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Structure of 868662-36-6
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This boronate moiety features a trifluoromethyl group at the 6-position of pyridin-3-yl, enhancing electron deficiency and metabolic stability. It enables efficient Suzuki-Miyaura coupling under standard conditions, delivering arylated products with high fidelity. The compound exhibits bench-stable handling and compatibility with diverse reaction matrices.
(6-(Trifluoromethyl)pyridin-3-yl)boronic acid is a stable, bench-ready building block that facilitates Suzuki-Miyaura coupling reactions with high efficiency. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable for constructing bioactive heterocycles in medicinal chemistry. The boronic acid functional group exhibits excellent compatibility with diverse electrophiles and tolerates common protecting groups, enabling straightforward access to complex scaffolds in API development.
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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: