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Structure of 503309-11-3
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2-Fluoro-4-(trifluoromethyl)phenylboronic acid features a boronate moiety appended to an electron-deficient aryl ring, enabling efficient Suzuki-Miyaura coupling under standard conditions. The trifluoromethyl group enhances metabolic stability and modulates electronic properties, while the ortho-fluorine facilitates directed functionalization. This bench-stable reagent integrates readily into complex molecule synthesis, particularly in pharmaceutical and agrochemical discovery workflows.
2-Fluoro-4-(trifluoromethyl)phenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its fluorinated aryl core enhances metabolic stability and modulates electronic properties, while the boronic acid functionality offers excellent bench stability and compatibility with diverse reaction conditions. Ideal for medicinal chemistry and materials science applications requiring halogenated, electron-deficient aryl linkages.
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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: