2,3,4,6-Tetrafluorobenzenemethanol is an organic compound characterized by the presence of a benzene ring substituted with four fluorine atoms and a hydroxymethyl group (-CH2OH). The fluorine substitutions significantly influence the compound's physical and chemical properties, including increased electronegativity and altered reactivity compared to non-fluorinated analogs. This compound is likely to be a colorless or pale yellow liquid or solid, depending on its specific form and purity. Its high fluorine content contributes to its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, where fluorinated compounds are valued for their stability and unique interactions. The presence of the hydroxymethyl group suggests potential for hydrogen bonding, which may affect solubility in polar solvents. Additionally, the compound's structure may impart specific biological activities, making it of interest for further research in medicinal chemistry. Safety data should be consulted for handling and storage, as fluorinated compounds can exhibit unique toxicity profiles.

2,3,4,6-Tetrafluorobenzenemethanol

53001-70-0: 2,3,4,6-Tetrafluorobenzenemethanol, 2,3,4,6-Tetrafluorobenzyl alcohol, Benzenemethanol, 2,3,4,6-Tetrafluoro-, (2,3,4,6-Tetrafluorophenyl)methanol

(2,3,4,6-Tetrafluorophenyl)methanol

2,3,4,6-Tetrafluorobenzyl alcohol

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CAS 53001-70-0: 2,3,4,6-Tetrafluorobenzenemethanol

(2,3,4,6-Tetrafluorophenyl)methanol

Ref: IN-DA003FDS

2,3,4,6-Tetrafluorobenzyl alcohol

Ref: 54-PC904651

2,3,4,6-Tetrafluorobenzyl Alcohol

Ref: 3D-FT80998

2,3,4,6-Tetrafluorobenzyl Alcohol

Ref: 3B-T1942

(2,3,4,6-Tetrafluorophenyl)methanol

Ref: 10-F721157