1606994-77-7

Basic information

• Product Name: 2-(4-bromophenyl)-1-tosyl-1H-indole
• Synonyms: 2-(4-bromophenyl)-1-tosyl-1H-indole
• CAS NO: 1606994-77-7
• Molecular Weight: 426.334
• Mol File: 1606994-77-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(4-bromophenyl)-1-tosyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromophenyl)-1-tosyl-1H-indole(1606994-77-7)
• EPA Substance Registry System: 2-(4-bromophenyl)-1-tosyl-1H-indole(1606994-77-7)

Safety Data

• Hazardous Substances Data: 1606994-77-7(Hazardous Substances Data)

Upstream product

• 1236044-94-2 N-{2-[(4-bromophenyl)ethynyl]phenyl}-4-methylbenzenesulfonamide 
• 615-43-0 2-iodophenylamine 
• 766-96-1 4-bromo-1-ethynylbenzene 
• 586-75-4 4-chlorobenzoyl chloride 
• 243844-35-1 N-[2-(chloromethyl)-phenyl]-4-methylbenzene-1-sulfonamide 

Relevant articles and documents

Tandem Phospha-Michael Addition/N-Acylation/ Intramolecular Wittig Reaction of aza-o-Quinone Methides: Approaches to 2,3-Disubstituted Indoles

A tandem phospha-Michael addition/N-acylation/intramolecular Wittig reaction of in situ formed aza-o-QMs is disclosed. This approach features high functional group tolerance and provides a convenient and practical access to biologically significant indole derivatives (37 examples, up to 91% yield) under mild reaction conditions. (Figure presented.).

A robust, well-defined homogeneous silver(I) catalyst for mild intramolecular hydroamination of 2-ethynylanilines leading to indoles

A highly efficient, chemically stable and well-defined homogeneous silver(I) catalyst is reported for the room temperature, intramolecular hydroamination of 2-alkynylanilines leading to indole derivatives. Copyright