474688-73-8

Basic information

• Product Name: 9-Bromo-10-(2-naphthyl)anthracene
• Synonyms: 9-Bromo-10-(2-naphthyl)anthracene;9-Bromo-10-(naphthyl-2-yl)anthracene;9-Bromo-10-(naphthalen-2-yl)anthracen;9-Bromo-10-(2-naphth;10-BroMo-9-(naphthalen-2-yl )anthracene;9-BroMo-10-naphthalen-2-yl-anthracene;9-BroMo-10-(naphth-2-yl)anthracene;10-BroMo-9-(naphthalene-2-yl)Anthracene
• CAS NO: 474688-73-8
• Molecular Formula: C₂₄H₁₅Br
• Molecular Weight: 383.28
• EINECS: 1312995-182-4
• Product Categories: Electronic Chemicals
• Mol File: 474688-73-8.mol

Chemical Properties

• Melting Point: 169.0 to 173.0 °C
• Boiling Point: 518.85 °C at 760 mmHg
• Flash Point: 261.106 °C
• Appearance: /
• Density: 1.403 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.757
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Toluene
• CAS DataBase Reference: 9-Bromo-10-(2-naphthyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Bromo-10-(2-naphthyl)anthracene(474688-73-8)
• EPA Substance Registry System: 9-Bromo-10-(2-naphthyl)anthracene(474688-73-8)

Safety Data

• Hazardous Substances Data: 474688-73-8(Hazardous Substances Data)

Usage

Uses

Used in Chemical Analysis:
9-Bromo-10-(2-naphthyl)anthracene is used as a reagent for the determination of amines. Its chemical structure allows it to interact with amine compounds, making it a valuable tool in the identification and quantification of these important organic compounds in various chemical and biological processes.
Used in Research and Development:
Due to its unique chemical properties, 9-Bromo-10-(2-naphthyl)anthracene is also utilized in research and development for the synthesis of new compounds and materials. It can serve as a building block or intermediate in the creation of more complex organic molecules with specific functions and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 9-Bromo-10-(2-naphthyl)anthracene may be employed as a starting material or intermediate in the synthesis of novel drug candidates. Its unique structure can be exploited to design and develop new therapeutic agents with potential applications in various medical conditions.
Used in Material Science:
9-Bromo-10-(2-naphthyl)anthracene can also be used in the field of material science, where its properties can be harnessed to develop new materials with specific characteristics. These materials could have applications in areas such as electronics, optics, or even as components in advanced composites.

InChI:InChI=1/C24H15Br/c25-24-21-11-5-3-9-19(21)23(20-10-4-6-12-22(20)24)18-14-13-16-7-1-2-8-17(16)15-18/h1-15H

Upstream product

• 7424-72-8 9-(naphthyl-2-yl)anthracene 
• 580-13-2 2-bromonaphthalene 
• 32316-92-0 naphthalene-2-boronic acid 
• 135-19-3 β-naphthol 
• 128-08-5 N-Bromosuccinimide 
• 1564-64-3 9-Bromoanthracene 
• 523-27-3 9,10-Dibromoanthracene 
• 5419-55-6 Triisopropyl borate 
• 100622-34-2 anthracene-9-boronic acid 
• 90-44-8 anthracen-9(10H)-one 

Downstream Products

• 862501-00-6 9-biphenyl-10-(2-naphthyl)anthracene 
• 948860-10-4 C₃₀H₂₁N 
• 1087347-02-1 1-phenyl-2-(4-benz[a]anthracen-4-yl-phenyl)benzimidazole 
• 936854-62-5 9-(4-bromophenyl)-10-(naphthalen-2-yl)anthracene 
• 1335315-07-5 N-(4-(10-naphthalen-2-yl)anthracen-9-yl)phenyl-N-phenylnaphthalen-2-amine 
• 922518-84-1 4,4,5,5-tetramethyl-2-(10-(naphthalen-2-yl)anthracen-9-yl)-1,3,2-dioxaborolane 
• 1263386-55-5 1-phenyl-2-(4-benz[a]anthracen-8-ylphenyl)benzimidazole 
• 948860-11-5 C₃₀H₂₀O 
• 1297374-60-7 C₄₄H₃₀O₂ 
• 1297373-96-6 C₄₄H₂₈O 
• 1432475-70-1 2',5'-dimethyl-4'-(10-(naphthalen-2-yl)anthracen-9-yl)-N,N-diphenyl-[1,1'-biphenyl]-4-amine 
• 1197175-44-2 2-(4-(10-(naphthalen-2-yl)anthracen-9-yl)phenyl)-1-phenyl-1H-phenanthro[9,10-d]imidazole 
• 1197177-38-0 C₅₁H₃₂N₂ 

Relevant articles and documents

New blue host materials based on anthracene-containing dibenzothiophene

A series of novel host blue-emitting materials based on anthracene have been synthesized and investigated in which, a π-electron-rich dibenzothiophene moiety was introduced as a side group to fine adjust the HOMO/LUMO levels of the anthracene and enhance the ability of hole-transport and electron-injection. These materials exhibit good film-forming capabilities, and display strong blue fluorescence in solution. To explore the electroluminescent properties of these materials, sky blue devices of 2-TNATA (60 nm)/NPB (10 nm)/Host: BUBD-1 (40 nm)/Alq3 (15 nm)/LiF (1 nm)/Al (150 nm) were fabricated. For the device with 9, 10-bis(dibenzothiophen-4-yl)anthracene as the host, an electroluminescence efficiency of 13.14 cd/A and 6.76 lm/W at 20 mA/cm2 and 6.09 V were achieved, with Commission Internationale d'Eclairage (CIEx,y) color coordinates of (x = 0.15, y = 0.30).

Compound, organic luminescent material and organic electroluminescent device

The invention provides a compound as shown in a general formula (I), which has a mother structure of sym-triphenyl substituted anthracene, is high in bond energy among atoms, has good thermal stability, is beneficial to solid-state accumulation among molecules, is large in bandwidth, has a light-emitting region in a blue light region, is high in light-emitting intensity, and has a proper energy level with adjacent levels. And injection and migration of excitons are facilitated. When the compound is used as a blue light host material in a luminescent layer, the driving voltage of an organic electroluminescent device can be effectively reduced, the luminous efficiency is improved, and the service life is prolonged. The invention also provides an organic electroluminescent device and a display device containing the compound of the general formula (I).

Novel compound and organic light emitting device comprising the same

The present invention provides a novel compound and an organic light emitting device using the same. The present invention provides a compound represented by chemical formula 1. The compound represented by chemical formula 1 described above can be used as a material for an organic layer of the organic light emitting device, and can improve efficiency, low driving voltage, and/or lifespan characteristics in the organic light emitting device.

Organic compound and electronic element and electronic device using same (by machine translation)

The invention belongs to the technical field of organic materials, and particularly relates to an organic compound and an electronic element and an electronic device using the same, wherein the organic compound has the structure shown 1. When the compound is used as an electron transport layer for preparing an organic electroluminescent device, the service life of the organic electroluminescent device can be effectively prolonged, and the luminous efficiency or the driving voltage can be improved to a certain extent. (by machine translation)

Antracene derivatives having heteroaryl substituted phenyl group and organic light-emitting diode including the same

The present invention relates to an antracene derivative represented by the following [Formula A] and an organic light-emitting diode including the same. Z , Y, and L are the same as defined in the detailed description of the invention.

Asymmetric antracene derivatives having two naphthyl groups and organic light-emitting diode including the same

The present invention relates to antracene derivatives represented by [Formula A] and [Formula B], and an organic light-emitting diode including the same. Substituents X_1 to X_14, Y, and Z are the same as defined in the detailed description.

Asymmetric antracene derivatives having two naphthyl groups and organic light-emitting diode including the same

The present invention relates to an antracene derivative represented by the following [Formula A] or [Formula B], and an organic light-emitting diode including the same. Substituents X_1 to X_7 , Y, and Z are the same as defined in the detailed description of the invention.

Semiconducting Material Comprising a Phosphine Oxide Matrix and Metal Salt

The present invention is directed to a semiconducting material comprising: i) a compound according to formula (I) wherein R1, R2 and R3 are independently selected from C1-C30-alkyl, C3-C30 cycloalkyl, C2-C30-heteroalkyl, C6-C30-aryl, C2-C30-heteroaryl, C1-C30-alkoxy, C3-C30-cycloalkyloxy, C6-C30 aryloxy, and from structural unit having general formula E-A-, wherein—A is a C6-C30 phenylene spacer unit, and—E is an electron transporting unit that is selected from C10-C60 aryl and C6-C60 heteroaryl comprising up to 6 heteroatoms independently selected from O, S, P, Si and B and that comprises a conjugated system of at least 10 delocalized electrons, and—at least one group selected from R1, R2 and R3 has the general formula E-A-; and ii) at least one complex of a monovalent metal having formula (II) wherein—M+ is a positive metal ion bearing a single elementary charge, and each of A1, A2, A3 and A4 is independently selected from H, substituted or unsubstituted C6-C20 aryl and substituted or unsubstituted C2-C20 heteroaryl, wherein a heteroaryl ring of at least 5 ring-forming atoms of the substituted or unsubstituted C2-C20 heteroaryl comprises at least one hetero atom selected from O, S and N.

Organic light emitting device

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

3,5-bis(10-naphthalenyl-anthracen-9-yl)pyridine compounds as hosts for light-emitting devices

Optionally substituted 3-(10-(aryl)anthracen-9-yl)-5-(10-(aryl)anthracen-9-yl)pyridine compounds may be used as host compounds for devices such as organic light-emitting devices.