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Structure of 1044210-57-2
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3-Bromo-5-cyclopropylpyridine features a cyclopropyl group that enhances metabolic stability while the bromo substituent enables efficient cross-coupling reactions. This electron-deficient pyridine derivative integrates readily into complex heterocycles and serves as a key intermediate in medicinal chemistry applications.
3-Bromo-5-cyclopropylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to install aryl and heteroaryl extensions. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the cyclopropyl group enhances metabolic stability and modulates lipophilicity. Bench-stable and readily purified by flash chromatography, it functions reliably in the synthesis of kinase inhibitors and other bioactive heterocycles.
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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: