1,6-Anhydro-2,3-O-(1-isopropylidene)-4-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-β-D-mannopyranose (CAS 67591-05-3)

1,6-Anhydro-2,3-O-(1-isopropylidene)-4-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-β-D-mannopyranose is a multifunctional synthetic sugar derivative extensively used in the field of carbohydrate chemistry for the exploration of complex oligosaccharide synthesis. This compound features an anhydro bridge, linking the first and sixth carbon atoms of the mannopyranose ring, which imparts notable stability and reactivity to the molecule, facilitating its use in challenging glycosylation reactions. The structure of this chemical includes isopropylidene and acetyl protective groups which play crucial roles in its application. These groups protect the hydroxyl functionalities during synthesis, allowing for selective activation and subsequent bond formation with other sugar units. This selectivity is pivotal for constructing specific glycosidic linkages that are essential in the study of carbohydrate-based interactions. Researchers utilize this compound primarily to investigate the synthesis pathways and structural behaviors of mannose-containing polysaccharides. The insights gained from such studies are fundamental for understanding the underlying principles of carbohydrate molecular recognition and assembly, critical for advancing basic scientific knowledge in fields such as materials science and synthetic biology. The chemical serves as a key tool in designing and synthesizing novel carbohydrate polymers and materials, exploring their physical properties and interactions.