922721-28-6

Basic information

• Product Name: 9-phenyl-3-(pyridin-2-yl)-9H-carbazole
• Synonyms: 9-phenyl-3-(pyridin-2-yl)-9H-carbazole
• CAS NO: 922721-28-6
• Molecular Weight: 320.393
• Mol File: 922721-28-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9-phenyl-3-(pyridin-2-yl)-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-phenyl-3-(pyridin-2-yl)-9H-carbazole(922721-28-6)
• EPA Substance Registry System: 9-phenyl-3-(pyridin-2-yl)-9H-carbazole(922721-28-6)

Safety Data

• Hazardous Substances Data: 922721-28-6(Hazardous Substances Data)

Upstream product

• 854952-58-2 N-phenyl-9H-carbazol-3-boronic acid 
• 109-04-6 2-bromo-pyridine 
• 591-50-4 iodobenzene 
• 1153-85-1 3-bromo-9-phenyl-9H-carbazole 
• 17997-47-6 2-tri-n-butylstannylpyridine 
• 86-74-8 9H-carbazole 
• 1150-62-5 N-phenylcarbazole 

Downstream Products

• 1240116-78-2 Pt(C₆H₄(C₆H₄NC₆H₃)C₅H₄N)(CH₃COCHCOCH₃) 

Relevant articles and documents

A highly efficient and aerobic protocol for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives via a palladium-catalyzed ligand-free Suzuki reaction

A palladium-catalyzed aerobic and ligand-free Suzuki reaction in aqueous ethanol has been developed for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives. A number of N-heteroaryl halides, namely 2-halogenated pyridines, 2-bromoquinoline, 5-bromopyrimidine and 2-chloropyrazine, were coupled with 4-(9H-carbazol-9-yl)phenylboronic acid (CPBA) or 9-phenyl-9H-carbazol-3-ylboronic acid (PCBA) efficiently to afford good to excellent yields in a short reaction time. Moreover, the catalytic system of Pd(OAc)2-EtOH/H2O-K2CO3 was successfully extended to the cross-couplings of N-heteroaryl halides with various arylboronic acids. The results demonstrated that the cross-coupling reaction in the present protocol was promoted by oxygen.

Multifunctional iridium complexes based on carbazole modules as highly efficient electrophosphors

(Figure Presented) Getting the green light: Highly efficient organic light-emitting diodes (OLEDs) have been synthesized from robust green-electrophosphorescent IrIII complexes based on carbazole derivatives (see picture, HT = hole transporting, EL = electroluminescence). The combination of short triplet lifetime, high emission efficiency, and improved charge-transporting properties allows these OLEDs to achieve peak efficiencies of 12% photons per electron and 38 cd A-1.