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Structure of 915720-54-6
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1-(5-Fluoropyridin-2-yl)ethanone features a fluorinated pyridine ring linked to a ketone-bearing ethyl group, enabling direct integration into pharmaceutical intermediates. The electron-deficient aromatic system enhances reactivity in nucleophilic substitution and transition-metal-catalyzed coupling processes. This bench-stable compound serves as a key building block for bioactive heterocycles.
1-(5-Fluoropyridin-2-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. Its ketone functionality supports direct functionalization, including nucleophilic additions and enolization reactions, while the 5-fluoropyridine moiety offers enhanced metabolic stability and favorable electronic properties. The compound exhibits excellent bench stability and compatibility with standard synthetic protocols, facilitating integration into multi-step synthesis workflows for API development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P405-P501
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Lot numbers can be found on the outside label of a product: