CAS 90366-30-6
:5,6-dihydroxycyclohexane-1,2,3,4-tetrayl tetraacetate
Description:
5,6-Dihydroxycyclohexane-1,2,3,4-tetrayl tetraacetate, with the CAS number 90366-30-6, is a chemical compound characterized by its structure, which includes a cyclohexane ring with four hydroxyl groups and four acetate groups attached. This compound is a derivative of cyclohexane, featuring dihydroxy substitutions at the 5 and 6 positions, which contribute to its reactivity and solubility properties. The presence of acetate groups enhances its ability to form esters, making it useful in various chemical applications, including as a potential intermediate in organic synthesis. The hydroxyl groups provide sites for hydrogen bonding, influencing its physical properties such as solubility in polar solvents. Additionally, the compound may exhibit biological activity due to its functional groups, which can interact with biological systems. Overall, 5,6-dihydroxycyclohexane-1,2,3,4-tetrayl tetraacetate is a versatile compound with potential applications in both industrial and research settings.
Formula:C14H20O10
InChI:InChI=1/C14H20O10/c1-5(15)21-11-9(19)10(20)12(22-6(2)16)14(24-8(4)18)13(11)23-7(3)17/h9-14,19-20H,1-4H3
SMILES:CC(=O)OC1C(C(C(C(C1OC(=O)C)OC(=O)C)OC(=O)C)O)O
Synonyms:- 1,4,5,6-Tetraacetate
- 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL
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Found 3 products.
3,4,5,6-Tetra-O-acetyl myo-Inositol
CAS:Controlled ProductFormula:C14H20O10Color and Shape:NeatMolecular weight:348.33,4,5,6-Tetra-O-acetyl myo-inositol
CAS:<p>3,4,5,6-Tetra-O-acetyl myo-inositol is a synthetic compound that functions as a methyl donor for the modification of saccharides and polysaccharides. It is used in click chemistry reactions to modify oligosaccharides with fluorinated alkyne moieties. 3,4,5,6-Tetra-O-acetyl myo-inositol is also used in glycosylation reactions to produce complex carbohydrates. This chemical has CAS number 90366-30-6.</p>Formula:C14H20O10Purity:Min. 95%Molecular weight:348.3 g/mol


