Ethyl 3-(3,4-difluorophenyl)propanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethyl alcohol) and a carboxylic acid. This compound features a propanoate backbone with a phenyl ring that has two fluorine substituents at the 3 and 4 positions, contributing to its unique chemical properties. The presence of fluorine atoms typically enhances the compound's lipophilicity and may influence its reactivity and stability. Ethyl 3-(3,4-difluorophenyl)propanoate is likely to be a colorless to pale yellow liquid with a pleasant odor, commonly used in organic synthesis and potentially in pharmaceuticals or agrochemicals. Its molecular structure suggests it may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. As with many fluorinated compounds, it may also possess distinct physical properties, such as altered boiling and melting points compared to its non-fluorinated analogs. Safety data should be consulted for handling and usage, as fluorinated compounds can have specific environmental and health considerations.

ethyl 3-(3,4-difluorophenyl)propanoate

803687-25-4: Ethyl 3-(3,4-difluorophenyl)propanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethyl alcohol) and a carboxylic acid. This compound features a propanoate backbone with a phenyl ring that has two fluorine substituents at the 3 and 4 positions, contributing to its unique chemical properties. The presence of fluorine atoms typically enhances the compound's lipophilicity and may influence its reactivity and stability. Ethyl 3-(3,4-difluorophenyl)propanoate is likely to be a colorless to pale yellow liquid with a pleasant odor, commonly used in organic synthesis and potentially in pharmaceuticals or agrochemicals. Its molecular structure suggests it may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. As with many fluorinated compounds, it may also possess distinct physical properties, such as altered boiling and melting points compared to its non-fluorinated analogs. Safety data should be consulted for handling and usage, as fluorinated compounds can have specific environmental and health considerations.

CAS 803687-25-4

ethyl 3-(3,4-difluorophenyl)propanoate