849223-96-7

Basic information

• Product Name: Anthracene, 9-[1,1'-biphenyl]-2-yl-
• CAS NO: 849223-96-7
• Molecular Formula: C26H18
• Molecular Weight: 330.429
• Mol File: 849223-96-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Anthracene, 9-[1,1'-biphenyl]-2-yl-(CAS DataBase Reference)
• NIST Chemistry Reference: Anthracene, 9-[1,1'-biphenyl]-2-yl-(849223-96-7)
• EPA Substance Registry System: Anthracene, 9-[1,1'-biphenyl]-2-yl-(849223-96-7)

Safety Data

• Hazardous Substances Data: 849223-96-7(Hazardous Substances Data)

Usage

Uses

Used in Organic Electronic Devices:
Anthracene, 9-[1,1'-biphenyl]-2-ylis used as a component in the development of organic electronic devices due to its unique molecular structure and properties. It has been studied for its potential use in:
Organic Light-Emitting Diodes (OLEDs): Anthracene, 9-[1,1'-biphenyl]-2-ylcontributes to the efficiency and performance of OLEDs, which are used in display and lighting technologies.
Organic Thin-Film Transistors: It plays a role in enhancing the functionality of organic thin-film transistors, which are utilized in flexible electronics and sensors.
Organic Solar Cells: Anthracene, 9-[1,1'-biphenyl]-2-ylis considered for its potential to improve the efficiency and stability of organic solar cells, contributing to the advancement of renewable energy technologies.
Used in Chemical Reactions and Synthesis:
Anthracene, 9-[1,1'-biphenyl]-2-ylis used as a building block for the synthesis of other organic molecules and in various chemical reactions. Its unique molecular structure allows for further exploration and development of new compounds with potential applications in different industries.
Further research is necessary to fully understand the properties and potential applications of Anthracene, 9-[1,1'-biphenyl]-2-yl-, as its unique characteristics may lead to innovative solutions in the fields of organic electronics, chemical synthesis, and beyond.

Upstream product

• 2052-07-5 2-Bromobiphenyl 
• 716-53-0 9-chloroanthracene 
• 4688-76-0 2-Biphenylboronic acid 
• 914675-52-8 2‐{[1,1'‐biphenyl]‐2‐yl}‐4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolane 
• 1564-64-3 9-Bromoanthracene 

Downstream Products

• 400607-16-1 9-([1,1′-biphenyl]-2-yl)-10-bromoanthracene 
• 400607-48-9 10-([1,1'-biphenyl]-2-yl)-9-anthracenylboronic acid 
• 1184301-61-8 C₃₂H₂₉BO₂ 

Relevant articles and documents

Organic light emitting device

The present invention relates to an organic light emitting device having improved driving voltage, efficiency and lifetime.

Mixed phosphine/N-heterocyclic carbene palladium complexes: Synthesis, characterization and catalytic use in aqueous Suzuki-Miyaura reactions

A series of N-heterocyclic carbene (NHC)/PR3 palladium(ii) and palladium(0) complexes has been synthesized and fully characterized. X-ray crystallographic data have allowed comparison of ligand steric properties. The NHC ligand was found to vary its steric properties as a function of the phosphine co-ligand. These complexes display interesting catalytic properties in the Suzuki-Miyaura reaction performed in aqueous media. The pre-catalyst [PdCl2(IPr)(XPhos)] (IPr = N,N′-bis-(2,6-diisopropylphenyl) imidazol-2-ylidene; XPhos = 2-dicyclohexylphosphino-2′,4′,6′- triisopropylbiphenyl) was found to be the most efficient system, promoting the coupling of a wide range of aryl chlorides with boronic acids in aqueous media with a typical catalyst loading of 0.03 mol%.

LUMINESCENT COMPOUNDS AND ELECTROLUMINESCENT DEVICE USING THE SAME

The present invention relates to organic electroluminescent compounds and organic electroluminescent devices employing the same. More specifically, the invention relates to organic electroluminescent compounds containing an anthracenyl group or an aryl group having an anthracenyl substituent m the aryl ring of fluorene or indenofluorene, as a blue electroluminescent material in an organic electroluminescent layer. The electroluminescent compounds according to the invention exhibit high luminous efficiency and excellent life property, so that an OLED device having very good operation lifetime can be prepared therefrom.

Highly efficient carbazolyl-derived phosphine ligands: Application to sterically hindered biaryl couplings

A new family of phosphine ligands bearing a bulky carbazolyl scaffold is described. With the combination of ligand 2a and Pd(OAc)2, difficult tri-ortho-substituted biaryl couplings are accomplished smoothly. In particular, the catalyst loading as low as 0.02 mol% of Pd for non-activated 2,6-disubstituted aryl chloride coupling can be achieved.

Platinum-catalysed diborylation of arynes: Synthesis and reaction of 1,2-diborylarenes

Arynes are found to be facilely inserted into bis(pinacolato)diboron by using a platinum-isocyanide catalyst, affording diverse 1,2-diborylarenes, which can be converted into o-terphenyls via Suzuki-Miyaura coupling reaction.

Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of sterically hindered aryl bromides

(Chemical Equation Presented) A highly general, active, and stable catalytic system was realized in the palladium-catalyzed Suzuki-Miyaura reactions of sterically hindered aryl bromides with arylboronic acids using biphenylene-substituted di-tert-butylrut