3,4-Difluorophenylacetic acid methyl ester is an organic compound characterized by the presence of a phenyl ring substituted with two fluorine atoms at the 3 and 4 positions, along with an acetic acid moiety esterified with a methyl group. This compound typically exhibits properties associated with both aromatic and carboxylic acid derivatives, including moderate polarity due to the electronegative fluorine substituents, which can influence its reactivity and solubility in various solvents. The presence of the methyl ester group suggests that it may participate in esterification and hydrolysis reactions. Additionally, the fluorine atoms can enhance the compound's biological activity and lipophilicity, making it of interest in pharmaceutical research. Its molecular structure allows for potential interactions with biological targets, which may be relevant in drug design. Safety data and handling precautions should be observed, as with many fluorinated compounds, due to potential toxicity and environmental impact. Overall, 3,4-Difluorophenylacetic acid methyl ester is a compound of interest in both synthetic organic chemistry and medicinal chemistry.

3,4-Difluorophenylacetic acid methyl ester

210530-71-5: Methyl (3,4-Difluorophenyl)Acetate

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CAS 210530-71-5: 3,4-Difluorophenylacetic acid methyl ester

3,4-Difluorophenylacetic acid methyl ester

Ref: 54-PC400704

Methyl (3,4-Difluorophenyl)Acetate

Ref: 3D-FM81804

3,4-Difluorophenylacetic acid methyl ester

Ref: 10-F094445

Benzeneacetic acid, 3,4-difluoro-, methyl ester

Ref: IN-DA002KTY