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Structure of 5398-36-7
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Ethyl 2-aminothiazole-4-carboxylate features a reactive amino group flanked by a thiazole ring and an ester-functionalized carboxylate, enabling direct incorporation into heterocyclic scaffolds. This bench-stable intermediate delivers efficient access to bioactive thiazole derivatives through straightforward derivatization pathways.
Ethyl 2-aminothiazole-4-carboxylate serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The molecule combines a nucleophilic amino group with an electrophilic ester, enabling sequential functionalization via alkylation, acylation, or coupling reactions. Its thiazole core provides structural rigidity and metabolic stability, while the ethyl ester facilitates downstream transformations such as hydrolysis or amidation. Bench-stable and readily purified by recrystallization, it functions efficiently in standard synthetic workflows for API intermediate 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: