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Structure of 37619-24-2
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Methyl 1-methylpyrrole-2-carboxylate features a pyrrole ring bearing both methyl and ester functionalities at the 1- and 2-positions, respectively. This electron-rich heterocycle serves as a key scaffold in synthetic routes to bioactive molecules, offering enhanced solubility and stability under standard conditions. The ester group enables straightforward derivatization via hydrolysis or nucleophilic substitution, facilitating integration into complex architectures.
Methyl 1-methylpyrrole-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyrrole-based heterocycles and bioactive scaffolds. The ester functionality facilitates standard transformations such as hydrolysis, reduction, and coupling reactions, while the N-methylpyrrole core exhibits good bench stability and compatibility with diverse reaction conditions. Its defined regiochemistry supports predictable reactivity in electrophilic substitution and transition-metal-catalyzed processes, making it a reliable intermediate for medicinal chemistry and process development.
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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: