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Structure of 107351-82-6
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2-Bromo-5-phenylpyridine features a phenyl-substituted pyridine core with a bromine atom at the 2-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations, while the ortho-bromo substitution facilitates selective C–C bond formation. This bench-stable, moisture-tolerant scaffold serves as a key building block for pharmaceutical intermediates and functional materials.
2-Bromo-5-phenylpyridine serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki, Stille, and Negishi conditions. The bromine substituent exhibits high reactivity with palladium catalysts, while the phenylpyridine scaffold provides structural rigidity and favorable electronic properties for further functionalization. Bench-stable and readily purified by recrystallization, it functions effectively in the synthesis of biaryl motifs and complex heterocyclic systems relevant to medicinal chemistry and materials science.
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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: