78395-75-2

Basic information

• Product Name: 3-(4-nitrophenyldiazenyl)-1-methyl-2-phenyl-1H-indole
• Synonyms: 3-(4-nitrophenyldiazenyl)-1-methyl-2-phenyl-1H-indole
• CAS NO: 78395-75-2
• Molecular Weight: 356.384
• Mol File: 78395-75-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(4-nitrophenyldiazenyl)-1-methyl-2-phenyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-nitrophenyldiazenyl)-1-methyl-2-phenyl-1H-indole(78395-75-2)
• EPA Substance Registry System: 3-(4-nitrophenyldiazenyl)-1-methyl-2-phenyl-1H-indole(78395-75-2)

Safety Data

• Hazardous Substances Data: 78395-75-2(Hazardous Substances Data)

Upstream product

• 14368-49-1 p-nitrobenzenediazonium 
• 56656-06-5 1-methyl-3-(methylthio)-2-phenyl-1H-indole 
• 82946-81-4 3-(p-dimethylaminobenzyl)-1-methyl-2-phenylindole 
• 67335-20-0 3,3'-(phenylmethylene)bis(1-methyl-2-phenyl-1H-indole) 
• 78395-78-5 1-methyl-2-phenyl-3-hydroxymethylindole 
• 948-65-2 2-phenyl-indole 
• 4677-05-8 3-(phenyldiazenyl)-1-methyl-2-phenyl-1H-indole 
• 67335-29-9 bis(1-methyl-2-phenyl-1H-indol-3-yl)methane 
• 1757-72-8 1-methyl-2-phenyl-1H-indole-3-carbaldehyde 
• 3558-24-5 1-methyl-2-phenyl-1H-indole 
• 100-01-6 4-nitro-aniline 
• 2684-02-8 benzenediazonium 

Downstream Products

• 78395-74-1 1-methyl-2-phenyl-3,5-dinitroindole 
• 78395-71-8 1-methyl-2-phenyl-3-nitro-1H-indole 

Relevant articles and documents

Phenylazoindole dyes 3: Determination of azo-hydrazone tautomers of new phenylazoindole dyes in solution and solid state

A new two series of phenylazo indole dyes was synthesized and the structures of the dyes were confirmed by UV-vis, FT-IR, HRMS and 1H/13C NMR spectroscopic techniques. Five of these dyes (I, I′, II′, III and III′) were also characterized in solid state by using single crystal X-ray diffraction studies besides other spectroscopic techniques. The geometries of the azo and hydrazone tautomeric forms of the dyes were optimized by using Density Functional Theory (DFT). In addition, the effects of the donor and acceptor groups on the azo and hydrazone forms of the dyes were evaluated experimentally and theoretically. The results indicate that the phenylazoindole dyes derived from 2-phenyl indole as coupling component exist as azo form in solution, gas phase and solid state.

Electrophilic ipso-Substitutions. Part 1. Reaction of 3-Substituted Indoles with Nitronium and Nitrosonium Ions

3-Substituted indoles react with nitronium and nitrosonium ions to yield 3-nitroindole.In both cases the reaction was interpreted as an electrophilic ipso-substitution.The reaction mechanism is interpreted by hypothesizing the formation of a ?-complex-like intermediate, wich is some cases is preceded by an electron-transfer process.An order for the leaving abilities of the different electrofugal groups is discussed.