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Structure of 1227598-69-7
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This trifluoromethylpyridine derivative features a reactive primary alcohol group positioned ortho to a strongly electron-withdrawing trifluoromethylpyridine moiety. The combination imparts enhanced solubility and stability under standard conditions, enabling efficient incorporation into pharmaceutical intermediates and functional materials through straightforward derivatization.
(3-(Trifluoromethyl)pyridin-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient incorporation of a polar trifluoromethylpyridine motif. The primary alcohol functionality facilitates straightforward derivatization via esterification, ether formation, or oxidation to the carboxylic acid. Its bench-stable nature and compatibility with standard coupling reactions make it a practical choice for constructing bioactive heterocyclic scaffolds and functionalizing APIs.
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GHS Pictogram :
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GHS No : GHS03,GHS05,GHS09
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Signal Word : Danger
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UN#: 1479
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Class : 5.1
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Packing Group : Ⅲ
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Hazard Statements : H272-H314-H410
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Precautionary Statements : P210-P220-P260-P264-P273-P280-P301+P330+P331-P304+P340-P363-P370+P378-P391-P405-P501
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Lot numbers can be found on the outside label of a product: