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CAS 14307-09-6

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2-Amino-2-deoxy-D-altrose

Description:
2-Amino-2-deoxy-D-altrose, with the CAS number 14307-09-6, is an amino sugar that is structurally related to D-altrose, a hexose sugar. This compound features an amino group (-NH2) at the second carbon position, replacing a hydroxyl group (-OH), which is characteristic of amino sugars. It is a white, crystalline solid that is soluble in water, reflecting the polar nature of its functional groups. The presence of the amino group imparts unique reactivity, allowing it to participate in various biochemical processes, including glycosylation reactions. 2-Amino-2-deoxy-D-altrose can serve as a building block in the synthesis of glycosides and other biologically relevant molecules. Its role in biological systems may include involvement in cell signaling and structural functions in polysaccharides. As with many amino sugars, it may exhibit biological activity, potentially influencing metabolic pathways. Proper handling and storage are essential, as with all chemical substances, to ensure safety and stability.
Formula:C6H13NO5
Synonyms:
  • 2-Amino-2-deoxy-D-altrose
  • D-Altrosamine
  • D-Altrose, 2-amino-2-deoxy-
  • Altrosamine
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Found 1 products.
  • 2-Amino-2-deoxy-D-altrose

    CAS:
    <p>2-Amino-2-deoxy-D-altrose (2AD) is a molecule with the chemical formula C6H14N2O4. It belongs to the class of compounds known as uronic acids. 2AD is an acetylated molecule that has been structurally studied by X-ray crystallography and NMR spectroscopy. The molecule contains a ring of six carbon atoms, two of which are epoxide groups. The nature of this compound is glycosidic, with focus on hexamethylphosphoramide and diamino oligosaccharides. 2AD has been shown to have anti-inflammatory activities in animals, but its exact mechanism of action remains unknown. This compound may act through a ring-opening reaction or by inhibiting prostaglandin synthesis.</p>
    Formula:C6H13NO5
    Purity:Min. 95%
    Molecular weight:179.17 g/mol

    Ref: 3D-MA32651

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