55035-42-2

Basic information

• Product Name: 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline)
• Synonyms: 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline);9,10-p-bis(p-N,N-diphenylaminostyryl)benzene
• CAS NO: 55035-42-2
• Molecular Formula: C₄₆H₃₆N₂
• Molecular Weight: 616.79144
• Mol File: 55035-42-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 172 °C
• Appearance: /
• CAS DataBase Reference: 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline)(55035-42-2)
• EPA Substance Registry System: 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline)(55035-42-2)

Safety Data

• Hazardous Substances Data: 55035-42-2(Hazardous Substances Data)

Usage

General Description

4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline) is a chemical compound that belongs to the family of bisanilines. It is composed of two 1,4-phenylenebis(ethene-2,1-diyl) groups connected by a nitrogen nucleus, and each group is substituted with a diphenylaniline moiety. 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline) is commonly used as a dopant in organic semiconductors and as a component in the production of electronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells. It exhibits good thermal stability and high charge carrier mobility, making it a promising material for use in various organic electronic applications. However, it is important to handle and use this compound with caution, as it may pose some health and environmental risks if not properly managed.

Upstream product

• 624-38-4 para-diiodobenzene 
• 25069-74-3 N,N-diphenyl-N-(4-vinylphenyl)amine 

Downstream Products

• 119564-42-0 1,4-bis[2-(4-N,N-diphenylaminophenyl) ethyl]benzene 

Relevant articles and documents

TPA-active D-π-D fluorophores with rigid, planar cores from phenylene to indenofluorene and indolocarbazole

A series of D-π-D quadrupolar fluorophores with systematically varied π-conjugated cores were prepared using the Heck reaction and their single- and two-photon photophysical properties were examined. Introduction of extended π-conjugated cores such as indenofluorene/indolocarbazole was found to induce only small shifts in the absorption and emission maxima versus the phenylene linked fluorophore but greatly enhance their single- and two-photon absorption cross-sections. The effects of positional substitution on the properties of the indolocarbazole derivatives were also investigated.