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Structure of 321-37-9
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1-(4-Chlorophenyl)-2,2,2-trifluoroethan-1-one features a trifluoromethyl ketone group flanked by an electron-deficient chlorophenyl ring, enabling efficient coupling in cross-coupling reactions. This bench-stable compound serves as a key building block for fluorinated aromatic synthons in medicinal chemistry and materials science.
1-(4-Chlorophenyl)-2,2,2-trifluoroethan-1-one serves as a valuable building block in synthetic organic chemistry, enabling efficient access to fluorinated aryl ketones and heterocyclic scaffolds. Its trifluoromethyl ketone functionality exhibits high reactivity in nucleophilic additions and condensation reactions, with excellent bench stability and straightforward purification. This compound functions effectively in standard coupling and cyclization protocols, offering predictable reactivity for medicinal chemistry and process development 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: