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CAS 91143-71-4

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(2R)-2-(4-acetylphenoxy)propanoate

Description:
(2R)-2-(4-acetylphenoxy)propanoate, identified by its CAS number 91143-71-4, is an organic compound characterized by its ester functional group. This substance features a propanoate backbone, which is a three-carbon chain with a carboxylate group, and is substituted with a 4-acetylphenoxy group. The presence of the acetyl group indicates that it has a ketone functional group, contributing to its reactivity and potential applications in organic synthesis. The stereochemistry of the compound is specified as (2R), indicating that it has a specific spatial arrangement around the chiral center, which can influence its biological activity and interactions. This compound may exhibit properties typical of esters, such as volatility and solubility in organic solvents, and could be utilized in various chemical reactions, including esterification and acylation processes. Its unique structure may also suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. However, specific biological or industrial applications would require further investigation.
Formula:C11H11O4
InChI:InChI=1/C11H12O4/c1-7(12)9-3-5-10(6-4-9)15-8(2)11(13)14/h3-6,8H,1-2H3,(H,13,14)/p-1/t8-/m1/s1
SMILES:CC(=O)c1ccc(cc1)O[C@H](C)C(=O)[O-]
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