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Structure of 27063-98-5
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3-Bromo-4,5-dimethylpyridine features a bromine atom at the 3-position and methyl groups at the 4- and 5-positions of the pyridine ring, delivering enhanced reactivity in cross-coupling processes. The electron-rich aromatic core supports efficient palladium-catalyzed transformations, while the steric profile from adjacent methyl substituents improves selectivity in complex synthetic sequences. This bench-stable compound integrates seamlessly into medicinal chemistry and materials synthesis workflows.
3-Bromo-4,5-dimethylpyridine serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. The bromine substituent enables reliable Suzuki, Stille, and Negishi couplings, while the methyl groups enhance solubility and influence electronic properties. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of functionalized heterocycles and advanced intermediates for API development.
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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: