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Structure of 1033203-40-5
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2-Bromo-4-chloro-5-methylpyridine features a pyridine core functionalized with bromo, chloro, and methyl groups at positions 2, 4, and 5 respectively. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a key building block for pharmaceutical intermediates and agrochemical scaffolds. The strategically positioned halogens enable selective derivatization under palladium-catalyzed conditions.
2-Bromo-4-chloro-5-methylpyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its orthogonal halogenation pattern enables selective cross-coupling reactions, facilitating the construction of complex pyridyl scaffolds. The methyl group enhances metabolic stability, while the bromo and chloro substituents offer complementary reactivity in Pd-catalyzed transformations. Bench-stable and amenable to purification by distillation or chromatography, it functions reliably in standard synthetic workflows for API development and library synthesis.
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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: