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Structure of 18087-76-8
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6-Chloro-3-nitroimidazo[1,2-b]pyridazine features a fused heterocyclic core bearing a chloro group at the 6-position and a nitro substituent at the 3-position. This electron-deficient scaffold integrates readily into medicinal chemistry campaigns targeting kinase inhibitors and antiparasitic agents, offering enhanced metabolic stability and favorable binding affinity in biological assays.
6-Chloro-3-nitroimidazo[1,2-b]pyridazine serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical synthesis. Its dual functional groups—electrophilic chlorine and electron-deficient nitro moiety—enable selective nucleophilic substitution and coupling reactions under mild conditions. The scaffold exhibits good bench stability and facilitates efficient derivatization, making it well-suited for constructing complex nitrogen-rich frameworks in API development pipelines.
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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: