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Structure of 408502-43-2
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3-Bromo-2-iodopyridine features a dual halogen substitution pattern on the pyridine ring, enabling selective cross-coupling reactions. The bromo group at C3 and iodo group at C2 offer orthogonal reactivity for sequential functionalization. This molecule serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical scaffolds.
3-Bromo-2-iodopyridine serves as a versatile diaryl building block in cross-coupling chemistry, enabling efficient access to biaryl scaffolds via Pd-catalyzed reactions. The orthogonal halogen reactivity allows sequential functionalization—bromine engages in Suzuki or Stille couplings, while iodine facilitates rapid Negishi or Sonogashira transformations. Its bench-stable crystalline form and predictable regioselectivity make it ideal for iterative synthesis of complex heterocycles and pharmaceutical intermediates.
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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: