400607-04-7

Basic information

• Product Name: ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)-
• Synonyms: ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)-;9-Bromo-10-(1-naphthalenyl)anthracene;9-Bromo-10-(naphthalen-1-yl)anthracene;9-BroMo-10-(1-naphthyl)anth racene;10-BroMo-9-(naphthalene-1-yl)Anthracene;10-broMo-9-(phthalen-1-yl)anthracene;10-(naphthalen-1-yl)anthracen-9-broMine;BA1N
• CAS NO: 400607-04-7
• Molecular Formula: C₂₄H₁₅Br
• Molecular Weight: 383.286
• EINECS: 1312995-182-4
• Product Categories: organic chemicals and derivatives/others;OLED
• Mol File: 400607-04-7.mol
• Article Data: 35

Chemical Properties

• Melting Point: 177.0 to 181.0 °C
• Boiling Point: 508 °C at 760 mmHg
• Flash Point: 254.3 °C
• Appearance: Pale yellow/Solid
• Density: 1.403 g/cm³
• Refractive Index: 1.756
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Toluene
• CAS DataBase Reference: ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)-(CAS DataBase Reference)
• NIST Chemistry Reference: ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)-(400607-04-7)
• EPA Substance Registry System: ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)-(400607-04-7)

Safety Data

• Hazardous Substances Data: 400607-04-7(Hazardous Substances Data)

Usage

Chemical Properties

Off-white powder

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

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 13922-41-3 1-Naphthylboronic acid 
• 90-11-9 1-Bromonaphthalene 
• 7424-70-6 10-(naphthalen-1-yl)anthracene 
• 1564-64-3 9-Bromoanthracene 

Downstream Products

• 1149804-35-2 4,4,5,5-tetramethyl-2-(10-naphthalene-1-yl-anthracene-9-yl)-[1,3,2]dioxaborolane 
• 400607-46-7 9-(naphthalen-1-yl)anthracen-10-yl-10-boronic acid 
• 1225375-02-9 C₃₇H₂₃N 
• 1225375-01-8 C₃₆H₂₄ 
• 1445997-83-0 C₅₅H₄₅NSi 
• 1445998-20-8 C₂₈H₂₄Si 
• 1445998-19-5 C₂₆H₂₁ClSi 
• 1261580-75-9 9-(9-phenylcarbazole-3-yl)-10-(naphthalene-1-yl)anthracene 
• 1581768-77-5 9-naphthalen-1-yl-10-(5,6,7,8-tetrahydro-naphthalene-1-yl)-anthracene 

Relevant articles and documents

ANTHRACENE COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING SAME

The present specification relates to an anthracene compound represented by chemical formula 1 and an organic light emitting device including the same.

Blue light electroluminescent material and application thereof

The invention relates to a blue light electroluminescent material and an application thereof. A structural formula of the blue light electroluminescent material is represented by a chemical formula 1shown in the specification. The blue light electroluminescent material provided by the invention has the advantages of high luminous efficiency, high color saturation, good film-forming performance, better thermal stability and the like; compared with a conventional blue host material, the blue light electroluminescent material provided by the invention has the characteristics of high luminous efficiency and long service life of a prepared device; and inventors also find that when a deuterium element is introduced into the material structure, by using the characteristics of the deuterium element, the quantum efficiency, color saturation, service life and the like can be improved, and at the same time, the material has higher tolerance when used for preparing the device.

Preparation method and purification method of 9,10-substituted anthracene

The invention belongs to the technical field of organic synthesis and catalysis, and particularly relates to a preparation method for synthesizing 9-(naphthalene-1-yl)-10-(4-(naphthalene-2-yl)phenyl)anthracene through a five-step reaction, and a purification method. The method provided by the invention has the advantages of less catalyst dosage, high synthesis yield, less reaction by-products (impurities) (the content of removed boric acid products is less than 1%, and boric acid self-coupling products are not generated), high product purity (the HPLC purity is greater than or equal to 99.99%)and the like, and can be directly applied to OLED terminal materials of devices, and is simple, easy to operate and suitable for large-scale industrial production.

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

The present invention relates to an anthracene derivative represented by Chemical Formula A and an organic light-emitting device including the same, wherein substituents X1 to X5, Y, and Z are the same as defined in detailed explanation of the invention.

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)

DOUBLE-DECKER SILSESQUIOXANE DERIVATIVE AND SYNTHESIZING METHOD THEREOF

A double-deck silsesquioxane derivative represented by chemical formula 1, a method for preparing the same, and an organic light emitting diode including the derivative are provided. Chemical Formula 1. R is the same as in the above formula. 1 Is a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group. R2 is possible. . Or. Me. (by machine translation)

Anthracene derivatives and organic light emitting devices comprising the same

An anthracene derivative represented by Formula 1 is disclosed. An organic light-emitting device including an anode, a cathode, and an organic layer between the anode and the cathode, where the organic layer includes at least one anthracene derivative represented by Formula 1, is also disclosed. A method of manufacturing the organic light-emitting device is also disclosed.

Phenanthridine Derivatives and organic light-emitting diode including the same

PURPOSE: A phenanthridine derivative compound is provided to obatin an organic light emitting diode with excellent light emitting property. CONSTITUTION: A phenanthridine derivative compound is denoted by chemical formula 1 or 2. An organic light emitting diode contains an anode, a cathode, and the phenanthridine derivative compounds inserted between the anode and cathode. The organic light emitting diode further contains a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, or an electron injection layer formed by monomer deposition or solution process.

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.

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.