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Structure of 313545-72-1
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2-Chloro-4-fluorophenylboronic acid features a boronic acid group flanked by chlorine and fluorine substituents, enabling efficient cross-coupling under standard conditions. This electron-deficient arylboronic acid delivers high reactivity in Suzuki-Miyaura reactions, particularly with challenging substrates. The ortho-chloro and para-fluoro pattern enhances stability and selectivity, streamlining access to complex fluorinated biaryl architectures.
2-Chloro-4-fluorophenylboronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its orthogonal reactivity allows selective functionalization in the presence of other halogens, while its bench-stable solid form facilitates handling and purification. Widely used in medicinal chemistry and agrochemical synthesis, it provides access to substituted aryl scaffolds with enhanced metabolic stability and targeted bioactivity.
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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: