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Structure of 1008140-70-2
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This trifluoromethoxy-substituted pyridyl boronic acid features enhanced stability and solubility in polar solvents, enabling efficient Suzuki-Miyaura cross-coupling reactions. The electron-deficient pyridine ring facilitates regioselective functionalization, while the boronic acid moiety integrates readily into complex molecular architectures under mild conditions.
(6-(Trifluoromethoxy)pyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. Its trifluoromethoxy group imparts enhanced metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications. The boronic acid functionality offers reliable reactivity under mild conditions, good bench stability, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular scaffolds.
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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: