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Structure of 2854-10-6
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tert-Butyl 4-oxopentanoate features a ketone-functionalized aliphatic chain flanked by a robust tert-butyl ester group, enabling straightforward deprotection and integration into complex molecular architectures. This stable, bench-ready reagent facilitates efficient access to β-keto ester intermediates through controlled hydrolysis or reduction pathways.
tert-Butyl 4-oxopentanoate serves as a versatile synthon in synthetic organic chemistry, enabling efficient access to γ-keto ester derivatives and functionalized heterocycles. Its α,β-unsaturated ketone moiety facilitates Michael additions and aldol-type condensations, while the tert-butyl ester group offers excellent bench stability and ease of subsequent deprotection under mild acidic conditions. The molecule functions reliably in multistep sequences requiring orthogonal functionality and is widely employed in the construction of bioactive scaffolds and complex natural product intermediates.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: