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Structure of 153035-56-4
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering high functional group tolerance and stability under standard conditions. The propyl-substituted biphenyl scaffold enhances solubility and facilitates purification, enabling efficient synthesis of complex biaryl architectures in medicinal chemistry and materials science applications.
(4'-Propyl-1,1'-biphenyl-4-yl)boronic acid serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its biphenyl architecture provides enhanced stability and solubility, while the propyl substituent offers favorable lipophilicity for medicinal chemistry applications. The boronic acid functions reliably in diverse reaction environments, facilitating the synthesis of complex biaryl scaffolds with high reproducibility and ease of purification.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: