1440422-65-0

Basic information

• Product Name: ethyl 7-methoxy-2-phenyl-1H-indole-3-carboxylate
• Synonyms: ethyl 7-methoxy-2-phenyl-1H-indole-3-carboxylate
• CAS NO: 1440422-65-0
• Molecular Weight: 295.338
• Mol File: 1440422-65-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 7-methoxy-2-phenyl-1H-indole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 7-methoxy-2-phenyl-1H-indole-3-carboxylate(1440422-65-0)
• EPA Substance Registry System: ethyl 7-methoxy-2-phenyl-1H-indole-3-carboxylate(1440422-65-0)

Safety Data

• Hazardous Substances Data: 1440422-65-0(Hazardous Substances Data)

Upstream product

• 1383986-85-3 (Z)-ethyl 3-((2-methoxyphenyl)amino)-3-phenylacrylate 
• 90-04-0 2-methoxy-phenylamine 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 57183-44-5 β-o-anisidino-cinnamic acid ethyl ester 

Relevant articles and documents

Base-promoted, CBr4-mediated tandem bromination/intramolecular Friedel-Crafts alkylation ofN-aryl enamines: a facile access to 1H- And 3H-indoles

Described here is a general and highly efficient method for the synthesis of 1H- and 3H-indoles. In the presence of CBr4and a suitable base, the cyclization ofN-aryl enamines proceeds with high efficiency. Unlike previous intramolecular cross d

Iodide-Ion-Catalyzed carbon-carbon bond-forming cross-dehydrogenative coupling for the synthesis of indole derivatives

The nBu4NI-catalyzed intramolecular cross-dehydrogenative coupling (CDC) reaction has been applied to the synthesis of 1H-indole derivatives. Intramolecular oxidative coupling of N-arylenamines proceeded in the presence of a catalytic amount of nBu4NI and tert-butyl hydroperoxide (TBHP) to afford the corresponding 1H-indole derivatives in good-to-excellent yields. A preliminary study of the synthesis of 3H-indole is also reported. This is a rare example of the nBu4NI-catalyzed C-C bond-forming CDC reaction. Copyright