1287777-24-5

Basic information

• Product Name: tetra-(3-pyridylphenyl)ethylene
• Synonyms: tetra-(3-pyridylphenyl)ethylene;Tetrakis[3-(4-phenylphenyl)pyridine]ethylene;Tetra-(3-pyridylbiphenyl)ethylene
• CAS NO: 1287777-24-5
• Molecular Formula: C₄₆H₃₂N₄
• Molecular Weight: 640.77308
• EINECS: -0
• Mol File: 1287777-24-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 807.9±65.0 °C(Predicted)
• Appearance: /
• Density: 1.187±0.06 g/cm3(Predicted)
• PKA: 5.50±0.10(Predicted)
• CAS DataBase Reference: tetra-(3-pyridylphenyl)ethylene(CAS DataBase Reference)
• NIST Chemistry Reference: tetra-(3-pyridylphenyl)ethylene(1287777-24-5)
• EPA Substance Registry System: tetra-(3-pyridylphenyl)ethylene(1287777-24-5)

Safety Data

• Hazardous Substances Data: 1287777-24-5(Hazardous Substances Data)

Usage

General Description

Tetra-(3-pyridylphenyl)ethylene is a chemical compound, typically used in scientific research, with a particular interest in the field of molecular engineering and organic electronics. Classified as an organic compound, it features a complex structure made of hydrogen, carbon, and nitrogen atoms. As a derivative of ethylene, it belongs to the broad class of compounds known as aromatic ethers which are aromatic compounds containing an ether group substituted with an aromatic group. Typically, it has applications in the creation of advanced materials, particularly in the fabrication of organic semiconductors and light-emitting diodes (LEDs).

Upstream product

• 129013-83-8 3-(4-bromophenyl)pyridine 
• 61326-44-1 1,1,2,2-tetrakis(4-bromophenyl)ethene 
• 329214-79-1 3-(4,4,5,5,-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine 
• 1692-25-7 3-pyridylboronic acid 

Relevant articles and documents

Drum-like Metallacages with Size-Dependent Fluorescence: Exploring the Photophysics of Tetraphenylethylene under Locked Conformations

Materials with aggregation-induced emission (AIE) properties are of growing interest due to their widespread applications. AIEgens, such as tetraphenylethylene units, display varying emission behaviors during their conformational changes. However, the str

Coordination-enhanced luminescence on tetra-phenylethylene-based supramolecular assemblies

Materials with aggregation-induced emission (AIE) properties have received increased attention recently due to their potential applications in light-emitting devices, chemo/biosensors and biomedical diagnostics. In general, AIE requires the forced aggrega

Tetrapyridyl tetraphenylethylenes: Supramolecular building blocks with aggregation-induced emission properties

Two tetrapyridyl-substituted tetraphenylethylenes have been prepared via Suzuki coupling between tetrabromo tetraphenylethylene and 3- or 4-pyridine boronic acid. Both compounds exhibit aggregation-induced emission as determined by solid state fluorescenc