860530-98-9

Upstream product

• 60-29-7 diethyl ether 
• 572-83-8 2-bromoanthracene-9,10-dione 
• 108-86-1 bromobenzene 
• 117-79-3 2-aminoanthraquinone 
• 591-51-5 phenyllithium 

Downstream Products

• 43217-28-3 2-chloro-9,10-diphenylanthracene 
• 1404222-74-7 4-[4-(9H-carbazol-9-yl)phenyl]-4'-(9,10-diphenyl-2-anthryl)triphenylamine 
• 1404222-73-6 N-[4-(9,10-diphenyl-2-anthryl)phenyl]-N,N',N'-triphenylbenzidine 
• 1123921-75-4 2-(3-{N-[4-(carbazol-9-yl)phenyl]-N-phenylamino}phenyl)-9,10-diphenylanthracene 
• 1123921-73-2 2-{3-[N-phenyl-N-(9-phenylcarbazol-3-yl)amino]phenyl}-9,10-diphenylanthracene 
• 1136225-77-8 2-(4-{N-[4-(carbazol-9-yl)phenyl]-N-phenylamino}phenyl)-9,10-diphenylanthracene 
• 1123921-71-0 2-[4-[N-phenyl-N-(9-phenylcarbazol-3-yl)amino]phenyl]-9,10-diphenylanthracene 
• 1123921-70-9 2-{4-[N-(4-diphenylaminophenyl)-N-phenylamino]phenyl}-9,10-diphenylanthracene 
• 1123921-69-6 2-iodo-9,10-diphenylanthracene 
• 1123921-74-3 2-(3-bromophenyl)-9,10-diphenylanthracene 
• 1123921-68-5 2-(4-bromophenyl)-9,10-diphenylanthracene 
• 201731-79-5 2-bromo-9,10-diphenylanthracene 

Relevant academic research and scientific papers

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

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 purpose of the present invention is to provide a novel anthracene derivative having excellent light emitting efficiency and durability. To this end, provided is an anthracene derivative represented by chemical formula 1. In the chemical formula 1, definition of each subsistent is the same as defined in the specification.(DD) Light emitting layer(EE) Hole transporting layer(FF) Hole injection layer(GG) Positive electrode(HH) Organic layer(CC) Electron transfer layer(BB) Electron injection layer(AA) Negative electrodeCOPYRIGHT KIPO 2015

Light emitting compound and organic light-emitting diode including the same

PURPOSE: A light emitting compound is provided to ensure excellent luminous efficiency, power efficiency and brightness, to be used as a host material of a light-emitting layer and to increase service life of an organic electroluminescence device. CONSTITUTION: A light emitting compound is represented by chemical formula(1). In chemical formula(1), X1 - X4 are selected from the group consisting of C1-19 substituted or unsubstituted alkyl group, C1-19 substituted or unsubstituted alkoxy group, cyano group, C1-19 substituted or unsubstituted silyl group, nitro group, hydroxyl group, C1-19 substituted or unsubstituted amino group, C1-19 substituted or unsubstituted sulfonic acid group, halogen, deuterium, hydrogen C1-19 substituted or unsubstituted aryl group, heteroaryl group and heterocycle group; A1 and A2 are independently selected from the group consisting of C, N, S, O, Si and Ge; and L1 and L2 are selected from the group consisting of substituted or unsubstituted C3-40 aryl group, heteroaryl group, and heterocyclic group.

Anthracene derivatives and light-emitting devices using the anthracene derivatives

The present invention provides novel anthracene derivatives. In particular, the present invention provides light-emitting elements with high luminous efficiency, and light-emitting elements with long lifetime. Further, the present invention provides light-emitting devices and electronic devices having long lifetime by using these light-emitting elements. An anthracene derivative represented by the general formula (1) is provided. In addition, since the anthracene derivative represented by the general formula (1) has high luminous efficiency, a light-emitting element using the anthracene derivative represented by the general formula (1) can also have high luminous efficiency. By using the anthracene derivative represented by the general formula (1), light-emitting elements with long lifetime can be provided.

BLUE ELECTROLUMINESCENT COMPOUNDS WITH HIGH EFFICIENCY AND DISPLAY DEVICE USING THE SAME

The present invention relates to novel organic electroluminescent compounds and display devices comprising the same. The organic electroluminescent compounds according to the present invention exhibit high luminous efficiency and excellent life property, so that an OLED device having very good operation life can be prepared therefrom.

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:

Anthracene Derivative, Light-Emitting Material, Material for Light-Emitting Element, Composition for Coating, Light-Emitting Element, Light-Emitting Device, and Electronic Appliance

A novel anthracene derivative with a large energy gap is provided. An anthracene derivative represented by General Formula (G1) below is provided. In the formula, Ar1 and Ar2 independently represent an aryl group with 6 to 13 carbon atoms in a ring, R1 and R2 independently represent any of hydrogen, an alkyl group with 1 to 4 carbon atoms, or an aryl group with 6 to 13 carbon atoms in a ring, and each of Ar1, Ar2, R1, and R2 may have a substituent and the two substituents may be bonded to each other to form a ring.

ANTHRACENE DERIVATIVE, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, AND ELECTRONIC APPLIANCE

Novel anthracene derivatives are provided. Further, a light-emitting element, a light-emitting device, and an electronic appliance each using the novel anthracene derivative are provided. Anthracene derivatives represented by general formulae (G11) and (G21) are provided. The anthracene derivatives represented by the general formulae (G11) and (G21) each emit blue light with high color purity and have a carrier-transporting property. Therefore, each of the anthracene derivatives represented by the general formulae (G11) and (G21) is suitable for use in a light-emitting element, a light-emitting device, and an electronic appliance.

Anthracene Derivatives and Light-Emitting Devices Using the Anthracene Derivatives

The present invention provides novel anthracene derivatives. In particular, the present invention provides light-emitting elements with high luminous efficiency, and light-emitting elements with long lifetime. Further, the present invention provides light-emitting devices and electronic devices having long lifetime by using these light-emitting elements. An anthracene derivative represented by the general formula (1) is provided. In addition, since the anthracene derivative represented by the general formula (1) has high luminous efficiency, a light-emitting element using the anthracene derivative represented by the general formula (1) can also have high luminous efficiency. By using the anthracene derivative represented by the general formula (1), light-emitting elements with long lifetime can be provided.