(4-Fluorophenyl)(phenyl)acetic acid, with the CAS number 723-69-3, is an organic compound characterized by the presence of both a fluorophenyl and a phenyl group attached to an acetic acid moiety. This compound typically appears as a white to off-white solid and is known for its aromatic properties due to the presence of the phenyl rings. The fluorine atom on the para position of the phenyl ring can influence the compound's reactivity and solubility, often enhancing its lipophilicity. It is soluble in organic solvents such as ethanol and dichloromethane but may have limited solubility in water. The compound is of interest in medicinal chemistry and pharmaceutical research, particularly for its potential biological activities, including anti-inflammatory and analgesic properties. As with many organic acids, it can participate in various chemical reactions, including esterification and amidation, making it a versatile building block in organic synthesis. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with fluorinated compounds.

(4-fluorophenyl)(phenyl)acetic acid

723-69-3: (4-Fluorophenyl)(phenyl)acetic acid, with the CAS number 723-69-3, is an organic compound characterized by the presence of both a fluorophenyl and a phenyl group attached to an acetic acid moiety. This compound typically appears as a white to off-white solid and is known for its aromatic properties due to the presence of the phenyl rings. The fluorine atom on the para position of the phenyl ring can influence the compound's reactivity and solubility, often enhancing its lipophilicity. It is soluble in organic solvents such as ethanol and dichloromethane but may have limited solubility in water. The compound is of interest in medicinal chemistry and pharmaceutical research, particularly for its potential biological activities, including anti-inflammatory and analgesic properties. As with many organic acids, it can participate in various chemical reactions, including esterification and amidation, making it a versatile building block in organic synthesis. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with fluorinated compounds.

CAS 723-69-3

(4-fluorophenyl)(phenyl)acetic acid

2-(4-Fluorophenyl)-2-phenylacetic acid

Ref: IN-DA005U08

(4-Fluoro-phenyl)-phenyl-acetic acid

Ref: 10-F058723