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Structure of 5711-41-1
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4-(4-Methoxyphenyl)-4-oxobut-2-enoic acid features a conjugated enone system linked to a para-methoxyphenyl group, enabling efficient integration into Michael addition cascades. The electron-rich aromatic moiety enhances solubility and reactivity in polar media, while the α,β-unsaturated ketone serves as a key electrophilic handle for bioconjugation and synthetic transformations under mild conditions.
4-(4-Methoxyphenyl)-4-oxobut-2-enoic acid serves as a versatile synthetic building block for conjugated enone systems and heterocyclic scaffolds. Its α,β-unsaturated ketone functionality enables Diels-Alder reactions, Michael additions, and condensation processes under mild conditions. The methoxyphenyl group provides steric and electronic modulation, enhancing solubility and reactivity in multi-step synthesis. Bench-stable and readily purified by recrystallization, it functions effectively in medicinal chemistry campaigns requiring extended conjugation or electrophilic carbon centers.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: