528609-98-5

Usage

Uses

Used in Organic Synthesis:
2,6-dibromo-9,10-diphenyl-9,10-dihydroanthracene is used as a building block in organic synthesis for the production of a wide range of compounds. Its unique structure allows for the formation of diverse organic molecules, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-dibromo-9,10-diphenyl-9,10-dihydroanthracene is used as a versatile intermediate for the development of new drugs. Its unique structure and reactivity enable the synthesis of various pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
2,6-dibromo-9,10-diphenyl-9,10-dihydroanthracene is also utilized as an intermediate in the agrochemical industry for the synthesis of pesticides and other agrochemical products. Its ability to form a variety of compounds makes it a valuable component in the development of effective and environmentally friendly agrochemicals.
Used in Advanced Materials:
This chemical is used as a key intermediate in the production of advanced materials, such as organic semiconductors, due to its unique electronic and optical properties. Its potential applications in the development of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs) make it an important component in the advancement of modern technology.
Safety Precautions:
It is crucial to handle 2,6-dibromo-9,10-diphenyl-9,10-dihydroanthracene with caution due to its reactivity and potential hazards. Proper safety measures should be taken during its synthesis, storage, and use to minimize risks associated with its handling.

Upstream product

• 633-70-5 2,6-dibromoanthraquinone 
• 5794-88-7 5-Bromo-2-aminobenzoic acid 
• 63617-45-8 2,5-diphenyl-6H-1,3,4-oxadiazin-6-one 
• 591-51-5 phenyllithium 
• 131-14-6 2,6-diamino-9,10-anthraquinone 
• 1158648-68-0 C₂₆H₁₈Br₂O₂ 

Downstream Products

• 1074021-14-9 C₆₆H₄₂O₂ 
• 1245526-43-5 2,6-di(2-nitrophenyl)-9,10-diphenylanthracene 
• 1245526-44-6 C₃₈H₂₄N₂ 
• 1380245-00-0 2,2'-(9,10-diphenylanthracene-2,6-diyl)bis(N-(4-decylphenyl)aniline) 

Relevant academic research and scientific papers

NOVEL MATERIALS FOR ORGANIC ELECTROLUMINESCENCE DEVICES

The present invention relates to a compound of the formula (1) and (2) The invention further relates to a process to produce the compound. The invention additionally relates and an electronic device containing the compound of the formula (1) or (2). The electronic device can be an organic electroluminescence devices, particularly a blue emitting device, in which compounds are used as host materials or dopants in the emitting layer and/or as hole transport materials and/or as electron transport materials.

Antracene derivative and organic electroluminescent device including the same

The subject of the present invention is providing a novel anthracene derivative with excellent light emitting efficiency and excellent durability compared with an existing material. Provided is an anthracene derivative presented by chemical formula 1. In chemical formula 1, definition of each substituent is the same as defined in the detailed specification of the invention.(AA) Negative electrode(BB) Electron injection layer(CC) Electron transfer layer(DD) Light emitting layer(EE) Hole transporting layer(FF) Hole injection layer(GG) Positive electrode(HH) Organic layerCOPYRIGHT KIPO 2015

Antracene derivative and organic electroluminescent device including the same

The subject of the present invention is providing a novel anthracene derivative with excellent light emitting efficiency and excellent durability compared with an existing material. Provided is an anthracene derivative presented by chemical formula 1. In chemical formula 1, definition of each substituent is the same as defined in the detailed specification of the invention.(AA) Negative electrode(BB) Electron injection layer(CC) Electron transfer layer(DD) Light emitting layer(EE) Hole transporting layer(FF) Hole injection layer(GG) Positive electrode(HH) Organic filmCOPYRIGHT KIPO 2015

Herocyclic compound and organic light emitting device comprising same

The present invention provides a new compound useful for an electron injection material or an electron transport material; and an organic light emitting device comprising the compound, which has high efficiency, low voltage, high brightness and a long life. Disclosed are a compound represented by chemical formula 1 or chemical formula 2, and an organic light emitting device comprising the compound. Information about chemical formula 1 and chemical formula 2 is referred to in the detailed description of the present invention.COPYRIGHT KIPO 2015

Condensed-cyclic compound and organic light emitting diode having organic layer including the same

A condensed-cyclic compound represented by Formula 1 and an organic light emitting diode including the same:

CONDENSED-CYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DIODE HAVING ORGANIC LAYER INCLUDING THE SAME

A condensed-cyclic compound represented by Formula 1 and an organic light emitting diode including the same:

Organic Light-Emitting Device

The present invention provides a heterocyclic compound and an organic light-emitting device including the heterocyclic compound. The organic light-emitting devices using the heterocyclic compounds have high-efficiency, low driving voltage, high luminance and long lifespan.

Synthesis and characterization of a new series of blue fluorescent 2, 6-linked 9, 10-diphenylanthrylenephenylene copolymers and their application for polymer light-emitting diodes

A series of new 9, 10-diphenylanthracene-based, 2, 6-linked blue-light-emitting copolymers bearing hole- or electron-transporter as well as bulky substituent were successfully synthesized. Photophysical, thermal, electrochemical, and electroluminescence (EL) properties of these copolymers were studied and characterized. Bright and efficient blue fluorescence in the solid state was achieved by incorporating bulky substituent into the copolymer backbone. Both hole- and electron-transport-substituted copolymers apparently enhanced the electroluminescent performance of their polymeric light-emitting diodes (PLEDs). A diphenylvinyl-bearing copolymer (pDPV) PLED exhibited sky-blue EL (λETmax=473 nm, CIEx,y=0.16,0.28) with peak luminous efficiency of 2.21 cd/A; a N-carbazole bearing copolymer (pCBZ) PLED displayed a blue EL (λELmax469 nm, CIEx,y=0.15, 0.22) with peak luminous efficiency of 2.15 cd/A OXD-7 (1,3-bis(2-(4-tertbutylphenyl)-1,3,4-oxadiazol-5-yl)benzene) as an electron-transporting dopant was found to improve the performance of PLED significantly. A better balanced hole/electron charge carrier was ascribed to electrontransporting, 1, 3, 4-oxadiazole-bearing copolymer (pOXD) PLED. It showed a very mild efficiency rolls off: only 0.13 cd/A luminous efficiency drops from current densities of 10-100 mA/cm2, corresponding to EL brightness of 169-1558 cd/m2.

The most stable and fully characterized functionalized heptacene

(Chemical Equation Presented) Lucky seven: Crystals of heptacene, which consists of seven linearly fused benzene rings, remain stable for at least 21 days in mineral oil and 24 h in degassed solution when the oligoacene is functionalized with phenyl and t

Organic electroluminescence device

Disclosed is an organic electroluminescent device comprising a structure having an anode, an emitting layer, and a cathode stacked therein, wherein a fluorescent compound represented by Formula 1 is used as a emitting material of the emitting layer or used as a dopant of the emitting layer: wherein A 1 and A 2 are independently selected from a substituted or unsubstituted C 1 -C 6 aliphatic group, a C 6 -C 20 aromatic group and a C 5 -C 19 heterocyclic group containing N, S or O, A 3 is selected from a substituted or unsubstituted C 1 -C 6 aliphatic group, a C 6 -C 20 aromatic group, a C 5 -C 19 heterocyclic group containing N, S or O, and a hydrogen atom, and substituents of A 1 , A 2 and A 3 are respectively one or more and the substituent is selected from the group consisting of C 1 -C 10 alkyl, C 1 -C 1 alkoxy, C 1 -C 10 alkylamino, C 1 -C 10 alkylsilyl, a halogen atom, C 6 -C 10 aryl, C 6 -C 10 aryloxy, C 6 -C 10 arylamino, C 6 -C 10 arylsilyl and a hydrogen atom. Disclosed is an organic electroluminescent device comprising a structure having an anode, an emitting layer, and a cathode stacked therein, wherein a fluorescent compound represented by Formula 1 is used as a dopant of the emitting layer and a fluorescent compound by Formula 2 is used as a host of the emitting layer: where in A is independently selected from a substituted or unsubstituted C 6 -C 30 aromatic group, B is independently selected from a substituted or unsubstituted C 6 -C 30 aromatic group and a hydrogen atom, and substituents of A and B may be one or more, respectively, and the substituent is selected from the group consisting of C 1 -C 10 alkyl and a hydrogen atom.