10H-Phenothiazine, 10-(4-bromophenyl)-, with the CAS number 63524-03-8, is a chemical compound that belongs to the phenothiazine class, which is characterized by a tricyclic structure containing sulfur and nitrogen atoms. This compound features a bromophenyl group at the 10-position of the phenothiazine core, which can influence its chemical reactivity and biological activity. Typically, phenothiazines exhibit properties such as antipsychotic and antihistaminic effects, and the presence of the bromine substituent may enhance these properties or alter the compound's pharmacokinetics. The compound is likely to be a solid at room temperature, with moderate solubility in organic solvents. Its molecular structure allows for potential interactions with various biological targets, making it of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as halogenated compounds can exhibit varying degrees of toxicity. Overall, 10H-Phenothiazine, 10-(4-bromophenyl)- is a notable compound for research in both chemical and pharmaceutical contexts.

10H-Phenothiazine, 10-(4-bromophenyl)-

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10-(4-Bromophenyl)phenothiazine (contains 10% 10-(4-Iodophenyl)phenothiazine at maximum)

Phenothiazine is a heterocyclic aromatic organic compound with the molecular formula C12H8N2. It is a colorless solid that is sparingly soluble in water, but soluble in common organic solvents. Phenothiazine has been found to be a transition metal catalyst for the synthesis of amines from cyanide and amines. The reaction requires no additional reagents, such as acids or bases, and proceeds under mild conditions. This reaction can also be conducted on an industrial scale, making it an economically viable process. Additionally, phenothiazine is able to catalyze the conversion of amines to nitriles using hydrogen peroxide as the oxidant. This reaction occurs in two steps: first, hydrogen peroxide oxidizes the amine to an iminium ion followed by oxidation of the iminium ion to a nitrile. Phenothiazine has been shown to enhance this reaction by increasing the rate at which hydrogen peroxide reacts with

CAS 63524-03-8: 10H-Phenothiazine, 10-(4-bromophenyl)-

10-(4-Bromophenyl)phenothiazine (contains 10% 10-(4-Iodophenyl)phenothiazine at maximum)

Ref: 3B-B5374

10-(4-Bromophenyl)phenothiazine phenothiazine at maximum)

Ref: 3D-NCA52403

10-(4-Bromophenyl)phenothiazine (contains 10% 10-(4-Iodophenyl)phenothiazine at maximum)

Ref: IN-DA01FND1