(4-Fluoro-2,6-dimethyl-phenyl)methanol is an organic compound characterized by the presence of a phenolic structure with a hydroxymethyl group attached to a substituted aromatic ring. The compound features a fluorine atom at the para position and two methyl groups at the ortho positions relative to the hydroxymethyl group on the benzene ring. This substitution pattern influences its physical and chemical properties, such as solubility, boiling point, and reactivity. Typically, compounds like this exhibit moderate polarity due to the hydroxyl group, which can engage in hydrogen bonding, enhancing solubility in polar solvents. The presence of the fluorine atom can also impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological systems. Additionally, the methyl groups contribute to steric hindrance, which may influence the compound's conformation and reactivity. Overall, (4-fluoro-2,6-dimethyl-phenyl)methanol is of interest in various fields, including pharmaceuticals and materials science, due to its unique structural features.

(4-fluoro-2,6-dimethyl-phenyl)methanol

773868-67-0: (4-Fluoro-2,6-dimethyl-phenyl)methanol is an organic compound characterized by the presence of a phenolic structure with a hydroxymethyl group attached to a substituted aromatic ring. The compound features a fluorine atom at the para position and two methyl groups at the ortho positions relative to the hydroxymethyl group on the benzene ring. This substitution pattern influences its physical and chemical properties, such as solubility, boiling point, and reactivity. Typically, compounds like this exhibit moderate polarity due to the hydroxyl group, which can engage in hydrogen bonding, enhancing solubility in polar solvents. The presence of the fluorine atom can also impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological systems. Additionally, the methyl groups contribute to steric hindrance, which may influence the compound's conformation and reactivity. Overall, (4-fluoro-2,6-dimethyl-phenyl)methanol is of interest in various fields, including pharmaceuticals and materials science, due to its unique structural features.

CAS 773868-67-0

(4-fluoro-2,6-dimethyl-phenyl)methanol

Benzenemethanol,4-fluoro-2,6-dimethyl-

Ref: IN-DA005BKS

2,6-Dimethyl-4-fluorobenzyl alcohol

Ref: 54-PC5427

4-Fluoro-2,6-dimethyl-benzyl alcohol

Ref: 10-F478759