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

• 119-61-9 benzophenone 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 919789-80-3 (2-(4-aminophenyl)ethene-1,1,2-triyl)tribenzene 
• 881-42-5 diphenylmethyllithium 
• 1016-77-9 3-bromobenzophenone 
• 1607-57-4 Triphenylvinyl bromide 
• 5467-74-3 4-Bromophenylboronic acid 
• 101-81-5 Diphenylmethane 
• 2116-36-1 1-benzyl-4-bromo-benzene 
• 1391632-33-9 C₂₆H₂₁BrO 
• 1137-41-3 (4-aminophenyl)(phenyl)methanone 
• 589-87-7 1,4-bromoiodobenzene 
• 501-65-5 diphenyl acetylene 
• 98-80-6 phenylboronic acid 

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 
• 1274702-35-0 9-(4-bromophenyl)-10-phenylphenanthrene 
• 1332830-69-9 4'-[4'-(1,2,2-triphenylvinyl)-(1,1'-biphenyl)-4-yl]-2,2':6',2''-terpyridine 
• 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 
• 1416785-75-5 1,4-dimethyl-2,5-bis[4-(1,2,2-triphenylvinyl)phenyl]benzene 
• 1416785-74-4 1,4-bis(hexyloxy)-2,5-bis[4-(1,2,2-triphenylvinyl)phenyl]benzene 
• 1416785-73-3 1,5-bis[4-(1,2,2-triphenylvinyl)phenyl]naphthalene 
• 174676-07-4 9,10-bis(4-(1,2,2-triphenylvinyl)phenyl)anthracene 
• 1426396-32-8 N-(4-(1,2,2-triphenylvinyl)phenyl)benzenamine 

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

Enantiomeric selectivity of ruthenium (II) chiral complexes with antitumor activity, in vitro and in vivo

Different enantiomers of chiral drugs show distinctive activities. Here, a pair of chiral ruthenium Λ-[Ru(phen)2(TPEPIP)]2+ (Λ-Ru), and Δ-[Ru(phen)2(TPEPIP)]2+ (Δ-Ru) (phen = 1,10-phenanthroline; TPEPIP = 2-(4′-(1,2,2-triphenylvinyl)-[1,1′-biphenyl]-4-yl)-1H-imidazo[4,5-f][1,10]phenanthroline) compounds have been prepared and characterized. Both have aggregation-induced emission characteristics, although Λ-Ru exhibits much higher activity, towards duplex DNA extracted from SGC-7901 cancer cells. In vitro experiments demonstrate that both Λ-Ru and Δ-Ru can induce the apoptosis of tumor cells with Λ-Ru showing greater activity than Δ-Ru. Λ-Ru aggregates in the cell nucleus of SGC-7901 within 5 h which shows that nucleic acids may be the effective target of Λ-Ru. In vivo experiments with nude mice showed that Λ-Ru can inhibit the growth and proliferation of a tumor, in tumor-bearing mice as well as targeting the tumor site, as demonstrated by fluorescence. These results demonstrate the dual-function of Λ-Ru, which could be used for real-time visualization of a chemotherapeutic agent.

Tetraphenylethylene AIEgen bearing thiophenylbipyridine receptor for selective detection of copper(ii) ion

Highly emissive tetraphenylethylene chromophore appended thiophenylbipyridine pendant as a receptor (1) site has been successfully synthesized via a multistep reaction pathway. The synthesized chromophore 1 was well characterized by modern spectroscopy. I