CAS 102185-26-2
:3-Acetamido-3-deoxy-D-allose
Description:
3-Acetamido-3-deoxy-D-allose is a monosaccharide derivative characterized by the presence of an acetamido group at the C-3 position of the D-allose sugar backbone. This compound is a hexose, which means it contains six carbon atoms, and it is an epimer of other sugars due to the specific configuration of its hydroxyl groups. The acetamido substitution introduces a functional group that can participate in various chemical reactions, making it useful in biochemical applications. It is typically white to off-white in appearance and is soluble in water, which is common for many sugars and their derivatives. The presence of the acetamido group also suggests potential applications in medicinal chemistry and biochemistry, particularly in the synthesis of glycosylated compounds or as a building block in carbohydrate chemistry. Its molecular structure contributes to its reactivity and interactions with other biomolecules, making it a subject of interest in research related to glycoproteins and other carbohydrate-based materials.
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3-Acetamido-3-deoxy-D-allose
CAS:<p>3-Acetamido-3-deoxy-D-allose is a ringed sugar that is nucleophilic and reacts with hydroxide solution to form a dithioacetal. It has been analyzed using deuterium and cyclic voltammetry. 3-Acetamido-3-deoxy-D-allose can be oxidized by periodate to form an alditol acetal and then reacted with ammonium hydroxide to produce the corresponding amine. This reaction was used to generate the compound in large quantities.</p>Formula:C8H15NO6Purity:Min. 95%Molecular weight:221.21 g/mol
