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Structure of 465515-31-5
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2-Carboxythiophene-5-boronic acid delivers a strategically positioned boronic acid group conjugated to a carboxylic acid-functionalized thiophene scaffold. This dual-functionalized architecture enables direct incorporation into Suzuki-Miyaura coupling reactions while preserving solubility and stability under standard conditions. The electron-deficient thiophene ring enhances reactivity, facilitating efficient cross-coupling with aryl and heteroaryl halides. Ideal for synthesizing bioactive conjugated systems and functional materials in medicinal chemistry and materials science workflows.
2-Carboxythiophene-5-boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its dual functionality—carboxylic acid and boronic acid—supports orthogonal reactivity and facilitates downstream derivatization. The compound exhibits good bench stability and is compatible with standard aqueous workups, making it well-suited for synthetic applications in medicinal chemistry and materials science.
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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: