1323975-44-5

Basic information

• Product Name: 1-(2-iodo-4-methylphenyl)-1H-pyrrole
• Synonyms: 1-(2-iodo-4-methylphenyl)-1H-pyrrole
• CAS NO: 1323975-44-5
• Molecular Weight: 283.112
• Mol File: 1323975-44-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(2-iodo-4-methylphenyl)-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-iodo-4-methylphenyl)-1H-pyrrole(1323975-44-5)
• EPA Substance Registry System: 1-(2-iodo-4-methylphenyl)-1H-pyrrole(1323975-44-5)

Safety Data

• Hazardous Substances Data: 1323975-44-5(Hazardous Substances Data)

Upstream product

• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 13194-69-9 2-iodo-5-methylaniline 
• 29289-13-2 2-iodo-4-methylaniline 

Relevant articles and documents

Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne-carbonyl metathesis

The strategic use of a sequential Sonogashira coupling/intramolecular alkyne-carbonyl metathesis process for the synthesis of a pyridine ring from 1-(2-haloaryl)-1H-pyrrole-2-carbaldehydes allowed ready access to diverse novel benzo-fused indolizines, pyr

Palladium-Catalyzed Synthesis of Tetrasubstituted Olefins by Triple Domino Process

An efficient, highly regio- and stereoselective protocol for the synthesis of tetrasubstituted olefins was developed to take place by a palladium(0)-catalyzed triple domino process. It involves the formation of three new C?C bonds through double carbopalladation and C?H activation across 2-bromoaryl alkynyl biaryls/heteroaryls with norbornene. This method is practically simple with broad substrate scope and tolerates a wide range of substituents. The products bearing 9H-pyrrolo[1,2-a]indole motifs reveal intriguing solid state fluorescence properties and thus form a new class of aggregation induced emission (AIE) fluorophores. (Figure presented.).