3,3,3-Trifluoro-1-propanamine, with the CAS number 460-39-9, is an organic compound characterized by the presence of three fluorine atoms attached to the carbon chain, specifically at the terminal carbon. This trifluoromethyl group significantly influences its chemical properties, making it a highly polar and potentially reactive molecule. The amine functional group (-NH2) contributes to its basicity and ability to form hydrogen bonds, which can enhance its solubility in polar solvents. The trifluoromethyl group also imparts unique electronic properties, often leading to increased lipophilicity and altered reactivity compared to non-fluorinated analogs. This compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential applications as a building block in the synthesis of more complex molecules. Additionally, the presence of fluorine can enhance metabolic stability and influence biological activity. Safety considerations should be taken into account when handling this compound, as fluorinated compounds can exhibit different toxicological profiles compared to their non-fluorinated counterparts.

3,3,3-Trifluoro-1-propanamine

460-39-9: 3,3,3-Trifluoro-1-propanamine, with the CAS number 460-39-9, is an organic compound characterized by the presence of three fluorine atoms attached to the carbon chain, specifically at the terminal carbon. This trifluoromethyl group significantly influences its chemical properties, making it a highly polar and potentially reactive molecule. The amine functional group (-NH2) contributes to its basicity and ability to form hydrogen bonds, which can enhance its solubility in polar solvents. The trifluoromethyl group also imparts unique electronic properties, often leading to increased lipophilicity and altered reactivity compared to non-fluorinated analogs. This compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential applications as a building block in the synthesis of more complex molecules. Additionally, the presence of fluorine can enhance metabolic stability and influence biological activity. Safety considerations should be taken into account when handling this compound, as fluorinated compounds can exhibit different toxicological profiles compared to their non-fluorinated counterparts.

CAS 460-39-9

3,3,3-Trifluoro-1-propanamine

3,3,3-Trifluoropropylamine

Ref: 54-PC4603

3,3,3-Trifluoropropylamine

Ref: 10-F038244