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(Z)-3-(2-chlorophenyl)-2-(4-chlorophenyl)acrylonitrile is an organic compound characterized by its molecular formula C15H9Cl2N. (Z)-3-(2-chlorophenyl)-2-(4-chlorophenyl)acrylonitrile features a conjugated triple bond (C≡C) between two phenyl rings, with one phenyl ring substituted at the 2-position with a chlorine atom and the other at the 4-position. The molecule exhibits a Z-configuration, indicating that the two chlorine atoms are on the same side of the double bond. It is a colorless to pale yellow solid with a melting point of 70-72°C. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, such as herbicides and insecticides, due to its reactive nature and potential to form stable derivatives.

2958-44-3

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2958-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2958-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2958-44:
(6*2)+(5*9)+(4*5)+(3*8)+(2*4)+(1*4)=113
113 % 10 = 3
So 2958-44-3 is a valid CAS Registry Number.

2958-44-3Downstream Products

2958-44-3Relevant academic research and scientific papers

Direct C–S Bond Functionalization of Benzyl Mercaptan

Choudhuri, Khokan,Mal, Prasenjit,Pramanik, Milan

, (2020)

Cleavage of a C–S bond of benzyl mercaptan led to formation of a new C–C bond during (Z)-selective alkenylation of nitriles using 1,10-phenanthroline as organocatalyst and tBuOK as a base. Furthermore, we have shown that the cascaded functionalization of benzylic C–S and aryl–halide bonds could be done in one pot. 1H NMR study and kinetic experiments also helped to establish the mechanism of the reaction.

CuCl-catalyzed regio- and stereoselective aminohalogenation of α,β-unsaturated nitriles

Han, Jian-Lin,Zhi, San-Jun,Wang, Le-Yong,Pan, Yi,Li, Guigen

, p. 1332 - 1337 (2008/09/17)

α,β-Unsat1urated nitriles were found to be suitable substrates for aminochlorination with N,N-dichloro-p-toluenesulfonamide (4-TsNCl 2) in the presence of CuCl as the catalyst (10 mol-%) and 4 A molecular sieves. The reaction is very convenient

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