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Structure of 313545-32-3
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This boronic acid features a chloro-fluoro-substituted phenyl core, enabling efficient coupling in palladium-catalyzed cross-coupling reactions. The ortho-chloro and para-fluoro groups enhance reactivity and stability under standard conditions. Designed for streamlined synthesis of bioactive arylated compounds in medicinal chemistry and materials science applications.
(2-Chloro-6-fluorophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-chloro and fluoro substituents provide enhanced stability and predictable reactivity, facilitating functional group tolerance and ease of purification. Ideal for constructing biaryl scaffolds in medicinal chemistry and materials science, it functions reliably in both solution-phase and solid-phase synthesis workflows.
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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: