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Structure of 131747-57-4
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This trifluoromethyl-substituted pyridylmethanol features a reactive alcohol group positioned ortho to the electron-withdrawing trifluoromethyl moiety, enhancing its utility in cross-coupling and functionalization reactions. The molecule exhibits enhanced stability and solubility in polar organic solvents, enabling straightforward incorporation into complex molecular architectures under standard conditions.
(2-(Trifluoromethyl)pyridin-3-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient incorporation of a trifluoromethylated pyridine motif into target molecules. Its benzyl alcohol functionality facilitates straightforward derivatization via oxidation, protection, or coupling reactions. The molecule exhibits good bench stability and functional group tolerance, supporting its use in multi-step syntheses of bioactive compounds and API intermediates.
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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: