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

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.

METHOD FOR PRODUCING 9-(1-NAPHTHYL)-9H-CARBAZOLE DERIVATIVE

PROBLEM TO BE SOLVED: To provide a method for producing 9-(1-naphthyl)-9H-carbazole derivatives. SOLUTION: The production method includes causing a reaction to occur between a 9H-carbazole derivative and 1-halonaphthalene in the presence of a palladium compound, a biarylphosphine represented by formula (4), and a lithium base. (R3: a C4-10 linear, branched or cyclic alkyl. R4 and R5: H or a benzene ring formed together with bonded C. R6, R7, R8, R9 and R10: H, a C1-3 alkyl or the like). SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT