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Structure of 550998-53-3
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Methyl 7-bromobenzo[b]thiophene-2-carboxylate features a brominated benzo[b]thiophene core with a methyl ester at the 2-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient thiophene ring enhances reactivity in palladium-catalyzed transformations, while the ester group provides a handle for downstream derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced materials.
Methyl 7-bromobenzo[b]thiophene-2-carboxylate serves as a versatile building block for the synthesis of biologically relevant heterocycles and functionalized pharmaceutical intermediates. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports selective transformations. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex scaffolds in medicinal chemistry and materials science 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-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: