Cyclohexanol msds fisher. The parent of the class of cyclohexanols.

Cyclohexanol msds fisher Jun 13, 2005 · Generic Name Cyclohexanol DrugBank Accession Number DB03703 Background Monohydroxy derivatives of cyclohexanes that contain the general formula R-C6H11O. Soc. ; Holmes, J. It is a colorless, viscous liquid or cristalline solid with a camphor-like odor that is very soluble in most organic solvents. May 20, 2025 · cyclohexanol - cas 108-93-0, synthesis, structure, density, melting point, boiling point Sep 25, 2025 · Cyclohexanol (CAS 108-93-0) information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses, prices, suppliers, SDS and more, available at Chemicalbook. Am. They have a camphorlike odor and are used in making soaps, insecticides, germicides, dry cleaning, and plasticizers. Since there is only one possible arrangement of the atoms in cyclohexanol, it does not require a numerical prefix to specify its position or number of functional groups. Alcohols exhibit both weak acid and weak base behavior. ; Morgan, R. Cyclohexanol may be used in the preparation of ε-caprolactam and adipic acid, important precursors for the industrial synthesis of nylon-6 and nylon-6. , 1975, 97, 4936. [PubChem] Modality Small Molecule Groups Experimental Structure 3D Download CYCLOHEXANOL is an alcohol. , 1975 Derrick, P. It is a secondary alcohol and a member of cyclohexanols. Derrick, Holmes, et al. Cyclohexanol has a single hydroxyl (-OH) functional group attached to a cyclohexane ring, and its molecular formula is C6H12O. L. Aug 14, 2024 · Cyclohexanol is an organic compound with the chemical formula C6H12O. , Kinetics and mechanisms of the loss of water from the cyclohexanol radical ion at times from 50 picoseconds to 10 microseconds following field ionization, J. [4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature. [4] Cyclohexanol is an alcohol that consists of cyclohexane bearing a single hydroxy substituent. They react with oxoacids and carboxylic acids to form esters plus water. J. Cyclohexanol is the organic compound with the formula HOCH (CH 2) 5. P. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group. . Oxidizing agents convert them to aldehydes or ketones. [all data] Jun 13, 2005 · Generic Name Cyclohexanol DrugBank Accession Number DB03703 Background Monohydroxy derivatives of cyclohexanes that contain the general formula R-C6H11O. It has a role as a solvent. Chem. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. The parent of the class of cyclohexanols. Cyclohexanol is the organic compound with the formula HOCH (CH 2) 5. 6, respectively.