158080-71-8

Usage

Chemical Properties

Pale Yellow Solid

Uses

The (S)-enantiomer metabolite of Propafenone.

InChI:InChI=1/C21H27NO4.ClH/c1-2-12-22-14-18(24)15-26-21-11-9-17(23)13-19(21)20(25)10-8-16-6-4-3-5-7-16;/h3-7,9,11,13,18,22-24H,2,8,10,12,14-15H2,1H3;1H/t18-;/m0./s1

Upstream product

• 93885-31-5 (E)-1-(5-Benzyloxy-2-oxiranylmethoxy-phenyl)-3-phenyl-propenone 
• 490-78-8 2,5-Dihydroxyacetophenone 
• 30992-63-3 5-benzyloxy-2-hydroxyacetophenone 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 

Relevant academic research and scientific papers

Studies on the metabolism of propafenone. 1st comm.: Synthesis and chromatographic/mass spectrometric properties of the labelled compound and of the reference substances

The synthesis of 14C-propafenone and 2H-propafenone (propafenone: 2-(2'-hydroxy-3'-propylamino-propoxy)-ω-phenyl-propiophenone hydrochloride) and some reference compounds is described. The thin-layer chromatographic, high-performance liquid and gas chromatographic properties of the substances are described. Propafenone and the reference substances were studied by mass spectrometry and compared with each other, with respect to structural elucidation of the metabolites. The chromatographic and mass spectrometric data (key ions) enables the metabolites of propafenone to be identified in biological material.