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Structure of 38696-20-7
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5-Bromo-2-phenylpyrimidine features a bromine atom at the 5-position and a phenyl group at the 2-position, conferring enhanced reactivity for cross-coupling applications. This electron-deficient pyrimidine scaffold enables efficient C–C bond formation under palladium catalysis, delivering complex heterocyclic architectures with high regiocontrol.
5-Bromo-2-phenylpyrimidine serves as a versatile building block in medicinal chemistry and cross-coupling synthesis, enabling efficient access to biologically active heterocycles. The bromine substituent facilitates palladium-catalyzed coupling reactions such as Suzuki, Stille, and Negishi transformations, while the pyrimidine core provides structural rigidity and hydrogen-bonding capacity. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step synthetic sequences targeting kinase inhibitors and other pharmaceutical scaffolds.
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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: