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Structure of 1458-16-8
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Methyl 3-amino-6-iodopyrazine-2-carboxylate features a pyrazine core functionalized with amino, iodo, and ester groups, enabling direct coupling in cross-coupling reactions. The electron-deficient pyrazine ring enhances reactivity in palladium-catalyzed transformations. This bench-stable compound integrates readily into complex molecular architectures under standard conditions.
Methyl 3-amino-6-iodopyrazine-2-carboxylate serves as a versatile building block for constructing pyrazine-based heterocycles in medicinal chemistry and materials science. The iodine handle enables palladium-catalyzed cross-coupling reactions, while the amino and ester groups offer orthogonal reactivity for further functionalization. Bench-stable and readily purified by recrystallization, it facilitates efficient synthesis of complex scaffolds under standard conditions.
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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: