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Structure of 113853-16-0
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Ethyl 2-aminooxazole-5-carboxylate features a fused oxazole ring bearing both amino and ethyl ester functionalities, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key intermediate in the synthesis of bioactive oxazoles, offering enhanced solubility and reactivity in nucleophilic substitution and cyclization reactions.
Ethyl 2-aminooxazole-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to oxazole-based scaffolds relevant to medicinal chemistry and agrochemical development. The molecule combines a readily functionalizable amino group with a carboxylate ester, facilitating nucleophilic substitution, amidation, and coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthetic sequences and scale-up applications.
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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: