858641-06-2

Basic information

• Product Name: 4-(9H-carbazol-9-yl)-N-phenylaniline
• Synonyms: 4-(9H-carbazol-9-yl)-N-phenylaniline;4-carbazol-9-yl-N-phenylaniline;N-phenyl-N-[4-(9-carbazolyl)phenyl]amine;4-(9H-Carbazol-9-yl)-N-phenylbenzenamine
• CAS NO: 858641-06-2
• Molecular Formula: C₂₄H₁₈N₂
• Molecular Weight: 334.41312
• EINECS: -0
• Mol File: 858641-06-2.mol
• Article Data: 28

Chemical Properties

• Boiling Point: 539.8±42.0 °C(Predicted)
• Appearance: /
• Density: 1.14±0.1 g/cm3(Predicted)
• PKA: -0.26±0.40(Predicted)
• CAS DataBase Reference: 4-(9H-carbazol-9-yl)-N-phenylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(9H-carbazol-9-yl)-N-phenylaniline(858641-06-2)
• EPA Substance Registry System: 4-(9H-carbazol-9-yl)-N-phenylaniline(858641-06-2)

Safety Data

• Hazardous Substances Data: 858641-06-2(Hazardous Substances Data)

Usage

General Description

4-(9H-carbazol-9-yl)-N-phenylaniline is a chemical compound that belongs to the class of carbazoles, which are aromatic heterocyclic compounds. It is a derivative of carbazole and aniline, containing both a carbazole and a phenyl group. 4-(9H-carbazol-9-yl)-N-phenylaniline has potential applications in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells, due to its electron transporting properties and good film-forming ability. It is also studied for its potential use in organic semiconductors and organic field-effect transistors. Additionally, research is being conducted on its potential therapeutic applications, such as its use as a pharmaceutical intermediate and in the development of new drugs. Overall, 4-(9H-carbazol-9-yl)-N-phenylaniline is a versatile chemical with promising uses in various industries and scientific fields.

Upstream product

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Downstream Products

• 934817-18-2 N,N',N-triphenyl-N,N',N-tris[4-(carbazol-9-yl)phenyl]-benzene-1,3,5-triamine 
• 1136225-77-8 2-(4-{N-[4-(carbazol-9-yl)phenyl]-N-phenylamino}phenyl)-9,10-diphenylanthracene 
• 1123921-75-4 2-(3-{N-[4-(carbazol-9-yl)phenyl]-N-phenylamino}phenyl)-9,10-diphenylanthracene 
• 18628-07-4 9-(9H-carbazol-3-yl)-9H-carbazole 
• 1246635-28-8 4-(benzo[d]oxazol-2-yl)-4'-(9H-carbazol-9-yl)triphenylamine 
• 1246635-32-4 4-(9H-carbazol-9-yl)-4'-(1-phenyl-1H-benzo[d]imidazol-2-yl)triphenylamine 
• 1246635-29-9 4-(imidazo[1,2-a]pyridine-2-yl)-4'-(9H-carbazol-9-yl)triphenylamine 
• 1290615-09-6 C₄₂H₂₉N₃ 
• 1246055-77-5 4-(9H-carbazol-9-yl)-4'-(3-phenyl-1,2,4-oxadiazol-5-yl)triphenylamine 

Relevant articles and documents

Nitrogen-containing compound, organic electroluminescent device, and electronic device

The invention provides a nitrogen-containing compound, an organic electroluminescent device and an electronic device, and belongs to the technical field of organic materials. The structure of the nitrogen-containing compound is represented by Chemical Formula 1: wherein X1, X2, Y1, Y2 are the same or different from each other and are each independently a single bond, O, S, N(R3), C(R4R5), Ge(R6R7), Si(R8R9), Se, wherein X1 and Y1 are not single bonds simultaneously and X2 and Y2 are not single bonds simultaneously.

Organic electroluminescent material and OLED (organic electroluminescent device) comprising same

The invention provides an organic electroluminescent material and an OLED (organic electroluminescent device) comprising the same. The structural formula of the organic electroluminescent material isshown in the description. Compared with a monoamine structure containing adamantly, a diamine structure contained in the material has higher HOMO energy and hole mobility and can show higher efficiency and longer service life than a device made of a monoamine material. The OLED comprising the organic electroluminescent material has lower driving voltage, higher luminous efficiency and longer service life.

METHOD FOR PRODUCING 9-(ARYLAMINO)ARYL-9H-CARBAZOLE

PROBLEM TO BE SOLVED: To efficiently produce 9-(arylamino)aryl-9H-carbazole. SOLUTION: A haloarylamine represented by formula (1) is reacted with a carbazole derivative in the presence of a palladium compound, a phosphine compound, and a metal alkoxide. (Each Ar is independently a phenylene group or the like, provided that the phenylene group or the like may be substituted with a C1-4 alkyl group or the like; each X is independently Cl, Br or I; p and q are each independently 1 or 2; each R1 is independently a C1-6 alkyl group, a phenyl group, a naphthyl group, a biphenylyl group or a pyridyl group; m is 1 or 2; n is 0 or 1; and m+n=2 is satisfied.) SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT