Tetrafluorocatechol, with the CAS number 1996-23-2, is a fluorinated derivative of catechol, characterized by the presence of four fluorine atoms substituting the hydrogen atoms on the aromatic ring. This compound typically exhibits a high degree of chemical stability due to the strong C-F bonds, which also contribute to its unique reactivity and solubility properties. Tetrafluorocatechol is often used in various chemical applications, including as an intermediate in the synthesis of fluorinated compounds and in research related to fluorinated materials. Its polar nature, resulting from the electronegative fluorine atoms, enhances its solubility in polar solvents. Additionally, tetrafluorocatechol may exhibit interesting biological activities, making it a subject of study in medicinal chemistry. Safety considerations are important when handling this compound, as fluorinated compounds can pose environmental and health risks. Overall, tetrafluorocatechol is a significant compound in the field of fluorochemistry, with potential applications in various industrial and research settings.

Tetrafluorocatechol

1996-23-2: Tetrafluoropyrocatechol, 3,4,5,6-Tetrafluorobenzene-1,2-Diol, Tetrafluorobenzene-1,2-diol

Tetrafluorobenzene-1,2-diol

1,2-Benzenediol, 3,4,5,6-tetrafluoro-

1,2-Dihydroxytetra-fluoro-benzene is an organic molecule with a protonated hydroxy group and two bidentate ligands. This compound has been used as a solid catalyst in cationic polymerization reactions because it has a high flow rate. The cyclopentadienyl ligand activates the 1,2-dihydroxytetra-fluoro-benzene to catalyze the polymerization of olefins. 1,2-Dihydroxytetra-fluoro-benzene can be synthesized by reacting ethylene glycol with boronic ester and nitrogen gas in an organic solvent at room temperature.

CAS 1996-23-2: Tetrafluorocatechol

Tetrafluorobenzene-1,2-diol

Ref: 10-F010525

Tetrafluorobenzene-1,2-diol

Ref: 54-PC9657

1,2-Benzenediol, 3,4,5,6-tetrafluoro-

Ref: IN-DA002C81

1,2-Dihydroxytetra-fluoro-benzene

Ref: 3D-FD32233