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Structure of 404-24-0
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2,2,2-Trifluoro-N-phenylacetamide features a trifluoromethyl group flanking a carbonyl-linked phenylamine moiety, delivering enhanced stability and lipophilicity. This structural combination facilitates efficient integration into bioactive scaffolds, particularly in medicinal chemistry applications requiring metabolic resistance and membrane permeability.
2,2,2-Trifluoro-N-phenylacetamide serves as a stable, bench-ready building block for trifluoromethylated aromatic amides. It enables direct incorporation of the trifluoromethyl group into complex scaffolds via standard amide coupling protocols or nucleophilic substitution reactions. The molecule exhibits excellent functional group tolerance and facilitates purification due to its crystalline nature, making it well-suited for iterative synthesis in medicinal chemistry and process development 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: