1432521-55-5

Basic information

• Product Name: methyl 3-iodo-1-tosyl-1H-indole-6-carboxylate
• Synonyms: methyl 3-iodo-1-tosyl-1H-indole-6-carboxylate
• CAS NO: 1432521-55-5
• Molecular Weight: 455.273
• Mol File: 1432521-55-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 3-iodo-1-tosyl-1H-indole-6-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-iodo-1-tosyl-1H-indole-6-carboxylate(1432521-55-5)
• EPA Substance Registry System: methyl 3-iodo-1-tosyl-1H-indole-6-carboxylate(1432521-55-5)

Safety Data

• Hazardous Substances Data: 1432521-55-5(Hazardous Substances Data)

Upstream product

• 850374-98-0 3-iodo-1H-indole-6-carboxylic acid methyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 50820-65-0 indole-6-carboxylic acid methyl ester 

Downstream Products

• 1432521-31-7 methyl 3-(2-(2,2-dibromovinyl)phenyl)-1-tosyl-1H-indole-6-carboxylate 
• 1432521-44-2 methyl 3-(2-formylphenyl)-1-tosyl-1H-indole-6-carboxylate 
• 1038997-75-9 3-phenylindole-6-carboxylic acid methyl ester 

Relevant articles and documents

Design and Synthesis of 2,2′-Diindolylmethanes to Selectively Target Certain G-Quadruplex DNA Structures

G-quadruplex (G4) structures carry vital biological functions, and compounds that selectively target certain G4 structures have both therapeutic potential and value as research tools. Along this line, 2,2′-diindolylmethanes have been designed and synthesi

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.