2-Oxo-2-piperidin-1-ylethanamine hydrochloride, also known by its CAS number 5437-48-9, is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features an oxo group (C=O) and an amino group (NH2) attached to an ethyl chain, contributing to its reactivity and potential biological activity. As a hydrochloride salt, it is typically more soluble in water, enhancing its utility in various applications, particularly in pharmaceuticals. The presence of the piperidine moiety suggests potential interactions with biological systems, making it of interest in medicinal chemistry. Its properties may include moderate to high polarity, influencing its solubility and interaction with biological targets. Additionally, the compound may exhibit basic characteristics due to the amino group, allowing it to participate in protonation and deprotonation reactions. Overall, 2-oxo-2-piperidin-1-ylethanamine hydrochloride is a compound of interest for research and development in the fields of organic chemistry and pharmacology.

2-oxo-2-piperidin-1-ylethanamine hydrochloride

5437-48-9: 2-Amino-1-(1-piperidinyl)-ethanone HCl, 2-Amino-1-(piperidin-1-yl)ethan-1-one hydrochloride, 2-Amino-1-(piperidin-1-yl)ethanone hydrochloride, 2-Amino-1-(piperidin-1-yl)ethanone hydrochloride (1:1), 2-Amino-1-Piperidin-1-Yl-Ethanone Hcl, 2-Amino-1-piperidino-1-ethanone hydrochloride, Ethanone, 2-amino-1-(1-piperidinyl)-, hydrochloride (1:1), Ethanone, 2-amino-1-(1-piperidinyl)-, hydrochloride (1:1)2-Amino-1-(1-piperidinyl)-ethanone HCl, Piperidine, 1-(aminoacetyl)-, monohydrochloride, Piperidine, 1-glycyl-, hydrochloride, Piperidine, 1-glycyl-, monohydrochloride

2-Amino-1-(1-piperidinyl)-1-ethanone hydrochloride is an achiral and enantioselective chiral catalyst. It has been shown to catalyze the transfer of alkyl groups from one molecule to another, including imine, initially alkylated, and chiral substrates. 2-Amino-1-(1-piperidinyl)-1-ethanone hydrochloride has been used in asymmetric synthesis of levobupivacaine with high optical purity.

CAS 5437-48-9: 2-oxo-2-piperidin-1-ylethanamine hydrochloride

2-Amino-1-(1-piperidinyl)-1-ethanone hydrochloride

Ref: 3D-FAA43748

2-AMINO-1-PIPERIDIN-1-YL-ETHANONE HCL

Ref: IN-DA00DAMV

2-Amino-1-piperidin-1-yl-ethanone hydrochloride

Ref: 10-F024984

2-Amino-1-(piperidin-1-yl)ethan-1-one hydrochloride

Ref: 54-OR1021203