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Structure of 933041-13-5
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4-Bromo-6-chloropyridazin-3(2H)-one features a fused heterocyclic core with strategically positioned halogen substituents, enabling direct functionalization in cross-coupling and derivatization workflows. This bench-stable compound integrates readily into bioactive scaffolds, offering enhanced metabolic stability and tunable electronic properties for medicinal chemistry applications.
4-Bromo-6-chloropyridazin-3(2H)-one serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The molecule exhibits excellent bench stability and compatibility with diverse reaction conditions, facilitating the construction of complex pyridazinone scaffolds. Its orthogonal reactivity profile supports sequential derivatization, making it ideal for the synthesis of targeted API candidates and functionalized heterocycles in high-throughput screening campaigns.
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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: