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Structure of 1008361-77-0
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3-Bromo-6-iodo-2-methylpyridine features a sterically accessible pyridine core with complementary halogen handles enabling sequential cross-coupling. The ortho-methyl group enhances regiochemical control, while the bromo and iodo substituents facilitate efficient Pd-catalyzed transformations under standard conditions. This bifunctional scaffold enables rapid access to complex heterocyclic architectures in medicinal chemistry and materials synthesis.
3-Bromo-6-iodo-2-methylpyridine serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling sequential functionalization of heteroaromatic scaffolds. The ortho-bromo and para-iodo substituents provide complementary reactivity for Pd- or Ni-catalyzed coupling protocols, while the methyl group offers a handle for further derivatization. Its bench-stable nature and high regioselectivity facilitate efficient synthesis of complex pyridine-based architectures relevant to medicinal chemistry and materials science.
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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-H320-H335
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: