932406-43-4

Basic information

• Product Name: benzyl (6-chloro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridin-4-yl)(2-fluoro-4-nitrophenyl)acetate
• Synonyms: benzyl (6-chloro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridin-4-yl)(2-fluoro-4-nitrophenyl)acetate
• CAS NO: 932406-43-4
• Molecular Weight: 638.091
• Mol File: 932406-43-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl (6-chloro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridin-4-yl)(2-fluoro-4-nitrophenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (6-chloro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridin-4-yl)(2-fluoro-4-nitrophenyl)acetate(932406-43-4)
• EPA Substance Registry System: benzyl (6-chloro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridin-4-yl)(2-fluoro-4-nitrophenyl)acetate(932406-43-4)

Safety Data

• Hazardous Substances Data: 932406-43-4(Hazardous Substances Data)

Upstream product

• 369-34-6 3,4-difluoronitrobenzene 
• 372-48-5 2-fluoropyridine 
• 892414-50-5 6-chloro-4-nitro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine 
• 892414-49-2 4-nitro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 892414-45-8 1,1,1-trifluoro-2-(2-fluoropyridin-3-yl)-3-nitropropan-2-ol 
• 892414-46-9 3-(trifluoromethyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-3-ol 
• 932406-33-2 2,2,2-trifluoro-1-(2-fluoropyridin-3-yl)ethane-1,1-diol 
• 892414-48-1 3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 892414-47-0 3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine 
• 932406-45-6 benzyl (2-fluoro-4-nitrophenyl)acetate 
• 892414-51-6 6-chloro-4-nitro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine 

Relevant articles and documents

Synthesis and derivatization of 3-perfluoroalkyl-substituted 7-azaindoles

An expedient large-scale synthesis of 3-perfluoroalkyl-7-azaindoles starting from 2-fluoropyridine is presented. The activation as 6-chloro-4-nitro derivative allows the further derivatization by nucleophilic aromatic substitution in the 4-position. Georg