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Structure of 3168-85-2
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Methyl 2-methyl-1H-pyrrole-3-carboxylate features a bench-stable pyrrole core with a methyl group at the 2-position and a methyl ester at the 3-position. This electron-rich heterocycle integrates readily into synthetic sequences requiring polar, aromatic scaffolds. The ester functionality enables direct derivatization or reduction to the corresponding alcohol, offering access to diverse analogs in medicinal chemistry and materials science.
Methyl 2-methyl-1H-pyrrole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles via cross-coupling and functional group interconversions. The methyl ester facilitates straightforward derivatization, while the 2-methyl substituent enhances stability and directs electrophilic substitution. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for medicinal chemistry campaigns and process development.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: