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Structure of 2243753-57-1
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This trifluoromethylpyrazolyl boronic acid features a stable boronate moiety integrated into an electron-deficient pyrazole scaffold, enabling direct C–H borylation and efficient Suzuki-Miyaura coupling. The trifluoromethyl group enhances metabolic stability and modulates electronic properties, making this reagent ideal for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
(1-(Trifluoromethyl)-1H-pyrazol-4-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of trifluoromethyl-substituted biaryls and heterocycles. Its stability under ambient conditions and compatibility with diverse functional groups facilitate straightforward purification and integration into complex molecular architectures. This boronic acid functions effectively in late-stage diversification for medicinal chemistry and materials science applications.
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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: