[5-(Trifluoromethyl)-3-pyridyl]methanamine, identified by its CAS number 766513-53-5, is an organic compound characterized by the presence of a pyridine ring substituted with a trifluoromethyl group and an amine functional group. The trifluoromethyl group (-CF3) is known for its electron-withdrawing properties, which can significantly influence the compound's reactivity and polarity. The pyridine ring contributes to the compound's aromaticity and can participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. The amine group (-NH2) enhances the compound's basicity and can engage in hydrogen bonding, affecting its solubility and interaction with biological systems. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its unique structural features suggest potential applications in drug development, particularly in targeting specific biological pathways. Overall, the combination of these functional groups imparts distinctive chemical behavior and potential utility in various fields, including pharmaceuticals and agrochemicals.

[5-(trifluoromethyl)-3-pyridyl]methanamine

766513-53-5: [5-(Trifluoromethyl)-3-pyridyl]methanamine, identified by its CAS number 766513-53-5, is an organic compound characterized by the presence of a pyridine ring substituted with a trifluoromethyl group and an amine functional group. The trifluoromethyl group (-CF3) is known for its electron-withdrawing properties, which can significantly influence the compound's reactivity and polarity. The pyridine ring contributes to the compound's aromaticity and can participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. The amine group (-NH2) enhances the compound's basicity and can engage in hydrogen bonding, affecting its solubility and interaction with biological systems. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its unique structural features suggest potential applications in drug development, particularly in targeting specific biological pathways. Overall, the combination of these functional groups imparts distinctive chemical behavior and potential utility in various fields, including pharmaceuticals and agrochemicals.

CAS 766513-53-5

[5-(trifluoromethyl)-3-pyridyl]methanamine

C-(5-Trifluoromethyl-pyridin-3-yl)-methylamine

Ref: IN-DA005AOV