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Structure of 2374134-99-1
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5-Chloro-8-iodoimidazo[1,2-c]pyrimidine features a dual halogenated imidazopyrimidine core, enabling facile cross-coupling and functionalization in medicinal chemistry. The electron-deficient scaffold supports efficient Pd-catalyzed transformations, while the chloro and iodo substituents offer orthogonal reactivity for sequential derivatization. This compound serves as a key building block in the synthesis of bioactive heterocycles and advanced pharmaceutical intermediates.
5-Chloro-8-iodoimidazo[1,2-c]pyrimidine serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The chloro and iodo substituents facilitate sequential functionalization, with the iodo group exhibiting high reactivity in Suzuki, Stille, and Negishi couplings. Bench-stable and amenable to purification by flash chromatography, it functions reliably in the synthesis of pharmaceutical intermediates and kinase inhibitor scaffolds.
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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: