1160294-96-1

Basic information

• Product Name: N-(4-(phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-aMine
• Synonyms: N-(4-(phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-aMine;3-[4-(4-Biphenylylamino)phenyl]-9-phenylcarbazole;Biphenyl-4-yl-[4-(9-phenyl-9H-carbazol-3-yl)-phenyl]-amine;[1,1'-Biphenyl]-4-amine,N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-
• CAS NO: 1160294-96-1
• Molecular Formula: C₃₆H₂₆N₂
• Molecular Weight: 486.60504
• EINECS: -0
• Mol File: 1160294-96-1.mol
• Article Data: 17

Chemical Properties

• Melting Point: 178.0 to 187.0 °C
• Boiling Point: 706℃
• Flash Point: 381℃
• Appearance: /
• Density: 1.13
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 0.86±0.50(Predicted)
• CAS DataBase Reference: N-(4-(phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-(phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-aMine(1160294-96-1)
• EPA Substance Registry System: N-(4-(phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-aMine(1160294-96-1)

Safety Data

• Hazardous Substances Data: 1160294-96-1(Hazardous Substances Data)

Usage

Chemical Properties

Off-white powder

Uses

N-(4-(9-Phenyl-9H-carbazol-3-yl)phenyl)-[1,1''-biphenyl]-4-amine is used as a reactant in the synthesis of imidazopyridines for organic light-emitting diode display devices.

Upstream product

• 1028647-93-9 3-(4-bromophenyl)-9-phenyl-9H-carbazole 
• 92-67-1 4-phenylalanine 
• 1153-85-1 3-bromo-9-phenyl-9H-carbazole 
• 854952-58-2 N-phenyl-9H-carbazol-3-boronic acid 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 106-40-1 4-bromo-aniline 
• 589-87-7 1,4-bromoiodobenzene 
• 1160294-93-8 N-(4-bromophenyl)-[1,1'-biphenyl]-4-amine 

Downstream Products

• 1160294-92-7 (4-(9-phenyl-fluoren-9-yl)-phenyl)-(4-(9-phenyl-9H-carbazol-3-yl)-phenyl)-biphenyl-4-yl-amine 

Relevant articles and documents

Effect of arylamino-carbazole containing hole transport materials on the device performance and lifetime of OLED

We synthesized four hyper-conjugated aromatic hole transporting materials with different molecular geometry and energy levels by attaching arylamino moiety attached to the carbazole core. A brominated carbazole moiety reacted with an arylamino moiety using a Buchwald-Hartwig reaction. The characteristics of these hole transporting materials were investigated using TGA, DSC, UV–Vis and luminescence spectroscopy. The energy levels of all materials used in this study were estimated from cyclic voltammograms and absorption spectra. The hole transporting properties of the synthesized molecules were measured using single-carrier devices. All four hole transporting materials showed similar hole mobility. The effectiveness of hole transporting materials was compared by fabricating green-emitting organic light emitting diode (OLED) devices. It turned out that the device performances were critically dependent on the relative energy levels of the hole transporting layer and emission layer. However, the molecular geometry greatly influenced the device lifetime, determining thermally induced crystallization by the heat produced during device operation.

ARYLATION METHOD

The present invention relates to a selective method for carrying out the Buchwald-Hartwig coupling of biphenyl derivatives.

Novel compound for capping layer and organic light emitting device including same

The present invention relates to a novel compound for a capping layer and an organic light emitting device including the same. The compound according to an embodiment of the present invention is a compound in which carbazole is boned to one side of amine