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Structure of 278183-12-3
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Ethyl 4-amino-2-methyl-1,3-thiazole-5-carboxylate features a bifunctional thiazole scaffold with an electron-rich amino group and a sterically accessible methyl substituent. This bench-stable derivative integrates readily into heterocyclic synthesis, enabling efficient access to bioactive analogs through nucleophilic substitution or coupling reactions under standard conditions.
Ethyl 4-amino-2-methyl-1,3-thiazole-5-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted thiazoles via standard functional group transformations. Its amino and ester groups offer orthogonal reactivity for coupling, cyclization, and derivatization, facilitating the synthesis of heterocyclic scaffolds relevant to pharmaceutical research. The compound exhibits good bench stability and is amenable to purification by standard chromatographic methods, supporting scalable 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: