107275-11-6

Basic information

• Product Name: (2-methyl-5-methoxyl-1H-indol-3-yl)(phenyl)methanone
• Synonyms: (2-methyl-5-methoxyl-1H-indol-3-yl)(phenyl)methanone
• CAS NO: 107275-11-6
• Molecular Weight: 265.312
• Mol File: 107275-11-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2-methyl-5-methoxyl-1H-indol-3-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-methyl-5-methoxyl-1H-indol-3-yl)(phenyl)methanone(107275-11-6)
• EPA Substance Registry System: (2-methyl-5-methoxyl-1H-indol-3-yl)(phenyl)methanone(107275-11-6)

Safety Data

• Hazardous Substances Data: 107275-11-6(Hazardous Substances Data)

Upstream product

• 20771-77-1 1-phenyl-3-N-(p-methoxyphenylimino)-1-butanone 
• 98-88-4 benzoyl chloride 
• 104-94-9 4-methoxy-aniline 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 14277-02-2 N-(4-methoxyphenyl)acetimidamide 
• 1076-74-0 5-methoxy-2-methyl-1H-indole 

Downstream Products

• 360054-28-0 3-benzoyl-5-methoxy-1,2-dimethyl-4-nitroindole 

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

Controlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones

A series of substituted 3-(4-nitrophenyloxy)methylindole-4,7-diones (Q) were synthesised. The effects of substitution patterns on the indole core on rates of elimination of 4-nitrophenol as a model for drug release following fragmentation of a phenolic et