2-Amino-6-ethoxy-4-trifluoromethylpyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of an amino group (-NH2) at the 2-position and an ethoxy group (-OCH2CH3) at the 6-position contributes to its reactivity and solubility in polar solvents. The trifluoromethyl group (-CF3) at the 4-position enhances the compound's lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its unique functional groups suggest potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The trifluoromethyl group is particularly notable for imparting unique electronic properties, which can affect the compound's interaction with biological targets. As with many nitrogen-containing heterocycles, it may also participate in hydrogen bonding, influencing its solubility and reactivity in various chemical environments.

2-AMINO-6-ETHOXY-4-TRIFLUOROMETHYLPYRIDINE

117519-14-9: 2-Amino-6-ethoxy-4-trifluoromethylpyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of an amino group (-NH2) at the 2-position and an ethoxy group (-OCH2CH3) at the 6-position contributes to its reactivity and solubility in polar solvents. The trifluoromethyl group (-CF3) at the 4-position enhances the compound's lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its unique functional groups suggest potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The trifluoromethyl group is particularly notable for imparting unique electronic properties, which can affect the compound's interaction with biological targets. As with many nitrogen-containing heterocycles, it may also participate in hydrogen bonding, influencing its solubility and reactivity in various chemical environments.

CAS 117519-14-9

2-AMINO-6-ETHOXY-4-TRIFLUOROMETHYLPYRIDINE