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Structure of 210037-58-4
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Methyl 5-bromopyrazine-2-carboxylate features a pyrazine core bearing bromo and ester functionalities, enabling direct incorporation into cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the methyl ester group offers convenient downstream derivatization. This bench-stable reagent delivers efficient access to complex nitrogen-containing architectures.
Methyl 5-bromopyrazine-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromo group reactivity. The methyl ester functionality offers compatibility with standard hydrolysis and derivatization protocols. Its stability under ambient conditions and ease of purification make it suitable for iterative synthetic strategies in medicinal chemistry and materials science applications.
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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: