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Structure of 22367-82-4
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Ethyl 3-methyl-1-benzofuran-2-carboxylate features a fused benzofuran scaffold with a methyl group at the 3-position and an ester-functionalized C2 carbon. This electron-rich heterocycle serves as a key building block in medicinal chemistry, enabling efficient access to bioactive molecules through direct functionalization or cross-coupling reactions under standard conditions.
Ethyl 3-methyl-1-benzofuran-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted benzofuran scaffolds. Its ester functionality facilitates standard transformations including hydrolysis, reduction, and nucleophilic substitution, while the methyl group provides regiochemical control in electrophilic aromatic substitution. The molecule exhibits good bench stability and compatibility with common reaction conditions, making it a practical choice for medicinal chemistry and process development workflows.
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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
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Precautionary Statements : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: