(2-Trifluoromethyl-phenylthio)-acetic acid, with the CAS number 13334-00-4, is an organic compound characterized by the presence of a trifluoromethyl group and a phenylthio moiety attached to an acetic acid backbone. This compound typically exhibits properties associated with both acidic and aromatic functionalities, making it a versatile intermediate in organic synthesis. The trifluoromethyl group contributes to its lipophilicity and can enhance biological activity, while the phenylthio group may influence its reactivity and solubility in various solvents. The presence of the carboxylic acid functional group allows for potential hydrogen bonding and reactivity in esterification or amidation reactions. Additionally, the compound may exhibit unique electronic properties due to the electron-withdrawing nature of the trifluoromethyl group, which can affect its behavior in chemical reactions and interactions with biological systems. Overall, (2-trifluoromethyl-phenylthio)-acetic acid is of interest in pharmaceutical and agrochemical research due to its potential applications in drug development and synthesis.

(2-TRIFLUOROMETHYL-PHENYLTHIO)-ACETIC ACID

13334-00-4: (2-Trifluoromethyl-phenylthio)-acetic acid, with the CAS number 13334-00-4, is an organic compound characterized by the presence of a trifluoromethyl group and a phenylthio moiety attached to an acetic acid backbone. This compound typically exhibits properties associated with both acidic and aromatic functionalities, making it a versatile intermediate in organic synthesis. The trifluoromethyl group contributes to its lipophilicity and can enhance biological activity, while the phenylthio group may influence its reactivity and solubility in various solvents. The presence of the carboxylic acid functional group allows for potential hydrogen bonding and reactivity in esterification or amidation reactions. Additionally, the compound may exhibit unique electronic properties due to the electron-withdrawing nature of the trifluoromethyl group, which can affect its behavior in chemical reactions and interactions with biological systems. Overall, (2-trifluoromethyl-phenylthio)-acetic acid is of interest in pharmaceutical and agrochemical research due to its potential applications in drug development and synthesis.

CAS 13334-00-4

(2-TRIFLUOROMETHYL-PHENYLTHIO)-ACETIC ACID

Acetic acid, 2-[[2-(trifluoromethyl)phenyl]thio]-

Ref: IN-DA0014PE