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Structure of 89283-31-8
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3-Chloro-5-methylpyridazine is a heterocyclic building block featuring a chlorinated pyridazine core with a methyl group at the 5-position. This electron-deficient scaffold integrates readily into medicinal chemistry campaigns, offering enhanced metabolic stability and tunable reactivity in cross-coupling transformations. The pendant chlorine enables direct functionalization under palladium-catalyzed conditions, while the methyl substituent modulates lipophilicity and steric profile.
3-Chloro-5-methylpyridazine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. The chloropyridazine core exhibits excellent bench stability and tolerates a range of functional groups, facilitating downstream derivatization. Its reactivity profile supports reliable incorporation into bioactive molecules, particularly in the development of kinase inhibitors and targeted therapeutics.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS08
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335-H351
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Precautionary Statements : P201-P202-P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P308+P313-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: