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Structure of 4347-31-3
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering functionalized thiophene scaffolds with high efficiency. The aldehyde group enables downstream derivatization via condensation or reductive amination, enhancing synthetic versatility in pharmaceutical and materials chemistry applications.
(2-Formylthiophen-3-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biologically relevant thiophene-containing scaffolds. The pendant aldehyde group offers orthogonal functionality for downstream derivatization via reductive amination or condensation reactions. Its stability under standard reaction conditions and compatibility with common protecting groups facilitate streamlined synthesis 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-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: