1228392-67-3

Basic information

• Product Name: 3-(1-methyl-1H-pyrrol-2-yl)-1-(phenylsulfonyl)-1H-indole
• Synonyms: 3-(1-methyl-1H-pyrrol-2-yl)-1-(phenylsulfonyl)-1H-indole
• CAS NO: 1228392-67-3
• Molecular Weight: 336.414
• Mol File: 1228392-67-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(1-methyl-1H-pyrrol-2-yl)-1-(phenylsulfonyl)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-methyl-1H-pyrrol-2-yl)-1-(phenylsulfonyl)-1H-indole(1228392-67-3)
• EPA Substance Registry System: 3-(1-methyl-1H-pyrrol-2-yl)-1-(phenylsulfonyl)-1H-indole(1228392-67-3)

Safety Data

• Hazardous Substances Data: 1228392-67-3(Hazardous Substances Data)

Upstream product

• 99655-68-2 3-bromo-1-phenylsulfonyl indole 
• 118486-97-8 1-methyl-2-(tributyltin)pyrrole 

Relevant articles and documents

An efficient low-temperature stille-migita cross-coupling reaction for heteroaromatic compounds by Pd-PEPPSI-IPent

The reactivity of Pd-PEPPSI (Pyridine, Enhanced, Precatalyst, Preparation, Stabilization, and Initiation) precatalysts in the Stille-Migita crosscoupling reaction between heteroaryl stannanes and aryl or heteroaryl halides was evaluated. In general, PdPEPPSI-IPent (IPent = diisopentylphenylimidazolium derivative) demonstrated high efficiency over a variety of challenging aryl or heteroaryl halides with thiophene-, furan-, pyrrole-, and thiazole-based organostannanes when compared with Pd-PEPPSI-IPr (IPr = diisopropylphenylimidazolium derivative). The transformations proceeded at appreciably lower temperatures (3080°C) than triarylphosphine-based Pd catalysts, improving the scope of this useful carbon-carbon bond-forming process.