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Structure of 56041-57-7
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1-(2,3-Dichlorophenyl)ethanone features a dichlorinated aromatic ring fused to a ketone-bearing ethyl side chain, delivering enhanced lipophilicity and metabolic stability. This configuration supports direct integration into bioactive scaffolds, particularly in medicinal chemistry campaigns targeting CNS-penetrant molecules. The ortho-dichloro substitution pattern influences electronic distribution and steric profile, enabling predictable reactivity in nucleophilic addition and coupling processes under standard conditions.
1-(2,3-Dichlorophenyl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient construction of biologically relevant scaffolds. Its aryl ketone functionality supports standard transformations including nucleophilic additions, reductions, and coupling reactions. The dichloro substitution pattern enhances metabolic stability and modulates lipophilicity, offering favorable properties for drug discovery applications. This compound exhibits excellent bench stability and is compatible with common purification 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: