1334298-38-2

Basic information

• Product Name: 4-methyl-N-(2-(1-methyl-5-phenyl-1H-indol-3-yl)ethyl)benzenesulfonamide
• Synonyms: 4-methyl-N-(2-(1-methyl-5-phenyl-1H-indol-3-yl)ethyl)benzenesulfonamide
• CAS NO: 1334298-38-2
• Molecular Weight: 404.533
• Mol File: 1334298-38-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-methyl-N-(2-(1-methyl-5-phenyl-1H-indol-3-yl)ethyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-(2-(1-methyl-5-phenyl-1H-indol-3-yl)ethyl)benzenesulfonamide(1334298-38-2)
• EPA Substance Registry System: 4-methyl-N-(2-(1-methyl-5-phenyl-1H-indol-3-yl)ethyl)benzenesulfonamide(1334298-38-2)

Safety Data

• Hazardous Substances Data: 1334298-38-2(Hazardous Substances Data)

Upstream product

• 117235-22-0 methyl 2-(5-bromo-1H-indole-3-yl)acetate 
• 1334298-69-9 methyl 2-(5-bromo-1-methyl-1H-indol-3-yl)acetate 
• 1334298-70-2 methyl 2-(1-methyl-5-phenyl-1H-indol-3-yl)acetate 
• 1368633-66-2 C₁₇H₁₅NO₂ 
• 1334298-76-8 2-(1-methyl-5-phenyl-1H-indol-3-yl)-N-tosylacetamide 
• 40432-84-6 (5-bromo-1H-indol-3-yl)-acetic acid 

Relevant articles and documents

Organocatalyzed enantioselective fluorocyclizations

Enantioenriched fluorinated heterocycles can be prepared through fluorocyclizations of prochiral indoles (see scheme; Ts=tosyl, Bn=benzyl, Boc=tert-butoxycarbonyl). More than twenty examples for this cascade fluorination-cyclization, which is catalyzed by cinchona alkaloids and employs N-fluorobenzenesulfonimide as the electrophilic fluorine source have been explored, and an unprecedented catalytic asymmetric difluorocyclization has also been identified.