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Structure of 27063-92-9
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5-Bromo-2,4-dimethylpyridine features a brominated pyridine core with methyl groups at the 2- and 4-positions, enhancing electron density at key sites for cross-coupling reactions. This bench-stable heterocycle integrates readily into pharmaceutical intermediates and agrochemical scaffolds, offering predictable reactivity under palladium-catalyzed conditions.
5-Bromo-2,4-dimethylpyridine serves as a versatile building block in medicinal chemistry and catalysis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic site. The bromine atom facilitates Suzuki, Stille, and Negishi couplings with high efficiency, while the methyl groups stabilize the pyridine core and enhance solubility. Its bench-stable nature and compatibility with diverse functional groups make it ideal for constructing complex heterocyclic scaffolds in API development and process chemistry workflows.
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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: