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Structure of 306934-95-2
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This boronate moiety features a phenylthiophene scaffold, delivering enhanced stability and solubility in polar organic media. The electron-rich thiophene ring facilitates efficient coupling under Suzuki-Miyaura conditions, enabling direct integration into complex heterocyclic architectures with minimal byproduct formation.
(5-Phenylthiophen-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its phenylthiophene core provides enhanced stability and orthogonal reactivity, facilitating the construction of biaryl scaffolds with high functional group tolerance. The boronic acid moiety enables straightforward purification and compatibility with diverse reaction setups, making it a reliable reagent for medicinal chemistry and materials synthesis 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-H315-H319-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: