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Structure of 934236-35-8
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Methyl 2-chlorooxazole-4-carboxylate features a chlorinated oxazole core that enables direct functionalization at the C2 position. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring electron-deficient heterocycles. The ester group facilitates downstream transformations, while the chlorine atom serves as a reactive handle for nucleophilic substitution or cross-coupling reactions.
Methyl 2-chlorooxazole-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to oxazole-containing scaffolds via nucleophilic substitution or transition-metal-catalyzed coupling. The chloro group at the C2 position provides high reactivity for further functionalization, while the ester functionality offers stability and ease of purification. This compound functions effectively in medicinal chemistry campaigns requiring robust, bench-stable intermediates for API 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: