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CAS 349-22-4

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4-(4-fluoro-3-methylphenyl)-4-oxobutanoic acid

Description:
4-(4-Fluoro-3-methylphenyl)-4-oxobutanoic acid, with the CAS number 349-22-4, is an organic compound characterized by its distinctive structure, which includes a butanoic acid backbone with a ketone functional group and a substituted aromatic ring. The presence of a fluorine atom and a methyl group on the aromatic ring contributes to its unique chemical properties, influencing its reactivity and potential applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functional group. It can participate in various chemical reactions, including esterification and acylation, making it useful in synthetic organic chemistry. Additionally, the fluorine substitution can enhance the compound's biological activity, potentially making it relevant in pharmaceutical research. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken.
Formula:C11H11FO3
InChI:InChI=1/C11H11FO3/c1-7-6-8(2-3-9(7)12)10(13)4-5-11(14)15/h2-3,6H,4-5H2,1H3,(H,14,15)
SMILES:Cc1cc(ccc1F)C(=O)CCC(=O)O
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