4,5,5,5-Tetrafluoro-4-(trifluoromethyl)pentan-1-ol, with the CAS number 29819-73-6, is a fluorinated organic compound characterized by its unique structure that includes multiple fluorine atoms and a hydroxyl group. This compound features a pentane backbone with four fluorine atoms attached to the carbon chain, significantly influencing its physical and chemical properties. The presence of the trifluoromethyl group enhances its lipophilicity and stability, making it useful in various applications, including as a solvent or in the synthesis of other fluorinated compounds. Its high electronegativity due to fluorine substitution contributes to its potential as a reagent in organic synthesis and its utility in materials science. Additionally, the hydroxyl group provides the compound with polar characteristics, which can affect its solubility and reactivity in different environments. Overall, this compound exemplifies the unique properties of fluorinated organic molecules, including increased thermal stability and altered reactivity compared to their non-fluorinated counterparts.

4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentan-1-ol

29819-73-6: 4,5,5,5-Tetrafluoro-4-(trifluoromethyl)pentan-1-ol, with the CAS number 29819-73-6, is a fluorinated organic compound characterized by its unique structure that includes multiple fluorine atoms and a hydroxyl group. This compound features a pentane backbone with four fluorine atoms attached to the carbon chain, significantly influencing its physical and chemical properties. The presence of the trifluoromethyl group enhances its lipophilicity and stability, making it useful in various applications, including as a solvent or in the synthesis of other fluorinated compounds. Its high electronegativity due to fluorine substitution contributes to its potential as a reagent in organic synthesis and its utility in materials science. Additionally, the hydroxyl group provides the compound with polar characteristics, which can affect its solubility and reactivity in different environments. Overall, this compound exemplifies the unique properties of fluorinated organic molecules, including increased thermal stability and altered reactivity compared to their non-fluorinated counterparts.

<p>4,5,5,5-Tetrafluoro-4-(trifluoromethyl)pentan-1-ol</p>

CAS 29819-73-6

4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentan-1-ol

4,5,5,5-Tetrafluoro-4-(trifluoromethyl)pentan-1-ol

Ref: 54-PC6932G