4-Hydroxy-3-(trifluoromethyl)benzenamine, also known by its CAS number 1535-76-8, is an organic compound characterized by the presence of a hydroxyl group (-OH) and an amino group (-NH2) attached to a benzene ring that also features a trifluoromethyl group (-CF3). This compound is a derivative of aniline, where the trifluoromethyl group significantly influences its chemical properties, including increased lipophilicity and altered reactivity. The hydroxyl group contributes to its potential as a phenolic compound, which can participate in hydrogen bonding and may enhance solubility in polar solvents. The trifluoromethyl group is known for imparting unique electronic properties, making the compound of interest in various applications, including pharmaceuticals and agrochemicals. Additionally, the presence of both functional groups allows for potential derivatization, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence.

4-hydroxy-3-(trifluoromethyl)benzenamine

1535-76-8: 4-Hydroxy-3-(trifluoromethyl)benzenamine, also known by its CAS number 1535-76-8, is an organic compound characterized by the presence of a hydroxyl group (-OH) and an amino group (-NH2) attached to a benzene ring that also features a trifluoromethyl group (-CF3). This compound is a derivative of aniline, where the trifluoromethyl group significantly influences its chemical properties, including increased lipophilicity and altered reactivity. The hydroxyl group contributes to its potential as a phenolic compound, which can participate in hydrogen bonding and may enhance solubility in polar solvents. The trifluoromethyl group is known for imparting unique electronic properties, making the compound of interest in various applications, including pharmaceuticals and agrochemicals. Additionally, the presence of both functional groups allows for potential derivatization, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence.

CAS 1535-76-8

4-hydroxy-3-(trifluoromethyl)benzenamine

4-Amino-2-(trifluoromethyl)phenol

Ref: IN-DA00AKUE

4-Amino-2-(trifluoromethyl)phenol

Ref: 54-PC103311

4-Amino-2-(trifluoromethyl)phenol

Ref: 10-F608961