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Structure of 117846-56-7
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2,3-Dibromo-5,6-dimethylpyridine features a highly substituted pyridine core with bromine atoms at the 2 and 3 positions and methyl groups flanking the nitrogen. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions, offering robust reactivity under mild conditions. The steric bulk from the methyl substituents enhances regioselectivity and improves stability during handling.
2,3-Dibromo-5,6-dimethylpyridine serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the pyridine ring due to its activated bromine substituents. The molecule exhibits enhanced bench stability and facilitates palladium-catalyzed cross-coupling reactions with high regioselectivity, making it valuable for constructing complex nitrogen-containing scaffolds in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: