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Structure of 5118-06-9
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Methyl 3-hydroxythiophene-2-carboxylate features a hydroxylated thiophene core with a methyl ester handle, enabling direct functionalization in heterocyclic synthesis. The electron-rich ring system supports transition-metal-catalyzed couplings, while the pendant hydroxyl group offers sites for derivatization or coordination. This bench-stable compound serves as a versatile intermediate in medicinal chemistry and materials development.
Methyl 3-hydroxythiophene-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the C3 position via oxidation or esterification. The pendant hydroxyl group offers orthogonal reactivity for derivatization, while the methyl ester facilitates subsequent transformations. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for medicinal chemistry campaigns and API intermediate 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 : 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: