154201-40-8

Upstream product

• 5102-18-1 1-(5-hydroxy-2-methyl-1-phenyl-1H-indol-3-yl)ethanone 
• 75-36-5 acetyl chloride 

Downstream Products

• 154201-43-1 3,6-diacetyl-5-ethyoxycarbonylmethoxy-2-methyl-1-phenylindole 
• 849148-73-8 3,7-diacetyl-2,8-dimethyl-1-phenyl-1H-pyrano[2,3-f]indol-6-one 
• 154201-46-4 3,6-diacetyl-2-methyl-1-phenylindol-5-yloxyacetic acid 

Relevant academic research and scientific papers

Synthesis and antimicrobial activity of novel linearly fused 5-substituted- 7-acetyl-2,6-dimethyloxazolo[4,5-f]indoles

The exclusive formation of l-substituted-6-α-oximinoethylindoles 3a-d from the reaction of 3,6-diacetylindoles with hydroxylamine reveals the chemoselectivity of C6-acetyl function over that of C3-acetyl function towards the nucleophilic attack

Synthesis and antimicrobial activity of furoindole derivatives

8-Bromofuroindole derivatives (5a-d) have been prepared by cyclodehydration of 5-benzoylmethoxy-6-bromoindoles (4a-d) with PPA at 90-100 deg C. 3,6-Diacetyl-5-hydroxyindoles (6a-c) on reaction with ethyl chloroacetate followed by hydrolysis with aq