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(E)-1-carboethoxy-2-(4'-chlorophenyl)-1-nitroethene is a synthetic chemical compound with the molecular formula C11H10ClNO4. It is an organic molecule characterized by a nitro group (-NO2), a chlorophenyl group (C6H4Cl), and a carbethoxy group (-COOCH3) attached to a double-bonded ethene (C2H4) backbone. The "E" in its name indicates that the molecule has a trans configuration, meaning the substituents on the double bond are on opposite sides. (E)-1-carboethoxy-2-(4'-chlorophenyl)-1-nitroethene is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

60859-73-6

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60859-73-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60859-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60859-73:
(7*6)+(6*0)+(5*8)+(4*5)+(3*9)+(2*7)+(1*3)=146
146 % 10 = 6
So 60859-73-6 is a valid CAS Registry Number.

60859-73-6Relevant academic research and scientific papers

Catalytic Enantioselective Synthesis of 3,4,5-Trisubstituted Isoxazoline N-Oxides and Regioselective Synthesis of 3,4,5-Trisubstituted Isoxazoles

Sahoo, Subas Chandra,Pan, Subhas Chandra

supporting information, p. 1385 - 1389 (2019/01/09)

An efficient catalytic asymmetric synthesis of 3,4,5-trisubstituted isoxazoline N-oxides and regioselective synthesis of 3,4,5-trisubstituted isoxazoles has been described. α-Nitrocinnamates and α-nitrobenzophenones were utilized as Michael acceptors resp

Study of geometric isomerism of ethyl β-aryl(hetaryl)-α-nitroacrylates by 1H NMR spectroscopy method

Baichurin,Berestovitskaya,Baichurina,Aboskalova,Berestovitskaya

, p. 51 - 57 (2016/03/12)

Features of Z→E isomerization of ethyl α-nitrocinnamates as well as their furyl and thienyl heteroanalogs depending on the nature of the substituent in the β-position of α-nitroacrylates, deuterated solvent and duration of exposure of the sample were stud

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