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Structure of 1246349-89-2
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1-(2,4-Dichloropyridin-3-yl)ethanone features a pyridine ring bearing two chlorine substituents at the 2- and 4-positions, creating a highly electron-deficient heterocyclic core. This structure integrates a ketone group at the 3-position, enabling direct coupling in cross-coupling reactions or nucleophilic addition processes. The compound exhibits enhanced stability under standard bench conditions and serves as a key intermediate in the synthesis of bioactive molecules and functionalized pharmaceuticals.
1-(2,4-Dichloropyridin-3-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. Its electrophilic acyl group facilitates nucleophilic substitution and condensation reactions, particularly in the synthesis of heterocyclic compounds. The 2,4-dichloro substitution pattern provides enhanced reactivity and orthogonal functionalization potential, while the ketone functionality offers stability and compatibility with standard purification methods. This compound functions effectively in late-stage modifications and is well-suited for scalable synthetic processes.
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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: