N-methyl-2-(trifluoromethoxy)aniline is an organic compound characterized by its aniline structure, which includes an amino group (-NH2) attached to a benzene ring. In this specific compound, the amino group is methylated, resulting in the N-methyl substitution. The presence of a trifluoromethoxy group (-O-CF3) at the 2-position of the aniline ring significantly influences its chemical properties, including increased lipophilicity and potential reactivity. This trifluoromethoxy group is known for its electron-withdrawing characteristics, which can affect the compound's acidity and reactivity in various chemical reactions. N-methyl-2-(trifluoromethoxy)aniline may be utilized in the synthesis of pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Its unique structure may also impart specific biological activities, making it of interest in medicinal chemistry. As with many fluorinated compounds, it may exhibit stability under various conditions, but safety and handling precautions should be observed due to potential toxicity and environmental impact.

N-methyl-2-(trifluoromethoxy)aniline

175278-04-3: N1-Methyl-2-(trifluoromethoxy)aniline, 2-Methyl-5-(Trifluoromethoxy)Aniline

Benzenamine, N-methyl-2-(trifluoromethoxy)-

N-Methyl-2-(trifluoromethoxy)aniline

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CAS 175278-04-3: N-methyl-2-(trifluoromethoxy)aniline

Benzenamine, N-methyl-2-(trifluoromethoxy)-

Ref: IN-DA0020TR

N-Methyl-2-(trifluoromethoxy)aniline

Ref: 54-PC5171E

N-Methyl-2-(trifluoromethoxy)aniline

Ref: 10-F006836

N-Methyl-2-(trifluoromethoxy)aniline

Ref: 3D-FM86417