaminoglycans (GAGs), such as heparin and heparan sulfate mimetics, which are crucial components of the extracellular matrix and play essential roles in numerous biological processes, including cell signaling and inflammation. Additionally, this compound has been employed in the assembly of glycolipids, glycoproteins, and glycosylated natural products, facilitating the study of their structure-function relationships and biological activities. Its versatility and significance in carbohydrate chemistry research contribute to advancements in glycobiology and provide valuable tools for elucidating the roles of carbohydrates in various biological systems.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Methyl 2,3,4-Tri-O-acetyl-β-D-glucuronic Acid Methyl Ester, 25 mg | sc-211828 | 25 mg | $360.00 |