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Structure of 193965-30-9
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This boronate moiety integrates a methoxy-substituted benzo[b]thiophene scaffold, offering enhanced solubility and stability in aqueous-organic media. The electron-donating methoxy group modulates reactivity, enabling efficient Suzuki-Miyaura coupling under mild conditions. Designed for synthetic versatility, it facilitates the construction of complex heteroaryl architectures in pharmaceutical and materials applications.
(5-Methoxybenzo[b]thiophen-2-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl architectures. The methoxy group enhances solubility and modulates electronic properties, while the boronic acid moiety provides reliable reactivity under standard Suzuki-Miyaura conditions. Its bench-stable solid form facilitates handling and purification, making it well-suited for iterative 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: