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Structure of 72054-60-5
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Ethyl 2-amino-5-methylthiazole-4-carboxylate features a fused thiazole core with complementary amino and ester functionalities, enabling direct integration into heterocyclic scaffolds. The electron-rich nitrogen atoms facilitate metal-catalyzed coupling reactions, while the methyl group enhances solubility and steric profile. This bench-stable intermediate supports rapid access to bioactive thiazole derivatives in medicinal chemistry and materials synthesis.
Ethyl 2-amino-5-methylthiazole-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to thiazole-based scaffolds prevalent in medicinal chemistry. Its amino and ester functionalities offer orthogonal reactivity for derivatization via coupling, cyclization, or substitution reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for scalable applications in API intermediate development and combinatorial library generation.
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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: