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Structure of 957060-85-4
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2-Fluoro-4-methanesulfonylphenylboronic acid features a boronic acid group flanked by electron-withdrawing fluorine and methanesulfonyl substituents, enhancing its stability and reactivity in Suzuki-Miyaura coupling. This combination enables efficient cross-coupling under mild conditions, delivering arylated products with high fidelity. The molecule exhibits bench-stable handling and compatibility with diverse reaction matrices, making it ideal for complex molecular assembly in synthetic and medicinal chemistry workflows.
2-Fluoro-4-methanesulfonylphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The fluorine and methanesulfonyl groups provide orthogonal reactivity and enhanced stability, facilitating selective transformations and simplifying purification. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for the synthesis of complex aryl scaffolds 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: