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Structure of 33332-31-9
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2-Chloro-5-methoxypyrazine features a pyrazine core functionalized with chlorine and methoxy groups, delivering enhanced electron deficiency and tailored reactivity. This bench-stable heterocycle integrates readily into synthetic routes requiring polar, electron-deficient scaffolds, enabling efficient access to complex molecular architectures in medicinal chemistry and materials science applications.
2-Chloro-5-methoxypyrazine serves as a versatile heterocyclic building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for C–C bond formation. Its chlorine atom facilitates nucleophilic substitution under mild conditions, while the methoxy group provides orthogonal reactivity and enhanced solubility. The compound exhibits excellent bench stability and is compatible with diverse functional groups, making it well-suited for modular synthesis of bioactive scaffolds and pharmaceutical intermediates.
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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: