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Structure of 39736-29-3
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Ethyl 4-amino-2-(methylthio)thiazole-5-carboxylate features a thiazole core functionalized with an electron-rich amino group and a moisture-tolerant methylthio substituent, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key intermediate in the synthesis of bioactive thiazole-based compounds, particularly within medicinal chemistry and agrochemical development workflows.
Ethyl 4-amino-2-(methylthio)thiazole-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling access to thiazole-based scaffolds prevalent in medicinal chemistry. The amino and methylthio groups offer orthogonal reactivity for derivatization, while the ester functionality supports transformations including hydrolysis, amidation, and coupling reactions. Bench-stable and readily purified by flash chromatography, it functions effectively in standard synthetic workflows requiring functional group tolerance and predictable reactivity.
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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: