2-Piperidino-5-(trifluoromethyl)aniline, with the CAS number 1496-40-8, is an organic compound characterized by its piperidine and aniline functional groups. This substance features a trifluoromethyl group, which significantly influences its chemical properties, including increased lipophilicity and potential biological activity. The presence of the piperidine ring contributes to its basicity and potential as a nucleophile in various chemical reactions. The trifluoromethyl group enhances the compound's stability and can affect its reactivity, making it useful in medicinal chemistry and material science. Typically, compounds like this may exhibit interesting pharmacological properties, potentially acting as intermediates in the synthesis of pharmaceuticals or agrochemicals. Its molecular structure suggests that it may participate in hydrogen bonding and other intermolecular interactions, which can influence its solubility and reactivity in different solvents. Overall, 2-piperidino-5-(trifluoromethyl)aniline is a versatile compound with applications in various fields, particularly in the development of new chemical entities.

2-piperidino-5-(trifluoromethyl)aniline

1496-40-8: 2-Piperidino-5-(trifluoromethyl)aniline, with the CAS number 1496-40-8, is an organic compound characterized by its piperidine and aniline functional groups. This substance features a trifluoromethyl group, which significantly influences its chemical properties, including increased lipophilicity and potential biological activity. The presence of the piperidine ring contributes to its basicity and potential as a nucleophile in various chemical reactions. The trifluoromethyl group enhances the compound's stability and can affect its reactivity, making it useful in medicinal chemistry and material science. Typically, compounds like this may exhibit interesting pharmacological properties, potentially acting as intermediates in the synthesis of pharmaceuticals or agrochemicals. Its molecular structure suggests that it may participate in hydrogen bonding and other intermolecular interactions, which can influence its solubility and reactivity in different solvents. Overall, 2-piperidino-5-(trifluoromethyl)aniline is a versatile compound with applications in various fields, particularly in the development of new chemical entities.

CAS 1496-40-8

2-piperidino-5-(trifluoromethyl)aniline

Benzenamine, 2-(1-piperidinyl)-5-(trifluoromethyl)-

Ref: IN-DA001LVA

2-(Piperidin-1-yl)-5-(trifluoromethyl)aniline

Ref: 54-PC1100E

N-(2-Amino-4-trifluoromethylphenyl)piperidine

Ref: 10-F004031