22034-43-1

Basic information

• Product Name: 9-(1-Naphthyl) carbazole
• Synonyms: 9-(1-Naphthyl) carbazole;9-(naphthalen-1-yl)-9H-carbazole;9-(1-naphthalenyl)-9H-Carbazole;9H-Carbazole, 9-(1-naphthalenyl)-
• CAS NO: 22034-43-1
• Molecular Formula: C22H15N
• Molecular Weight: 293.3612
• Mol File: 22034-43-1.mol
• Article Data: 14

Chemical Properties

• Melting Point: 126.0 to 131.0 °C
• Boiling Point: 503.7°C at 760 mmHg
• Flash Point: 258.4°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 2.85E-10mmHg at 25°C
• Refractive Index: 1.669
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 9-(1-Naphthyl) carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(1-Naphthyl) carbazole(22034-43-1)
• EPA Substance Registry System: 9-(1-Naphthyl) carbazole(22034-43-1)

Safety Data

• Hazardous Substances Data: 22034-43-1(Hazardous Substances Data)

Usage

Uses

9-(Naphthalen-1-yl)-9H-carbazole is a useful research chemical.

InChI:InChI=1/C22H15N/c1-2-10-17-16(8-1)9-7-15-20(17)23-21-13-5-3-11-18(21)19-12-4-6-14-22(19)23/h1-15H

Upstream product

• 90-11-9 1-Bromonaphthalene 
• 86-74-8 9H-carbazole 
• 13029-09-9 2,2'-dibromobiphenyl 
• 134-32-7 1-amino-naphthalene 
• 623-03-0 4-Cyanochlorobenzene 
• 1413355-67-5 Cu₂[P(m-tol)₃]₄(carbazolide)₂ 
• 189999-35-7 [1,1'-biphenyl]-2,2'-iodonium trifluoromethanesulfonate 
• 2113-51-1 2-iodobiphenyl 
• 13029-08-8 2,2'-Dichlorobiphenyl 
• 90-14-2 1-Iodonaphthalene 
• 90-13-1 1-Chloronaphthalene 

Downstream Products

• 934545-83-2 3-bromo-9-(naphthalen-1-yl)-9H-carbazole 

Relevant articles and documents

Light-emitting conjugated molecule containing 1,3,4-oxadiazole, carbazole and naphthalene units

A novel π-conjugated small molecule VNCO, 2,5-bis{3′-[3″-vinyl-9″-(α-naphthyl)carbazolyl]phenyl} -1,3,4-oxadiazole, containing hole-transporting carbazole moieties, electron-injecting 1,3,4-oxadiazole moieties and chromophore naphthalene was designed and synthesized by Wittig reaction of 2,5-bis(3-tolylene-triphenylphosphonium bromide)-1,3,4-oxadiazole and 3-formyl-9-(α-naphthyl)carbazole. The UV-vis absorption, fluorescence excitation and emission spectra have been obtained in solution for VNCO. The photoluminescence (PL) of VNCO were examined in different solvents and the luminescence quantum yield was 0.746 in chloroform. It emitted blue and blue-green light, with the band gap of 3.30 eV estimated from the onset absorption. In addition, the light-emitting can be quenched by both electron donor (N,N-dimethylaniline) and electron acceptor (dimethylterephalate). Furthermore, the molecular interactions of VNCO with fullerene (C60) or carbon nanotubes (CNTs) were also carefully investigated.

CARBAZOLE AND ACRIDINE PHOTOREDOX CATALYSTS FOR SMALL MOLECULE AND MACROMOLECULAR TRANSFORMATIONS

The present invention provides photocatalysts, methods for their preparation, and methods for preparing linear polymers with high propagation rate.

Palladium-Catalysed Amination of Hindered Aryl Halides with 9H-Carbazole

Palladium-catalysed Buchwald–Hartwig amination of ortho-substituted hindered aryl bromides or chlorides with 9H-carbazole has been investigated. In the amination of 1-bromo- or chloronaphthalene with 9H-carbazole, the combined use of Pd2(dba)s