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Structure of 313546-16-6
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This boronic acid features a methoxy-substituted aryl group paired with a trifluoromethyl moiety, delivering enhanced stability and solubility in organic media. The electron-deficient ring facilitates efficient Suzuki-Miyaura coupling under mild conditions, enabling reliable C–C bond formation in complex molecule synthesis.
(4-Methoxy-2-(trifluoromethyl)phenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the methoxy substituent provides favorable electronic modulation. The boronic acid functionality offers excellent bench stability, straightforward purification, and broad functional group tolerance, making it ideal 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-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: