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Structure of 936-12-9
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Ethyl 2-methyl-1H-pyrrole-3-carboxylate serves as a versatile heterocyclic building block in synthetic organic chemistry. Featuring a methyl-substituted pyrrole core and an ester handle, it enables efficient access to functionalized pyrrolidines and fused polycycles under standard conditions. The electron-rich aromatic system supports palladium-catalyzed couplings and conjugate additions.
Ethyl 2-methyl-1H-pyrrole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles via standard functional group transformations. Its stability under routine reaction conditions and compatibility with palladium-catalyzed couplings facilitate downstream derivatization. The ester functionality allows for selective hydrolysis or reduction, while the methyl group provides a handle for further alkylation or oxidation, making it well-suited for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07,GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P312-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: