51958-51-1

Basic information

• Product Name: 1-Bromophenanthrene
• Synonyms: 1-Bromophenanthrene;1-bromophennathrene
• CAS NO: 51958-51-1
• Molecular Formula: C₁₄H₉Br
• Molecular Weight: 257.12526
• Mol File: 51958-51-1.mol
• Article Data: 9

Chemical Properties

• Melting Point: 108-109℃
• Appearance: /
• CAS DataBase Reference: 1-Bromophenanthrene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromophenanthrene(51958-51-1)
• EPA Substance Registry System: 1-Bromophenanthrene(51958-51-1)

Safety Data

• Hazardous Substances Data: 51958-51-1(Hazardous Substances Data)

Usage

Description

1-Bromophenanthrene is an organic compound that belongs to the class of polycyclic aromatic hydrocarbons. It is characterized by the presence of a bromine atom attached to a phenanthrene molecule, which is a tricyclic aromatic hydrocarbon. 1-Bromophenanthrene is known for its unique chemical properties and reactivity, making it a valuable intermediate in various chemical reactions and synthesis processes.

Uses

1-Bromophenanthrene is used as an important reagent in the synthesis of heteroaryl compounds for organic light-emitting devices (OLEDs). The expression is: 1-Bromophenanthrene is used as a reagent for the synthesis of heteroaryl compounds in the production of OLEDs.
Used in Electronics Industry:
1-Bromophenanthrene is used as a key intermediate in the synthesis of various organic materials for the electronics industry, particularly in the development and manufacturing of OLEDs. Its role in this application is to facilitate the formation of heteroaryl compounds, which are essential components in the construction of OLEDs, enhancing their performance and efficiency.

Upstream product

• 4176-53-8 1-aminophenanthrene 
• 78602-28-5 1-bromo-2-(2-phenylethenyl)benzene 
• 2489-86-3 1-allylnaphthalene 
• 213599-19-0 1-bromo-2-(2,2-dibromovinyl)benzene 
• 6630-33-7 ortho-bromobenzaldehyde 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 36901-75-4 (2-bromobenzyl)triphenylphosphonium bromide 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 3366-65-2 2-aminophenanthrene 
• 54737-45-0 (E)-2-bromostilbene 
• 51958-50-0 2-Amino-1-bromophenanthren 

Downstream Products

• 85-01-8 phenanthrene 
• 146746-66-9 1-(2-fluoro-6-hydroxyphenyl)phenanthrene triflate 
• 146746-65-8 1-(2-fluoro-6-hydroxyphenyl)phenanthrene 
• 194-69-4 benzo[c]chrysene 
• 959926-12-6 2-(1-Phenanthryl)benzaldehyde 
• 146746-64-7 1-(2-fluoro-6-methoxyphenyl)phenanthrene 

Relevant articles and documents

Extremely deep-blue fluorescent emitters with CIEy?≤?0.04 for non-doped organic light-emitting diodes based on an indenophenanthrene core

The fluorescent molecules 7,7-dimethyl-N,N-diphenyl-7H-indeno[1,2-a] phenanthren-9-amine (DIP) and 4-(7,7-dimethyl-7H-indeno[1,2-a]phenanthren-9-yl)-N,N-diphenylaniline (TIP), with indenophenanthrene cores and attached arylamine structures, were synthesiz

Construction of Phenanthrenes and Chrysenes from β-Bromovinylarenes via Aryne Diels-Alder Reaction/Aromatization

A highly efficient transition-metal-free general method for the synthesis of polycyclic aromatic hydrocarbons like phenanthrenes and chrysenes (and tetraphene) from β-bromovinylarenes and arynes has been developed. The reactions proceed via an aryne Diels-Alder (ADA) reaction, followed by a facile aromatization. This is the first report on direct construction of chrysenes (and tetraphene) using the ADA approach. Unlike the literature method which is limited to only 9/10-substituted derivatives, this method gives access to a wide variety of functionalized phenanthrenes.

Amine-based compound and organic light-emitting diode including the same

An amine-based compound is represented by Formula 1: An organic light-emitting diode includes a first electrode, a second electrode, and an organic layer between the first electrode and the second electrode. The organic layer includes an emission layer an