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Structure of 5006-57-5
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3,6-Dibromo-2,4-dimethylpyridine features two bromine substituents at electron-deficient positions flanking a methylated pyridine core. This sterically shielded scaffold enables direct functionalization in cross-coupling reactions under mild conditions. The molecule exhibits enhanced stability and solubility in organic solvents, facilitating use in synthesis of advanced heterocyclic architectures.
3,6-Dibromo-2,4-dimethylpyridine serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the C3 and C6 positions via palladium-catalyzed cross-coupling reactions. The methyl groups at C2 and C4 provide steric and electronic modulation, enhancing regioselectivity in subsequent transformations. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for use in medicinal chemistry campaigns and API intermediate development.
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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: