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Structure of 1065076-49-4
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This fluorinated phenyl ketone features a hydroxy and methoxy group positioned ortho to the carbonyl, enhancing polarity and enabling hydrogen bonding. The 2-fluoro substitution imparts electron-withdrawing character, stabilizing adjacent reaction intermediates. Its bench-stable nature supports reliable use in synthetic transformations involving nucleophilic addition or coupling reactions under standard conditions.
1-(2-Fluoro-4-hydroxy-5-methoxyphenyl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles and pharmaceutical scaffolds. Its phenolic hydroxyl group facilitates direct derivatization, while the ketone functionality supports nucleophilic addition and condensation reactions. The molecule exhibits good bench stability and compatibility with common protecting group strategies, making it suitable for multi-step synthesis workflows requiring functional group tolerance and predictable reactivity.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: