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Structure of 1260664-82-1
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2-Bromo-5-chloro-3-methylpyrazine features a triheterocyclic core with complementary halogen and methyl substituents, enabling selective cross-coupling reactions under mild conditions. The electron-deficient pyrazine ring enhances reactivity in palladium-catalyzed transformations, while the ortho-halogen arrangement facilitates regioselective functionalization. This bench-stable compound serves as a key building block for advanced heterocyclic architectures in medicinal chemistry and materials science.
2-Bromo-5-chloro-3-methylpyrazine serves as a versatile heterocyclic building block in medicinal chemistry and agrochemical synthesis. Its dual halogenation pattern enables selective cross-coupling reactions, including Suzuki and Stille couplings, under mild conditions. The methyl group provides a handle for further functionalization, while the pyrazine core offers enhanced metabolic stability and favorable pharmacophore characteristics. Bench-stable and readily purified by flash chromatography, it facilitates efficient assembly of complex molecular architectures in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: