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Structure of 161942-89-8
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This bromothiophene-acetic acid derivative features a reactive carboxylic acid group flanked by a brominated thiophene ring, enabling direct incorporation into cross-coupling reactions. The electron-deficient thiophene moiety enhances compatibility with palladium-catalyzed transformations, while the bench-stable structure simplifies handling in synthetic workflows.
2-(4-Bromothiophen-2-yl)acetic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds and pharmaceutical intermediates. Its brominated thiophene moiety enables efficient palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates direct derivatization or salt formation. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis in medicinal chemistry and process development 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-P302+P352
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Lot numbers can be found on the outside label of a product: