2-O-(2-Deoxy-2-N-phthalimido-3,4,6-tri-O-acetyl-beta-D-glucopyranosyl)-3-O-benzyl-4,6-O-benzylidene-α-D-mannose (CAS 865488-82-0)

2-O-(2-Deoxy-2-N-phthalimido-3,4,6-tri-O-acetyl-β-D-glucopyranosyl)-3-O-benzyl-4,6-O-benzylidene-α-D-mannose is a complex synthetic carbohydrate derivative exemplifying the complex maneuvers possible in carbohydrate chemistry. This compound is synthesized through a series of protection and deprotection steps, crucial for the selective modification of specific hydroxyl groups within the sugar molecules. Its structure incorporates phthalimido and benzylidene groups, which serve as protective groups that can be selectively removed or modified. The presence of these groups also potentially modifies the physical properties and reactivity of the carbohydrate core, making it a valuable tool in the study of carbohydrate interactions and functions. In research, such molecules are primarily used to probe the biochemical pathways involving carbohydrates, to understand the mechanisms of carbohydrate recognition by proteins, and to explore the synthesis of complex glycostructures. The derivative′s elaborate structure allows scientists to study stereochemical outcomes during synthesis processes and helps in the elucidation of interaction patterns in biological systems, thereby contributing to fundamental research in biochemistry and organic chemistry, particularly in the field of glycoscience where the manipulation of carbohydrate structures is essential for exploring biological phenomena.