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Structure of 84331-14-6
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1-(6-Fluoropyridin-3-yl)ethanone features a fluorinated pyridine ring paired with a ketone-functionalized ethyl side chain, enabling direct integration into heterocyclic synthesis. The electron-deficient aromatic core enhances reactivity in nucleophilic substitution and transition metal-catalyzed coupling reactions. This bench-stable compound serves as a key building block for pharmaceutical intermediates and functional materials.
1-(6-Fluoropyridin-3-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles via nucleophilic substitution or palladium-catalyzed coupling. The fluorinated pyridine moiety enhances metabolic stability and modulates electronic properties, while the acetyl group provides a handle for further functionalization. Bench-stable and compatible with standard purification techniques, it facilitates scalable synthesis of target molecules in drug discovery programs.
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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: