4-(Trifluoromethyl)quinolin-2-amine is an organic compound characterized by the presence of a quinoline ring system substituted with a trifluoromethyl group and an amino group. The trifluoromethyl group (-CF3) is known for its electron-withdrawing properties, which can significantly influence the compound's reactivity and stability. The amino group (-NH2) is a basic functional group that can participate in hydrogen bonding and may enhance the compound's solubility in polar solvents. This compound is typically used in medicinal chemistry and research due to its potential biological activity, including antimicrobial and anticancer properties. Its unique structure allows for various synthetic modifications, making it a valuable intermediate in the development of pharmaceuticals. Additionally, the presence of fluorine atoms can improve the metabolic stability of the compound, making it an interesting subject for further studies in drug design and development. Overall, 4-(Trifluoromethyl)quinolin-2-amine exhibits a combination of properties that make it significant in both chemical research and potential therapeutic applications.

4-(Trifluoromethyl)quinolin-2-amine

211449-19-3: 2-Quinolinamine, 4-(Trifluoromethyl)-

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CAS 211449-19-3: 4-(Trifluoromethyl)quinolin-2-amine

4-(Trifluoromethyl)quinolin-2-amine

Ref: IN-DA00C14L

4-(Trifluoromethyl)quinolin-2-amine

Ref: 10-F225479

4-(Trifluoromethyl)quinolin-2-amine

Ref: 3D-FT82463