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((Perfluorophenyl)methylene)dibenzene is a complex organic compound characterized by its unique molecular structure. It features a dibenzene core, which is essentially two benzene rings fused together, with a perfluorophenyl group attached to it through a methylene bridge. The perfluorophenyl group consists of a benzene ring where all the hydrogen atoms have been replaced by fluorine atoms, which significantly influences the compound's chemical and physical properties. This molecule is known for its high thermal stability, resistance to chemical reactions, and unique electronic properties, making it a subject of interest in various fields, including materials science and organic chemistry. Due to its specific structure, it may have potential applications in the development of new materials with tailored properties, such as high-performance polymers or specialized coatings.

4707-19-1

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4707-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4707-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4707-19:
(6*4)+(5*7)+(4*0)+(3*7)+(2*1)+(1*9)=91
91 % 10 = 1
So 4707-19-1 is a valid CAS Registry Number.

4707-19-1Relevant academic research and scientific papers

Copper(I)-Catalyzed Alkylation of Polyfluoroarenes through Direct C - H Bond Functionalization

Xu, Shuai,Wu, Guojiao,Ye, Fei,Wang, Xi,Li, Huan,Zhao, Xia,Zhang, Yan,Wang, Jianbo

, p. 4669 - 4672 (2015/04/14)

The copper(I)-catalyzed alkylation of electron-deficient polyfluoroarenes with N-tosylhydrazones and diazo compounds has been developed. This reaction uses readily available starting materials and is operationally simple, thus representing a practical method for the construction of C(sp2) - C(sp3) bonds with polyfluoroarenes through direct C - H bond functionalization. Mechanistically, copper(I) carbene formation and subsequent migratory insertion are proposed as the key steps in the reaction pathway.

The Reduction of Fluorine-containing Triarylmethanols by Formic Acid

Andrews, Adrian F.,Mackie, Raymond K.,Walton, John C.

, p. 96 - 102 (2007/10/02)

Triarylmethanols containing one or more fluorine substituents in the para-positions are converted by 90 percent formic acid into a mixture of the fluorine-containing triarylmethane, and a second component in which one fluorine has been replaced by a hydro

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