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Structure of 7126-44-5
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Ethyl 3-cyano-1H-pyrrole-2-carboxylate features a pyrrole core with strategically positioned electron-withdrawing cyano and ester groups, enabling efficient incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates direct functionalization in transition-metal-catalyzed cross-couplings and serves as a key building block for bioactive nitrogen-containing compounds.
Ethyl 3-cyano-1H-pyrrole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrrole-based scaffolds through standard functional group transformations. Its cyano and ester groups offer orthogonal reactivity for alkylation, hydrolysis, and coupling reactions, facilitating the construction of complex medicinal chemistry intermediates. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step syntheses requiring high reproducibility and scalability.
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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: