1133057-98-3

Basic information

• Product Name: [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid
• Synonyms: [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid;[9-(2-Naphthalenyl)-9H-carbazol-3-yl]-boronic acid;[9-(2-phthalenyl)-9H-carbazol-3-yl]-Boronic acid;[9-(2-phthalenyl)-9H-carbazole-3-yl] boronic acid;3-Boronic acid-9-(2-naphthalenyl)carbazole
• CAS NO: 1133057-98-3
• Molecular Formula: C22H16BNO2
• Molecular Weight: 337.17894
• EINECS: 200-258-5
• Mol File: 1133057-98-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 548.4±56.0 °C(Predicted)
• Appearance: /
• Density: 1.22±0.1 g/cm3 (20 ºC 760 Torr)
• PKA: 8.82±0.30(Predicted)
• CAS DataBase Reference: [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid(1133057-98-3)
• EPA Substance Registry System: [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid(1133057-98-3)

Safety Data

• Hazardous Substances Data: 1133057-98-3(Hazardous Substances Data)

Usage

General Description

[9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid is a chemical compound that consists of a boronic acid group attached to a carbazole derivative with a naphthalene group. It is commonly used in organic synthesis as a reagent for Suzuki-Miyaura coupling reactions, which are important for the formation of carbon-carbon bonds in the production of various organic compounds. [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid has potential applications in the pharmaceutical industry, as boronic acids are known to have biological activity and can be used in drug discovery and development. Additionally, [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid may also have uses in materials science, for example in the production of organic light-emitting diodes (OLEDs) and other organic electronic devices.

Upstream product

• 121-43-7 Trimethyl borate 
• 934545-80-9 3-bromo-9-(naphthalen-2-yl)-9H-carbazole 
• 1592-95-6 3-bromo-9H-carbazole 
• 612-55-5 2-iodonaphthalene 
• 580-13-2 2-bromonaphthalene 
• 86-74-8 9H-carbazole 
• 34292-03-0 (9-(naphthalene-2-yl)-carbazole) 

Relevant articles and documents

Organic compound, and organic electroluminescent device and electronic device using the same

The present invention relates to an organic compound and an organic electroluminescent device and an electronic device using the same, wherein the organic compound has a structure formed by combining an indole carbazole-based planar conjugated group in a fused manner and a dibenzofuran substituted with an aryl group. The structure has higher hole mobility and higher energy transfer efficiency, and is suitable for being used as a light-emitting host material in an organic electroluminescent device. When the organic compound is used as a light emitting host material in an organic electroluminescent device, the light emitting efficiency and the service life of the device can be effectively improved, and the working voltage is reduced.

ORGANIC LIGHT EMITTING DEVICE AND DISPLAY DEVICE HAVING THE SAME

An organic light emitting device and a display device including the same, the organic light emitting device including a first electrode; a hole controlling layer on the first electrode; an emission layer on the hole controlling layer; an electron controlling layer on the emission layer; and a second electrode on the electron controlling layer, wherein the emission layer includes a hole transport host material, an electron transport host material, a bipolar host material, and at least one dopant material.

A HOLE TRANSPORT MATERIAL AND AN ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

The present invention relates to a hole transport material and an organic electroluminescent device comprising the same. By using the hole transport material according to the present invention, an organic electroluminescent device having significantly improved operational lifespan while maintaining low driving voltage and high current and power efficiencies can be produced.