103012-26-6

Basic information

• Product Name: 3-phenyl-9H-carbazole
• Synonyms: 3-phenyl-9H-carbazole;-phenyl-9H-carbazole;3-Phenyl carbazole;3-phenyl-9H-carabazole
• CAS NO: 103012-26-6
• Molecular Formula: C₁₈H₁₃N
• Molecular Weight: 243.30252
• Mol File: 103012-26-6.mol
• Article Data: 43

Chemical Properties

• Melting Point: 222.8-224.1℃
• Boiling Point: 474.3±14.0 °C(Predicted)
• Appearance: /
• Density: 1.208±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 16.97±0.30(Predicted)
• CAS DataBase Reference: 3-phenyl-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-9H-carbazole(103012-26-6)
• EPA Substance Registry System: 3-phenyl-9H-carbazole(103012-26-6)

Safety Data

• Hazardous Substances Data: 103012-26-6(Hazardous Substances Data)

Usage

Uses

3-Phenyl-9H-carbazole is a useful research chemical.

Chemical Properties

off-white powder

Upstream product

• 108993-46-0 3-diazo-3H-carbazole 
• 71-43-2 benzene 
• 55542-85-3 6-phenyl-2,3,4,9-tetrahydro-1H-carbazole 
• 17223-85-7 9H-carbazol-9-amine 
• 32228-99-2 4-phenyldiphenylamine 
• 2788-23-0 9-nitroso-9H-carbazole 
• 86-74-8 9H-carbazole 
• 92-67-1 4-phenylalanine 
• 14221-01-3 tetrakis(triphenylphosphine) palladium⁽⁰⁾ 
• 1592-95-6 3-bromo-9H-carbazole 
• 96042-30-7 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 
• 98-80-6 phenylboronic acid 
• 1160823-30-2 N-(2-chlorophenyl)[1,1′-biphenyl]-4-amine 
• 4894-75-1 1-phenyl-4-cyclohexanone 

Downstream Products

• 1218786-27-6 CzPAP 
• 1215232-06-6 3-phenyl-9-[4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenyl]-9H-carbazole 
• 1215232-01-1 9-[4-(benzoxazol-2-yl)phenyl]-3-phenyl-9H-carbazole 
• 1319015-92-3 methyl 2-(3-bromo-6-phenyl-9H-carbazolyl)benzoate 
• 1319015-94-5 2-[2-(3-bromo-6-phenylcarbazol-9-yl)phenyl]propan-2-ol 
• 1319016-13-1 8,8-Dimethyl-6-phenyl-8H-indolo[3,2,1-de]acridine-3-boronic acid 
• 1319015-91-2 methyl 2-(3-phenyl-9H-carbazolyl)benzoate 
• 1319015-96-7 6-bromo-8,8-dimethyl-3-phenyl-8H-indolo[3,2,1-de]acridine 
• 1028648-09-0 3,9-diphenyl-9H-carbazole 

Relevant articles and documents

Rh(I)-catalyzed decarbonylation synthesis of carbazoles via C-N cleavage

A one-pot Rh(I)-catalyzed synthesis of 9-H carbazoles via C-N bond cleavage by activation of aldehyde C-H bonds is reported. This protocol offers good yields and tolerates a broad range of functional groups. Based on the extensive control experiments, we propose a plausible decarbonylation mechanism.

Carbazole synthesis by platinum-catalyzed C-H functionalizing reaction using water as reoxidizing reagent

Treatment of 1-aminobiphenyl and diphenylamine with catalytic amount of Pt/C in hydrothermal water (250 °C, 4 MPa) affords 9H-carbazole in good yield. In this catalytic cycle, water works as reoxidizing reagent for platinum catalyst. Copyright

Synthesis of Carbazoles by a Diverted Bischler-Napieralski Cascade Reaction

An unforeseen twist in a seemingly trivial Bischler-Napieralski reaction led to the selective formation of an unexpected carbazole product. The reaction proved to be general, providing access to a range of diversely substituted carbazoles from readily available substrates. Judicious variation of substituents revealed a complex cascade mechanism comprising no less than 10 elementary steps, that could be diverted in multiple ways toward various other carbazole derivatives.

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE

The present invention relates to a compound for an organic optoelectronic device, represented by Chemical Formula 1; a composition for an organic optoelectronic device, including same; an organic optoelectronic device; and a display device. The description of Chemical Formula 1 is the same as that defined in the specification.

An organoelectro luminescent compounds and organoelectro luminescent device using the same

The present invention relates to an organic light emitting compound represented by chemical formula I to III, and to an organic electroluminescent device including the same. According to the present invention, the organic electroluminescent device including the organic light emitting compound uses low driving voltages and has excellent efficiency of light emission.