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Structure of 71637-38-2
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This brominated thiophene-acetic acid derivative integrates a reactive carboxylate group with a sterically accessible bromine substituent. The para-brominated thiophene moiety enables direct functionalization in cross-coupling reactions, while the pendant acetic acid facilitates conjugation or derivatization under standard conditions. Bench-stable and moisture-tolerant, it serves as a key building block for bioactive heterocycles and advanced materials synthesis.
2-(5-Bromothiophen-2-yl)acetic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized thiophene derivatives. Its bromo-substituted heterocyclic core facilitates palladium-catalyzed cross-coupling reactions, while the pendant acetic acid group offers direct handle for amidation, esterification, or further derivatization. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: