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Structure of 76360-43-5
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Methyl 2-bromothiophene-3-carboxylate features a brominated thiophene core that enables direct functionalization in cross-coupling reactions. The ester group provides a handle for further derivatization, while the electron-deficient ring enhances reactivity in palladium-catalyzed transformations. This bench-stable compound serves as a key intermediate in heterocyclic synthesis.
Methyl 2-bromothiophene-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromo functionality. The methyl ester group offers orthogonal reactivity for selective transformations, while the thiophene core provides structural rigidity and electronic properties relevant to pharmaceutical and agrochemical scaffolds. Bench-stable and compatible with standard synthetic workflows, it facilitates efficient access to substituted thiophenes under mild conditions.
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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: