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Structure of 1330750-56-5
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6-Bromo-5-methylimidazo[1,2-a]pyrazine features a fused heterocyclic core with bromine and methyl substituents at strategic positions, enabling direct functionalization in cross-coupling reactions. The electron-deficient imidazopyrazine scaffold enhances reactivity in transition-metal-catalyzed transformations, while the bench-stable nature supports reliable handling in synthetic workflows.
6-Bromo-5-methylimidazo[1,2-a]pyrazine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances metabolic stability and modulates electronic properties. The fused imidazopyrazine core provides structural rigidity and favorable pharmacophoric characteristics. This compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard synthetic workflows involving C–X bond formation and functional group interconversions.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: