1454704-55-2

Basic information

• Product Name: (E)-2-(4-chlorostyryl)-N,N-dimethyl-1H-indole-1-carboxamide
• Synonyms: (E)-2-(4-chlorostyryl)-N,N-dimethyl-1H-indole-1-carboxamide
• CAS NO: 1454704-55-2
• Molecular Weight: 324.81
• Mol File: 1454704-55-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-2-(4-chlorostyryl)-N,N-dimethyl-1H-indole-1-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(4-chlorostyryl)-N,N-dimethyl-1H-indole-1-carboxamide(1454704-55-2)
• EPA Substance Registry System: (E)-2-(4-chlorostyryl)-N,N-dimethyl-1H-indole-1-carboxamide(1454704-55-2)

Safety Data

• Hazardous Substances Data: 1454704-55-2(Hazardous Substances Data)

Upstream product

• 1073-67-2 4-vinylbenzyl chloride 
• 70957-05-0 1-(N,N?dimethylcarbamoyl)indole 
• 120-72-9 indole 

Relevant articles and documents

Regioselective C2 oxidative olefination of indoles and pyrroles through cationic rhodium(III)-Catalyzed C-H bond activation

Be economic with your atoms! An efficient Rh-catalyzed oxidative olefination of indoles and pyrroles with broad substrate scope and tolerance is reported (see scheme). The catalytic reaction proceeds with excellent regio- and stereoselectivity. The directing group N,N-dimethylcarbamoyl was crucial for the reaction and could be removed easily. Copyright

Aerobic Ru-catalyzed direct C2-olefination of N-heteroarenes with alkenes directed by a removable N-dimethylcarbamoyl group

A highly efficient and selective Ru-catalyzed direct C2-olefination of indoles, pyrroles, and carbazoles assisted by a removable N-dimethylcarbamoyl group has been developed by using O2 as the terminal oxidant. Both electron-deficient and unactivated alkenes are applicable to the protocol. The Royal Society of Chemistry 2013.