2-Deoxy-1,3:4,5-di-O-isopropylidene-2-oxamoylamino-D-mannitol (CAS 128741-75-3)

2-Deoxy-1,3:4,5-di-O-isopropylidene-2-oxamoylamino-D-mannitol is a multifunctional synthetic sugar derivative primarily utilized in organic chemistry research, focusing on the study of complex glycosylation reactions and the synthesis of novel glycoconjugates. The structure includes isopropylidene groups that protect the mannitol molecule′s vicinal diols, thereby stabilizing the sugar ring against harsh chemical environments and facilitating selective modifications. The oxamoylamino group introduces nitrogen functionality, which is particularly valuable for investigating nucleophilic addition reactions and the formation of amide bonds in biomimetic syntheses. This compound serves as a crucial tool for exploring new dimensions in carbohydrate chemistry, particularly in the development of amide linkage-based polymers and glycomimetics, which mimic natural carbohydrate functions but with enhanced stability and modified properties. Researchers leverage this compound to study the interaction between sugar hydroxyl groups and various reagents, enhancing our understanding of carbohydrate reactivity and enabling the design of targeted organic synthesis strategies. Such studies contribute significantly to the fields of materials science and biotechnology, where engineered sugar derivatives are crucial for creating innovative materials, such as biodegradable plastics and responsive gel matrices. These applications are strictly research-oriented, focusing on the fundamental aspects of sugar chemistry and materials development.