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Structure of 52661-56-0
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(E)-3-(5-Nitrofuran-2-yl)acrylaldehyde features a conjugated enal system fused to a nitro-substituted furan ring, delivering high electrophilicity at the aldehyde terminus. This electron-deficient scaffold enables efficient Michael additions and Diels-Alder cycloadditions, serving as a key building block in heterocyclic synthesis. The planar structure enhances π-stacking interactions in supramolecular systems.
(E)-3-(5-Nitrofuran-2-yl)acrylaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to fused polycyclic systems via Diels-Alder and Michael addition reactions. The conjugated enal functionality exhibits high reactivity with nucleophiles and dienes, while the nitrofuran moiety provides inherent stability and facilitates downstream functionalization. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: