CAS 495-75-0
:2,5-anhydro-D-mannose
Description:
2,5-Anhydro-D-mannose is a monosaccharide and a sugar derivative that is classified as an anhydro sugar. It is characterized by its five-membered ring structure, which is formed by the dehydration of D-mannose, resulting in the loss of a water molecule. This compound is a white crystalline solid that is soluble in water, exhibiting a sweet taste. It is often used in biochemical research and has potential applications in the food and pharmaceutical industries due to its ability to act as a sugar substitute and its role in glycosylation processes. The molecular formula of 2,5-anhydro-D-mannose is C6H10O5, and it has a specific stereochemistry that contributes to its biological activity. Additionally, it can participate in various chemical reactions, including oxidation and reduction, making it a versatile compound in organic synthesis. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application.
Formula:C6H10O5
InChI:InChI=1/C6H10O5/c7-1-3-5(9)6(10)4(2-8)11-3/h1,3-6,8-10H,2H2/t3-,4-,5-,6-/m1/s1
SMILES:C(=O)[C@@H]1[C@H]([C@@H]([C@@H](CO)O1)O)O
Synonyms:- D-mannose, 2,5-anhydro-
- 2,5-Anhydro-D-mannose
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Found 5 products.
2,5-Anhydro-D-mannose
CAS:2,5-Anhydro-D-mannosePurity:≥95%Color and Shape:SolidMolecular weight:162.14g/mol2,5-Anhydro-D-mannose
CAS:<p>Stability Very Hygroscopic<br>Applications This compound is a mixture of the acetal and aldehyde forms.<br>References Zamani, A., et al.: J. Agric. Food Chem., 56, 8314 (2008), Nowicki, M., et al.: Bioorg. Med. Chem., 16, 5050 (2008),<br></p>Formula:C6H10O5Color and Shape:NeatMolecular weight:162.142,5-Anhydro-D-mannofuranose
CAS:<p>2,5-Anhydro-D-mannofuranose is a biologically active compound that belongs to the group of inorganic acids. It has been shown to be an inhibitor of heparin-induced thrombocytopenia. 2,5-Anhydro-D-mannofuranose inhibits platelet aggregation and prolongs bleeding time in rats by blocking glycosidic bond formation. This compound is also found as a constituent of oligosaccharides and nitrous oxide. Structural analysis has revealed that this molecule contains reactive groups and is acidic in nature. The analytical method for this compound is α1-acid glycoprotein. Monoclonal antibodies against fatty acid have been used for its detection in human serum.</p>Formula:C6H10O5Purity:Min. 85 Area-%Color and Shape:PowderMolecular weight:162.14 g/mol



