1097245-00-5

Basic information

• Product Name: 3-bromo-9-phenyl-6-(triphenylsilyl)-9-carbazole
• Synonyms: 3-bromo-9-phenyl-6-(triphenylsilyl)-9-carbazole
• CAS NO: 1097245-00-5
• Molecular Weight: 580.599
• Mol File: 1097245-00-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-bromo-9-phenyl-6-(triphenylsilyl)-9-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-9-phenyl-6-(triphenylsilyl)-9-carbazole(1097245-00-5)
• EPA Substance Registry System: 3-bromo-9-phenyl-6-(triphenylsilyl)-9-carbazole(1097245-00-5)

Safety Data

• Hazardous Substances Data: 1097245-00-5(Hazardous Substances Data)

Upstream product

• 76-86-8 Triphenylsilyl chloride 
• 57103-20-5 3,6-dibromo-9-phenyl-9H-carbazole 

Relevant articles and documents

This polycarbazole-phosphine oxide compound and an organic electroluminescence element including (by machine translation)

The present invention relates to a carbazole-based phosphine oxide compound, and an organic electroluminescent device including the same. According to the present invention, provided are a compound for an organic electroluminescent device which can improve unstable thermal stability and low efficiency characteristics which are the problems of known compounds for an organic electroluminescent device, and particularly, can implement excellent efficiency characteristics in a pure blue phosphorescent device, by using the carbazole-based phosphine oxide compound of the compound for the organic electroluminescent device, and the organic electroluminescent device. According to one aspect of the present invention, the carbazole-based phosphine oxide compound of the compound for the organic electroluminescent device is provided, and the organic electroluminescent device containing the same which can implement thermal stability and high efficiency characteristics is also provided.

Silanylamine-based compound, method of preparing the same and organic light emitting device including organic layer comprising the silanylamine-based compound

Silanylamine-based compounds represented by Formula I are provided. Methods of preparing the compounds and organic light emitting devices including organic layers comprising the silanylamine-based compounds are also provided. The silanylamine-based compounds have excellent electrical stability and hole transporting capabilities. Thus, the silanylamine-based compounds may be effectively used for red, green, blue, and white fluorescent and phosphorescent materials used to form hole injection layers, hole transport layers, and emissive layers in organic light emitting devices. Organic light emitting devices using these compounds have high efficiency, low driving voltages, high luminance and long lifetimes.