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Structure of 1114563-59-5
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6-Chloro-2,5-dimethylpyridazin-3(2H)-one features a chlorinated pyridazinone core with methyl substituents at positions 2 and 5, delivering enhanced electron-withdrawing character and steric shielding. This bench-stable scaffold integrates readily into medicinal chemistry libraries, enabling efficient access to bioactive heterocycles through nucleophilic displacement or cross-coupling reactions under standard conditions.
6-Chloro-2,5-dimethylpyridazin-3(2H)-one serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to pyridazinone-based scaffolds. Its chlorine atom facilitates nucleophilic substitution under mild conditions, while the 2,5-dimethyl substitution pattern enhances metabolic stability and modulates physicochemical properties. The compound exhibits excellent bench stability and compatibility with common coupling reactions, facilitating rapid diversification for drug discovery 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: