The chemical substance known as "4-[4-(4-chloro-2,3,5,6-tetradeuteriophenyl)-4-hydroxy-1-oxidopiperidin-1-ium-1-yl]-1-(4-fluorophenyl)butan-1-one" with CAS number 1246815-56-4 is a complex organic compound characterized by its multi-functional groups and specific isotopic labeling. It features a piperidine ring that is substituted with a hydroxy group and a quaternary ammonium moiety, indicating its potential as a cationic species. The presence of a chloro substituent on the aromatic ring and a fluorine atom further enhances its chemical reactivity and may influence its biological activity. The incorporation of deuterium atoms suggests applications in isotopic labeling for studies in pharmacokinetics or metabolic pathways. This compound's structural complexity may contribute to unique properties, such as solubility, stability, and interaction with biological targets, making it of interest in medicinal chemistry and drug development. Its specific characteristics, including melting point, solubility, and reactivity, would require empirical investigation to fully understand its behavior in various environments.

4-[4-(4-chloro-2,3,5,6-tetradeuteriophenyl)-4-hydroxy-1-oxidopiperidin-1-ium-1-yl]-1-(4-fluorophenyl)butan-1-one

1246815-56-4: The chemical substance known as "4-[4-(4-chloro-2,3,5,6-tetradeuteriophenyl)-4-hydroxy-1-oxidopiperidin-1-ium-1-yl]-1-(4-fluorophenyl)butan-1-one" with CAS number 1246815-56-4 is a complex organic compound characterized by its multi-functional groups and specific isotopic labeling. It features a piperidine ring that is substituted with a hydroxy group and a quaternary ammonium moiety, indicating its potential as a cationic species. The presence of a chloro substituent on the aromatic ring and a fluorine atom further enhances its chemical reactivity and may influence its biological activity. The incorporation of deuterium atoms suggests applications in isotopic labeling for studies in pharmacokinetics or metabolic pathways. This compound's structural complexity may contribute to unique properties, such as solubility, stability, and interaction with biological targets, making it of interest in medicinal chemistry and drug development. Its specific characteristics, including melting point, solubility, and reactivity, would require empirical investigation to fully understand its behavior in various environments.

CAS 1246815-56-4

4-[4-(4-chloro-2,3,5,6-tetradeuteriophenyl)-4-hydroxy-1-oxidopiperidin-1-ium-1-yl]-1-(4-fluorophenyl)butan-1-one

Haloperidol-d4 N-Oxide

Ref: 4Z-H-0110