2-(2,2,2-Trifluoroethoxy)pyridin-3-amine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of the trifluoroethoxy group introduces significant electronegativity and steric effects due to the three fluorine atoms, which can influence the compound's reactivity and solubility. This compound typically exhibits moderate polarity, making it soluble in polar organic solvents. The amino group at the 3-position of the pyridine ring can participate in hydrogen bonding, enhancing its potential interactions in biological systems or with other chemical entities. The trifluoroethoxy substituent may also impart unique properties, such as increased lipophilicity and altered electronic characteristics, which can be beneficial in medicinal chemistry applications. Overall, this compound's structure suggests potential utility in various fields, including pharmaceuticals and agrochemicals, where modifications to the pyridine scaffold can lead to diverse biological activities.

2-(2,2,2-trifluoroethoxy)pyridin-3-amine

154584-73-3: 2-(2,2,2-Trifluoroethoxy)pyridin-3-amine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of the trifluoroethoxy group introduces significant electronegativity and steric effects due to the three fluorine atoms, which can influence the compound's reactivity and solubility. This compound typically exhibits moderate polarity, making it soluble in polar organic solvents. The amino group at the 3-position of the pyridine ring can participate in hydrogen bonding, enhancing its potential interactions in biological systems or with other chemical entities. The trifluoroethoxy substituent may also impart unique properties, such as increased lipophilicity and altered electronic characteristics, which can be beneficial in medicinal chemistry applications. Overall, this compound's structure suggests potential utility in various fields, including pharmaceuticals and agrochemicals, where modifications to the pyridine scaffold can lead to diverse biological activities.

<p>2-(2,2,2-Trifluoroethoxy)pyridin-3-amine</p>

CAS 154584-73-3

2-(2,2,2-trifluoroethoxy)pyridin-3-amine

2-(2,2,2-Trifluoroethoxy)pyridin-3-amine

Ref: 54-PC102606

2-(2,2,2-Trifluoroethoxy)pyridin-3-amine

Ref: 10-F603015