1023674-80-7

Basic information

• Product Name: 9-(3-broMophenyl)-10-phenyl-anthracene
• Synonyms: 9-(3-broMophenyl)-10-phenyl-anthracene;9-phenyl-10-(3-bromophenyl)anthracene
• CAS NO: 1023674-80-7
• Molecular Formula: C₂₆H₁₇Br
• Molecular Weight: 409.31718
• Mol File: 1023674-80-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 182.0 to 186.0 °C
• Boiling Point: 498.5±14.0 °C(Predicted)
• Appearance: /
• Density: 1.344±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 9-(3-broMophenyl)-10-phenyl-anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(3-broMophenyl)-10-phenyl-anthracene(1023674-80-7)
• EPA Substance Registry System: 9-(3-broMophenyl)-10-phenyl-anthracene(1023674-80-7)

Safety Data

• Hazardous Substances Data: 1023674-80-7(Hazardous Substances Data)

Usage

General Description

9-(3-broMophenyl)-10-phenyl-anthracene, abbreviated as BMPA, is a synthetic, organic chemical compound. Its molecular structure comprises two phenyl groups (simple rings of carbon and hydrogen), an anthracene group (three-fused benzene rings), and a bromine atom attached to one of the phenyl groups. The compound is associated with the field of Photochemistry, specifically organobromine compounds (organic compounds that contain carbon bonded to bromine). It often serves as a building block or intermediate in chemical synthesis. Specific properties, toxicity, and applications can vary and are largely dependent on the specifics of the synthesis process, the addition of functional groups or other chemicals, and the intended use.

Upstream product

• 1564-64-3 9-Bromoanthracene 
• 602-55-1 9-phenylanthracene 
• 98-80-6 phenylboronic acid 
• 334658-75-2 10-phenylanthracene-9-boronic acid 
• 108-36-1 1,3-dibromobenzene 
• 23674-20-6 9-bromo-10-phenylanthracene 
• 591-18-4 1-Bromo-3-iodobenzene 

Downstream Products

• 1620010-90-3 C₃₁H₂₆Si 
• 1620010-93-6 C₃₆H₂₂Br₂ 
• 1620010-51-6 C₅₀H₃₂ 
• 1620010-91-4 C₂₈H₁₈ 
• 1620010-92-5 C₃₅H₂₂O 
• 905947-49-1 {3-(10-phenylanthracen-9-yl)phenyl}boronic acid 
• 910897-93-7 9-[3-(10-phenyl-9-anthryl)phenyl]-9H-carbazole 
• 1382763-45-2 6-[3-(10-phenyl-9-anthryl)phenyl]-benzo[b]naphtho[1,2-d]furan 
• 1364890-86-7 3-(dibenzofuran-4-yl)-9-[3-(10-phenyl-9-anthryl)phenyl]-9H-carbazole 
• 1364890-85-6 3-(dibenzothiophen-4-yl)-9-[3-(10-phenyl-9-anthryl)phenyl]-9H-carbazole 

Relevant articles and documents

ORGANIC LIGHT-EMITTING DEVICE

An organic light-emitting device including: a first electrode; a second electrode; and an organic layer disposed between the first electrode and the second electrode, wherein the organic layer includes an emission layer, wherein the emission layer includes a polycyclic compound represented by Formula 1 and a host, and wherein an amount of the polycyclic compound is less than an amount of the host in the emission layer, wherein Formula 1 is as provided herein.

NOVEL ANTHRACENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, MATERIAL SOLUTION FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC APPARATUS

PROBLEM TO BE SOLVED: To provide a novel anthracene derivative, and a material for an organic electroluminescent element that uses the same and can form an organic thin film by an application method. SOLUTION: The present invention provides an anthracene derivative represented by the formula (1). SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2018,JPOandINPIT

COMPOUND FOR ORGANIC ELECTROLUMINESCENT ELEMENT AND ORGANIC ELECTROLUMINESCENT ELEMENT USING THE SAME

PROBLEM TO BE SOLVED: To provide a compound for an organic electroluminescent element which allows a sufficiently long driving life to be obtained when used as a constituent material of an organic electroluminescent element, and to provide an organic electroluminescent element using the compound. SOLUTION: The compound for an organic electroluminescent element is an anthracene compound having at least one substituent represented by general formula (2). The organic electroluminescent element uses the compound. (L is a linking group and is a single bond, a substituted/unsubstituted arylene group, a substituted/unsubstituted divalent group having a heterocyclic skeleton, or the like; and R1 and R2 are each independently H, a substituted/unsubstituted alkyl group, or the like.) SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT