2,3,4,6-Tetra-O-acetyl-D-mannopyranose (CAS 140147-37-1)

2,3,4,6-Tetra-O-acetyl-D-mannopyranose is a chemical compound commonly utilized in research within the fields of carbohydrate chemistry and glycobiology. As a derivative of D-mannopyranose, it serves as a versatile building block for the synthesis of various carbohydrate derivatives and glycoconjugates. Its acetyl groups protect the hydroxyl moieties of the mannose ring, allowing for selective functionalization at specific positions. Researchers often employ this compound in the synthesis of complex oligosaccharides, glycopeptides, and glycolipids for studying molecular recognition events, such as protein-carbohydrate interactions and host-pathogen interactions. Additionally, it serves as a valuable precursor for the preparation of glycosyl donors and acceptors in enzymatic and chemical glycosylation reactions. Studies utilizing 2,3,4,6-Tetra-O-acetyl-D-mannopyranose contribute to advancing our understanding of carbohydrate structure-function relationships, as well as the development of carbohydrate-based materials with potential applications in drug delivery, diagnostics, and materials science. Its chemical properties and versatility make it an indispensable tool in carbohydrate chemistry research, facilitating the synthesis of diverse carbohydrate derivatives for various applications in biological and materials sciences.