3-Pyridinamine, N-(2,2,2-trifluoroethyl)-, also known by its CAS number 77262-40-9, is an organic compound characterized by the presence of a pyridine ring substituted with an amino group and a trifluoroethyl group. The molecular structure features a six-membered aromatic ring containing nitrogen, which contributes to its basicity and potential reactivity. The trifluoroethyl substituent introduces significant electronegativity due to the presence of three fluorine atoms, which can influence the compound's polarity and solubility in various solvents. This compound may exhibit unique chemical properties, including potential applications in pharmaceuticals or agrochemicals, owing to the trifluoromethyl group’s ability to enhance biological activity and metabolic stability. Additionally, the presence of the amino group allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Safety and handling considerations are important, as fluorinated compounds can exhibit different toxicological profiles compared to their non-fluorinated counterparts. Overall, 3-pyridinamine, N-(2,2,2-trifluoroethyl)- is a compound of interest in various chemical research fields.

3-pyridinamine, N-(2,2,2-trifluoroethyl)-

77262-40-9: 3-Pyridinamine, N-(2,2,2-trifluoroethyl)-, also known by its CAS number 77262-40-9, is an organic compound characterized by the presence of a pyridine ring substituted with an amino group and a trifluoroethyl group. The molecular structure features a six-membered aromatic ring containing nitrogen, which contributes to its basicity and potential reactivity. The trifluoroethyl substituent introduces significant electronegativity due to the presence of three fluorine atoms, which can influence the compound's polarity and solubility in various solvents. This compound may exhibit unique chemical properties, including potential applications in pharmaceuticals or agrochemicals, owing to the trifluoromethyl group’s ability to enhance biological activity and metabolic stability. Additionally, the presence of the amino group allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Safety and handling considerations are important, as fluorinated compounds can exhibit different toxicological profiles compared to their non-fluorinated counterparts. Overall, 3-pyridinamine, N-(2,2,2-trifluoroethyl)- is a compound of interest in various chemical research fields.

CAS 77262-40-9

3-pyridinamine, N-(2,2,2-trifluoroethyl)-

N-(2,2,2-trifluoroethyl)pyridin-3-amine

Ref: 10-F495976