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Structure of 73956-17-9
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Ethyl 2-formylthiazole-4-carboxylate features a reactive aldehyde group flanked by electron-deficient thiazole and ester functionalities, enabling direct coupling in heterocyclic synthesis. This bench-stable reagent integrates readily into multistep sequences for bioactive molecule construction.
Ethyl 2-formylthiazole-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted thiazoles and fused ring systems. The orthogonal functionality of the formyl and ester groups facilitates sequential transformations—such as Wittig reactions, nucleophilic additions, and cyclizations—under mild conditions. Its bench-stable nature and compatibility with common reaction protocols make it suitable for both medicinal chemistry lead optimization and process-scale applications.
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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: