2,3-Diamino-5-trifluoromethylpyridine is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted with two amino groups and a trifluoromethyl group. The molecular structure features a six-membered aromatic ring containing nitrogen atoms, which contributes to its basicity and potential reactivity. The trifluoromethyl group enhances the compound's lipophilicity and can influence its electronic properties, making it a valuable building block in medicinal chemistry and agrochemicals. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its amino groups can participate in hydrogen bonding, affecting its interactions with other molecules. Additionally, the presence of fluorine atoms can impart unique characteristics, such as increased metabolic stability and altered pharmacokinetics in biological systems. Overall, 2,3-Diamino-5-trifluoromethylpyridine is of interest in various fields, including pharmaceuticals, due to its potential applications in drug development and synthesis.

2,3-Diamino-5-trifluoromethylpyridine

107867-51-6: 2,3-Pyridinediamine, 5-(Trifluoromethyl)-, 5-(Trifluoromethyl)pyridine-2,3-diamine

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CAS 107867-51-6: 2,3-Diamino-5-trifluoromethylpyridine

5-(Trifluoromethyl)-2,3-Pyridinediamine

Ref: 3D-FT84979

5-(Trifluoromethyl)pyridine-2,3-diamine

Ref: 10-F219326

2,3-Pyridinediamine, 5-(trifluoromethyl)-

Ref: IN-DA00HB1L

5-(Trifluoromethyl)pyridine-2,3-diamine

Ref: 54-PC51080