1431882-00-6

Basic information

• Product Name: N-(1-allyl-1H-indol-2-yl)-N-(4-bromo-2-iodophenyl)-4-methylbenzenesulfonamide
• Synonyms: N-(1-allyl-1H-indol-2-yl)-N-(4-bromo-2-iodophenyl)-4-methylbenzenesulfonamide
• CAS NO: 1431882-00-6
• Molecular Weight: 607.31
• Mol File: 1431882-00-6.mol

Chemical Properties

• CAS DataBase Reference: N-(1-allyl-1H-indol-2-yl)-N-(4-bromo-2-iodophenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-allyl-1H-indol-2-yl)-N-(4-bromo-2-iodophenyl)-4-methylbenzenesulfonamide(1431882-00-6)
• EPA Substance Registry System: N-(1-allyl-1H-indol-2-yl)-N-(4-bromo-2-iodophenyl)-4-methylbenzenesulfonamide(1431882-00-6)

Safety Data

• Hazardous Substances Data: 1431882-00-6(Hazardous Substances Data)

Upstream product

• 16886-08-1 1-allylindole 
• 1426138-88-6 N-(4-bromo-2-iodophenyl)-4-methylbenzenesulfonamide 

Downstream Products

• 1431882-23-3 6-allyl-2-bromo-5-tosyl-5,6-dihydroindolo[2,3-b]indole 

Relevant articles and documents

Apparent Carbon Monoxide Insertion via Double Isocyanide Incorporation during Palladium-Catalyzed Construction of Indoloquinoline Ring in a Single Pot: Synthesis of New Cytotoxic Agents

The formation of an amide bond via incorporation of two isocyanide units during a palladium-catalyzed construction of the indoloquinoline ring afforded N-substituted 6H-indolo[2,3-b]quinoline-11-carboxamides as new cytotoxic agents. The solvent and base play a key role in the selective and unprecedented synthesis of this class of amides. (Figure presented.).

Conformationally restricted functionalized heteroaromatics: A direct access to novel indoloindoles via Pd-mediated reaction

A new, versatile and direct Pd-mediated method involving intramolecular cyclization of N-(2-iodoaryl)-N-(1-alkyl-1H-indol-2-yl)alkane/arene/heteroarene sulfonamide has been developed leading to a diverse and unique class of indolo[2,3-b]indoles for the potential inhibition of sirtuins.