(1-Fluorocyclohexyl)methanol is an organic compound characterized by the presence of a cyclohexyl ring substituted with a fluorine atom and a hydroxymethyl group. This compound features a cyclohexane structure, which contributes to its cyclic nature and potential for conformational isomerism. The fluorine atom introduces unique electronic properties, influencing the compound's reactivity and polarity. The hydroxymethyl group (-CH2OH) enhances its solubility in polar solvents and can participate in hydrogen bonding, affecting its physical properties such as boiling and melting points. (1-Fluorocyclohexyl)methanol may exhibit interesting biological activities due to its structural features, making it a subject of interest in medicinal chemistry and drug design. Its synthesis typically involves the introduction of the fluorine atom and subsequent functionalization of the cyclohexane ring. As with many fluorinated compounds, it may also exhibit stability against metabolic degradation, which can be advantageous in pharmaceutical applications. However, specific safety and handling guidelines should be followed due to the potential toxicity associated with fluorinated organic compounds.

(1-FLUOROCYCLOHEXYL)METHANOL

117169-30-9: (1-Fluorocyclohexyl)methanol is an organic compound characterized by the presence of a cyclohexyl ring substituted with a fluorine atom and a hydroxymethyl group. This compound features a cyclohexane structure, which contributes to its cyclic nature and potential for conformational isomerism. The fluorine atom introduces unique electronic properties, influencing the compound's reactivity and polarity. The hydroxymethyl group (-CH2OH) enhances its solubility in polar solvents and can participate in hydrogen bonding, affecting its physical properties such as boiling and melting points. (1-Fluorocyclohexyl)methanol may exhibit interesting biological activities due to its structural features, making it a subject of interest in medicinal chemistry and drug design. Its synthesis typically involves the introduction of the fluorine atom and subsequent functionalization of the cyclohexane ring. As with many fluorinated compounds, it may also exhibit stability against metabolic degradation, which can be advantageous in pharmaceutical applications. However, specific safety and handling guidelines should be followed due to the potential toxicity associated with fluorinated organic compounds.

CAS 117169-30-9

(1-FLUOROCYCLOHEXYL)METHANOL

(1-Fluorocyclohexyl)methanol

Ref: IN-DA000DUA

(1-Fluorocyclohex-1-yl)methanol

Ref: 54-PC49014

(1-Fluorocyclohexyl)methanol

Ref: 10-F067773