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Structure of 64038-64-8
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Ethyl 2-mercapto-1H-imidazole-4-carboxylate features a reactive thiol group flanked by electron-rich imidazole and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient coupling in synthetic routes targeting bioactive nitrogen-containing compounds.
Ethyl 2-mercapto-1H-imidazole-4-carboxylate serves as a versatile heterocyclic building block in medicinal chemistry and synthetic organic chemistry. Its thiol functionality enables facile metal-catalyzed coupling reactions, while the ester group supports selective transformations under mild conditions. The imidazole core provides structural rigidity and hydrogen-bonding capacity, enhancing molecular recognition potential. This compound exhibits good bench stability, ease of purification, and compatibility with diverse functional groups, facilitating efficient access to imidazole-based scaffolds relevant to pharmaceutical research.
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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 : H315-H319-H335
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Precautionary Statements : P233-P260-P261-P264-P271-P280-P302+P352-P304+P340-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: