5-Trifluoromethyl-pyridin-3-ylamine is an organic compound characterized by the presence of a pyridine ring 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) introduces basicity and potential for hydrogen bonding, making the compound relevant in various chemical reactions and applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. Its unique structure allows it to participate in diverse chemical transformations, making it of interest in medicinal chemistry and material science. Additionally, the trifluoromethyl substitution can enhance lipophilicity, potentially affecting the compound's biological activity and pharmacokinetics. Overall, 5-Trifluoromethyl-pyridin-3-ylamine is a versatile compound with significant implications in research and industrial applications.

5-Trifluoromethyl-pyridin-3-ylamine

112110-07-3: 3-Pyridinamine, 5-(Trifluoromethyl)-, 5-(Trifluoromethyl)pyridin-3-amine, 5-(Trifluoromethyl)-3-pyridinamine, 5-(Trifluoromethyl)-3-Aminopyridine

5-(Trifluoromethyl)-3-aminopyridine

5-(Trifluoromethyl)-3-pyridinamine is an analog of the natural product, phenol. It has been shown to inhibit the growth of plasmodium falciparum and may be useful for the treatment of malaria. 5-(Trifluoromethyl)-3-pyridinamine is synthesized from an intermediate in the synthesis of methylamine. This compound was isolated from a strain of Australian plasmodium falciparum.

CAS 112110-07-3: 5-Trifluoromethyl-pyridin-3-ylamine

5-(Trifluoromethyl)-3-aminopyridine

Ref: 10-F077693

5-(Trifluoromethyl)-3-pyridinamine

Ref: 3D-FT74980

5-(Trifluoromethyl)pyridin-3-amine

Ref: IN-DA007CEE

3-Amino-5-(trifluoromethyl)pyridine

Ref: 54-PC301200