91107-10-7

Basic information

• Product Name: 1H-Indole, 4,6-dimethoxy-2,3-diphenyl-
• CAS NO: 91107-10-7
• Molecular Formula: C22H19NO2
• Molecular Weight: 329.398
• Mol File: 91107-10-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 4,6-dimethoxy-2,3-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 4,6-dimethoxy-2,3-diphenyl-(91107-10-7)
• EPA Substance Registry System: 1H-Indole, 4,6-dimethoxy-2,3-diphenyl-(91107-10-7)

Safety Data

• Hazardous Substances Data: 91107-10-7(Hazardous Substances Data)

Upstream product

• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 10272-07-8 3.5-dimethoxyaniline 
• 501-65-5 diphenyl acetylene 
• 6293-83-0 2-iodo-4-nitrophenylamine 

Downstream Products

• 123613-02-5 2-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-1-pyrroline 
• 123613-01-4 [1-(4,6-Dimethoxy-2,3-diphenyl-1H-indol-7-yl)-1-phenyl-meth-(E)-ylidene]-phenyl-amine 
• 91107-13-0 7-(indol-2'-yl)-4,6-dimethoxy-2,3-diphenylindole 
• 159114-43-9 4,6-dimethoxy-2,3-diphenyl-1H-indole-7-glyoxyloyl chloride 
• 91107-18-5 4,6-dimethoxy-7-(4',6'-dimethoxyindol-2'-yl)-2,3-diphenylindole 
• 123613-03-6 4,6-dimethoxy-7-(5-methyl-1-pyrrolin-2-yl)-2,3-diphenylindole 
• 146255-91-6 1-benzyl-4,6-dimethoxy-2,3-diphenylindole 
• 123612-99-7 4,6-dimethoxy-2,3-diphenyl-7-(phenyliminomethyl)indole 
• 176696-08-5 4,6-dimethoxy-7-(4',4'-dimethyl-4',5'-dihydro-oxazol-2'-yl)-2,3-diphenylindole 
• 51206-73-6 2-chloro-3-methyl-1H-indole 

Relevant articles and documents

Synthesis and antioxidant screening of Novel indole amines

Novel indoles amines have been synthesized and screened for antioxidant activity. Chiron approach is used to synthesis enantiopure heterocycles. Newly synthesized indole amines showed good antioxidant potential as compared to standard drugs. Novel indole

Synthesis, characterization, UV–Vis absorption and cholinesterase inhibition properties of bis-indolyl imine ligand systems

A number of bis-indolyl imine helical structures has successfully been synthesized employing Schiff base reaction conditions starting from 4,6-dimethoxy-2,3-diphenylindole with different o-phenyl diamines as π-spacer bridged. The structures of targeted co

Rh-Catalyzed oxidative C-H activation/annulation: Converting anilines to indoles using molecular oxygen as the sole oxidant

A practical and efficient Rh(iii)-catalyzed aerobic C-H activation has been developed for the facile synthesis of a broad range of indoles from simple anilines and alkynes. The protocol could be conducted under mild conditions and used environmentally friendly oxygen as the sole clear oxidant.