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Structure of 74290-67-8
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5-Bromo-3-methylpyrazin-2-amine features a bromine substituent at the 5-position and a methyl group at the 3-position on a pyrazine core, enabling selective functionalization in heterocyclic synthesis. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and ligand frameworks, offering enhanced reactivity in palladium-catalyzed couplings.
5-Bromo-3-methylpyrazin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The pyrazine core provides a rigid, electron-deficient heterocyclic scaffold with enhanced metabolic stability. Its methyl and amino groups offer orthogonal functionalization sites, facilitating downstream derivatization. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis campaigns in API development.
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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: