38829-72-0

Basic information

• Product Name: 5,6-dimethyl-2,3-diphenyl-1H-indole
• Synonyms: 5,6-dimethyl-2,3-diphenyl-1H-indole
• CAS NO: 38829-72-0
• Molecular Weight: 297.4
• Mol File: 38829-72-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5,6-dimethyl-2,3-diphenyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-dimethyl-2,3-diphenyl-1H-indole(38829-72-0)
• EPA Substance Registry System: 5,6-dimethyl-2,3-diphenyl-1H-indole(38829-72-0)

Safety Data

• Hazardous Substances Data: 38829-72-0(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 501-65-5 diphenyl acetylene 
• 374924-94-4 acetic acid N'-(3,4-dimethylphenyl)hydrazide 
• 95-64-7 4-amino-o-xylene 
• 60481-51-8 3,4-dimethylphenylhydrazine hydrochloride 
• 99-51-4 4-nitro-o-xylene 

Relevant articles and documents

Step and redox efficient nitroarene to indole synthesis

Step and redox efficiencies are a rising priority in synthetic method development, in order to make synthetic processes more sustainable and more affordable. Herein, a step and redox efficient nitroarene to indole synthesis is developed, in sharp contrast to the rich literature on the construction of indoles. Elemental zinc was found to be the best terminal reductant. This journal is

Indole synthesis by rhodium(III)-catalyzed hydrazine-directed C-H activation: Redox-neutral and traceless by N-N bond cleavage

Fishing for complements! There is an alternative to the useful Fischer indole synthesis. The new method utilizes the same retrosynthetic disconnection but is based on a RhIII-catalyzed directed C-H activation step and a successive coupling with alkynes. Copyright