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Structure of 1114563-58-4
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6-Chloro-2,4-dimethylpyridazin-3(2H)-one features a chlorinated pyridazinone core with methyl substituents at C2 and C4, offering enhanced electron-withdrawing character and improved metabolic stability. This scaffold integrates readily into bioactive molecules, serving as a key pharmacophore in kinase inhibitors and targeted therapeutics. The chlorine at C6 enables site-specific functionalization via cross-coupling reactions.
6-Chloro-2,4-dimethylpyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazinones via palladium-catalyzed cross-coupling. Its chloro group facilitates C–C bond formation under mild conditions, while the enaminone functionality supports further functionalization. The compound exhibits excellent bench stability and compatibility with diverse reaction conditions, simplifying purification and integration into multi-step syntheses 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: