Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Cyclohexanol is the organic compound with the formula HOCH(CH2)5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group.[4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature. Millions of tonnes are produced annually, mainly as a precursor to nylon.[5]
^Merck Index, 11th Edition, 2731.
^ abcdNIOSH Pocket Guide to Chemical Hazards. "#0165". National Institute for Occupational Safety and Health (NIOSH).
^"Cyclohexanol". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
^Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
^Michael Tuttle Musser "Cyclohexanol and Cyclohexanone" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.
Cyclohexanol is the organic compound with the formula HOCH(CH2)5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl...
using cobalt catalysts: C6H12 + O2 → (CH2)5CO + H2O This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol...
than benzene. In the laboratory, it can be prepared by dehydration of cyclohexanol. C6H11OH → C6H10 + H2O Benzene is converted to cyclohexylbenzene by acid-catalyzed...
undergoes catalytic oxidation to produce cyclohexanone and cyclohexanol. The cyclohexanone–cyclohexanol mixture, called "KA oil", is a raw material for adipic...
In enzymology, a cyclohexanol dehydrogenase (EC 1.1.1.245) is an enzyme that catalyzes the chemical reaction cyclohexanol + NAD+ ⇌ {\displaystyle \rightleftharpoons...
Adipic acid is produced by oxidation of a mixture of cyclohexanone and cyclohexanol, which is called KA oil, an abbreviation of ketone-alcohol oil. Nitric...
Isobornyl cyclohexanol (IBCH, Sandenol) is an organic compound used primarily as a fragrance because of its aroma which is similar to sandalwood oil. Its...
methoxyphenyl)ethyl]cyclohexanol, though it is sometimes referred to as (±)-1-[a-[a-(dimethylamino)methyl]-p-methoxybenzyl]cyclohexanol. It consists of two...
a solvent choice of cyclohexanol. Curiously they found that when they used lower-purity (e.g. technical grade, 98%) cyclohexanol, the reaction proceeded...
Erythromycin is an antibiotic used for the treatment of a number of bacterial infections. This includes respiratory tract infections, skin infections,...
proceed via carbocation]]ic intermediates as shown for the dehydration of cyclohexanol. Some alcohols are prone to dehydration. 3-Hydroxylcarbonyls, called...
nitrite is an organic compound, with formula C6H11NO2. It is the ester of cyclohexanol and nitrous acid, i.e. it is an alkyl nitrite. Like amyl nitrite and...
It is a colorless liquid. Cyclohexyl chloride can be prepared from cyclohexanol by treatment with hydrogen chloride. Henry Gilman and W. E. Catlin (1926)...
The molecular formula C6H12O may refer to: Cyclohexanol Cyclopentyl methyl ether Ethyl isopropyl ketone Hexanal 2-Hexanone 3-Hexanone cis-3-Hexen-1-ol...
hydrolyzed, releasing carbon dioxide. The metabolite at this step is cyclohexanol which, being relatively non-toxic, is advantageous to the design of the...
phenylalanine, trans-cinnamate, benzamide, salicylate, cyclohexanone, cyclohexanol and cyclohexane-2-carboxylate. Ramana, Ch. V. (1 September 2006). "Rubrivivax...
of the following isomeric organic compounds with the formula C6H13OH: Cyclohexanol Amyl alcohol This set index article lists chemical compounds articles...
(OTC) Identifiers IUPAC name trans-4-(2-Amino-3,5-dibromobenzylamino)-cyclohexanol CAS Number 18683-91-5 N PubChem CID 2132 ChemSpider 10276826 Y UNII 200168S0CL...
+ 3 H2 → C6H11NH2 It is also prepared by alkylation of ammonia using cyclohexanol. Cyclohexylamine is used as an intermediate in synthesis of other organic...
process involves electrophilic aromatic substitution using a tethered cyclohexanol group using diphosphorus pentoxide, which closes the central ring onto...
these date to 1947 by Givaudan in Switzerland. The resulting isobornyl cyclohexanol can be distinguished from santolol, but is much cheaper. Since then other...
catalytic amounts of copper(II) salts. The phenol can be converted to cyclohexanol, which is a starting material for nylon synthesis. Benzoate plasticizers...
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