(1R)-2,2,2-Trifluoro-1-(3-pyridyl)ethylamine is a chemical compound characterized by its unique trifluoromethyl and pyridine functionalities. The presence of the trifluoromethyl group contributes to its lipophilicity and potential biological activity, while the pyridine ring can participate in various interactions due to its nitrogen atom, which can act as a hydrogen bond donor or acceptor. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents, which makes it useful in various chemical reactions and applications, particularly in medicinal chemistry and drug development. The specific stereochemistry indicated by the (1R) configuration suggests that it has a defined spatial arrangement, which can significantly influence its biological properties and interactions with biological targets. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit unique toxicological profiles. Overall, this compound's structural features make it of interest in the synthesis of pharmaceuticals and agrochemicals.

(1R)-2,2,2-TRIFLUORO-1-(3-PYRIDYL)ETHYLAMINE

1212813-98-3: (1R)-2,2,2-Trifluoro-1-(3-pyridyl)ethylamine is a chemical compound characterized by its unique trifluoromethyl and pyridine functionalities. The presence of the trifluoromethyl group contributes to its lipophilicity and potential biological activity, while the pyridine ring can participate in various interactions due to its nitrogen atom, which can act as a hydrogen bond donor or acceptor. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents, which makes it useful in various chemical reactions and applications, particularly in medicinal chemistry and drug development. The specific stereochemistry indicated by the (1R) configuration suggests that it has a defined spatial arrangement, which can significantly influence its biological properties and interactions with biological targets. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit unique toxicological profiles. Overall, this compound's structural features make it of interest in the synthesis of pharmaceuticals and agrochemicals.

CAS 1212813-98-3

(1R)-2,2,2-TRIFLUORO-1-(3-PYRIDYL)ETHYLAMINE