474688-76-1

Basic information

• Product Name: 2-Bromo-9,10-bis(2-naphthalenyl)anthracene
• Synonyms: 2-broMo-9,10-di(naphthalen-2-yl)anthracene (BDNA);2-broMo-9,10-di(phthalen-2-yl)anthracene;2-BroMo-9,10-bis(2-napthalenyl)anthracene;BDNA;2-Bromo-9,10-bis(2-naphthyl)anthracene;2-Bromo-9,10-di-2-phthalenylanthracene;2-Bromo-9,10-bis(2-naphthalenyl); Anthracene, 2-bromo-9,10-di-2-naphthalenyl-
• CAS NO: 474688-76-1
• Molecular Formula: C₃₄H₂₁Br
• Molecular Weight: 509.43
• EINECS: 1592732-453-0
• Product Categories: Electronic Chemicals
• Mol File: 474688-76-1.mol

Chemical Properties

• Boiling Point: 630.082 °C at 760 mmHg
• Flash Point: 322.452 °C
• Appearance: /
• Density: 1.367 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.768
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-Bromo-9,10-bis(2-naphthalenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-9,10-bis(2-naphthalenyl)anthracene(474688-76-1)
• EPA Substance Registry System: 2-Bromo-9,10-bis(2-naphthalenyl)anthracene(474688-76-1)

Safety Data

• Hazardous Substances Data: 474688-76-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C34H21Br/c35-28-17-18-31-32(21-28)34(27-16-14-23-8-2-4-10-25(23)20-27)30-12-6-5-11-29(30)33(31)26-15-13-22-7-1-3-9-24(22)19-26/h1-21H

Upstream product

• 109-72-8 n-butyllithium 
• 580-13-2 2-bromonaphthalene 
• 124-38-9 carbon dioxide 
• 572-83-8 2-bromoanthracene-9,10-dione 
• 90-11-9 1-Bromonaphthalene 

Downstream Products

• 624744-67-8 2-(9,10-di(naphthalene-2-yl)anthracene-2-yl)4,4,5,5-tetramethyl-1,3,2-dioxa-borolane 
• 867044-28-8 (9,10-di (naphthalene-2-yl) anthracene-2-yl)boronic acid 
• 1265734-70-0 2-(2-nitrophenyl)-9,10-di(2-naphthyl)anthracene 
• 1228263-74-8 C₆₁H₃₈N₂ 
• 1573176-40-5 5,15-bis{9,10-di(naphth-2-yl)anthr-2-ylethynyl}-10,20-bis(3,5-di-tert-butylphenyl)porphyrin Ni(II) 
• 274905-73-6 2-tert-butyl-9,10-bis-(β-naphthyl)-anthracene 

Relevant articles and documents

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

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.

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 COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME

The present invention discloses an anthracene compound which can be used as emitting material in organic electroluminescence devices is disclosed. The mentioned anthracene compound is represented by the following formula [I] Wherein Ar1 and Ar2 are the same or different and each is selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted anthryl group.