2-Methyl-4-(trifluoromethoxy)benzyl alcohol is an organic compound characterized by its aromatic structure, which includes a benzyl alcohol moiety substituted with a trifluoromethoxy group and a methyl group. The presence of the trifluoromethoxy group significantly influences its chemical properties, including increased lipophilicity and potential reactivity in various chemical reactions. This compound is likely to exhibit moderate to high polarity due to the hydroxyl (-OH) group, which can engage in hydrogen bonding, enhancing its solubility in polar solvents. The trifluoromethoxy group can also impart unique electronic properties, making it a useful building block in medicinal chemistry and material science. Additionally, the compound may exhibit interesting biological activities, although specific biological data would depend on empirical studies. Its synthesis typically involves the introduction of the trifluoromethoxy group onto the aromatic ring, followed by the reduction of a suitable precursor to yield the alcohol. As with many fluorinated compounds, it may have specific environmental and safety considerations due to the presence of fluorine atoms.

2-METHYL-4-(TRIFLUOROMETHOXY)BENZYL ALCOHOL

261951-94-4: 2-Methyl-4-(trifluoromethoxy)benzyl alcohol is an organic compound characterized by its aromatic structure, which includes a benzyl alcohol moiety substituted with a trifluoromethoxy group and a methyl group. The presence of the trifluoromethoxy group significantly influences its chemical properties, including increased lipophilicity and potential reactivity in various chemical reactions. This compound is likely to exhibit moderate to high polarity due to the hydroxyl (-OH) group, which can engage in hydrogen bonding, enhancing its solubility in polar solvents. The trifluoromethoxy group can also impart unique electronic properties, making it a useful building block in medicinal chemistry and material science. Additionally, the compound may exhibit interesting biological activities, although specific biological data would depend on empirical studies. Its synthesis typically involves the introduction of the trifluoromethoxy group onto the aromatic ring, followed by the reduction of a suitable precursor to yield the alcohol. As with many fluorinated compounds, it may have specific environmental and safety considerations due to the presence of fluorine atoms.

2-Methyl-4-(trifluoromethoxy)benzyl alcohol

CAS 261951-94-4

2-METHYL-4-(TRIFLUOROMETHOXY)BENZYL ALCOHOL

2-Methyl-4-(trifluoromethoxy)benzyl alcohol

Ref: 54-PC0420