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Structure of 1257072-34-6
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6-Bromo-3-chloropyrazine-2-carbonitrile features a highly functionalized pyrazine core with complementary halogen and nitrile handles. This electron-deficient heterocycle enables efficient coupling in cross-coupling reactions, particularly under palladium catalysis. The strategic placement of bromo and chloro groups facilitates sequential functionalization, while the carbonitrile moiety provides a robust anchor for further derivatization. Bench-stable and moisture-tolerant, this compound serves as a key building block in medicinal chemistry and materials science.
6-Bromo-3-chloropyrazine-2-carbonitrile serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its dual halogenation (Br, Cl) at adjacent positions enables sequential cross-coupling reactions, while the nitrile group provides a handle for derivatization via hydrolysis or nucleophilic addition. The molecule exhibits good bench stability and facilitates efficient functional group interconversions in standard synthetic workflows.
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Lot numbers can be found on the outside label of a product: