Ethyl 5-(3-fluoro-4-methyl-phenyl)-5-oxo-pentanoate is an organic compound characterized by its ester functional group, which is typical of many compounds in the ester category. This substance features a pentanoate backbone, indicating a five-carbon chain with a ketone (5-oxo) and an ethyl ester group. The presence of a 3-fluoro-4-methyl-phenyl substituent suggests that the compound has both halogen and alkyl groups attached to a phenyl ring, which can influence its reactivity and physical properties. The fluorine atom may impart unique electronic characteristics, potentially enhancing the compound's lipophilicity or altering its interaction with biological systems. Ethyl 5-(3-fluoro-4-methyl-phenyl)-5-oxo-pentanoate may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its molecular structure suggests potential applications in various fields, including pharmaceuticals and agrochemicals, although specific applications would depend on further studies and evaluations of its biological activity and safety profile.

ethyl 5-(3-fluoro-4-methyl-phenyl)-5-oxo-pentanoate

898752-58-4: Ethyl 5-(3-fluoro-4-methyl-phenyl)-5-oxo-pentanoate is an organic compound characterized by its ester functional group, which is typical of many compounds in the ester category. This substance features a pentanoate backbone, indicating a five-carbon chain with a ketone (5-oxo) and an ethyl ester group. The presence of a 3-fluoro-4-methyl-phenyl substituent suggests that the compound has both halogen and alkyl groups attached to a phenyl ring, which can influence its reactivity and physical properties. The fluorine atom may impart unique electronic characteristics, potentially enhancing the compound's lipophilicity or altering its interaction with biological systems. Ethyl 5-(3-fluoro-4-methyl-phenyl)-5-oxo-pentanoate may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its molecular structure suggests potential applications in various fields, including pharmaceuticals and agrochemicals, although specific applications would depend on further studies and evaluations of its biological activity and safety profile.

CAS 898752-58-4

ethyl 5-(3-fluoro-4-methyl-phenyl)-5-oxo-pentanoate