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Structure of 18112-31-7
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3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine features a fused heterocyclic core bearing bromo and chloro substituents at electron-deficient positions, enabling selective cross-coupling reactions. The methyl group enhances solubility and modulates reactivity, while the halogen pattern supports sequential functionalization under palladium catalysis. This scaffold serves as a key building block in medicinal chemistry for targeted kinase inhibitors and bioactive heterocycles.
3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical research. Its orthogonal halogen handles enable 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 requiring precise functionalization.
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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: