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Structure of 97305-12-9
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Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate features a conjugated enone system flanked by a sterically hindered difluorophenyl group and an ethyl ester. This electron-deficient β-ketoester integrates readily into Michael additions and Claisen condensations under mild conditions. The ortho-fluorine substitution enhances metabolic stability and modulates electronic properties for use in pharmaceutical intermediates and functional materials synthesis.
Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate serves as a versatile building block in medicinal chemistry, enabling efficient construction of fluorinated heterocycles and bioactive scaffolds. Its α,β-unsaturated ketone functionality facilitates Michael additions, condensations, and cyclizations under mild conditions. The molecule exhibits good bench stability, ease of purification, and compatibility with diverse functional groups, making it well-suited for iterative synthesis campaigns and scale-up applications.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: