2,2,2-Trifluoro-1,1-bis(4-fluorophenyl)ethanol, with the CAS number 733-83-5, is an organic compound characterized by its unique structure featuring multiple fluorine substituents. This compound is a colorless to pale yellow solid at room temperature and is known for its high stability and low volatility due to the presence of fluorine atoms, which enhance its chemical resilience. It exhibits significant hydrophobic properties, making it less soluble in water but more soluble in organic solvents. The presence of the hydroxyl (-OH) group contributes to its potential as a hydrogen bond donor, influencing its reactivity and interactions with other molecules. Additionally, the compound's fluorinated aromatic rings can impart unique electronic properties, making it of interest in various applications, including pharmaceuticals and agrochemicals. Its synthesis typically involves multi-step reactions that require careful handling due to the reactivity of fluorinated intermediates. Overall, 2,2,2-trifluoro-1,1-bis(4-fluorophenyl)ethanol is notable for its distinctive chemical properties and potential utility in advanced material science and medicinal chemistry.

2,2,2-trifluoro-1,1-bis(4-fluorophenyl)ethanol

733-83-5: 2,2,2-Trifluoro-1,1-bis(4-fluorophenyl)ethanol, with the CAS number 733-83-5, is an organic compound characterized by its unique structure featuring multiple fluorine substituents. This compound is a colorless to pale yellow solid at room temperature and is known for its high stability and low volatility due to the presence of fluorine atoms, which enhance its chemical resilience. It exhibits significant hydrophobic properties, making it less soluble in water but more soluble in organic solvents. The presence of the hydroxyl (-OH) group contributes to its potential as a hydrogen bond donor, influencing its reactivity and interactions with other molecules. Additionally, the compound's fluorinated aromatic rings can impart unique electronic properties, making it of interest in various applications, including pharmaceuticals and agrochemicals. Its synthesis typically involves multi-step reactions that require careful handling due to the reactivity of fluorinated intermediates. Overall, 2,2,2-trifluoro-1,1-bis(4-fluorophenyl)ethanol is notable for its distinctive chemical properties and potential utility in advanced material science and medicinal chemistry.

<p>Bis(4-fluorophenyl)trifluoromethyl carbinol</p>

CAS 733-83-5

2,2,2-trifluoro-1,1-bis(4-fluorophenyl)ethanol

Bis(4-fluorophenyl)trifluoromethyl carbinol

Ref: 54-PC1227JE