2-[Chloro(dideuterio)methyl]-1-(trideuteriomethyl)piperidine is a synthetic organic compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The presence of deuterium, a stable isotope of hydrogen, in the molecule indicates that it has been isotopically labeled, which can be useful in various applications such as tracing studies in metabolic pathways or in NMR spectroscopy. The compound features a chloro substituent, which can influence its reactivity and solubility. The presence of multiple deuterated methyl groups suggests that it may exhibit unique physical and chemical properties compared to its non-deuterated counterparts, such as altered boiling and melting points, as well as changes in reactivity due to the kinetic isotope effect. Additionally, the specific arrangement of substituents on the piperidine ring can affect its biological activity and interactions with other molecules. Overall, this compound is of interest in both synthetic chemistry and potential pharmaceutical applications due to its unique isotopic labeling and structural characteristics.

2-[chloro(dideuterio)methyl]-1-(trideuteriomethyl)piperidine

1795025-62-5: 2-[Chloro(dideuterio)methyl]-1-(trideuteriomethyl)piperidine is a synthetic organic compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The presence of deuterium, a stable isotope of hydrogen, in the molecule indicates that it has been isotopically labeled, which can be useful in various applications such as tracing studies in metabolic pathways or in NMR spectroscopy. The compound features a chloro substituent, which can influence its reactivity and solubility. The presence of multiple deuterated methyl groups suggests that it may exhibit unique physical and chemical properties compared to its non-deuterated counterparts, such as altered boiling and melting points, as well as changes in reactivity due to the kinetic isotope effect. Additionally, the specific arrangement of substituents on the piperidine ring can affect its biological activity and interactions with other molecules. Overall, this compound is of interest in both synthetic chemistry and potential pharmaceutical applications due to its unique isotopic labeling and structural characteristics.

<p>Applications Reactant in the preparation of CB1 cannabinoid receptor agonists and brain imaging agents.<br>References Deng, H. et al; J. Med. Chem. 48, 6386 (2005)<br></p>

CAS 1795025-62-5

2-[chloro(dideuterio)methyl]-1-(trideuteriomethyl)piperidine

N-Methyl-2-piperidinemethyl-d5 Chloride

Ref: TR-M324812