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Structure of 1823-63-8
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2,2,2-Trifluoro-1-(4-hydroxyphenyl)ethanone features a trifluoromethyl group flanking a phenolic hydroxyl, delivering enhanced electron-withdrawing character and improved metabolic stability. This scaffold integrates readily into bioactive molecules requiring polar, lipophilic domains with controlled solubility and resistance to oxidative degradation under standard conditions.
2,2,2-Trifluoro-1-(4-hydroxyphenyl)ethanone serves as a valuable building block in medicinal chemistry, enabling the synthesis of fluorinated aryl ketones via standard condensation and coupling reactions. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the phenolic hydroxyl facilitates further derivatization. Its bench-stable nature and compatibility with common protecting group strategies streamline downstream functionalization in API 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-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: