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Benzene, 1-(2-chloro-2-nitroethenyl)-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22013-87-2

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22013-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22013-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22013-87:
(7*2)+(6*2)+(5*0)+(4*1)+(3*3)+(2*8)+(1*7)=62
62 % 10 = 2
So 22013-87-2 is a valid CAS Registry Number.

22013-87-2Downstream Products

22013-87-2Relevant academic research and scientific papers

Chlorination of Conjugated Nitroalkenes with PhICl 2and so 2Cl 2for the Synthesis of α-Chloronitroalkenes

Fadeeva, Anastasia A.,Ioffe, Sema L.,Tabolin, Andrey A.

, p. 2679 - 2688 (2020/11/02)

Chlorination of conjugated nitroalkenes with iodobenzene dichloride or sulfuryl chloride to give target α-chloronitroalkenes in good yields is described. Details of the procedure depend on the donating ability of the nitroalkene substituents. The activity of the described chlorinating agents increases in order 'PhICl 2/Py' 2Cl 2' 2Cl 2/HCl' with the former producing the best yields for highly donating substrates and the latter for non-activated groups. An autocatalytic role of hydrogen chloride and the chemoselectivity of chlorination were also demonstrated.

An expedient synthesis of β-chloro-β-nitroolefin derivatives

Kim, Jae Nyoung,Son, Ji Suk,Lee, Hong Jung,Jung, Keum Shin

, p. 1885 - 1891 (2007/10/03)

β-Chloro-β-nitroolefin derivatives 2 were prepared from the reaction of β-nitroolefins 1 with HCl/DMF/Oxone system in moderate to good yields.

SYNTHESIS OF 2-HALOGENO-2-NITROETHENYLARENES

Aleksiev, D. I.,Ivanova, S. M.

, p. 1845 - 1848 (2007/10/02)

A series of 2-halogeno-2-nitroethenylarenes were obtained as a result of the condensation of halogenonitromethanes with aromatic (heterocyclic) aldehydes in the presence of catalytic amounts of ethylenediamine and also by the addition of halogenonitromethanes to butylarylimines in acetic anhydride.

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