1,2,3,4,6-penta-O-acetyl-alpha-D-galactopyranose CAS:4163-59-1

Organic synthesis: It serves as a starting material or intermediate for the synthesis of other complex carbohydrates, glycosides, and glycoconjugates. By selectively deprotecting the acetyl groups, chemists can introduce different functional groups onto the sugar backbone, creating new compounds with desired properties.

Biochemical research: This compound is used in various biochemical studies to investigate the role of carbohydrates in biological processes. Its acetylated form provides stability, allowing researchers to manipulate and study specific interactions between carbohydrates and proteins or other biomolecules.

Medicinal chemistry: Due to its carbohydrate nature, 1,2,3,4,6-penta-O-acetyl-alpha-D-galactopyranose and its derivatives are studied for their potential therapeutic applications. They can be modified to mimic specific complex carbohydrates found in nature, which play important roles in cell communication, immune response, and disease progression. Understanding these interactions may lead to the development of new drugs or treatments.