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Structure of 3430-34-0
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3,5-Dibromo-2,6-dimethylpyridine features two bromine atoms at the 3 and 5 positions flanking a central nitrogen atom, with methyl groups at the 2 and 6 positions. This sterically hindered architecture enhances stability under standard conditions while enabling selective coupling reactions in cross-coupling methodologies. The electron-deficient pyridine core facilitates transition metal-catalyzed transformations, making it a robust scaffold for synthesizing functionalized heterocycles.
3,5-Dibromo-2,6-dimethylpyridine serves as a versatile building block in synthetic organic chemistry, enabling the construction of substituted pyridine scaffolds via palladium-catalyzed cross-coupling reactions. The bromo groups exhibit high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl substituents enhance stability and facilitate purification. Its ortho-directed substitution pattern supports regioselective functionalization, making it valuable for medicinal chemistry and materials science applications requiring controlled molecular architecture.
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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: