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Structure of 957062-52-1
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This boronic acid features a methoxycarbonyl-substituted thiophene core, offering enhanced solubility and stability in aqueous and polar organic media. The pendant boronic acid group enables efficient Suzuki-Miyaura cross-coupling reactions under mild conditions, facilitating rapid access to functionalized heteroaryl architectures in medicinal chemistry and materials synthesis.
(5-(Methoxycarbonyl)thiophen-3-yl)boronic acid serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The methoxycarbonyl group enhances solubility and facilitates downstream derivatization, while the boronic acid moiety exhibits good bench stability and functional group tolerance. Its utility in synthesizing pharmaceutically relevant thiophene-based scaffolds makes it a practical choice for 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: