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Structure of 13984-50-4
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Methyl 5-oxohexanoate is a versatile β-keto ester featuring a ketone group at the C5 position and a methyl ester terminus. This structural motif enables efficient enolization and participation in Claisen condensations, Michael additions, and asymmetric synthesis. The compound exhibits favorable stability under standard conditions and integrates readily into complex molecular architectures.
Methyl 5-oxohexanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to γ-keto ester derivatives and functionalized heterocycles. Its α,β-unsaturated carbonyl motif facilitates Michael additions, aldol reactions, and cyclizations under mild conditions. The methyl ester group provides stability and ease of purification, while the ketone functionality supports subsequent transformations including enolate alkylations and reductive couplings. This compound functions reliably in multi-step syntheses for natural product analogs and pharmaceutical 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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: