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Structure of 142137-17-5
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3-Bromo-5-phenylpyridine features a phenyl-substituted pyridine core with a bromine atom at the 3-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the sterically accessible site facilitates efficient coupling with diverse nucleophiles. This bench-stable building block integrates readily into complex molecular architectures for pharmaceutical and materials applications.
3-Bromo-5-phenylpyridine serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its bromine substituent facilitates reliable Suzuki, Stille, and Negishi couplings, while the phenyl group imparts enhanced stability and solubility. The molecule exhibits excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: