4-[2-(1-Piperidinyl)ethyl]benzenamine, also known by its CAS number 168897-21-0, is an organic compound characterized by its structure, which includes a benzene ring substituted with an amino group and a piperidinyl ethyl side chain. This compound typically exhibits properties associated with amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility in various solvents. The presence of the piperidine ring contributes to its potential biological activity, as piperidine derivatives are often found in pharmaceuticals and can interact with various biological targets. The compound may also display moderate lipophilicity due to the aromatic and aliphatic components of its structure, affecting its pharmacokinetic properties. Additionally, it may undergo typical reactions of amines, such as alkylation or acylation, making it a versatile intermediate in organic synthesis. Overall, 4-[2-(1-Piperidinyl)ethyl]benzenamine is of interest in medicinal chemistry and related fields for its potential applications.

4-[2-(1-Piperidinyl)ethyl]benzenamine

168897-21-0: 4-(2-Piperidinoethyl)aniline, 4-(2-Piperidinoethyl)phenylamine, 4-[2-(1-Piperidinyl)ethyl]benzenamine, Benzenamine, 4-[2-(1-Piperidinyl)Ethyl]-

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CAS 168897-21-0: 4-[2-(1-Piperidinyl)ethyl]benzenamine

4-(2-Piperidin-1-Yl-Ethyl)-Aniline

Ref: 3D-FP52001

Benzenamine, 4-[2-(1-piperidinyl)ethyl]-

Ref: IN-DA007V7J

4-(2-Piperidin-1-yl-ethyl)-phenylamine

Ref: 54-OR307778

4-(2-Piperidin-1-yl-ethyl)-aniline

Ref: 10-F737629