2-(Azepan-1-yl)-N-ethylethanamine, also known by its CAS number 55543-73-2, is a chemical compound characterized by its structure, which includes an azepane ring and an ethyl group attached to an amine. This compound features a seven-membered saturated nitrogen-containing heterocycle (azepane) that contributes to its potential biological activity. The presence of the ethyl group and the amine functional group suggests that it may exhibit basic properties, allowing it to participate in various chemical reactions, including those typical of amines, such as nucleophilic substitutions. The compound may also interact with biological systems, potentially influencing neurotransmitter pathways or exhibiting pharmacological effects. Its solubility, stability, and reactivity can vary based on environmental conditions, such as pH and temperature. As with many amines, it may have implications in medicinal chemistry, particularly in the development of pharmaceuticals or as a building block in organic synthesis. However, specific applications and safety profiles would require further investigation and analysis.

2-(azepan-1-yl)-N-ethylethanamine

55543-73-2: 2-(Azepan-1-yl)-N-ethylethanamine, also known by its CAS number 55543-73-2, is a chemical compound characterized by its structure, which includes an azepane ring and an ethyl group attached to an amine. This compound features a seven-membered saturated nitrogen-containing heterocycle (azepane) that contributes to its potential biological activity. The presence of the ethyl group and the amine functional group suggests that it may exhibit basic properties, allowing it to participate in various chemical reactions, including those typical of amines, such as nucleophilic substitutions. The compound may also interact with biological systems, potentially influencing neurotransmitter pathways or exhibiting pharmacological effects. Its solubility, stability, and reactivity can vary based on environmental conditions, such as pH and temperature. As with many amines, it may have implications in medicinal chemistry, particularly in the development of pharmaceuticals or as a building block in organic synthesis. However, specific applications and safety profiles would require further investigation and analysis.

CAS 55543-73-2

2-(azepan-1-yl)-N-ethylethanamine

N-(2-Azepan-1-ylethyl)-N-ethylamine

Ref: 3D-FCA54373