Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose (CAS 855662-12-3)

Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose is a chemical compound extensively used in carbohydrate chemistry research due to its utility in synthesizing and modifying fucose-containing molecules. The bromo substituent facilitates selective functionalization of the fucose moiety, allowing for site-specific modifications. This compound has been instrumental in the synthesis of complex fucosylated glycans and glycoconjugates, enabling the study of fucose-mediated biological processes such as cell-cell recognition, host-pathogen interactions, and immune response modulation. Researchers have utilized Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose as a precursor in the synthesis of fucose-containing glycolipids, glycoproteins, and glycomimetics for investigating their roles in various physiological and pathological processes. Additionally, its benzoyl groups provide protection to the hydroxyl groups, allowing for orthogonal deprotection strategies and sequential chemical modifications. Furthermore, this compound has been employed in the development of glycan microarrays and glycoprotein engineering approaches for elucidating fucose-dependent protein interactions and their implications in disease mechanisms. Overall, Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose serves as a valuable tool in carbohydrate research, facilitating the exploration of fucose biology and its significance in cellular recognition and signaling pathways.