This compound is a structural analog of vortioxetine, featuring a piperazine ring linked to a phenylthio moiety substituted with 2,5-dimethylphenyl groups. The sulfur bridge introduces a thioether functionality, while the dimethyl substitution on the aryl ring alters electronic and steric properties compared to the parent drug. The phenyl-piperazine scaffold retains partial pharmacophoric similarity but diverges in metabolic stability and solubility profiles. It serves as a critical HPLC reference standard for quantifying process-related impurities in vortioxetine API synthesis.
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