883903-22-8

Basic information

• Product Name: 4-(2-ethylhexyl)bromobenzene
• Synonyms: 4-(2-ethylhexyl)bromobenzene
• CAS NO: 883903-22-8
• Molecular Formula: C14H21Br
• Molecular Weight: 269.22054
• EINECS: -0
• Mol File: 883903-22-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(2-ethylhexyl)bromobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-ethylhexyl)bromobenzene(883903-22-8)
• EPA Substance Registry System: 4-(2-ethylhexyl)bromobenzene(883903-22-8)

Safety Data

• Hazardous Substances Data: 883903-22-8(Hazardous Substances Data)

Usage

Chemical Structure

Benzene ring with a bromine atom attached to the 4th carbon atom, and a side chain consisting of two ethyl groups and a hexyl group attached to a different carbon atom on the benzene ring.

Classification

Aromatic hydrocarbon

Common Uses

Intermediate in the production of various industrial chemicals
Research chemical

Toxicity

Should be handled with care
Can pose health risks if not handled properly

Upstream product

• 106-37-6 1.4-dibromobenzene 
• 123-04-6 3-(chloromethyl)heptane 
• 5467-74-3 4-Bromophenylboronic acid 
• 18908-66-2 3-bromomethylheptane 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 1620400-78-3 C₁₇H₂₄N₂ 

Relevant articles and documents

Ultrafast intramolecular energy transfer in a nanostructured organosilicon luminophore based on p -terphenyl and 1,4-bis(5-phenyloxazol-2-yl)benzene

We report on the first experimental and theoretical investigations of ultrafast intramolecular energy transfer for a novel class of highly luminescent materials-nanostructured organosilicon luminophores (NOLs). For this purpose we designed, synthesized an

ORGANIC COMPOUNDS, LIGHE EMITTING DIODE AND LIGHT EMITTING DEVICE HAVING THE COMPOUNDS

The present invention relates to an organic compound having an amine core substituted with three aromatic rings, wherein a part of the three aromatic rings is substituted with a functional group capable of a solution process while the rest of the three aromatic rings is substituted with a hetero-aromatic functional group; and a light-emitting diode and a light-emitting device having the organic compound applied to a light-emitting layer. The organic compound may be used to the light-emitting layer to eliminate the HOMO energy barrier between the light-emitting layer and another light-emitting layer adjacent thereto. Also, the organic compound, when it forms a light-emitting layer in combination with light-emitting particles, may improve interfacial properties between the light-emitting layer and an adjacent layer to improve morphological properties of the light-emitting diode. The organic compound of the present invention, by allowing holes and electrons to be transported and implanted into a light emitting material layer in a balanced manner, may implement light-emitting diodes and light-emitting devices with improved luminance efficiency and capable of low-voltage driving.(110) First electrode(120) Second electrode(AA) Smooth interface morphology ↑COPYRIGHT KIPO 2019

Synthesis and photovoltaic performance of pyrazinoquinoxaline containing conjugated thiophene-based dendrimers and polymers

Pyrazinoquinoxaline-based building blocks were incorporated into both π-conjugated dendrimers and polymers. The dendrimers were synthesized using a convergent/divergent approach whereas the donor/acceptor copolymers were synthesized via Stille cross-coupling reactions. The structurally defined dendrimers and the π-conjugated polymers were investigated with respect to their optical and electronic properties as well as their performance in photovoltaic devices. Because of the presence of the electron-deficient pyrazinoquinoxaline moiety, the absorption spectra of the materials under investigation were red-shifted with respect to the all thiophene-containing materials. Power conversion efficiencies up to 1.7 and 0.8% were obtained from blends of second-generation dendrimers and polymers with PC71BM, respectively.