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Structure of 92992-85-3
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2-Bromo-3,5-dimethylpyridine features a sterically hindered pyridine core with electron-rich methyl groups flanking the bromine substituent. This configuration enhances regioselectivity in palladium-catalyzed cross-coupling reactions. The compound exhibits bench-stable handling and compatibility with standard reaction conditions in synthetic organic chemistry workflows.
2-Bromo-3,5-dimethylpyridine serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic reactivity at the C2 position. The ortho-bromo functionality facilitates Suzuki, Stille, and Negishi couplings with high efficiency and functional group tolerance. The 3,5-dimethyl substitution pattern enhances stability and solubility, supporting straightforward purification and scalability. This compound functions reliably in the construction of substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical research.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: