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Structure of 1310384-18-9
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This boronate moiety features a trifluorinated aryl scaffold with orthogonal halogen handles, enabling selective cross-coupling under standard conditions. The chlorine and fluorine substituents enhance electrophilic reactivity while maintaining bench-stability and compatibility with diverse catalytic systems.
(3-Chloro-2,4-difluorophenyl)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-fluoro and chloro substituents enhance electrophilic reactivity while maintaining bench stability and compatibility with diverse functional groups. The compound facilitates the synthesis of complex arylated scaffolds commonly found in pharmaceutical intermediates and agrochemicals.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: