4,5,5,5-Tetrafluoro-4-trifluoromethyl-2-iodopentan-1-ol is a complex organic compound characterized by its unique fluorinated structure, which includes multiple fluorine atoms and an iodine substituent. This compound features a pentane backbone, with the presence of both hydroxyl (-OH) and iodine (-I) functional groups, contributing to its reactivity and potential applications in various chemical processes. The high electronegativity of the fluorine atoms imparts significant polarity to the molecule, influencing its solubility and interaction with other substances. Additionally, the presence of the iodine atom can enhance the compound's reactivity, making it a potential candidate for nucleophilic substitution reactions. The compound's unique properties may find applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. However, due to the presence of multiple halogens, careful handling and consideration of environmental impact are essential. As with many fluorinated compounds, it may exhibit distinct physical properties, such as altered boiling and melting points compared to non-fluorinated analogs.

4,5,5,5-TETRAFLUORO-4-TRIFLUOROMETHYL-2-IODOPENTAN-1-OL

114810-56-9: 4,5,5,5-Tetrafluoro-4-trifluoromethyl-2-iodopentan-1-ol is a complex organic compound characterized by its unique fluorinated structure, which includes multiple fluorine atoms and an iodine substituent. This compound features a pentane backbone, with the presence of both hydroxyl (-OH) and iodine (-I) functional groups, contributing to its reactivity and potential applications in various chemical processes. The high electronegativity of the fluorine atoms imparts significant polarity to the molecule, influencing its solubility and interaction with other substances. Additionally, the presence of the iodine atom can enhance the compound's reactivity, making it a potential candidate for nucleophilic substitution reactions. The compound's unique properties may find applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. However, due to the presence of multiple halogens, careful handling and consideration of environmental impact are essential. As with many fluorinated compounds, it may exhibit distinct physical properties, such as altered boiling and melting points compared to non-fluorinated analogs.

CAS 114810-56-9

4,5,5,5-TETRAFLUORO-4-TRIFLUOROMETHYL-2-IODOPENTAN-1-OL

1-Pentanol, 4,5,5,5-tetrafluoro-2-iodo-4-(trifluoromethyl)-

Ref: IN-DA000F9J

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

Ref: 54-PC10048