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Structure of 343566-56-3
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Ethyl 5-chloro-1,2-oxazole-3-carboxylate is a bench-stable heterocyclic ester featuring a chlorine atom at the 5-position of the oxazole ring. This electron-deficient scaffold integrates readily into synthetic sequences, serving as a key building block for bioactive molecules and functional materials.
Ethyl 5-chloro-1,2-oxazole-3-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical synthesis. Its chloro substituent at the C5 position enables directed functionalization via palladium-catalyzed cross-coupling or nucleophilic substitution. The oxazole ring exhibits excellent bench stability and compatibility with common protecting groups, facilitating efficient access to complex scaffolds. The ester moiety allows for selective hydrolysis or derivatization, enhancing its utility in modular synthesis workflows.
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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: