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Usage

Uses

Used in Optoelectronic Applications:
Tetrakis[4-(dimethylamino)phenyl]ethene is used as a component in the development of organic light-emitting diodes (OLEDs) for its strong fluorescence and high quantum yield.
Used in Chemical Sensors:
Tetrakis[4-(dimethylamino)phenyl]ethene is used as a sensing material in chemical sensors due to its unique photophysical properties.
Used in Biological Imaging:
Tetrakis[4-(dimethylamino)phenyl]ethene is used as a fluorescent tag in biological imaging for its strong fluorescence and high quantum yield.
Used in Bioconjugation Chemistry:
Tetrakis[4-(dimethylamino)phenyl]ethene is used as a fluorescent tag in bioconjugation chemistry for its strong fluorescence and high quantum yield.
Used in Research and Development:
Tetrakis[4-(dimethylamino)phenyl]ethene is used in research and development for its potential applications in various fields, including materials science, chemistry, and biology.

Upstream product

• 19422-49-2 1,1,2,2-tetrakis<4-(dimethylamino)phenyl>-1,2-ethanediol 
• 101-61-1 4,4'-methylene-bis(N,N-dimethylaniline) 
• 7647-01-0 hydrogenchloride 
• 6483-79-0 dichloro-bis-(4-dimethylamino-phenyl)-methane 
• 67-64-1 acetone 
• 64-19-7 acetic acid 
• 67-66-3 chloroform 
• 7732-18-5 water 
• 86669-21-8 tetrakisethylene dichloride 
• 7664-93-9 sulfuric acid 
• 859776-90-2 1,1,2,2-tetrakis-(4-dimethylamino-phenyl)-ethanol 
• 14500-16-4 4'-(dimethylamino)-2,2,2-trisacetophenone 
• 1226-46-6 thiomichlersketone 
• 90-94-8 bis(p-dimethylaminophenyl)methanone 

Downstream Products

• 107329-31-7 1,1,2,2-tetrakis-(4-dimethylamino-phenyl)-ethane 
• 86669-21-8 tetrakisethylene dichloride 

Relevant academic research and scientific papers

Some Biological Properties of the Impure Dichloride Salt of Tetrakisethylene and a Pinacolone

The impure dichloride salt of tetrakisethylene and a pinacolone that is a substituted acetophenone show several biological properties, one of which is activity against lymphosarcoma in mice.The involvement, if any, of free radicals in the biological properties of these substances is discussed.

Identification of the donor-substitution effect of tetraphenylethylene AIEgen: Synthesis, photophysical property analysis, and bioimaging applications

Various aggregation-induced emission luminogen (AIEgen) derivatives based on TPE (tetraphenylethylene) containing the electron-donating moiety (–NMe2, –OMe) and bromine (–Br) moiety were prepared, which are key intermediates for tuning the emis

Aggregation-induced emission rotors: Rational design and tunable stimuli response

A novel molecular design strategy is provided to rationally tune the stimuli response of luminescent materials with aggregation-induced emission (AIE) characteristics. A series of new AIE-active molecules (AIE rotors) are prepared by covalently linking di

Stereoselective synthesis of olefins by a reductive coupling reaction

Ketones and aldehydes are converted to symmetrical and (E)-olefins (1-15) by reaction with 2,4-bis(phenyl)-1,3-diselenadiphosphetane-2,4-diselenide (PhPSe2)2, Woollins' reagent, in refluxing toluene; use of diketones was demonstrated by the reaction of PhC(O)CH2C(O)Ph which gives 1,2,4,5-tetraphenylbenzene (16) in 83% yield. The Royal Society of Chemistry 2007.

Ytterbium Metal Mediated Desulfurization and Coupling Reaction of Diaryl Thioketones

Diaryl thioketones are selectively reduced with ytterbium metal to diarylmethanethiols, diarylmethanes or tetraarylethylenes, via thiometallacycle intermediates which undergo electrophilic coupling at thiocarbonyl carbon and sulfur.