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CAS 140147-37-1

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D-Mannopyranose, 2,3,4,6-tetraacetate

Description:
D-Mannopyranose, 2,3,4,6-tetraacetate is a derivative of D-mannose, a naturally occurring sugar. This compound is characterized by the presence of four acetyl groups attached to the hydroxyl groups at positions 2, 3, 4, and 6 of the mannopyranose ring. The acetylation enhances the lipophilicity of the molecule, which can influence its solubility and reactivity compared to the parent sugar. D-Mannopyranose itself is a six-membered cyclic form of mannose, a monosaccharide that plays a role in various biological processes, including cell recognition and signaling. The tetraacetate form is often used in synthetic organic chemistry and biochemistry for its stability and ease of handling. It can serve as an intermediate in the synthesis of more complex carbohydrates or glycosides. Additionally, the compound may exhibit specific interactions with enzymes or receptors due to its structural features, making it of interest in research related to carbohydrate chemistry and biochemistry.
Formula:C14H20O10
InChI:InChI=1S/C14H20O10/c1-6(15)20-5-10-11(21-7(2)16)12(22-8(3)17)13(14(19)24-10)23-9(4)18/h10-14,19H,5H2,1-4H3/t10-,11-,12+,13+,14?/m1/s1
InChI key:InChIKey=IEOLRPPTIGNUNP-JABUTEAWSA-N
SMILES:O(C(C)=O)[C@H]1[C@H](OC(C)=O)[C@@H](COC(C)=O)OC(O)[C@H]1OC(C)=O
Synonyms:
  • D-Mannopyranose, 2,3,4,6-tetraacetate
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