Ethyl (3,5-difluorobenzoyl)acetate is an organic compound characterized by its ester functional group, which is derived from the reaction of ethyl alcohol and 3,5-difluorobenzoylacetate. This compound features a benzene ring substituted with two fluorine atoms at the 3 and 5 positions, contributing to its unique chemical properties, such as increased lipophilicity and potential biological activity. The presence of the acetyl group enhances its reactivity, making it useful in various synthetic applications. Ethyl (3,5-difluorobenzoyl)acetate is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in organic solvents. Its molecular structure allows for potential applications in pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties compared to its non-fluorinated analogs, including altered boiling and melting points, as well as unique reactivity patterns. Safety data should be consulted for handling and usage, as fluorinated compounds can have specific health and environmental considerations.

Ehyl (3,5-difluorobenzoyl)acetate

359424-42-3: Ethyl (3,5-difluorobenzoyl)acetate is an organic compound characterized by its ester functional group, which is derived from the reaction of ethyl alcohol and 3,5-difluorobenzoylacetate. This compound features a benzene ring substituted with two fluorine atoms at the 3 and 5 positions, contributing to its unique chemical properties, such as increased lipophilicity and potential biological activity. The presence of the acetyl group enhances its reactivity, making it useful in various synthetic applications. Ethyl (3,5-difluorobenzoyl)acetate is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in organic solvents. Its molecular structure allows for potential applications in pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties compared to its non-fluorinated analogs, including altered boiling and melting points, as well as unique reactivity patterns. Safety data should be consulted for handling and usage, as fluorinated compounds can have specific health and environmental considerations.

Ethyl (3,5-difluorobenzoyl)acetate

<p>Ethyl 3-(3,5-difluorophenyl)-3-oxopropanoate</p>

CAS 359424-42-3

Ehyl (3,5-difluorobenzoyl)acetate

Ethyl (3,5-difluorobenzoyl)acetate

Ref: IN-DA00CAFE

Ethyl 3-(3,5-difluorophenyl)-3-oxopropanoate

Ref: 54-PC103591

Ethyl (3,5-difluorobenzoyl)acetate

Ref: 10-F231919