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Structure of 850568-00-2
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4-Fluoro-2-hydroxyphenylboronic acid features a boronate moiety ortho to a phenolic hydroxyl group, enabling efficient Suzuki-Miyaura coupling under standard conditions. The electron-withdrawing fluorine substituent enhances reaction kinetics while maintaining bench-stable handling. This structure facilitates direct incorporation into bioactive aryl scaffolds and functional polymers.
4-Fluoro-2-hydroxyphenylboronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. The ortho-hydroxyl group provides inherent directing capability and enhances solubility, while the boronic acid functionality offers excellent bench stability and compatibility with diverse functional groups. Its utility is well-established in the synthesis of substituted phenols and heterocyclic systems relevant to pharmaceutical development.
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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: