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Structure of 7152-15-0
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Ethyl 4-methyl-3-oxopentanoate features a β-keto ester scaffold with a methyl-substituted α-carbon, enabling facile enolization and nucleophilic addition. This structural motif supports efficient C–C bond formation in multicomponent reactions and serves as a key building block for heterocyclic synthesis under mild conditions.
Ethyl 4-methyl-3-oxopentanoate serves as a versatile β-keto ester building block in synthetic organic chemistry, enabling efficient construction of substituted cyclohexanones and heterocyclic scaffolds via intramolecular aldol condensation or Michael additions. Its well-defined enolization behavior and compatibility with standard catalytic systems facilitate reliable functional group manipulation. The molecule’s bench-stable nature and straightforward purification support scalable synthesis workflows for medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Warning
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UN#: 3272
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: