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Structure of 254993-59-4
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2-Chloro-4-(trifluoromethyl)phenylboronic acid features a boronate moiety paired with electron-withdrawing chlorine and trifluoromethyl groups, enhancing its stability and reactivity in Suzuki-Miyaura couplings. This bench-stable reagent integrates efficiently into C–C bond formation under standard conditions, enabling precise functionalization of aryl targets in medicinal chemistry and materials synthesis.
2-Chloro-4-(trifluoromethyl)phenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. The ortho-chloro substituent provides enhanced stability and facilitates downstream functionalization, while the trifluoromethyl group imparts favorable electronic and metabolic properties. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry and process development 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: