2-Methylsulfonyl-10-(1,1,2,3,3-pentadeuterioprop-2-enyl)phenothiazine is a chemical compound characterized by its phenothiazine backbone, which is a tricyclic structure known for its applications in pharmaceuticals, particularly as antipsychotic agents. The presence of a methylsulfonyl group enhances its solubility and may influence its biological activity. The compound also features a pentadeuterioprop-2-enyl substituent, indicating that it contains five deuterium atoms, which can be useful in studies involving isotopic labeling for tracing mechanisms in biological systems. This substitution can affect the compound's physical properties, such as its mass and stability. The overall structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the specific arrangement of substituents can influence the compound's reactivity, pharmacokinetics, and pharmacodynamics. As with many phenothiazine derivatives, it may exhibit a range of biological activities, including antipsychotic, antidepressant, or anti-inflammatory effects, depending on its specific interactions within biological systems.

2-methylsulfonyl-10-(1,1,2,3,3-pentadeuterioprop-2-enyl)phenothiazine

1794940-43-4: 2-Methylsulfonyl-10-(1,1,2,3,3-pentadeuterioprop-2-enyl)phenothiazine is a chemical compound characterized by its phenothiazine backbone, which is a tricyclic structure known for its applications in pharmaceuticals, particularly as antipsychotic agents. The presence of a methylsulfonyl group enhances its solubility and may influence its biological activity. The compound also features a pentadeuterioprop-2-enyl substituent, indicating that it contains five deuterium atoms, which can be useful in studies involving isotopic labeling for tracing mechanisms in biological systems. This substitution can affect the compound's physical properties, such as its mass and stability. The overall structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the specific arrangement of substituents can influence the compound's reactivity, pharmacokinetics, and pharmacodynamics. As with many phenothiazine derivatives, it may exhibit a range of biological activities, including antipsychotic, antidepressant, or anti-inflammatory effects, depending on its specific interactions within biological systems.

Phenothiazine Impurity 2-d5

<p>Applications By-product in the preparation of Metopimazine-d6 (M338762).<br></p>

CAS 1794940-43-4

2-methylsulfonyl-10-(1,1,2,3,3-pentadeuterioprop-2-enyl)phenothiazine

Phenothiazine Impurity 2-d5

Ref: 4Z-P-332009

N-(2-Propenyl)-2-methylsulfonyl-10H-phenothiazine-d5

Ref: TR-P768952