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Structure of 5308-63-4
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1-(5-Methylpyridin-2-yl)ethanone features a pyridine ring bearing a methyl group at the 5-position and an acetyl substituent at the 2-position, delivering a sterically accessible, electron-deficient heterocyclic scaffold. This configuration enables direct incorporation into pharmaceutical intermediates and ligand frameworks, offering enhanced solubility in polar organic solvents and stability under standard bench conditions.
1-(5-Methylpyridin-2-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-containing scaffolds via standard functional group interconversions. Its stability under routine reaction conditions and compatibility with common coupling protocols facilitate straightforward integration into complex molecular architectures. The ketone functionality reacts selectively with nucleophiles and participates in transition-metal-catalyzed transformations, making it valuable for constructing 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: