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Structure of 10304-09-3
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Potassium 2-methoxy-2-oxoacetate delivers a reactive enolate equivalent for C–C bond formation, featuring enhanced solubility in polar solvents and stability under ambient conditions. This bench-stable reagent enables efficient aldol-type reactions without requiring cryogenic temperatures, streamlining synthetic access to β-hydroxy esters and related building blocks in complex molecule assembly.
Potassium 2-methoxy-2-oxoacetate serves as a reliable synthon for α-alkoxy-α-keto ester derivatives, enabling efficient access to key intermediates in heterocyclic synthesis and carbonylative transformations. Its bench-stable solid form facilitates handling and purification, while the methoxy-substituted acetyl group exhibits predictable reactivity in nucleophilic addition and condensation reactions. Functions effectively in standard organic workflows requiring controlled enolization or Michael acceptor behavior.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H319-H334
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Precautionary Statements : P261-P264-P280-P285-P501
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Lot numbers can be found on the outside label of a product: