2,3,4-Trifluoro-5-(trifluoromethyl)aniline is an aromatic amine characterized by the presence of multiple fluorine substituents on its benzene ring. Specifically, it features three fluorine atoms at the 2, 3, and 4 positions, and a trifluoromethyl group (-CF3) at the 5 position. This compound is typically a solid at room temperature and exhibits a high degree of chemical stability due to the strong C-F bonds. The presence of fluorine atoms significantly influences its physical and chemical properties, including increased lipophilicity and potential reactivity in nucleophilic substitution reactions. Additionally, the trifluoromethyl group enhances the compound's electron-withdrawing characteristics, which can affect its reactivity and interaction with other chemical species. Due to its unique structure, 2,3,4-trifluoro-5-(trifluoromethyl)aniline may find applications in various fields, including pharmaceuticals and agrochemicals, where fluorinated compounds are often valued for their biological activity and stability. Safety data should be consulted, as fluorinated compounds can exhibit toxicity and environmental persistence.

2,3,4-trifluoro-5-(trifluoromethyl)aniline

123973-35-3: 2,3,4-Trifluoro-5-(trifluoromethyl)aniline is an aromatic amine characterized by the presence of multiple fluorine substituents on its benzene ring. Specifically, it features three fluorine atoms at the 2, 3, and 4 positions, and a trifluoromethyl group (-CF3) at the 5 position. This compound is typically a solid at room temperature and exhibits a high degree of chemical stability due to the strong C-F bonds. The presence of fluorine atoms significantly influences its physical and chemical properties, including increased lipophilicity and potential reactivity in nucleophilic substitution reactions. Additionally, the trifluoromethyl group enhances the compound's electron-withdrawing characteristics, which can affect its reactivity and interaction with other chemical species. Due to its unique structure, 2,3,4-trifluoro-5-(trifluoromethyl)aniline may find applications in various fields, including pharmaceuticals and agrochemicals, where fluorinated compounds are often valued for their biological activity and stability. Safety data should be consulted, as fluorinated compounds can exhibit toxicity and environmental persistence.

CAS 123973-35-3

2,3,4-trifluoro-5-(trifluoromethyl)aniline

2,3,4-Trifluoro-5-(trifluoromethyl)aniline

Ref: 10-F098562