869960-03-2

Upstream product

• 869959-91-1 1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amino] propanone 
• 869960-21-4 N-acetyl-1-(4-bromophenyl)-2-[(3,5-dimethoxyphenyl)amido] prpanone 
• 869959-93-3 1-acetyl-3-(4-bromophenyl)-4,6-dimethoxy-2-methylindole 
• 38786-67-3 2-bromo-1-(4-bromophenyl)propan-1-one 
• 845548-60-9 3-(4-bromophenyl)-4,6-dimethoxy-2-methylindole 

Downstream Products

• 902772-64-9 ethyl 2-[3-(4-bromophenyl)-4,6-dimethoxy-2-methylindol-7-yl]-2-[O-(2,4-dinitrophenyl)oxyimino]acetate 

Relevant academic research and scientific papers

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.