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Structure of 865449-63-4
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1-(4-Bromo-5-fluoro-2-hydroxyphenyl)ethanone features a hydroxylated aromatic core with orthogonal halogen substituents, enabling selective functionalization in late-stage derivatization. The ketone moiety provides a reactive handle for nucleophilic addition, while the electron-withdrawing bromo- and fluoro-groups enhance electrophilicity at adjacent positions. This scaffold offers high stability under standard bench conditions and facilitates integration into complex molecular architectures.
1-(4-Bromo-5-fluoro-2-hydroxyphenyl)ethanone serves as a versatile building block in medicinal chemistry, enabling direct incorporation of halogenated phenolic motifs into target molecules. The ketone functionality facilitates nucleophilic addition and enolization, while the ortho-hydroxyl group supports intramolecular coordination or directed functionalization. Its bench-stable nature and compatibility with standard cross-coupling protocols make it well-suited for iterative synthesis of bioactive heterocycles and API intermediates.
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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: