1201561-34-3

Basic information

• Product Name: 4-Phenyl-9H-carbazole
• Synonyms: 4-Phenyl-9H-carbazole
• CAS NO: 1201561-34-3
• Molecular Weight: 243.308
• EINECS: -0
• Mol File: 1201561-34-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 4-Phenyl-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Phenyl-9H-carbazole(1201561-34-3)
• EPA Substance Registry System: 4-Phenyl-9H-carbazole(1201561-34-3)

Safety Data

• Hazardous Substances Data: 1201561-34-3(Hazardous Substances Data)

Usage

General Description

4-Phenyl-9H-carbazole is a chemical compound with the molecular formula C20H15N. It is a carbazole derivative, which is a class of aromatic heterocyclic compounds. 4-Phenyl-9H-carbazole is often used in organic synthesis and materials science, where it acts as an intermediate in the production of various organic compounds and polymers. It has also been studied for its potential applications in organic electronic devices, such as light-emitting diodes (LEDs) and organic photovoltaics (OPVs). Additionally, 4-Phenyl-9H-carbazole has shown potential as a pharmaceutical compound, with research suggesting that it may have antioxidant and anti-inflammatory properties. Overall, 4-Phenyl-9H-carbazole is a versatile and valuable chemical with a range of potential uses in various fields of science and technology.

Upstream product

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Relevant articles and documents

A PLURALITY OF HOST MATERIALS AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

The present disclosure relates to a plurality of host materials comprising a first host material comprising a compound represented by formula 1, and a second host material comprising a compound represented by formula 2, and an organic electroluminescent device comprising the same. By comprising a specific combination of compounds as host materials, it is possible to provide an organic electroluminescent device having lower driving voltage, higher luminous efficiency, higher power efficiency, and/or superior lifespan characteristics compared to conventional organic electroluminescent devices.

PLURALITY OF HOST MATERIALS AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

The present disclosure relates to a plurality of host materials comprising a first host material comprising a compound represented by formula 1, and a second host material comprising a compound represented by formula 2, and an organic electroluminescent device comprising the same. By comprising a specific combination of compounds as host materials, it is possible to provide an organic electroluminescent device having higher luminous efficiency, higher power efficiency, and/or better lifetime properties, compared to conventional organic electroluminescent devices.

Intramolecular Remote C-H Activation via Sequential 1,4-Palladium Migration to Access Fused Polycycles

An unprecedented intramolecular remote C-H activation via sequential 1,4-palladium migration with an aromatic ring as a conveyor has been described. This reaction provides an efficient route to construct diverse polycyclic frameworks in moderate to good yield via palladium-catalyzed remote C-H activation/alkene insertion, arylation, alkenylation, and the Heck reaction. The preliminary mechanistic studies revealed that the 1,4-palladium migration process was reversible.