CAS 404958-08-3
:Hexanoic acid, 6-chloro-5-hydroxy-3-oxo-, 1,1-dimethylethyl ester, (5R)-
Description:
Hexanoic acid, 6-chloro-5-hydroxy-3-oxo-, 1,1-dimethylethyl ester, (5R)-, is a chemical compound characterized by its ester functional group derived from hexanoic acid. The presence of a chloro group and a hydroxy group indicates that it has potential for various chemical reactivity and biological activity. The compound features a chiral center, denoted by the (5R) configuration, which can influence its interactions in biological systems, making it relevant in pharmaceutical applications. Its esterification with 1,1-dimethylethanol suggests it may exhibit properties typical of esters, such as volatility and solubility in organic solvents. The presence of the keto group (3-oxo) adds to its reactivity, potentially allowing for further transformations in synthetic chemistry. Overall, this compound's unique structure may contribute to its utility in various chemical syntheses or as an intermediate in the production of more complex molecules.
Formula:C10H17ClO4
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Found 3 products.
tert-Butyl 6-Chloro-(R)-hydroxy-3-oxohexanoate
CAS:Controlled Product<p>Applications tert-Butyl 6-Chloro(R)-hydroxy-3-oxohexanoate is a chiral reagent used in the synthesis of callystatin A, a polyketide natural product that functions as an antibiotic. Also an impurity in the synthesis of Rosuvastatin (R700500), a selective, competitive HMG-CoA reductase inhibitor. Antilipemic.<br>References Watanabe, M., et al.: Bioorg. Med. Chem., 5, 437 (1997), Lee, E., et al.: Clin. Pharmacol. Ther., 78, 330 (2005), Ferdinand, K.C., et al.: Am. J. Cardiol., 97, 229 (2006); Enders, D. et al.: Chem. A. Eur. J., 8, 4274 (2002);<br></p>Formula:C10H17ClO4Color and Shape:NeatMolecular weight:236.69
