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1,2-di(2'-anthraquinoyl)ethylene is a synthetic organic compound characterized by its unique molecular structure, which consists of an ethylene backbone with two anthraquinone moieties attached to the 1 and 2 positions. Anthraquinone is a derivative of anthracene, a tricyclic aromatic hydrocarbon, and is known for its versatile chemical properties. 1,2-di(2'-anthraquinoyl)ethylene is of interest in various fields, including materials science and chemistry, due to its potential applications in the development of new dyes, pigments, and other specialty chemicals. The specific arrangement of the anthraquinone groups on the ethylene backbone can influence the compound's reactivity, solubility, and other physical properties, making it a subject of study for chemists looking to understand and exploit its unique characteristics.

4392-72-7

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4392-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4392-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4392-72:
(6*4)+(5*3)+(4*9)+(3*2)+(2*7)+(1*2)=97
97 % 10 = 7
So 4392-72-7 is a valid CAS Registry Number.

4392-72-7Relevant academic research and scientific papers

Ions derived from dianthrylethane species. How the mode of linking affects the intramolecular electron transfer

Becker, Bardo,Bohnen, Angelika,Ehrenfreund, Marianne,Wohlfarth, Werner,Sakata, Yoshiteru,Huber, Walter,Müllen, Klaus

, p. 1121 - 1127 (2007/10/02)

Chemical and electrochemical reduction of dianthryl compounds affords mono-, di-, tri-, and tetraanions via successive electron-transfer processes. The diamagnetic or paramagnetic ions are characterized by NMR and ESR spectroscopy, respectively, by cyclic voltammetry, and by quenching reactions. The title dianthryl systems have in common that two anthracene units are linked by ethane bridges in a sterically variable fashion. It appears that the mode of linking drastically affects the rate of intramolecular electron-transfer processes in radical monoanions as well as the charge-storage behavior.

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