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Structure of 1298031-94-3
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8-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine features a sterically constrained imidazopyridazine core bearing bromo and chloro substituents at electron-deficient positions, enabling selective cross-coupling reactions. The methyl group enhances solubility and modulates reactivity, making this scaffold valuable for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
8-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its orthogonal halogenation pattern enables sequential cross-coupling reactions, while the methyl group enhances metabolic stability. The molecule exhibits excellent bench stability and facilitates efficient purification, making it well-suited for iterative synthesis workflows in API development and functionalized scaffold construction.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: