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(E)-2-(4-methoxyphenyl)-1-(5-nitro-2-furyl)ethylene is a synthetic organic compound characterized by a conjugated diene structure. It features a 4-methoxyphenyl group attached to the double bond at one end and a 5-nitro-2-furyl group at the other. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique electronic and steric properties. The presence of the electron-donating methoxy group and the electron-withdrawing nitro group on the phenyl and furyl rings, respectively, contributes to its reactivity and stability. This chemical's structure allows for further functionalization and exploration in the field of organic chemistry, particularly in the development of new compounds with specific biological activities.

72481-45-9

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72481-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72481-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,8 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72481-45:
(7*7)+(6*2)+(5*4)+(4*8)+(3*1)+(2*4)+(1*5)=129
129 % 10 = 9
So 72481-45-9 is a valid CAS Registry Number.

72481-45-9Downstream Products

72481-45-9Relevant academic research and scientific papers

MECHANISM OF ALKENYLATION OF AROMATIC SUBSTRATES WITH 5-NITRO-2-FURYLVINYL BROMIDE

Hrabovsky, Jan,Kovac, Jaroslav,Povazanec, Frantisek

, p. 2013 - 2018 (2007/10/02)

Mechanism has been studied of electrophilic aromatic substitution with (Z)- and (E)-5-nitro-2-furylvinyl bromide in the presence of aluminium(III) chloride.From chemical findings and 1H NMR study it follows that the mechanism can be interpreted as an electrophilic addition-elimination pathway (AdE-E) from the point of view of the vinyl substitution.

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