1374335-74-6

Basic information

• Product Name: 1,N-di(tert-butoxycarbonyl)-5-bromo-2-chloro-N-(4-methoxyphenyl)indol-3-acetamide
• Synonyms: 1,N-di(tert-butoxycarbonyl)-5-bromo-2-chloro-N-(4-methoxyphenyl)indol-3-acetamide
• CAS NO: 1374335-74-6
• Molecular Weight: 563.876
• Mol File: 1374335-74-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,N-di(tert-butoxycarbonyl)-5-bromo-2-chloro-N-(4-methoxyphenyl)indol-3-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,N-di(tert-butoxycarbonyl)-5-bromo-2-chloro-N-(4-methoxyphenyl)indol-3-acetamide(1374335-74-6)
• EPA Substance Registry System: 1,N-di(tert-butoxycarbonyl)-5-bromo-2-chloro-N-(4-methoxyphenyl)indol-3-acetamide(1374335-74-6)

Safety Data

• Hazardous Substances Data: 1374335-74-6(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 1374335-88-2 C₁₆H₁₂BrClN₂O 
• 1391039-32-9 C₁₆H₁₀BrClN₂O₂ 
• 20870-78-4 5-bromo-2-indolin-2-one 
• 59-48-3 2-oxoindole 

Downstream Products

• 142273-20-9 kenpaullone 

Relevant articles and documents

Synthesis of paullone and kenpaullone derivatives by photocyclization of 2-(2-chloro-1H-indol-3-yl)-N-arylacetamides

An efficient synthesis of paullone and kenpaullone derivatives in moderate to high yields has been achieved through photocyclizations of (2-chloro-1H-indole-3-yl)-N-arylacetamides in acetone at room temperature. Paullone and kenpaullone have been obtained