869959-91-1

Basic information

• Product Name: 1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amino] propanone
• Synonyms: 1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amino] propanone
• CAS NO: 869959-91-1
• Molecular Weight: 364.239
• Mol File: 869959-91-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amino] propanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amino] propanone(869959-91-1)
• EPA Substance Registry System: 1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amino] propanone(869959-91-1)

Safety Data

• Hazardous Substances Data: 869959-91-1(Hazardous Substances Data)

Upstream product

• 10272-07-8 3.5-dimethoxyaniline 
• 38786-67-3 2-bromo-1-(4-bromophenyl)propan-1-one 

Downstream Products

• 845548-60-9 3-(4-bromophenyl)-4,6-dimethoxy-2-methylindole 
• 869960-03-2 ethyl 2-(3-(4-bromophenyl)-4,6-dimethoxy-2-methylindol-7-yl)glyoxylate 
• 869960-13-4 3-(4-bromophenyl)-4,6-dimethoxy-7-trifluoroacetylindole-2-carbaldehyde 
• 869960-00-9 3-(4-bromophenyl)-4,6-dimethoxy-2-methyl-7-trifluoroacetylindole 
• 869960-02-1 3-(4-bromophenyl)-4,6-dimethoxy-2-methyl-7-trichloroacetylindole 
• 869960-04-3 N,N-dimethyl-2-(3-(4-bromophenyl)-4,6-dimethoxy-2-methylindol-7-yl) glyoxylamide 
• 869959-97-7 7-(3-(4-bromophenyl)-4,6-dimethoxy-2-methyl-3-phenylindolyl)-ethanone 
• 869959-95-5 3-(4-bromophenyl)-7-hydroxymethyl-4,6-dimethoxy-2-methylindole 
• 869748-11-8 3-(4-bromophenyl)-4,6-dimethohy-2-methylindole-7-carbaldehyde 
• 869959-93-3 1-acetyl-3-(4-bromophenyl)-4,6-dimethoxy-2-methylindole 
• 869960-21-4 N-acetyl-1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amido] prpanone 

Relevant articles and documents

New reactivity patterns in activated indoles with 2-methyl substituents

The synthesis and reactive properties of two new 3-aryl-2-methyl-4,6- dimethoxyindoles are reported. These compounds show typical electrophilic substitution and addition reactions at C7, but not oxidative dimerisation because of the reactivity of the 2-methyl group. This methyl group can be effectively oxidised to a carbaldehyde by selenium dioxide, but formation of 7,7′-diindolylselenides also occurs.