937385-02-9

Upstream product

• 90919-20-3 4-(3-chloropropyl)benzoic acid 

Downstream Products

• 1447931-34-1 (2-butyl-5-iodobenzofuran-3-yl)-[4-(3-chloropropyl)phenyl]methanone 
• 1447931-36-3 (5-bromo-2-butylbenzofuran-3-yl)-[4-(3-chloropropyl)phenyl]methanone 
• 1447931-33-0 C₂₅⁽¹⁴⁾CH₂₉ClO₄ 
• 1447931-43-2 [¹⁴C]SSR₁₄₉₇₄₄ 
• 1447931-37-4 (2-butyl-5-iodobenzofuran-3-yl)-[4-(3-dibutylaminopropyl)phenyl]methanone 
• 1447931-38-5 (5-bromo-2-butylbenzofuran-3-yl)-[4-(3-dibutylaminopropyl)phenyl]methanone 
• 1376436-78-0 1-methylethyl 2-butyl-3-{[4-(3-chloropropyl)phenyl]carbonyl}indolizine-7-carboxylate 
• 937385-05-2 (2-butylindolizin-3-yl)[4-(3-chloropropyl)phenyl]methanone 
• 937385-01-8 (2-butyl-6-ethylindolizin-3-yl)[4-(3-chloropropyl)phenyl]methanone 
• 937385-04-1 (2-ethylindolizin-3-yl)[4-(3-chloropropyl)phenyl]methanone 

Relevant academic research and scientific papers

A convenient method to produce [14C]carbon monoxide and its application to the radiosynthesis of [carboxyl-14C]celivarone, [carboxyl-14C]SSR149744

[carboxyl-14C]Celivarone was synthesised from barium [ 14C]carbonate with overall radiochemical yields in the range 49-53%. The synthetic route involves [14C]carbonylation methodology, which both decreased the number of synthetic steps and increased the yields obtained from previous synthetic routes. [carboxyl-14C]Celivarone was synthesised from barium [14C]carbonate with overall radiochemical yields in the range 49-53%. The synthetic route involves [14C] carbonylation methodology, which both decreased the number of synthetic steps and increased the yields obtained from previous synthetic routes. Copyright