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Structure of 3284-51-3
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Ethyl 5-methyl-1H-pyrrole-2-carboxylate features a bench-stable pyrrole core with a methyl group at the 5-position and an ester-functionalized C2. This electron-rich heterocycle integrates readily into synthetic sequences requiring polar, aromatic scaffolds. The ester moiety enables downstream derivatization via hydrolysis or nucleophilic substitution.
Ethyl 5-methyl-1H-pyrrole-2-carboxylate serves as a versatile heterocyclic building block in synthetic organic chemistry, enabling efficient access to substituted pyrroles via standard functional group manipulations. Its methyl and ester groups offer orthogonal reactivity for further derivatization, while the inherent stability facilitates handling and purification. This compound functions effectively in transition-metal-catalyzed couplings and serves as a key intermediate in the synthesis of biologically relevant scaffolds.
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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: