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Structure of 711-38-6
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4-Trifluoroacetylanisole features a para-trifluoroacetyl group appended to an aromatic ring, delivering enhanced electron-withdrawing character and improved metabolic stability. This trifluoromethylated aryl ketone integrates readily into synthetic sequences requiring polar, sterically accessible functional handles. The molecule exhibits robust bench stability and compatibility with standard reaction conditions in medicinal chemistry workflows.
4-Trifluoroacetylanisole serves as a versatile building block in medicinal chemistry, enabling efficient access to trifluoromethylated aryl scaffolds. Its stability under standard reaction conditions and compatibility with palladium-catalyzed cross-coupling reactions facilitate the construction of complex biaryl architectures. The trifluoroacetyl group provides enhanced metabolic stability and modulates electronic properties, making it valuable for lead optimization in pharmaceutical development.
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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: