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Structure of 57864-39-8
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3,6-Dichloropyridin-2(1H)-one features a planar heteroaromatic core with two chlorine substituents at electron-deficient positions, enhancing its reactivity in nucleophilic substitution. This bench-stable compound integrates readily into synthetic scaffolds requiring halogen-directed functionalization or serves as a key intermediate in the development of bioactive molecules.
3,6-Dichloropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based heterocycles. Its dual chlorine substituents provide orthogonal reactivity for sequential functionalization, while the enolizable carbonyl supports nucleophilic substitution and coupling reactions. Bench-stable and readily purified, it facilitates scalable synthesis of API intermediates and complex scaffolds through well-established transformation pathways.
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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: