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Structure of 1209458-06-9
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(6-Bromopyrazin-2-yl)methanol features a brominated pyrazine core with a reactive hydroxymethyl group, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The pendant alcohol facilitates derivatization while maintaining compatibility with standard synthetic protocols. This bench-stable reagent integrates readily into complex molecular architectures requiring halogenated heterocyclic motifs.
(6-Bromopyrazin-2-yl)methanol serves as a versatile building block for the synthesis of pyrazine-based pharmaceutical intermediates and functionalized heterocycles. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the pendant hydroxymethyl functionality offers a handle for derivatization via oxidation or substitution. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process 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: