1092390-01-6

Basic information

• Product Name: 9-broMo-10-(4-(naphthalen-1-yl)phenyl)anthracene
• Synonyms: 9-broMo-10-(4-(naphthalen-1-yl)phenyl)anthracene;10-(4-(1-Naphthyl)phenyl)-9-bromoanthracene;9-Bromo-10-[4-(1-naphthalenyl)phenyl]anthracene;9-Bromo-10-[4-(1-naphthyl)phenyl]anthracene
• CAS NO: 1092390-01-6
• Molecular Formula: C30H19Br
• Molecular Weight: 459.37586
• Mol File: 1092390-01-6.mol
• Article Data: 7

Chemical Properties

• Melting Point: 213 °C
• Boiling Point: 609.7±24.0 °C(Predicted)
• Appearance: /
• Density: 1.356
• CAS DataBase Reference: 9-broMo-10-(4-(naphthalen-1-yl)phenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-broMo-10-(4-(naphthalen-1-yl)phenyl)anthracene(1092390-01-6)
• EPA Substance Registry System: 9-broMo-10-(4-(naphthalen-1-yl)phenyl)anthracene(1092390-01-6)

Safety Data

• Hazardous Substances Data: 1092390-01-6(Hazardous Substances Data)

Usage

General Description

9-bromo-10-(4-(naphthalen-1-yl)phenyl)anthracene is a chemical compound that belongs to the class of compounds known as polycyclic aromatic hydrocarbons. These chemicals contain multiple fused aromatic rings. Specifically, this compound consists of a brominated anthracene bearing additional phenyl and naphthyl substituents. It's not naturally occurring and must be synthesized in a lab. Information regarding its biological activity or potential uses is not comprehensive, as it appears to be primarily used for research purposes. Its specific physical properties like melting point, toxicity, or reactivity are not readily available and require further experimental investigation. It also needs to have safety data and environmental impact studies.

Upstream product

• 641144-16-3 (10-bromoanthracen-9-yl)boronic acid 
• 583-55-1 1-Bromo-2-iodobenzene 
• 1564-64-3 9-Bromoanthracene 
• 1092390-00-5 9-(4-naphthalen-1-yl)phenylanthracene 
• 870774-25-7 (4-(naphthalen-1-yl)phenyl)boronic acid 
• 523-27-3 9,10-Dibromoanthracene 

Downstream Products

• 1297374-17-4 C₅₀H₃₂O 

Relevant articles and documents

Spirobenzofluorene linked anthracene derivatives: Synthesis and application in blue fluorescent host materials

Blue light-emitting anthracene-based host materials with a spiro[benzo[c]fluorene-7,9′-fluorene] core, 5-(10-(naphthalen-2-yl) anthracen-9-yl)spiro[benzo[c]fluorene-7,9′-fluorene] (NA-SBFF) and 5-(10-(4-(naphthalen-1-yl)phenyl)anthracen-9-yl)spiro[benzo[c]fluorene-7, 9′-fluorene] (NPA-SBFF), were designed and synthesized via two-step Suzuki coupling reactions. Introduction of a spiro group into the structure of the anthracene moieties lead to a reduction in crystallization tendency, and a high glass transition temperature was observed. Typical blue fluorescent organic light emitting diodes with the configuration of ITO/N,N′-diphenyl-N, N′-bis[4-(phenyl-m-tolyl-amino)phenyl]biphenyl-4,4′-diamine (DNTPD)/N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine (NPB)/HOST: Dopant/tris(8-hydroxyquinoline)aluminum (Alq3)/LiF were developed using SBFF-type anthracene derivatives as a host material and N,N,N′,N′-tetraphenylspiro[benzo[c]fluorene-7,9′-fluorene]-5, 9-diamine (TPA-SBFF) as a dopant material. A device obtained from NA-SBFF doped with TPA-SBFF showed blue color purity of 0.146 and 0.167, a luminance efficiency of 8.65 cd/A, and an external quantum efficiency >6.01% at 8.0 V.

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)

A organic compounds and their organic electroluminescent device in the application of the

The invention relates to an organic compound as shown in a formula (I). In the formula, one of A and B is N, and the other one is a CH group or a CH group of which H is substituted by one of alkyl of C1-12, aryl of C6-30, heterocyclic aryl of C6-30, -CF3 and -SCH3; n is 1 or 2; Ar is selected from anthryl, anthrylene, anthracenediyl or anthracenediylene which can be substituted by one of phenyl, biphenyl, naphthyl and naphthyl phenyl; L is a bridging ligand, and is selected from single bond, arylidene, penta-heterocyclic or hexa-heterocyclic aryl, oxygen atoms, nitrogen atoms or sulfur atoms; Ar1 and Ar2 are independently selected from H, phenyl, naphthyl and biphenyl which can be substituted by one of alkyl of C1-12, -CF3, -SCH3, phenyl, biphenyl and naphthyl. The invention further provides application of the compound in organic electroluminescence devices, in particular electronic transmission materials of an OLED.

ELECTROACTIVE MATERIALS

There is provided an electroactive material having Formula I wherein: Q is the same or different at each occurrence and can be O, S, Se, Te, NR, SO, SO2, P, PO, PO2, and SiR2;R is the same or different at each occurrence a