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Structure of 108258-54-4
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Methyl 2,3-dichloroquinoxaline-6-carboxylate features a rigid, electron-deficient quinoxaline core with dual chloro substituents at the 2 and 3 positions, enabling high reactivity in cross-coupling and nucleophilic substitution reactions. The methyl ester group provides solubility and stability under standard conditions, facilitating its use as a key intermediate in heterocyclic synthesis and pharmaceutical development.
Methyl 2,3-dichloroquinoxaline-6-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of quinoxaline-based scaffolds. The dichloro substitution pattern facilitates selective nucleophilic aromatic substitution, while the ester group supports further functionalization via hydrolysis or coupling reactions. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry campaigns 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: