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Structure of 58101-23-8
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Ethyl 3-(2,4-difluorophenyl)-3-oxopropanoate features a conjugated β-keto ester framework flanked by electron-deficient aryl substituents, enabling efficient enolization and nucleophilic addition. This bench-stable reagent integrates readily into heterocyclic synthesis pathways, particularly in the construction of fluorinated pyran and quinoline derivatives under mild conditions.
Ethyl 3-(2,4-difluorophenyl)-3-oxopropanoate serves as a versatile β-keto ester building block for constructing fluorinated heterocycles and bioactive scaffolds. Its electrophilic α-carbon facilitates nucleophilic addition, condensation, and cyclization reactions under standard conditions. The 2,4-difluorophenyl moiety enhances metabolic stability and modulates electronic properties, making it valuable in medicinal chemistry campaigns. Bench-stable and amenable to straightforward purification, it functions reliably in multistep synthesis workflows.
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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 : P233-P260-P261-P264-P271-P280-P302+P352-P304+P340-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: