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Structure of 62353-75-7
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Methyl 3-methoxythiophene-2-carboxylate features a thiophene core with complementary methoxy and ester functionalities, enabling direct integration into cross-coupling and cyclization sequences. This bench-stable heterocycle delivers regioselective reactivity under standard conditions, serving as a key building block for functionalized thienyl architectures in synthetic medicinal chemistry and materials science.
Methyl 3-methoxythiophene-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to functionalized thiophene scaffolds. Its methoxy and ester groups provide orthogonal reactivity for downstream transformations, including palladium-catalyzed cross-couplings and selective reductions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic campaigns in medicinal chemistry and materials science.
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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: