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Structure of 53090-43-0
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Ethyl 3-(3,4-dichlorophenyl)-3-oxopropanoate features a conjugated enone system flanked by electron-withdrawing ester and aryl groups, enabling efficient Michael addition reactions. This bench-stable reagent integrates readily into synthetic sequences requiring ketone-based electrophilic coupling.
Ethyl 3-(3,4-dichlorophenyl)-3-oxopropanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted cyclohexanones and heterocyclic scaffolds via Claisen condensation and related transformations. Its dual electrophilic functionalities—ketone and ester—support sequential functionalization under mild conditions, while the 3,4-dichlorophenyl group enhances metabolic stability and provides a handle for further derivatization in medicinal chemistry applications. The compound exhibits excellent bench stability and facilitates straightforward purification by standard chromatographic methods.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: