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Structure of 1703-07-7
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6-Chloro-5-methylpyridazin-3(2H)-one features a fused heterocyclic core with orthogonal electron-withdrawing and electron-donating substituents, enabling selective reactivity in transition-metal-catalyzed couplings. The chloro group serves as a robust handle for cross-coupling transformations, while the methyl moiety enhances solubility and modulates electronic properties. This scaffold demonstrates stability under standard bench conditions and integrates efficiently into complex molecular architectures.
6-Chloro-5-methylpyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazinones via palladium-catalyzed cross-coupling reactions. The chloro group facilitates nucleophilic substitution under mild conditions, while the methyl and lactam functionalities provide orthogonal reactivity for downstream derivatization. This compound exhibits excellent bench stability and is compatible with common purification methods, making it well-suited for high-throughput synthesis of bioactive heterocycles.
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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: