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Structure of 947533-39-3
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This boronate moiety integrates a trifluoromethylpyridine scaffold, delivering enhanced stability and solubility in polar solvents. The electron-deficient pyridine ring enables efficient Suzuki-Miyaura coupling under mild conditions, while the trifluoromethyl group imparts metabolic resistance and improved lipophilicity for medicinal chemistry applications.
(2-(Trifluoromethyl)pyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. Its trifluoromethylpyridine motif imparts enhanced metabolic stability and modulated electronic properties, making it valuable for medicinal chemistry applications. The boronic acid functionality offers good bench stability, compatibility with diverse reaction conditions, and straightforward purification via recrystallization or chromatography.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: