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Structure of 1346270-08-3
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This boronate moiety integrates a trifluoromethyl-substituted pyrazole ring, delivering enhanced electron-withdrawing character and improved stability under standard conditions. The functional group enables efficient Suzuki-Miyaura coupling reactions, facilitating the construction of complex heteroaryl architectures in medicinal chemistry and materials science applications.
(5-(Trifluoromethyl)-1H-pyrazol-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications. The boronic acid functionality offers excellent bench stability, predictable reactivity, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: