{2-[(Trifluoromethyl)sulfanyl]phenyl}methanol, with the CAS number 239463-93-5, is an organic compound characterized by the presence of a phenolic structure substituted with a trifluoromethylthio group. This compound typically exhibits properties associated with both aromatic and alcohol functionalities, which can influence its reactivity and solubility. The trifluoromethyl group is known for imparting unique electronic properties, enhancing lipophilicity, and potentially increasing the compound's biological activity. The presence of the hydroxyl (-OH) group contributes to hydrogen bonding capabilities, affecting its solubility in polar solvents. Additionally, the compound may exhibit interesting chemical behavior, such as participating in nucleophilic substitution reactions or acting as a ligand in coordination chemistry. Its specific applications can vary, but it may be relevant in fields such as pharmaceuticals, agrochemicals, or materials science due to its unique structural features. Safety and handling precautions should be observed, as with many fluorinated compounds, due to potential toxicity and environmental concerns.

{2-[(trifluoromethyl)sulfanyl]phenyl}methanol

239463-93-5: {2-[(Trifluoromethyl)sulfanyl]phenyl}methanol, with the CAS number 239463-93-5, is an organic compound characterized by the presence of a phenolic structure substituted with a trifluoromethylthio group. This compound typically exhibits properties associated with both aromatic and alcohol functionalities, which can influence its reactivity and solubility. The trifluoromethyl group is known for imparting unique electronic properties, enhancing lipophilicity, and potentially increasing the compound's biological activity. The presence of the hydroxyl (-OH) group contributes to hydrogen bonding capabilities, affecting its solubility in polar solvents. Additionally, the compound may exhibit interesting chemical behavior, such as participating in nucleophilic substitution reactions or acting as a ligand in coordination chemistry. Its specific applications can vary, but it may be relevant in fields such as pharmaceuticals, agrochemicals, or materials science due to its unique structural features. Safety and handling precautions should be observed, as with many fluorinated compounds, due to potential toxicity and environmental concerns.

<p>2-(Trifluoromethylthio)benzyl alcohol</p>

CAS 239463-93-5

{2-[(trifluoromethyl)sulfanyl]phenyl}methanol

2-(Trifluoromethylthio)benzyl alcohol

Ref: 54-PC4769