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

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

Downstream Products

• 1149804-35-2 4,4,5,5-tetramethyl-2-(10-naphthalene-1-yl-anthracene-9-yl)-[1,3,2]dioxaborolane 
• 1225375-02-9 C₃₇H₂₃N 
• 1261580-75-9 9-(9-phenylcarbazole-3-yl)-10-(naphthalene-1-yl)anthracene 
• 400607-46-7 9-(naphthalen-1-yl)anthracen-10-yl-10-boronic acid 

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.

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.

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)