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Structure of 942206-07-7
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2-Bromo-5-iodo-4-methylpyridine features a sterically accessible pyridine core bearing strategically positioned halogens and a methyl group, enabling selective cross-coupling reactions. This configuration supports efficient Pd-catalyzed transformations in the synthesis of functionalized heterocycles.
2-Bromo-5-iodo-4-methylpyridine serves as a versatile building block for the construction of functionalized pyridine scaffolds in medicinal chemistry and materials science. Its complementary halogenation pattern enables sequential cross-coupling reactions, particularly Suzuki-Miyaura and Stille couplings, with high chemoselectivity and excellent functional group tolerance. The methyl group provides a site for oxidation or further derivatization, while the bench-stable solid form facilitates handling and purification in multi-step syntheses.
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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: