1201561-34-3

Usage

Uses

Used in Organic Synthesis and Materials Science:
4-Phenyl-9H-carbazole is used as an intermediate in the synthesis of various organic compounds and polymers, playing a vital role in the development of new materials with enhanced properties.
Used in Organic Electronic Devices:
4-Phenyl-9H-carbazole is utilized in the development of organic electronic devices such as light-emitting diodes (LEDs) and organic photovoltaics (OPVs), where its unique properties contribute to improved device performance and efficiency.
Used in Pharmaceutical Applications:
4-Phenyl-9H-carbazole is studied for its potential as a pharmaceutical compound, with research indicating its antioxidant and anti-inflammatory properties. These characteristics make it a promising candidate for the development of new drugs and therapeutic agents.

Upstream product

• 1201561-33-2 9H-carbazol-4-yl N,N-diethyl-O-carbamate 
• 98-80-6 phenylboronic acid 
• 1314146-67-2 1-(2-(2-hydroxy-4-phenylbut-3-ynyl)-1H-indol-3-yl)-2-methylpropan-1-one 
• 29957-84-4 2-methyl-1-(2-methyl-1H-indol-3-yl)propan-1-one 
• 56970-23-1 [1,1':2',1''-terphenyl]-2-amine 
• 26429-41-4 1,2-dibromo-3-nitrobenzene 
• 323191-82-8 1-iodo-2-phenyl-4-nitrobenzene 
• 29608-75-1 2-amino-5-nitro-biphenyl 
• 3652-89-9 4-bromo-9H-carbazole 
• 95-20-5 2-methyl-1H-indole 

Relevant academic research and scientific papers

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 d

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.

Regioselective Formation of Substituted Indoles: Formal Synthesis of Lysergic Acid

A Diels–Alder reaction-based strategy for the synthesis of indoles and related heterocycles is reported. An intramolecular cycloaddition of alkyne-tethered 3-aminopyrones gives 4-substituted indolines in good yield and with complete regioselectivity. Additional substitution is readily tolerated in the transformation, allowing synthesis of complex and non-canonical substitution patterns. Oxidative conditions give the corresponding indoles. The strategy also allows the synthesis of carbazoles. The method was showcased in a formal synthesis of lysergic acid.

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.

Organic compound, light-emitting element, light-emitting device, electronic device, and lighting device

A novel compound in which a delayed fluorescence component due to TTA accounts for a high proportion of emissive components is provided. The organic compound includes an anthracene skeleton, an arylene group, and a substituted or unsubstituted heterocyclic group including a carbazole skeleton. The anthracene skeleton and the substituted or unsubstituted heterocyclic group including the carbazole skeleton are bonded to each other through the arylene group. The anthracene skeleton includes an aryl group at the 2-position or the 3-position.

Efficient synthesis of aryl-substituted carbazoles via tandem double or triple suzuki coupling and cadogan cyclization

An efficient one-step method to prepare aryl-substituted carbazoles via tandem double or triple C[sbnd]C bond formations by multiple Suzuki couplings and C[sbnd]N bond formation by Cadogan cyclization has been developed. The developed method employs comme

A carbazole compound and its preparation method, the organic electroluminescent device (by machine translation)

This invention has offered a kind of carbazole compound, the carbazole compound of formula (1) structure. Compared with the prior art, the present invention provides the carbazole compound is introduced in the carbazole compound is connected with the ethe

Amino-directed RhIII-catalyzed C-H activation leading to one-pot synthesis of N-H carbazoles

One-pot synthesis: An efficient amino-directed one-pot synthesis of N-H carbazoles from unprotected 2-aminobiaryl compounds is reported. The free amino unit acts as both a directing group for ortho C-H activation and a functional group for construction of an N-heterocyclic ring (see scheme). Copyright

Gold-catalyzed deacylative cycloisomerization reactions of 3-acylindole/ynes: A new approach for carbazole synthesis

The synthesis of functionalized carbazoles through gold-catalyzed deacylative cycloisomerization of 3-acylindole/ynes is described. A mechanistic proposal for these transformations involving a novel carbonyl group facilitated heterolytic fragmentation upo