1423469-24-2

Basic information

• Product Name: 1-(2,6-dibromo-4-chlorophenyl)-1H-pyrrole
• Synonyms: 1-(2,6-dibromo-4-chlorophenyl)-1H-pyrrole
• CAS NO: 1423469-24-2
• Molecular Weight: 335.425
• Mol File: 1423469-24-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(2,6-dibromo-4-chlorophenyl)-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,6-dibromo-4-chlorophenyl)-1H-pyrrole(1423469-24-2)
• EPA Substance Registry System: 1-(2,6-dibromo-4-chlorophenyl)-1H-pyrrole(1423469-24-2)

Safety Data

• Hazardous Substances Data: 1423469-24-2(Hazardous Substances Data)

Upstream product

• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 874-17-9 4-chloro-2,6-dibromoaniline 

Downstream Products

• 1423469-61-7 6-chloro-3,9-bis(4-(hexyloxy)phenyl)indolizino[6,5,4,3-ija]quinoline 
• 1423470-06-7 3,9-bis(4-(hexyloxy)phenyl)-6-(thiophen-2-yl)indolizino[6,5,4,3-ija]quinoline 
• 1423470-23-8 5-(3,9-bis(4-(hexyloxy)phenyl)indolizino[6,5,4,3-ija]quinolin-6-yl)thiophene-2-carbaldehyde 
• 1423469-41-3 1-(4-chloro-2,6-bis((4-(hexyloxy)phenyl)ethynyl)phenyl)-1H-pyrrole 

Relevant articles and documents

Palladium-Catalyzed Annulation of Internal Alkynes: Direct Access to π-Conjugated Ullazines

A palladium-catalyzed cyclization reaction of 1-(2,6-dibromophenyl)-1H-pyrroles with alkynes has been developed to construct various π-conjugated indolizino[6,5,4,3-ija]quinolones (ullazines) with a reactive functional group tolerance. As illustrative examples, three new ullazine-based sensitizers are synthesized, and the performance of these dyes is examined in DSSC devices, which demonstrates the potential of direct C-H functionalization in the construction of organic optoelectronic materials.