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Structure of 2141956-21-8
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6-Bromopyrrolo[1,2-b]pyridazin-4-ol features a brominated heterocyclic core with a phenolic hydroxyl group, enabling direct functionalization in cross-coupling and bioconjugation workflows. The electron-deficient pyridazine ring facilitates nucleophilic substitution, while the bench-stable scaffold supports integration into pharmaceutical intermediates and advanced materials under standard conditions.
6-Bromopyrrolo[1,2-b]pyridazin-4-ol serves as a versatile building block in medicinal chemistry, enabling direct functionalization via palladium-catalyzed cross-coupling reactions. The bromine and hydroxyl groups offer orthogonal reactivity, facilitating sequential derivatization. Its stability under standard synthetic conditions and compatibility with diverse coupling partners make it ideal for constructing complex heterocyclic scaffolds relevant to kinase inhibitor and CNS-targeted drug discovery.
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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: