1357149-34-8

Basic information

• Product Name: methyl 2-[4-(1H-indol-2-yl)phenoxy]acetate
• Synonyms: methyl 2-[4-(1H-indol-2-yl)phenoxy]acetate
• CAS NO: 1357149-34-8
• Molecular Weight: 281.311
• Mol File: 1357149-34-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-[4-(1H-indol-2-yl)phenoxy]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-[4-(1H-indol-2-yl)phenoxy]acetate(1357149-34-8)
• EPA Substance Registry System: methyl 2-[4-(1H-indol-2-yl)phenoxy]acetate(1357149-34-8)

Safety Data

• Hazardous Substances Data: 1357149-34-8(Hazardous Substances Data)

Upstream product

• 40643-14-9 2-(4'-hydroxy-phenyl)-indole 
• 96-32-2 bromoacetic acid methyl ester 

Downstream Products

• 1357149-17-7 2-[4-(1H-indol-2-yl)phenoxy]-1-(pyrrolidin-1-yl)ethanone 
• 1357149-13-3 2-[4-(1H-indol-2-yl)phenoxy]-N-(pyridin-4-yl)acetamide 
• 1357149-14-4 2-[4-(1H-indol-2-yl)phenoxy]-N-(pyrazin-2-yl)acetamide 
• 1357149-11-1 2-[4-(1H-indol-2-yl)phenoxy]acetamide 
• 1357149-23-5 2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide 
• 1357149-22-4 2-[4-(1H-indol-2-yl)phenoxy]-N-{4-[N-(5-methylisoxazol-3-yl)sulfamoyl]phenyl}acetamide 
• 1357149-12-2 2-[4-(1H-indol-2-yl)phenoxy]-N-(2-hydroxyethyl)acetamide 
• 1357149-19-9 2-[4-(1H-indol-2-yl)phenoxy]-N'-acetylacetohydrazide 
• 1357149-20-2 2-{2-[4-(1H-indol-2-yl)phenoxy]acetyl}hydrazinecarbothioamide 
• 1357149-21-3 2-[4-(1H-indol-2-yl)phenoxy]-N-(4-sulfamoylphenyl)acetamide 
• 1357149-16-6 2-[4-(1H-indol-2-yl)phenoxy]-N,N-dimethylacetamide 
• 1357149-15-5 2-[4-(1H-indol-2-yl)phenoxy]-N,N-bis(2-hydroxyethyl)acetamide 
• 1357149-18-8 2-[4-(1H-indol-2-yl)phenoxy]-N'-phenylacetohydrazide 

Relevant articles and documents

Synthesis, molecular docking study and antitumor activity of novel 2-phenylindole derivatives

The starting material, 4-(1-indol-2-yl)phenol 1 was obtained via Fischer synthesis. Vilsmeir Haack's formylation of 1 gave the carboxaldehyde derivative 2 which was subjected to different reactions affording the 3-substituted compounds 3-10. Co