1-(3-Fluorophenyl)propan-1-ol, with the CAS number 701-38-2, is an organic compound characterized by its structure, which includes a propanol backbone with a fluorinated phenyl group. This compound features a hydroxyl (-OH) functional group, making it an alcohol, and the presence of the fluorine atom on the phenyl ring can influence its chemical reactivity and physical properties. Typically, such compounds exhibit moderate polarity due to the hydroxyl group, which allows for hydrogen bonding, potentially leading to higher boiling points compared to non-polar compounds. The fluorine substituent can enhance the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry. Additionally, 1-(3-fluorophenyl)propan-1-ol may participate in various chemical reactions, including nucleophilic substitutions and oxidation processes. Its applications could range from pharmaceuticals to agrochemicals, depending on the specific interactions and properties it exhibits in different environments. Safety data should be consulted for handling and storage, as with any chemical substance.

1-(3-fluorophenyl)propan-1-ol

701-38-2: 1-(3-Fluorophenyl)propan-1-ol, with the CAS number 701-38-2, is an organic compound characterized by its structure, which includes a propanol backbone with a fluorinated phenyl group. This compound features a hydroxyl (-OH) functional group, making it an alcohol, and the presence of the fluorine atom on the phenyl ring can influence its chemical reactivity and physical properties. Typically, such compounds exhibit moderate polarity due to the hydroxyl group, which allows for hydrogen bonding, potentially leading to higher boiling points compared to non-polar compounds. The fluorine substituent can enhance the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry. Additionally, 1-(3-fluorophenyl)propan-1-ol may participate in various chemical reactions, including nucleophilic substitutions and oxidation processes. Its applications could range from pharmaceuticals to agrochemicals, depending on the specific interactions and properties it exhibits in different environments. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 701-38-2

1-(3-fluorophenyl)propan-1-ol

1-(3-Fluorophenyl)propan-1-ol

Ref: IN-DA005XJQ

α-Ethyl-3-fluorobenzyl alcohol

Ref: 54-PC6641