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Structure of 24522-30-3
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2-Cyano-N-[4-(trifluoromethyl)phenyl]acetamide features a trifluoromethyl-substituted phenyl group paired with a cyano-acetamide functionality, delivering enhanced electron-withdrawing character and improved metabolic stability. This structure enables efficient integration into bioactive scaffolds, particularly in medicinal chemistry applications requiring high lipophilicity and resistance to oxidative degradation.
2-Cyano-N-[4-(trifluoromethyl)phenyl]acetamide serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via cyclization reactions. Its trifluoromethylphenyl moiety enhances metabolic stability and lipophilicity, while the nitrile and amide functionalities provide orthogonal reactivity for downstream transformations. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for high-throughput screening campaigns and process-scale synthesis.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: