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Structure of 18903-18-9
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Ethyl 5-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 derivative serves as a key intermediate in the synthesis of bioactive thiazole-based compounds, particularly in medicinal chemistry and agrochemical development workflows.
Ethyl 5-aminothiazole-4-carboxylate serves as a versatile building block in medicinal and synthetic chemistry, enabling efficient access to thiazole-based pharmacophores. The amino group facilitates direct derivatization via acylation, alkylation, or coupling reactions, while the ester functionality supports hydrolysis or further functionalization. Its stability under standard reaction conditions and compatibility with diverse transformations make it a practical scaffold for API development and heterocyclic synthesis.
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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: