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Structure of 141-30-0
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3,6-Dichloropyridazine features a rigid heteroaromatic core with two chlorine substituents at electron-deficient positions, enabling selective cross-coupling and nucleophilic substitution reactions. This configuration supports efficient functionalization in medicinal chemistry and agrochemical synthesis, where halogen-directed derivatization enhances target specificity and metabolic stability under standard conditions.
3,6-Dichloropyridazin serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through nucleophilic substitution. Its two orthogonal chlorine sites facilitate sequential functionalization under mild conditions, offering high regiocontrol and excellent stability during storage and handling. Widely used in the synthesis of kinase inhibitors and bioactive nitrogen-containing heterocycles, it functions reliably in standard coupling protocols and demonstrates broad compatibility with diverse functional groups.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: