CAS 16299-15-3
:A-D-idopyranose pentaacetate
Description:
A-D-idopyranose pentaacetate is a derivative of the sugar A-D-idopyranose, which is a six-membered cyclic form of D-idose, a monosaccharide. This compound is characterized by the acetylation of all five hydroxyl groups present in the sugar, resulting in a pentaacetate form. The acetylation enhances the lipophilicity of the molecule, making it more soluble in organic solvents compared to its parent sugar. A-D-idopyranose pentaacetate typically appears as a white to off-white crystalline solid and is stable under standard laboratory conditions. It is often used in organic synthesis and carbohydrate chemistry for various applications, including the study of glycosylation reactions and as a protecting group in the synthesis of more complex carbohydrates. The compound's structure can be analyzed using techniques such as NMR spectroscopy and mass spectrometry, which provide insights into its molecular configuration and purity. As with many acetylated sugars, it may exhibit different reactivity and properties compared to its unmodified counterpart.
Formula:C16H22O11
InChI:InChI=1/C16H22O11/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(27-12)26-11(5)21/h12-16H,6H2,1-5H3
SMILES:CC(=O)OCC1C(C(C(C(OC(=O)C)O1)OC(=O)C)OC(=O)C)OC(=O)C
Synonyms:- a-L-Idopyranose, Pentaacetate
- 1,2,3,4,6-penta-O-acetylhexopyranose
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Found 2 products.
Penta-O-acetyl-a-L-idopyranose
CAS:<p>Penta-O-acetyl-a-L-idopyranose is a monosaccharide that is synthesized from D-glucose and acetic anhydride. It has been modified with methylation, fluorination, and saccharide modification. Penta-O-acetyl-a-L-idopyranose is soluble in water, methanol, ethanol, and acetone. This compound has been shown to be useful for glycosylation reactions as well as click chemistry. CAS No. 16299-15-3.</p>Formula:C16H22O11Purity:Min. 95%Color and Shape:PowderMolecular weight:390.34 g/mol
