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Structure of 4422-32-6
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3-(3-Bromophenyl)pyridine features a brominated phenyl group attached to a pyridine core, enabling direct functionalization in cross-coupling reactions. This electron-deficient heteroaryl scaffold integrates readily into pharmaceutical intermediates and advanced materials. The bromine moiety offers high reactivity under palladium catalysis, while the pyridine nitrogen provides coordination versatility for metal complexation. Bench-stable and compatible with standard synthetic protocols.
3-(3-Bromophenyl)pyridine serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of biaryl scaffolds via palladium-catalyzed reactions. The bromo group exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the pyridine nitrogen provides coordination sites for metal catalysts and enhances solubility in organic media. Bench-stable and readily purified by flash chromatography, it functions effectively in the synthesis of pharmaceutical intermediates and functional materials.
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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: