2,3-Dichloro-6-(trifluoromethyl)aniline is an organic compound characterized by its aromatic amine structure, featuring a benzene ring substituted with two chlorine atoms and a trifluoromethyl group. The presence of the aniline functional group indicates that it contains an amino (-NH2) group attached to the aromatic ring, which can participate in various chemical reactions, including electrophilic substitutions. The dichloro substituents at the 2 and 3 positions of the ring contribute to the compound's reactivity and influence its physical properties, such as solubility and boiling point. The trifluoromethyl group, known for its electron-withdrawing properties, enhances the compound's stability and alters its electronic characteristics, making it useful in various applications, including agrochemicals and pharmaceuticals. Additionally, the compound's molecular structure suggests potential for interactions with biological systems, which may be relevant in toxicological studies. Overall, 2,3-dichloro-6-(trifluoromethyl)aniline is a complex molecule with significant implications in chemical synthesis and application.

2,3-dichloro-6-(trifluoromethyl)aniline

1017777-92-2: 2,3-Dichloro-6-(trifluoromethyl)benzenamine, 5,6-Dichloro-α,α,α-trifluoro-o-toluidine, Benzenamine, 2,3-dichloro-6-(trifluoromethyl)-, Zr Bg Cg Fxfff, 2,3-Dichloro-6-(trifluoromethyl)aniline

CAS 1017777-92-2: 2,3-dichloro-6-(trifluoromethyl)aniline

Benzenamine, 2,3-dichloro-6-(trifluoromethyl)-

Ref: IN-DA0005HL

2,3-Dichloro-6-(trifluoromethyl)aniline

Ref: 54-PC302220

2,3-Dichloro-6-(trifluoromethyl)aniline

Ref: 3D-SQB77792

2,3-Dichloro-6-(trifluoromethyl)aniline

Ref: 10-F342707