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(4-Chloro-phenyl)-(4-trifluoromethyl-phenyl)-diazene is a chemical compound characterized by its diazenyl functional group, which consists of a nitrogen-nitrogen double bond. (4-Chloro-phenyl)-(4-trifluoromethyl-phenyl)-diazene features a 4-chlorophenyl group and a 4-trifluoromethylphenyl group attached to the diazenyl moiety. The 4-chlorophenyl group contains a chlorine atom at the para position, while the 4-trifluoromethylphenyl group has a trifluoromethyl group at the para position. The combination of these substituents results in a molecule with unique electronic and steric properties, which can be relevant in various chemical and pharmaceutical applications.

1959-94-0

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1959-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1959-94-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1959-94:
(6*1)+(5*9)+(4*5)+(3*9)+(2*9)+(1*4)=120
120 % 10 = 0
So 1959-94-0 is a valid CAS Registry Number.

1959-94-0Downstream Products

1959-94-0Relevant academic research and scientific papers

Convenient Electrocatalytic Synthesis of Azobenzenes from Nitroaromatic Derivatives Using SmI2

Zhang, Yu-Feng,Mellah, Mohamed

, p. 8480 - 8486 (2017)

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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