1600501-10-7

Basic information

• Product Name: 11-methyl-6-(p-tolyl)-11H-indolo[3,2-c]quinoline
• Synonyms: 11-methyl-6-(p-tolyl)-11H-indolo[3,2-c]quinoline
• CAS NO: 1600501-10-7
• Molecular Weight: 322.409
• Mol File: 1600501-10-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 11-methyl-6-(p-tolyl)-11H-indolo[3,2-c]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 11-methyl-6-(p-tolyl)-11H-indolo[3,2-c]quinoline(1600501-10-7)
• EPA Substance Registry System: 11-methyl-6-(p-tolyl)-11H-indolo[3,2-c]quinoline(1600501-10-7)

Safety Data

• Hazardous Substances Data: 1600501-10-7(Hazardous Substances Data)

Upstream product

• 16096-33-6 1-phenyl-1H-indole 
• 87613-34-1 1-methyl-2-phenyl-1H-indole-3-carbonitrile 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 3558-24-5 1-methyl-2-phenyl-1H-indole 

Relevant articles and documents

Site-Selective Electrochemical C-H Cyanation of Indoles

An electrochemical approach for the site-selective C-H cyanation of indoles employing readily available TMSCN as cyano source has been developed. The electrosynthesis relies on the tris(4-bromophenyl)amine as a redox catalyst, which achieves better yield and regioselectivity. A variety of C2- and C3-cyanated indoles were obtained in satisfactory yields. The reactions are conducted in a simple undivided cell at room temperature and obviate the need for transition-metal reagent and chemical oxidant.