2-[(2,2-Difluoroethyl)thio]aniline is an organic compound characterized by the presence of an aniline group, which is an amino-substituted aromatic ring, and a thioether functional group linked to a difluoroethyl moiety. This compound features a sulfur atom that connects the aniline to the difluoroethyl group, imparting unique chemical properties. The difluoroethyl group introduces fluorine atoms, which can enhance the compound's lipophilicity and influence its reactivity and biological activity. The presence of the amino group allows for potential hydrogen bonding and reactivity in various chemical reactions, making it a candidate for applications in pharmaceuticals or agrochemicals. Additionally, the compound's structure suggests it may exhibit specific interactions with biological targets due to the presence of both electron-donating (amino) and electron-withdrawing (difluoroethyl) groups. Overall, 2-[(2,2-difluoroethyl)thio]aniline is notable for its unique combination of functional groups, which can lead to diverse chemical behavior and potential applications in various fields.

2-[(2,2-difluoroethyl)thio]aniline

1018142-89-6: 2-[(2,2-Difluoroethyl)thio]aniline is an organic compound characterized by the presence of an aniline group, which is an amino-substituted aromatic ring, and a thioether functional group linked to a difluoroethyl moiety. This compound features a sulfur atom that connects the aniline to the difluoroethyl group, imparting unique chemical properties. The difluoroethyl group introduces fluorine atoms, which can enhance the compound's lipophilicity and influence its reactivity and biological activity. The presence of the amino group allows for potential hydrogen bonding and reactivity in various chemical reactions, making it a candidate for applications in pharmaceuticals or agrochemicals. Additionally, the compound's structure suggests it may exhibit specific interactions with biological targets due to the presence of both electron-donating (amino) and electron-withdrawing (difluoroethyl) groups. Overall, 2-[(2,2-difluoroethyl)thio]aniline is notable for its unique combination of functional groups, which can lead to diverse chemical behavior and potential applications in various fields.

CAS 1018142-89-6

2-[(2,2-difluoroethyl)thio]aniline