Butanoic acid, 2-fluoro-3-oxo- (CAS 97070-48-9) is an organic compound characterized by its carboxylic acid functional group and the presence of a fluorine atom and a ketone group within its structure. This compound features a four-carbon straight-chain backbone, typical of butanoic acid derivatives, with a fluorine substituent at the second carbon and a keto group at the third carbon. The presence of the fluorine atom can influence the compound's reactivity, polarity, and potential biological activity, making it of interest in various chemical and pharmaceutical applications. Butanoic acid derivatives are often studied for their roles in organic synthesis and as intermediates in the production of more complex molecules. The compound is likely to exhibit typical properties of carboxylic acids, such as acidity and solubility in polar solvents, while the fluorine substitution may enhance its lipophilicity and alter its interaction with biological systems. Overall, this compound represents a unique combination of functional groups that can lead to diverse chemical behavior and applications.

Butanoic acid,2-fluoro-3-oxo-

97070-48-9: Butanoic acid, 2-fluoro-3-oxo- (CAS 97070-48-9) is an organic compound characterized by its carboxylic acid functional group and the presence of a fluorine atom and a ketone group within its structure. This compound features a four-carbon straight-chain backbone, typical of butanoic acid derivatives, with a fluorine substituent at the second carbon and a keto group at the third carbon. The presence of the fluorine atom can influence the compound's reactivity, polarity, and potential biological activity, making it of interest in various chemical and pharmaceutical applications. Butanoic acid derivatives are often studied for their roles in organic synthesis and as intermediates in the production of more complex molecules. The compound is likely to exhibit typical properties of carboxylic acids, such as acidity and solubility in polar solvents, while the fluorine substitution may enhance its lipophilicity and alter its interaction with biological systems. Overall, this compound represents a unique combination of functional groups that can lead to diverse chemical behavior and applications.