1432521-31-7

Basic information

• Product Name: methyl 3-(2-(2,2-dibromovinyl)phenyl)-1-tosyl-1H-indole-6-carboxylate
• Synonyms: methyl 3-(2-(2,2-dibromovinyl)phenyl)-1-tosyl-1H-indole-6-carboxylate
• CAS NO: 1432521-31-7
• Molecular Weight: 589.304
• Mol File: 1432521-31-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 3-(2-(2,2-dibromovinyl)phenyl)-1-tosyl-1H-indole-6-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(2-(2,2-dibromovinyl)phenyl)-1-tosyl-1H-indole-6-carboxylate(1432521-31-7)
• EPA Substance Registry System: methyl 3-(2-(2,2-dibromovinyl)phenyl)-1-tosyl-1H-indole-6-carboxylate(1432521-31-7)

Safety Data

• Hazardous Substances Data: 1432521-31-7(Hazardous Substances Data)

Upstream product

• 1432521-55-5 methyl 3-iodo-1-tosyl-1H-indole-6-carboxylate 
• 850374-98-0 3-iodo-1H-indole-6-carboxylic acid methyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 558-13-4 carbon tetrabromide 
• 1432521-44-2 methyl 3-(2-formylphenyl)-1-tosyl-1H-indole-6-carboxylate 

Relevant articles and documents

Domino C-H functionalization reactions of gem-dibromoolefins: Synthesis of N-fused benzo[c]carbazoles

A palladium-catalyzed domino transformation of gem-dibromoolefins leading to novel polycyclic benzo[c]carbazoles is described. A unique feature of the current reaction is the participation of both bromides in C-H functionalization processes. Mechanistic studies were conducted to ascertain the sequence of reaction events, and the results indicate that the (Z)-bromide likely reacts in preference to the (E)-bromide.