N-Methyl-4-(trifluoromethyl)-benzeneethanamine, also known by its CAS number 137069-25-1, is an organic compound characterized by the presence of a trifluoromethyl group attached to a benzene ring, along with an amine functional group. This compound typically exhibits properties associated with both aromatic and aliphatic amines, including potential basicity due to the nitrogen atom. The trifluoromethyl group contributes to its lipophilicity and can influence its reactivity and interaction with biological systems. The presence of the methyl group on the nitrogen enhances its steric properties, which may affect its ability to participate in hydrogen bonding. As a result, N-Methyl-4-(trifluoromethyl)-benzeneethanamine may exhibit unique solubility characteristics, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group can impart specific electronic effects, potentially influencing the compound's stability and reactivity in chemical reactions. Overall, this compound represents a fascinating example of how structural modifications can lead to diverse chemical behaviors.

N-Methyl-4-(trifluoroMethyl)-benzeneethanaMine

137069-25-1: N-Methyl-4-(trifluoromethyl)-benzeneethanamine, also known by its CAS number 137069-25-1, is an organic compound characterized by the presence of a trifluoromethyl group attached to a benzene ring, along with an amine functional group. This compound typically exhibits properties associated with both aromatic and aliphatic amines, including potential basicity due to the nitrogen atom. The trifluoromethyl group contributes to its lipophilicity and can influence its reactivity and interaction with biological systems. The presence of the methyl group on the nitrogen enhances its steric properties, which may affect its ability to participate in hydrogen bonding. As a result, N-Methyl-4-(trifluoromethyl)-benzeneethanamine may exhibit unique solubility characteristics, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group can impart specific electronic effects, potentially influencing the compound's stability and reactivity in chemical reactions. Overall, this compound represents a fascinating example of how structural modifications can lead to diverse chemical behaviors.

N-Methyl-4-(trifluoromethyl)benzeneethanamine

<p>Methyl({2-[4-(trifluoromethyl)phenyl]ethyl})amine</p>

CAS 137069-25-1

N-Methyl-4-(trifluoroMethyl)-benzeneethanaMine

N-Methyl-4-(trifluoromethyl)benzeneethanamine

Ref: IN-DA009VIY

Methyl({2-[4-(trifluoromethyl)phenyl]ethyl})amine

Ref: 54-PC108123