3-(4-Fluoro-2-methyl-phenyl)-propionic acid is an organic compound characterized by its propionic acid backbone substituted with a 4-fluoro-2-methylphenyl group. This compound features a carboxylic acid functional group, which imparts acidic properties, making it soluble in polar solvents. The presence of the fluorine atom enhances its lipophilicity and can influence its biological activity, potentially affecting interactions with biological targets. The methyl group on the phenyl ring contributes to steric hindrance, which may affect the compound's reactivity and binding affinity in various chemical environments. This compound is of interest in pharmaceutical research and development, particularly in the design of drugs that target specific biological pathways. Its unique structural features may also lend it utility in materials science or as a building block in organic synthesis. As with many organic acids, it may exhibit typical acid-base behavior, participating in proton transfer reactions and forming salts with bases. Safety and handling precautions should be observed due to its chemical nature and potential biological effects.

3-(4-FLUORO-2-METHYL-PHENYL)-PROPIONIC ACID

166251-34-9: 3-(4-Fluoro-2-methyl-phenyl)-propionic acid is an organic compound characterized by its propionic acid backbone substituted with a 4-fluoro-2-methylphenyl group. This compound features a carboxylic acid functional group, which imparts acidic properties, making it soluble in polar solvents. The presence of the fluorine atom enhances its lipophilicity and can influence its biological activity, potentially affecting interactions with biological targets. The methyl group on the phenyl ring contributes to steric hindrance, which may affect the compound's reactivity and binding affinity in various chemical environments. This compound is of interest in pharmaceutical research and development, particularly in the design of drugs that target specific biological pathways. Its unique structural features may also lend it utility in materials science or as a building block in organic synthesis. As with many organic acids, it may exhibit typical acid-base behavior, participating in proton transfer reactions and forming salts with bases. Safety and handling precautions should be observed due to its chemical nature and potential biological effects.

3-(4-Fluoro-2-methylphenyl)propionic acid

<p>3-(4-Fluoro-2-methylphenyl)propionic acid</p>

CAS 166251-34-9

3-(4-FLUORO-2-METHYL-PHENYL)-PROPIONIC ACID

3-(4-Fluoro-2-methylphenyl)propionic acid

Ref: IN-DA001WLD

3-(4-Fluoro-2-methylphenyl)propionic acid

Ref: 54-PC302265

3-(4-Fluoro-2-methylphenyl)propionic acid

Ref: 10-F342768