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1,2-bis(3,5-difluorophenyl)hydrazine is an organic compound with the chemical formula C12H8F4N2. It is a derivative of hydrazine, featuring two 3,5-difluorophenyl groups attached to the nitrogen atoms. 1,2-bis(3,5-difluorophenyl)hydrazine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the creation of more complex molecules. Due to its reactivity and the presence of fluorine atoms, it can influence the electronic properties and metabolic stability of the final products. The compound is typically synthesized through the reaction of 3,5-difluorobenzene with hydrazine, and it is used in research and development settings to explore new chemical entities with improved properties.

404-12-6

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404-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 404-12-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 404-12:
(5*4)+(4*0)+(3*4)+(2*1)+(1*2)=36
36 % 10 = 6
So 404-12-6 is a valid CAS Registry Number.

404-12-6Relevant academic research and scientific papers

Visible-light-promoted oxidative dehydrogenation of hydrazobenzenes and transfer hydrogenation of azobenzenes

Wang, Xianya,Wang, Xianjin,Xia, Chungu,Wu, Lipeng

supporting information, p. 4189 - 4193 (2019/08/07)

Azo compounds are widely used in the pharmaceutical and chemical industries. Here, we report the use of a non-metal photo-redox catalyst, Eosin Y, to synthesize azo compounds from hydrazine derivatives. The use of visible-light with air as the oxidant makes this process sustainable and practical. Moreover, the visible-light-driven, photo-redox-catalyzed transfer hydrogenation of azobenzenes is compatible with a series of hydrogen donors such as phenyl hydrazine and cyclic amines. Compared with traditional (thermal/transition-metal) methods, our process avoids the issue of over-reduction to aniline, which extends the applicability of photo-redox catalysis and confirms it as a useful tool for synthetic organic chemistry.

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