123863-99-0

Basic information

• Product Name: 9,9-DI-N-OCTYLFLUORENE
• Synonyms: 9,9-DI-N-OCTYLFLUORENE;9,9-Di-n-octylfluorene
• CAS NO: 123863-99-0
• Molecular Formula: C₂₉H₄₂
• Molecular Weight: 390.64
• Product Categories: Fluorenes;Fluorenes & Fluorenones
• Mol File: 123863-99-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 27-28 °C
• Boiling Point: 498.223°C at 760 mmHg
• Flash Point: 23 °C
• Appearance: /
• Density: 0.93g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.521
• Water Solubility: Insoluble in water
• CAS DataBase Reference: 9,9-DI-N-OCTYLFLUORENE(CAS DataBase Reference)
• NIST Chemistry Reference: 9,9-DI-N-OCTYLFLUORENE(123863-99-0)
• EPA Substance Registry System: 9,9-DI-N-OCTYLFLUORENE(123863-99-0)

Safety Data

• Hazardous Substances Data: 123863-99-0(Hazardous Substances Data)

Usage

General Description

9,9-DI-N-OCTYLFLUORENE is a chemical compound that belongs to the family of fluorene derivatives. It is composed of two octyl groups attached to the 9th position of the fluorene molecule. 9,9-DI-N-OCTYLFLUORENE is primarily used as a component in the production of organic light-emitting diodes (OLEDs) due to its high thermal stability and efficient energy transfer properties. It is also utilized in the field of organic electronics for its ability to form stable thin films with high charge carrier mobility. Additionally, 9,9-DI-N-OCTYLFLUORENE has potential applications in other fields such as photovoltaics and organic semiconductors. Overall, this chemical compound plays a crucial role in the development of advanced materials for next-generation electronic devices.

InChI:InChI=1/C29H42/c1-3-5-7-9-11-17-23-29(24-18-12-10-8-6-4-2)27-21-15-13-19-25(27)26-20-14-16-22-28(26)29/h13-16,19-22H,3-12,17-18,23-24H2,1-2H3

Upstream product

• 19742-08-6 N-methyl-N-octyloctan-1-amine hydrochloride 
• 198964-46-4 2,7-dibromo-9,9-dioctylfluorene 
• 109-72-8 n-butyllithium 

Downstream Products

• 278176-06-0 2,7-diiodo-9,9-dioctyl-9H-fluorene 
• 1447801-20-8 C₄₆H₅₃N 
• 1447801-25-3 C₄₆H₅₁AuClN 
• 1447801-14-0 C₅₄H₅₆AuN 
• 851042-10-9 9,9-dioctyl-9H-fluorene-2,7-diamine 
• 1326306-61-9 9,9-dioctyl-2-(4-(trifluoromethyl)phenyl)-3,9-dihydrofluoreno[3,2-d]imidazole 
• 1326306-60-8 2-(2,6-difluorophenyl)-9,9-dioctyl-3,9-dihydrofluoreno[3,2-d]imidazole 
• 1326306-59-5 4-(9,9-dioctyl-3,9-dihydrofluoreno[3,2-d]imidazol-2-yl)-N,N-dimethylbenzenamine 
• 1326306-58-4 2-(4-nitrophenyl)-9,9-dioctyl-3,9-dihydrofluoreno[3,2-d]imidazole 
• 1326306-57-3 9,9-dioctyl-2-phenyl-3,9-dihydrofluoreno[3,2-d]imidazole 
• 1326306-56-2 9,9-dioctyl-2-p-tolyl-3,9-dihydrofluoreno[3,2-d]imidazo 
• 1326306-55-1 2-(4-chlorophenyl)-9,9-dioctyl-3,9-dihydrofluoreno[3,2-d]imidazole 
• 1326306-54-0 2-(4-fluorophenyl)-9,9-dioctyl-3,9-dihydrofluoreno[3,2-d]imidazole 
• 196207-58-6 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-dioctylfluorene 

Relevant articles and documents

Synthesis of unsymmetrically substituted biaryls via sequential lithiation of dibromobiaryls using integrated microflow systems

A microflow system consisting of micromixers and microtube reactors provides an effective method for the introduction of two electrophiles onto dibromobiaryls. Selective monolithiation of dibromobiaryls, such as 2,2'-dibromobiphenyl, 4,4'-dibromobiphenyl, 2,7-dibromo-9,9-dioctylfluorene, 2,2'-dibromo-1,1'-binaphthyl, and 2,2'-dibromobibenzyl with 1 equiv of n-butyllithium followed by the reaction with electrophiles was achieved using a microflow system by virtue of fast micromixing and precise temperature control. Sequential introduction of two different electrophiles was achieved using an integrated microflow system composed of four micromixers and four microtube reactors to obtain unsymmetrically substituted biaryl compounds.

Method for purifying electroluminescent material, electroluminescent material and electroluminescent device

Objects of the present invention are to provide a purification process that enables Pd to be removed effectively, and to provide an electroluminescent material and an electroluminescent device obtained by employing the process. The present invention relates to a process for purifying an electroluminescent material, the process involving treating, with a phosphorus-containing material, an electroluminescent material that contains Pd as an impurity so as to remove the Pd.