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Structure of 1211529-34-8
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4-Bromo-5-chloro-2-methylpyridine features a sterically accessible pyridine core bearing bromo and chloro substituents at adjacent positions, enabling efficient cross-coupling transformations. The methyl group enhances regioselectivity in electrophilic substitution reactions. This bench-stable, moisture-tolerant heterocycle serves as a key building block for pharmaceutical intermediates and functional materials.
4-Bromo-5-chloro-2-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogenation pattern. The methyl group enhances regioselectivity in electrophilic substitution, while the bromo and chloro functionalities offer orthogonal reactivity for sequential functionalization. Bench-stable and readily purified by column chromatography, it facilitates efficient access to complex heterocyclic scaffolds relevant to drug discovery programs.
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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: