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Structure of 884494-42-2
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2-Bromo-3-iodo-4-methylpyridine features a halogenated pyridine core with distinct regiochemistry, enabling selective cross-coupling reactions in late-stage functionalization. The methyl group enhances solubility and modulates electronic properties, while the orthogonal bromo- and iodo-substituents allow sequential Pd-catalyzed transformations. This compound serves as a key scaffold for diversification in medicinal chemistry and materials science applications.
2-Bromo-3-iodo-4-methylpyridine serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient access to substituted pyridine scaffolds. The orthogonal halogen reactivity—bromine undergoing Suzuki-Miyaura or Stille coupling, while iodine facilitates Negishi or Sonogashira transformations—allows sequential functionalization. Bench-stable and readily purified by column chromatography, it functions reliably in the synthesis of pharmaceutical intermediates and agrochemical candidates requiring regioselective diversification.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: