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Structure of 20577-61-1
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Methyl 2,4-dioxopentanoate is a versatile β-keto ester featuring a reactive enolizable α-position flanked by two carbonyl groups. This structural motif enables facile alkylation and condensation reactions, making it a key building block in the synthesis of substituted pyrones, heterocycles, and complex natural product intermediates under standard conditions.
Methyl 2,4-dioxopentanoate serves as a versatile synthon in organic synthesis, enabling efficient construction of substituted β-keto ester frameworks. Its α,β-unsaturated carbonyl system facilitates Michael additions, aldol condensations, and heterocycle formation under mild conditions. The molecule exhibits good bench stability and compatibility with common functional groups, simplifying purification and integration into multi-step sequences. Functions as a key building block for bioactive heterocycles and natural product derivatives.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: