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2,3-bis4-[(4-fluorophenyl)ethynyl]phenylquinoxaline is a complex organic chemical compound characterized by its polyaromatic hydrocarbon structure. It features two quinoxaline rings linked by phenyl groups, each of which is substituted with fluorophenyl and ethynyl moieties. This unique molecular architecture endows it with distinctive electronic and optical properties, making it a candidate of interest for various high-tech applications.

194936-20-4

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194936-20-4 Usage

Uses

Used in Organic Electronic Devices:
2,3-bis4-[(4-fluorophenyl)ethynyl]phenylquinoxaline is used as a component in organic electronic devices for its electronic and optical properties. It is particularly suitable for applications in organic light-emitting diodes (OLEDs), where its ability to emit light upon the application of an electric current is utilized. Additionally, its properties make it a potential candidate for organic photovoltaics (OPVs), where it can contribute to the conversion of light into electricity, and organic field-effect transistors (OFETs), where it can be involved in the modulation of electrical current.
Used in Fluorescent Probes for Biological Imaging:
In the field of biological imaging, 2,3-bis4-[(4-fluorophenyl)ethynyl]phenylquinoxaline is studied for its potential as a fluorescent probe. Its unique molecular structure allows it to be used for visualizing and tracking specific biological processes or structures within living organisms, which is crucial for advancing our understanding of biological systems and for diagnostic applications.
Used in Molecular Sensors:
2,3-bis4-[(4-fluorophenyl)ethynyl]phenylquinoxaline is also considered for use in molecular sensors due to its distinctive properties. Its sensitivity to changes in the environment or interactions with other molecules can be harnessed to create sensors that can detect specific substances or conditions, which is valuable in fields such as environmental monitoring, medical diagnostics, and chemical analysis.
Further research is necessary to fully explore the potential applications and properties of 2,3-bis4-[(4-fluorophenyl)ethynyl]phenylquinoxaline in various fields, ensuring that its use is optimized and its benefits are fully realized.

Check Digit Verification of cas no

The CAS Registry Mumber 194936-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,9,3 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 194936-20:
(8*1)+(7*9)+(6*4)+(5*9)+(4*3)+(3*6)+(2*2)+(1*0)=174
174 % 10 = 4
So 194936-20-4 is a valid CAS Registry Number.

194936-20-4Downstream Products

194936-20-4Relevant academic research and scientific papers

New activated bisfluoroaromatic compounds

Rusanov,Keshtov,Belomoina,Mikitaev,Sarkisyan,Keshtova

, p. 777 - 779 (1997)

Bis(p-fluorophenylethynyl) derivatives were obtained by the reaction of bisbromoaromatic compounds with p-fluorophenylacetylene in the presence of a Pd catalyst. Subsequent oxidation of these products using an I2-DMSO system led to new bis(p-fl

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