34699-28-0

Basic information

• Product Name: 1-(4-BroMophenyl)-1,2,2-triphenylethylene
• Synonyms: 1-(4-BroMophenyl)-1,2,2-triphenylethylene;1-Bromo-4-(1,2,2-triphenylethenyl)benzene;1-(4-Bromophenyl)-1,2,2-triphenylethene;(2-(4-bromophenyl)ethene-1,1,2-triyl)tribenzene;TPE-Br
• CAS NO: 34699-28-0
• Molecular Formula: C₂₆H₁₉Br
• Molecular Weight: 411
• Mol File: 34699-28-0.mol
• Article Data: 92

Chemical Properties

• Melting Point: 157.0 to 161.0 °C
• Boiling Point: 460.9±14.0 °C(Predicted)
• Appearance: /
• Density: 1.278±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• Solubility: soluble in Toluene
• CAS DataBase Reference: 1-(4-BroMophenyl)-1,2,2-triphenylethylene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-BroMophenyl)-1,2,2-triphenylethylene(34699-28-0)
• EPA Substance Registry System: 1-(4-BroMophenyl)-1,2,2-triphenylethylene(34699-28-0)

Safety Data

• Hazardous Substances Data: 34699-28-0(Hazardous Substances Data)

Usage

General Description

1-(4-Bromophenyl)-1,2,2-triphenylethylene, also known as Brominated stilbene, is an organic compound that belongs to the group of stilbene derivatives. It is a white to off-white solid with a molecular formula C24H19Br and a molecular weight of 371.31 g/mol. This chemical is used in organic synthesis and as a liquid crystal material for displays and optoelectronic applications. It is also known for its potential application as a fluorescent probe for the detection of metal ions. Additionally, 1-(4-Bromophenyl)-1,2,2-triphenylethylene has been studied for its potential biological activities, including its role as an anti-tumor agent and in the treatment of neurodegenerative diseases.

Upstream product

• 1137-41-3 (4-aminophenyl)(phenyl)methanone 
• 1607-57-4 Triphenylvinyl bromide 
• 5467-74-3 4-Bromophenylboronic acid 
• 71-43-2 benzene 
• 586-76-5 4-Bromobenzoic acid 
• 1016-77-9 3-bromobenzophenone 
• 108-86-1 bromobenzene 
• 101-81-5 Diphenylmethane 
• 2116-36-1 1-benzyl-4-bromo-benzene 
• 881-42-5 diphenylmethyllithium 
• 119-61-9 benzophenone 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 1391632-33-9 C₂₆H₂₁BrO 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 1260865-91-5 4,4,5,5–tetramethyl–2–(4–(1,2,2–triphenylvinyl)phenyl)–1,3,2–dioxaborolane 
• 1227040-87-0 4-(1,2,2-triphenylvinyl)phenylboronic acid 
• 1225493-18-4 (2-(4-ethynylphenyl) ethane-1,1,2-triyl)tribenzene 
• 1351272-41-7 (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene 
• 1351272-44-0 C₂₈H₂₀Br₂ 
• 1289218-74-1 [1-(4-carbaldehydephenyl)-1,2,2-triphenyl]ethylene 
• 1421768-47-9 (E)-4-(4-(1,1,2-triphenylvinyl)styryl)pyridine 
• 1426396-32-8 N-(4-(1,2,2-triphenylvinyl)phenyl)benzenamine 
• 1598375-26-8 N-(4-(1,2,2-triphenylvinyl)-phenyl)naphthalen-1-amine 

Relevant articles and documents

High-Performance Emission/Color Dual-Switchable Polymer-Bearing Pendant Tetraphenylethylene (TPE) and Triphenylamine (TPA) Moieties

Electrofluorochromic (EFC) materials have aroused great interest owing to their interesting ability of tuning fluorescence in response to the applied potential. However, some crucial characteristics, such as response speed, fluorescence contrast, and swit

Triphenylethylene benzimidazole derivatives with aggregation-induced emission (AIE) characteristics: An effect of the aryl linker and application in cell imaging

Three triphenylethylene benzimidazole derivatives TPT-BI, TPPT-BI and TPB-BI with aggregation-induced emission properties were synthesized, and the effect of connecting aromatic rings was studied. Among these TPT-based luminescent agents, TPT-BI showed th

Aggregation-induced emission molecular compound, preparation method and application thereof

The invention discloses an aggregation-induced emission molecular compound. The aggregation-induced emission molecular compound comprises a monosubstituted tetraphenyl ethylene derivative taking tetraphenyl ethylene as a skeleton, or a heavy atom-containi

Biocompatible and noncytotoxic nucleoside-based AIEgens sensor for lighting-up nucleic acids

Aggregation-induced emission luminogens (AIEgens) have been used in biomacromolecules detection. Herein, TPE-dC and TPE-dU acted as the nucleoside-based AIEgens sensors in the first case, which can be used to detect ctDNA and rRNA in vitro and light up th