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1-(4-methoxyphenyl)-2-(4-(trifluoromethyl)phenyl)diazene is a chemical compound with the molecular formula C14H11F3N2O. It is an aromatic diazene derivative, characterized by the presence of a diazenyl group (-N=N-) connecting two phenyl rings. One of the phenyl rings is substituted with a methoxy group (-OCH3) at the para position, while the other phenyl ring has a trifluoromethyl group (-CF3) at the para position. 1-(4-methoxyphenyl)-2-(4-(trifluoromethyl)phenyl)diazene is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the preparation of other organic compounds. Due to its unique structure and properties, it has been the subject of research in the field of organic chemistry, particularly in the development of new synthetic methods and applications.

2022-04-0

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2022-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2022-04-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2022-04:
(6*2)+(5*0)+(4*2)+(3*2)+(2*0)+(1*4)=30
30 % 10 = 0
So 2022-04-0 is a valid CAS Registry Number.

2022-04-0Relevant academic research and scientific papers

Convenient Electrocatalytic Synthesis of Azobenzenes from Nitroaromatic Derivatives Using SmI2

Zhang, Yu-Feng,Mellah, Mohamed

, p. 8480 - 8486 (2017/12/08)

The synthesis of azobenzenes has been a long-standing challenge. Their current preparation at a preparative or industrial scale requires stoichiometric amounts of environmentally unfriendly reactants. Herein, we demonstrate that the catalytic use of electrogenerated samarium diiodide (SmI2) could promote, in one-step synthesis, the reduction of nitrobenzenes into azobenzenes in high yields under mild reaction conditions. This catalytic procedure contains many elements satisfying a sustainable chemical process for the preparation of one of the most widely wanted family of chemical compounds. The easy synthetic procedure, and the absence of precious metals, bases, and nonhazardous substances, already makes our catalytic procedure a serious alternative to currently available methods. This is a promising method for the efficient synthesis of both symmetrical and asymmetrical azo compounds with a high functional group tolerance.

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