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Structure of 62224-16-2
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Methyl 4-bromothiophene-2-carboxylate features a brominated thiophene core with a methyl ester group, offering a reactive handle for cross-coupling and functionalization. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring electron-deficient heterocyclic scaffolds.
Methyl 4-bromothiophene-2-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 synthetic flexibility for subsequent transformations, while the thiophene core provides stability and compatibility with standard reaction conditions. Its bench-stable nature and predictable reactivity make it suitable for iterative synthesis workflows 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: