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Structure of 623-15-4
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4-(Furan-2-yl)but-3-en-2-one features a conjugated enone system linked to a furan ring, enabling participation in Diels-Alder reactions and cross-coupling processes. This electron-deficient dienophile integrates readily into synthetic routes for heterocyclic architectures, offering high reactivity under mild conditions with predictable regioselectivity.
4-(Furan-2-yl)but-3-en-2-one serves as a versatile building block in heterocyclic synthesis, leveraging its α,β-unsaturated ketone functionality for Michael additions and cycloaddition reactions. The conjugated system enables efficient integration into fused polycyclic frameworks, while the furan moiety provides orthogonal reactivity for downstream modifications. Bench-stable and amenable to standard purification methods, it functions reliably in synthetic sequences requiring precise regiocontrol and functional group compatibility.
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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+H312+H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: