1092390-84-5

Basic information

• Product Name: 3-[(5-bromo-1H-indol-3-yl)(phenyl)methyl]-1-methyl-1H-indole
• Synonyms: 3-[(5-bromo-1H-indol-3-yl)(phenyl)methyl]-1-methyl-1H-indole
• CAS NO: 1092390-84-5
• Molecular Weight: 415.332
• Mol File: 1092390-84-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-[(5-bromo-1H-indol-3-yl)(phenyl)methyl]-1-methyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(5-bromo-1H-indol-3-yl)(phenyl)methyl]-1-methyl-1H-indole(1092390-84-5)
• EPA Substance Registry System: 3-[(5-bromo-1H-indol-3-yl)(phenyl)methyl]-1-methyl-1H-indole(1092390-84-5)

Safety Data

• Hazardous Substances Data: 1092390-84-5(Hazardous Substances Data)

Upstream product

• 603-76-9 1-methylindole 
• 10075-50-0 5-bromo-1H-indole 
• 1484-27-1 3-bromoindole 
• 100-52-7 benzaldehyde 
• 1172116-64-1 N-[(5-bromoindol-3-yl)-(phenyl)methyl]-4-methylbenzenesulfonamide 
• 1092390-75-4 C₂₁H₁₈BrN₃O₃ 

Relevant articles and documents

A facile iron-catalyzed dual C-C bond cleavage: An approach towards triarylmethanes

A facile iron-catalyzed dual C-C bond cleaving reaction involving 1,3-dicarbonyl units along with electron-rich and sterically bulky arenes as efficient carbon-based leaving groups has been developed. The scope of the dual C-C bond breaking reaction was s

Br?nsted acid catalyzed synthesis of unsymmetrical arylbis(3-indolyl)-methanes synthesis of unsymmetrical arylbis(3-indolyl) methanes

Unsymmetrical arylbis(3-indolyl)methanes have been synthesized via a Br?nsted acid catalyzed Friedel-Crafts alkylation of a-(3-indolyl) benzylamines with N-methylindole. With 5 mol% of the catalyst, the reaction proceeds smoothly under mild conditions, af