1,1,1,3,3,3-Hexafluoro-2-(3-nitrophenyl)propan-2-ol, with CAS number 2402-65-5, is a fluorinated organic compound characterized by the presence of multiple fluorine atoms and a nitrophenyl group. This compound features a hexafluoropropanol structure, which contributes to its unique chemical properties, including high thermal stability and low volatility. The presence of the nitrophenyl moiety enhances its potential for applications in various fields, such as pharmaceuticals and agrochemicals, due to its ability to participate in electrophilic aromatic substitution reactions. Additionally, the fluorinated nature of the compound may impart hydrophobic characteristics, making it useful in formulations requiring water resistance. Its synthesis typically involves the introduction of fluorine atoms into the propanol framework, followed by the attachment of the nitrophenyl group. Safety considerations are important when handling this compound, as fluorinated substances can exhibit toxicity and environmental persistence. Overall, this compound exemplifies the intersection of fluorine chemistry and functional group reactivity, making it a subject of interest in advanced chemical research.

1,1,1,3,3,3-hexafluoro-2-(3-nitrophenyl)propan-2-ol

2402-65-5: 1,1,1,3,3,3-Hexafluoro-2-(3-nitrophenyl)propan-2-ol, with CAS number 2402-65-5, is a fluorinated organic compound characterized by the presence of multiple fluorine atoms and a nitrophenyl group. This compound features a hexafluoropropanol structure, which contributes to its unique chemical properties, including high thermal stability and low volatility. The presence of the nitrophenyl moiety enhances its potential for applications in various fields, such as pharmaceuticals and agrochemicals, due to its ability to participate in electrophilic aromatic substitution reactions. Additionally, the fluorinated nature of the compound may impart hydrophobic characteristics, making it useful in formulations requiring water resistance. Its synthesis typically involves the introduction of fluorine atoms into the propanol framework, followed by the attachment of the nitrophenyl group. Safety considerations are important when handling this compound, as fluorinated substances can exhibit toxicity and environmental persistence. Overall, this compound exemplifies the intersection of fluorine chemistry and functional group reactivity, making it a subject of interest in advanced chemical research.

<p>1,1,1,3,3,3-Hexafluoro-2-(3-nitrophenyl)propan-2-ol</p>

CAS 2402-65-5

1,1,1,3,3,3-hexafluoro-2-(3-nitrophenyl)propan-2-ol

1,1,1,3,3,3-Hexafluoro-2-(3-nitrophenyl)propan-2-ol

Ref: 54-PC50362