2-Trifluroacetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl Fluoride (CAS 137686-91-0)

2-Trifluoroacetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl fluoride, a derivative of D-glucopyranosyl fluoride, is a valuable tool in glycobiology research, particularly in the synthesis of complex carbohydrates and glycoconjugates. Its mechanism of action centers around its structural similarity to natural glucose molecules, allowing it to serve as a versatile substrate for enzymatic glycosylation reactions. This compound is utilized as a glycosyl donor in the synthesis of glycoconjugates and glycosylated molecules, facilitating the investigation of carbohydrate-protein interactions and cellular recognition events. Moreover, its chemical properties, such as the trifluoroacetamide group, enable selective modifications of specific hydroxyl groups within the glucose framework, leading to the creation of tailored glycan structures for studying glycan function and molecular recognition. Additionally, 2-Trifluoroacetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl fluoride finds applications in carbohydrate synthesis strategies for accessing diverse carbohydrate libraries, contributing to the development of novel glycan-based materials. Through its versatile applications, this compound continues to advance our understanding of carbohydrate biology and pave the way for innovative research approaches aimed at unraveling the roles of glycans in various biological processes.