2-Nitro-4-(trifluoromethoxy)aniline is an organic compound characterized by the presence of both nitro and trifluoromethoxy functional groups attached to an aniline structure. Its molecular formula typically includes carbon, hydrogen, nitrogen, and fluorine atoms, reflecting its complex nature. The nitro group (-NO2) is known for its electron-withdrawing properties, which can influence the reactivity and stability of the compound. The trifluoromethoxy group (-OCF3) enhances the compound's lipophilicity and can significantly affect its solubility and interaction with biological systems. This compound is often utilized in various chemical syntheses and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its unique combination of functional groups can impart specific electronic and steric properties, making it valuable in research and industrial applications. Safety data should be consulted, as compounds with nitro and fluorinated groups can pose environmental and health risks.

2-nitro-4-(trifluoromethoxy)aniline

2267-23-4: 2-Nitro-4-trifluoromethoxyaniline

2-Nitro-4-(trifluoromethoxy)aniline

2-Nitro-4-(trifluoromethoxy)aniline is an asymmetric synthesis of an enamine. In this process, the nitro group is introduced to the α position of a secondary amine. The chiral center is then introduced to the β-carbon atom of the enamine by way of a cyclic ketone. 2-Nitro-4-(trifluoromethoxy)aniline has been shown to be a modulator of G protein signaling pathways in research and has demonstrated anti-inflammatory properties. It also inhibits ester hydrolysis, arylation and intramolecular reductive reactions.

CAS 2267-23-4: 2-nitro-4-(trifluoromethoxy)aniline

2-Nitro-4-(trifluoromethoxy)aniline

Ref: IN-DA0033EP

2-Nitro-4-(trifluoromethoxy)aniline

Ref: 3B-N0841

2-Nitro-4-(trifluoromethoxy)aniline

Ref: 3D-FN64353

2-Nitro-4-(trifluoromethoxy)aniline

Ref: 10-F006900

2-Nitro-4-(trifluoromethoxy)aniline

Ref: 54-PC5292