1533406-38-0

Basic information

• Product Name: 9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
• Synonyms: 9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole;9H-Carbazole, 9-[1,1'-biphenyl]-3-yl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;9-([1,1'-Biphenyl]-3-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole;9-([1,1'-Biphenyl]-3-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole;3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9-([1,1'-biphenyl]-3-yl)-carbazole;9-[1,1'-Biphenyl]-3-yl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole
• CAS NO: 1533406-38-0
• Molecular Formula: C30H28BNO2
• Molecular Weight: 445.35982
• EINECS: -0
• Mol File: 1533406-38-0.mol
• Article Data: 8

Chemical Properties

• Melting Point: 236.0 to 240.0 °C
• Boiling Point: 578.9±42.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(1533406-38-0)
• EPA Substance Registry System: 9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(1533406-38-0)

Safety Data

• Hazardous Substances Data: 1533406-38-0(Hazardous Substances Data)

Usage

General Description

9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is a chemical compound that contains a carbazole core with biphenyl and dioxaborolane groups attached to it. The biphenyl group consists of two connected phenyl rings, while the dioxaborolane group is a boron-containing heterocycle. 9-(Biphenyl-3-yl)-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole has potential applications in organic electronics and materials science due to its unique structure and properties. It may be used in the development of organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and other electronic devices. Additionally, it could be used as a building block for the synthesis of other functional materials.

Upstream product

• 98-80-6 phenylboronic acid 
• 185112-61-2 9-(3-bromophenyl)carbazole 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1428551-28-3 9-([1,1′-biphenyl]-3-yl)-3-bromo-9H-carbazole 
• 2113-57-7 3-bromobiphenyl 
• 86-74-8 9H-carbazole 
• 73183-34-3 bis(pinacol)diborane 
• 1221237-87-1 9-([1,1'-biphenyl]-3-yl)-9H-carbazole 

Downstream Products

• 1800580-10-2 9'-[1,1-biphenyl-3-yl]-9H,9'H-3,3'-bicarbazole 

Relevant articles and documents

Organic electroluminescent host material and application thereof in organic electroluminescent device

The invention relates to an organic electroluminescent host material. In an organic light-emitting device, in order to reduce the problems of exciton quenching, efficiency roll-off, device service life shortening and the like caused by too high exciton concentration in a light-emitting layer, a light-emitting layer structure generally adopts a host-guest doping mode. Aiming at different luminescent material systems/luminescent mechanisms, the requirements on the basic performance of the host material are different. The invention designs an organic electroluminescent host material based on a 3,3'-dicarbazole unit and a 9,9'-diphenyl fluorene steric hindrance group end capping. The dicarbazole unit endows the material with good carrier transport performance, and end group steric hindrance can effectively inhibit local aggregation of a light-emitting guest. According to different luminescent material systems, the polarity and size of molecules are adjusted by changing the difference of carbazole N-substituent (R), so that the comprehensive optimization of the device performance is realized.

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Fused ring organic compound and mixture and organic electronic device comprising same

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