91444-27-8

Upstream product

• 62655-56-5 2-(4'-methoxy-phenyl)-6-methoxy-indole 
• 75-03-6 ethyl iodide 
• 536-90-3 m-Anisidine 
• 881-43-6 2-bromo-1-(4-methoxyphenyl)butan-1-one 

Downstream Products

• 86111-42-4 1,3-Diethyl-2-(4-hydroxy-phenyl)-1H-indol-6-ol 
• 86111-36-6 Acetic acid 2-(4-acetoxy-phenyl)-1,3-diethyl-1H-indol-6-yl ester 

Relevant academic research and scientific papers

3-Substituted 2-phenylindoles: Synthesis and biological properties

Knoevenagel-reaction of indol-3-carbaldehydes 5a,b and 7a,b with nitromethane leads to the nitroethenes 12 and 14, the analogous reaction with malodinitrile to the methylidenemalonic acid dinitriles 16.- Michael-addition of nitromethane at 12 and 14 affor

2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat

A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions