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Structure of 1260817-66-0
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3-Bromo-2-(trifluoromethyl)imidazo[1,2-b]pyridazine features a trifluoromethyl group that enhances electron deficiency and metabolic stability, while the bromine atom provides a reactive handle for cross-coupling transformations. This scaffold integrates readily into complex heterocyclic architectures used in medicinal chemistry and agrochemical development.
3-Bromo-2-(trifluoromethyl)imidazo[1,2-b]pyridazine serves as a versatile building block for constructing biologically active heterocycles. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the bromo substituent enables palladium-catalyzed cross-coupling reactions. This compound exhibits bench stability and facilitates efficient functionalization in late-stage diversification, making it valuable for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
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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: