1542232-34-7

Basic information

• Product Name: [4-(3-bromo-[²H₆]-propoxy)-phenyl]-(2-butyl-5-nitrobenzofuran-3-yl)-methanone
• CAS NO: 1542232-34-7
• Molecular Weight: 466.277
• Mol File: 1542232-34-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [4-(3-bromo-[²H₆]-propoxy)-phenyl]-(2-butyl-5-nitrobenzofuran-3-yl)-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(3-bromo-[²H₆]-propoxy)-phenyl]-(2-butyl-5-nitrobenzofuran-3-yl)-methanone(1542232-34-7)
• EPA Substance Registry System: [4-(3-bromo-[²H₆]-propoxy)-phenyl]-(2-butyl-5-nitrobenzofuran-3-yl)-methanone(1542232-34-7)

Safety Data

• Hazardous Substances Data: 1542232-34-7(Hazardous Substances Data)

Upstream product

• 141645-16-1 2-n-butyl-3-(4-hydroxybenzoyl)-5-nitrobenzofuran 
• 120404-22-0 [²H₆]-1,3-dibromopropane 

Downstream Products

• 1542232-41-6 (2-butyl-5-nitro-benzofuran-3-yl)-[4-(3-di-1-[²H₂]-butylamino-1-[²H₆]-propoxy)-phenyl]-methanone 
• 1542232-38-1 (2-butyl-5-nitro-benzofuran-3-yl)-[4-(3-dibutylamino-[²H₆]-propoxy)-phenyl]-methanone 
• 1542232-40-5 (2-butyl-5-nitro-benzofuran-3-yl)-[4-(3-di-[²H₉]-butylamino-[²H₆]-propoxy)-phenyl]-methanone 
• 1542232-46-1 (5-amino-2-butylbenzofuran-3-yl)-[4-(3-di-[²H₉]-butylamino-[²H₆]-propoxy)-phenyl]-methanone 
• 1542232-47-2 (5-amino-2-butyl-benzofuran-3-yl)-[4-(3-dibutylamino-[²H₆]-propoxy)-phenyl]-methanone 
• 1542232-48-3 (5-amino-2-butyl-benzofuran-3-yl)-[4-(3-di-1-[²H₂]-butylamino-3-[²H₆]-propoxy)-phenyl]-methanone 
• 1542232-57-4 N-{2-butyl-3-[4-(3-di-[²H₉]-butylamino-[²H₆]-propoxy)-benzoyl]-benzofuran-5-yl}-methanesulfonamide hydrochloride 
• 1329809-23-5 N-{2-butyl-3-[4-(3-dibutylamino-[²H₆]-propoxy)-benzoyl]-benzofuran-5-yl}-methanesulfonamide hydrochloride 
• 1542232-58-5 N-{2-butyl-3-[4-(3-di-1-[²H₂]-butylamino-[²H₆]-propoxy)-benzoyl]-benzofuran-5-yl}-methanesulfonamide hydrochloride 

Relevant articles and documents

Effect of deuteration on the metabolism and clearance of some pharmacologically active compounds - Synthesis and in vitro metabolism of deuterated derivatives of dronedadrone

The synthesis and in vitro metabolism studies of a family of specifically deuterated derivatives of dronedarone are described. Metabolic stability and clearance of the parent compound are not sensitive to deuterium substitution, irrespective of the position of the heavy label. Copyright