67060-92-8

Basic information

• Product Name: 1H-Indole, 1,3-dibenzoyl-
• CAS NO: 67060-92-8
• Molecular Formula: C22H15NO2
• Molecular Weight: 325.367
• Mol File: 67060-92-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 1,3-dibenzoyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 1,3-dibenzoyl-(67060-92-8)
• EPA Substance Registry System: 1H-Indole, 1,3-dibenzoyl-(67060-92-8)

Safety Data

• Hazardous Substances Data: 67060-92-8(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 925-90-6 ethylmagnesium bromide 
• 1496-76-0 N-benzoylindole 
• 611-73-4 Benzoylformic acid 
• 91476-96-9 3-Phenyl-8-(toluene-4-sulfonyl)-8,8a-dihydro-3aH-isoxazolo[5,4-b]indole 
• 91477-17-7 phenyl(1-tosyl-1H-indol-3-yl)methanone 
• 91476-93-6 Phenyl-(3-phenyl-3a,8a-dihydro-isoxazolo[5,4-b]indol-8-yl)-methanone 
• 91476-98-1 3-Phenyl-3a,8a-dihydro-isoxazolo[5,4-b]indole-8-carboxylic acid methyl ester 
• 91477-16-6 N-ethoxycarbonyl-3-benzoylindole 
• 91476-90-3 1-(3-Phenyl-3a,8a-dihydro-isoxazolo[5,4-b]indol-8-yl)-ethanone 
• 91477-18-8 N-methoxycarbonyl-3-benzoylindole 
• 698-16-8 benzohydroximoyl chloride 
• 82414-15-1 3-Phenyl-3a,8a-dihydro-isoxazolo[5,4-b]indole-8-carboxylic acid ethyl ester 
• 31271-90-6 1-(p-toluenesulfonyl)-1H-indole 

Relevant articles and documents

Room temperature palladium-catalyzed decarboxylative acyl/aroylation using [Fe(III)(EDTA)(η2-O2)]3- as oxidant at biological pH

The purple-coloured iron peroxo complex [Fe(III)EDTA(η2- O2)]3- as a novel reagent system for Pd-catalyzed decarboxylative ortho-acylation of acetanilides with α-oxocarboxylic acids at room temperature in aqueous media has been realized. This reaction provides an effective access to ortho-acylacetanilides under mild conditions. Copyright

Acylation, cyanoethylation and alkylation of methyl and phenyl indolylmagnesium salts: Influence of the substituents on the C- and N- reaction products

Analysis of the influence of the substitution on indolylmagnesium salts in the reaction with benzoyl chloride, acrylonitrile and methyl iodide, giving the C- and N-derivatives, have been carried out. The yield in the C- and N-product depends upon the electronic character and position of the substituent (methyl or phenyl) on the indole ring and of the ethereal solvent as well as the concentration and molar ratio of the reagents. The 2- or 3- phenyl substituted indolylmagnesium salts with acrylonitrile always gave the 1-(2-cyanoethyl)indole derivative.