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Structure of 849020-87-7
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6-Hydroxy-4-(trifluoromethyl)nicotinic acid features a trifluoromethyl group at the 4-position and a hydroxyl moiety at the 6-position of the pyridine ring, delivering enhanced electron-withdrawing character and hydrogen-bonding capacity. This combination enables robust integration into bioactive scaffolds and functional materials requiring polar, stable heterocyclic motifs under standard bench conditions.
6-Hydroxy-4-(trifluoromethyl)nicotinic acid serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and functionalized pyridine scaffolds. Its hydroxyl and trifluoromethyl groups provide orthogonal reactivity for derivatization, while the carboxylic acid facilitates coupling reactions. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis workflows 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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: