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Structure of 6436-59-5
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Ethyl 2-methylthiazole-4-carboxylate features a thiazole core with complementary electron-rich and electrophilic sites, enabling direct functionalization at the C4 position. The ethyl ester group facilitates downstream transformations in synthetic sequences. This bench-stable reagent integrates efficiently into heterocyclic synthesis workflows, particularly for medicinal chemistry applications requiring nitrogen- and sulfur-containing scaffolds.
Ethyl 2-methylthiazole-4-carboxylate serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The thiazole core provides a rigid, electron-deficient scaffold ideal for constructing bioactive molecules. The ester functionality enables facile manipulation via hydrolysis, reduction, or coupling reactions. Its bench-stable nature and compatibility with standard reaction conditions facilitate integration into multi-step syntheses, particularly for kinase inhibitors and other pharmaceutical intermediates.
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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: