Cyclohexanol, 4-methoxy-, trans- is an organic compound characterized by a cyclohexane ring with a hydroxyl group (-OH) and a methoxy group (-OCH3) attached to the fourth carbon in a trans configuration. This compound is a colorless to pale yellow liquid with a characteristic odor, and it is soluble in organic solvents while exhibiting limited solubility in water. The presence of the hydroxyl group contributes to its properties as an alcohol, influencing its reactivity and hydrogen bonding capabilities. The methoxy group, being an electron-donating substituent, can affect the compound's reactivity and stability. Cyclohexanol derivatives are often used in the synthesis of various chemicals, including fragrances, pharmaceuticals, and as solvents. The trans configuration of the methoxy group relative to the hydroxyl group can impact the compound's physical properties, such as boiling point and melting point, as well as its biological activity. Overall, cyclohexanol, 4-methoxy-, trans- is a versatile compound with applications in both industrial and research settings.

Cyclohexanol, 4-methoxy-, trans-

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Trans-4-Methoxycyclohexanol

trans-4-Methoxycyclohexanol

Trans-4-methoxycyclohexanol (TMC) is a cyclohexanol derivative that reacts with hydrogen peroxide to form a reactive intermediate. The reaction of the TMC molecule with hydrogen peroxide forms an unstable bond, which is then cleaved by a nucleophilic attack from water molecules. The reaction time for this process is shorter than that of other cyclohexanol derivatives. This product has been shown to be effective at breaking down organic acids such as acetic acid and formic acid.

CAS 22188-03-0: Cyclohexanol, 4-methoxy-, trans-

Trans-4-Methoxycyclohexanol

Ref: 10-F988470

trans-4-Methoxycyclohexanol

Ref: IN-DA00BG44

trans-4-Methoxycyclohexanol

Ref: 3D-XAA18803

trans-4-Methoxycyclohexanol

Ref: TR-M409060