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Structure of 117873-72-0
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2,6-Dibromo-4-methoxypyridine features a pyridine core functionalized with bromine atoms at positions 2 and 6 and a methoxy group at C4, creating a sterically constrained, electron-deficient heterocycle. This configuration enables selective cross-coupling reactions in medicinal chemistry and materials synthesis, offering high reactivity under standard conditions with minimal side-product formation.
2,6-Dibromo-4-methoxypyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine derivatives via palladium-catalyzed cross-coupling reactions. The ortho-bromine atoms facilitate sequential functionalization, while the methoxy group provides a handle for selective transformations. Its bench-stable crystalline form and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development workflows.
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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: