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Chemical compound
Cyclohexanol is the organic compound with the formula (CH2)5CHOH or C6H11OH. The molecule is related to cyclohexane by replacement of one hydrogen atom
Cyclohexanol
Chemical compound
Isobornyl cyclohexanol (IBCH, Sandenol) is an organic compound used primarily as a fragrance because of its aroma which is similar to sandalwood oil ("sandalwood
Isobornyl_cyclohexanol
Chemical compound
trans-2-Phenyl-1-cyclohexanol is an organic compound. The two enantiomers of this compound are used in organic chemistry as chiral auxiliaries. The enantioselective
Trans-2-Phenyl-1-cyclohexanol
Chemical compound
hydrogen to cyclohexanol, which he wasn't able to isolate, and then oxidized by electrolytic oxygen. Cyclohexanone can be prepared from cyclohexanol by oxidation
Cyclohexanone
Chemical compound
4-Phenyl-4-(1-piperidinyl)cyclohexanol, also known as PPC, is an organic chemical which is a metabolite of phencyclidine (PCP). It can be detected in the
4-Phenyl-4-(1-piperidinyl)cyclohexanol
4-Phenyl-4-(1-piperidinyl)cyclohexanol
Chemical compound
than benzene. In the laboratory, it can be prepared by dehydration of cyclohexanol. C6H11OH → C6H10 + H2O Benzene is converted to cyclohexylbenzene by acid-catalyzed
Cyclohexene
In enzymology, a cyclohexanol dehydrogenase (EC 1.1.1.245) is an enzyme that catalyzes the chemical reaction cyclohexanol + NAD+ ⇌ {\displaystyle \rightleftharpoons
Cyclohexanol_dehydrogenase
Chemical compound
It is a colorless liquid. Cyclohexyl chloride can be prepared from cyclohexanol by treatment with hydrogen chloride. Henry Gilman and W. E. Catlin (1926)
Cyclohexyl_chloride
Organic compound; 6-sided hydrocarbon ring
autoxidation to give a mixture of cyclohexanone and cyclohexanol. The cyclohexanone–cyclohexanol mixture, called "KA oil", is a raw material for adipic
Cyclohexane
SNRI antidepressant
methoxyphenyl)ethyl]cyclohexanol, though it is sometimes referred to as (±)-1-[a-[a-(dimethylamino)methyl]-p-methoxybenzyl]cyclohexanol. It consists of two
Venlafaxine
Chemical compound (CH2)4(COOH)2
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
Adipic_acid
Stereogenic group placed on a molecule to encourage stereoselectivity in reactions
compound is difficult to prepare and as an alternative trans-2-phenyl-1-cyclohexanol was introduced by J. K. Whitesell in 1985. Chiral auxiliaries are incorporated
Chiral_auxiliary
Angiotensin II receptor antagonist
is hydrolyzed, releasing carbon dioxide. This reaction also produces cyclohexanol, a relatively non-toxic byproduct that contributes to the favorable safety
Candesartan
Class of enzymes
class is 6-oxohexanoate:NADP+ oxidoreductase. This enzyme is involved in cyclohexanol degradation in Acinetobacter. Enzyme 1.2.1.63 at KEGG Pathway Database
6-oxohexanoate_dehydrogenase
Chemical compound
a solvent choice of cyclohexanol. Curiously they found that when they used lower-purity (e.g. technical grade, 98%) cyclohexanol, the reaction proceeded
Cyclohexenone
Chemical compound
combustable liquid. Fluorocyclohexane can by prepared by reaction of cyclohexanol with hydrogen fluoride. Fluoroalkanes Fluorocyclopropane Fluorobenzene
Fluorocyclohexane
Chemical compound
extremely resistant to hydrolysis. DCFP can be produced by reaction of cyclohexanol with phosphoryl dichloride fluoride. Diisopropyl phosphorofluoridate
Dicyclohexyl phosphorofluoridate
Dicyclohexyl_phosphorofluoridate
Synthetic opioid
(systematic name 4-(4-bromophenyl)-4-(dimethylamino)-1-(2-phenylethyl)cyclohexanol; also known as bromadol) is a potent fully synthetic opioid with a distinctive
BDPC
Species of bacteria
phenylalanine, trans-cinnamate, benzamide, salicylate, cyclohexanone, cyclohexanol and cyclohexane-2-carboxylate. Ramana, Ch. V. (1 September 2006). "Rubrivivax
Rubrivivax_benzoatilyticus
liquids. The 2- and 3-isomers are chiral. Musser, Michael Tuttle (2000). "Cyclohexanol and Cyclohexanone". Ullmann's Encyclopedia of Industrial Chemistry. doi:10
Methylcyclohexanone
Chemical compound
11α-Hydroxyprogesterone (11α-OHP), or 11α-hydroxypregn-4-ene-3,20-dione is an endogenous steroid and metabolite of progesterone. It is a weak antiandrogen
11α-Hydroxyprogesterone
Index of chemical compounds with the same name
of the following isomeric organic compounds with the formula C6H13OH: Cyclohexanol Amyl alcohol This set index article lists chemical compounds articles
Hexanol
Pharmaceutical drug
7-12 h Identifiers IUPAC name trans-4-(2-Amino-3,5-dibromobenzylamino)-cyclohexanol CAS Number 18683-91-5 N PubChem CID 2132 DrugBank DB06742 Y ChemSpider
Ambroxol
Synthetic opioid pain medication
cyclohexanol] has two stereogenic centers at the cyclohexane ring. Thus, 2-(dimethylaminomethyl)-1-(3-methoxyphenyl)cyclohexanol may exist in
Tramadol
Genus of bacteria
taxonomy Microbiology Alicycliphilus denitrificans gen. nov., sp. nov., a cyclohexanol-degrading, nitrate-reducing β-proteobacterium Classification of Genera
Alicycliphilus
Chemical reaction in which water is produced as a byproduct
proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. Some alcohols are prone to dehydration. 3-Hydroxylcarbonyls, called
Dehydration_reaction
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Sorbitol
Chemical compound
hydroperoxide that is typically used to assist in industrially producing cyclohexanol and cyclohexanone. These compounds are then usually turned into the polymer
Cyclohexyl_hydroperoxide
Saturated alicyclic hydrocarbon
to produce high octane gasoline. In another major industrial process, cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt
Cycloalkane
American chemical company
phenol, and alpha-methylstyrene from the cumene process. They sell cyclohexanol and cyclohexanone made from phenol, caprolactam, as well as ammonium
AdvanSix
Organic compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Ethanol
Chemical compound
+ 3 H2 → C6H11NH2 It is also prepared by alkylation of ammonia using cyclohexanol. Cyclohexylamine is used as an intermediate in synthesis of other organic
Cyclohexylamine
Chemical compound
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
Cyclohexyl_nitrite
Comprehensive list of compounds structurally related to fentanyl
previous example of cyclohexanol, is the stereocenter at C-4 is indeed a true stereocenter here, whereas in the previous example of cyclohexanol as an analogy
List_of_fentanyl_analogues
Sugar alcohol used as a sweetener
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Maltitol
Chemical compound found in oil of lemon eucalyptus
p-Menthane-3,8-diol, also known as para-menthane-3,8-diol, PMD, citriodiol or geranodyle, is an organic compound classified as a diol and a terpenoid.
P-Menthane-3,8-diol
Organic compound (C6H5COOH)
catalytic amounts of copper(II) salts. The phenol can be converted to cyclohexanol, which is a starting material for nylon synthesis. Benzoate plasticizers
Benzoic_acid
Index of chemical compounds with the same molecular formula
The molecular formula C6H12O may refer to: Cyclohexanol Cyclopentyl methyl ether 3,3-Dimethylbutyraldehyde Ethyl isopropyl ketone Hexanal 2-Hexanone 3-Hexanone
C6H12O
Active ingredient in fermented drinks
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Alcohol_(drug)
Opioid analgesic
Oxymorphazone is an opioid analgesic drug related to oxymorphone. Oxymorphazone is a potent and long acting μ-opioid agonist which binds irreversibly to
Oxymorphazone
Chemical substance
Ouabain /wɑːˈbɑːɪn/ or /ˈwɑːbeɪn, ˈwæ-/ (from Somali waabaayo, "arrow poison" through French ouabaïo) also known as g-strophanthin, is a plant derived
Ouabain
Cannabinoid agonist compound
CP 47,497 or (C7)-CP 47,497 is a cannabinoid receptor agonist drug, developed by Pfizer in the 1980s. It has analgesic effects and is used in scientific
CP_47,497
Chemical compound
compounds Related compounds Cyclopropanol Cyclobutanol Cyclopentanol Cyclohexanol Cycloheptanol Cyclooctanone Except where otherwise noted, data are given
Cyclooctanol
Genus of flowering plant in the mistletoe family Santalaceae
Due to its high cost, it is often replaced in perfumery by Isobornyl cyclohexanol. 19 species are currently accepted: S. acuminatum A.DC. — desert quandong
Santalum
Chemical compound
ethoxide and nitromethane. The resulting sodium salt of 1-(nitromethyl)cyclohexanol is added to acetic acid and shaken with hydrogen gas in the presence
Cycloheptanone
Antidepressant
biochemical profile of the novel bicyclic compound Wy-45,030, an ethyl cyclohexanol derivative". Biochemical Pharmacology. 35 (24): 4493–4497. doi:10
Imipramine
Essential oil
present levels that the oil is used in food as flavorings. Isobornyl cyclohexanol, a synthetic sandalwood oil Sandalore, a synthetic sandalwood odorant
Sandalwood_oil
Polycyclic aromatic hydrocarbon composed of three fused benzene rings
process involves electrophilic aromatic substitution using a tethered cyclohexanol group using diphosphorus pentoxide, which closes the central ring onto
Phenanthrene
of alcohols including those that are difficult to halogenate, such as cyclohexanol, which normally decomposes to form cyclohexene if reacted with only SOCl2
Darzens_halogenation
Class of woods from trees in the genus Santalum
alternative sources lose their aroma within a few months or years. Isobornyl cyclohexanol is a synthetic fragrance chemical produced as an alternative to the natural
Sandalwood
Chemical compound
more environmentally friendly than the traditional method of oxidizing cyclohexanol or cyclohexanone with nitric acid or potassium permanganate, which produce
Aliquat_336
Index of chemical compounds with the same molecular formula
3-HO-PCP 4'-Methyl-α-pyrrolidinohexiophenone PCHP 4-Phenyl-4-(1-piperidinyl)cyclohexanol α-Pyrrolidinoheptaphenone Vesamicol This set index page lists chemical
C17H25NO
Index of chemical compounds with the same molecular formula
39 g/mol, exact mass: 236.2140 u) may refer to: Ambroxide Isobornyl cyclohexanol (IBCH) 5-Cyclohexadecenone Cedramber Cetalor This set index page lists
C16H28O
Chemical compound (nerve agent)
with the other capsule containing a mixture of cyclohexylamine and cyclohexanol. Iraq fielded munitions filled with a mixture of GB (sarin) and GF (cyclosarin)
Cyclosarin
Organic compound (C6H5OH)
13–40, ISBN 978-0-12-821632-3, retrieved 2025-05-15 Musser, Michael T. "Cyclohexanol and Cyclohexanone". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim:
Phenol
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Fucitol
Natural sweetener
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Xylitol
Chemical compound
mixture of cyclohexanol and cyclohexanone) which is obtained during the oxidation of cyclohexane. The reaction proceeds via cyclohexanol hydroperoxide
N-Hydroxyphthalimide
diphenylsilane 778-24-5 C14H17ClNO4PS2 dialifor 10311-84-9 C14H17F5OSi cyclohexanol dmpfps 71338-76-6 C14H17MnO2 cycloheptenecyclopentadienylmanganese dicarbonyl
List of compounds with carbon number 14
List_of_compounds_with_carbon_number_14
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
1-Octanol
Tschech A, Fuchs G (1989). "Enzyme-reactions involved in anaerobic cyclohexanol metabolism by a denitrifying Pseudomonas species". Arch. Microbiol. 152
Cyclohexane-1,3-dione hydrolase
Cyclohexane-1,3-dione_hydrolase
Simplest secondary alcohol
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Isopropyl_alcohol
Type of organic chemical reaction
Elimination reaction of cyclohexanol to cyclohexene with sulfuric acid and heat
Elimination_reaction
Measurements of stable atom orientations
trans compound had rates identical to those found in the monosubstituted cyclohexanol. Using the A-values of the hydroxyl and isopropyl subunit, the energetic
A_value
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
3-Methyl-1-pentanol
Chemical compound
Fluocinonide is a potent glucocorticoid used topically as an anti-inflammatory agent for the treatment of skin disorders such as eczema and seborrhoeic
Fluocinonide
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Glycerol
Tranquilizer based with herbs Valerian, hops, peppermint & phenobarbital, a barbiturate
isovalerate by carbonylation of isobutylene with carbon monoxide and cyclohexanol in the presence of Pd (PPh 3) 4‒PPh 3‒TsOH and its antimicrobial activity
Corvalol
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
List_of_alkanols
Class of chemical compounds
Synth. 63: 66. doi:10.15227/orgsyn.063.0066. Michael T. Musser (2005). "Cyclohexanol and Cyclohexanone". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim:
Hydroperoxide
Chemical compound
Alloxydim is a chemical compound. Its formula is C17H25NO5. A member of the cyclohexanedione herbicide class, alloxydim is a post-emergence herbicide.
Alloxydim
Chemical reaction
toluene, acrolein from propylene, acetone from cumene, cyclohexanone from cyclohexanol. In teaching laboratories and small scale operations, many reagents have
Alcohol_oxidation
Chemical compound
1-Adamantyl Calcium Halides and Their Addition to Ketones: 1-(1-Adamantyl)cyclohexanol". Org. Synth. 72: 147. doi:10.15227/orgsyn.072.0147. Mudryk, Boguslaw;
Biphenyl
Sugar alcohol that is used as a sweetener
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Erythritol
Organic compound with at least one hydroxyl (–OH) group
oxidases facilitate these conversions. Many industrial alcohols, such as cyclohexanol for the production of nylon, are produced by hydroxylation. In the Ziegler
Alcohol_(chemistry)
Medication for the treatment of atrial fibrillation
Vernakalant, sold under the brand name Brinavess, is medication used for acute conversion of atrial fibrillation. It is given as an intravenous infusion
Vernakalant
Dimer for protein manipulation
FK1012 is a dimer consisting of two molecules of tacrolimus (FK506) linked via their vinyl groups. It is used as a research tool in chemically induced
FK1012
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Neopentyl_alcohol
Highly corrosive mineral acid
large scale by oxidation of "KA oil"—a mixture of cyclohexanone and cyclohexanol—with nitric acid. Nitric acid has been used in various forms as the oxidizer
Nitric_acid
Type of thermodynamic potential
heat into an inherently endergonic reaction, such as the elimination of cyclohexanol to cyclohexene, can be seen as coupling an unfavorable reaction (elimination)
Gibbs_free_energy
Chemical compound
case study using platinum(ii) acetylacetonate in mixtures of acetone, cyclohexanol, 1,2,3,4-tetrahydronaphthalene and propylene carbonate". Green Chemistry
Platinum(II) bis(acetylacetonate)
Platinum(II)_bis(acetylacetonate)
NGO enabling communication about chemistry
"hexane" (C 6H 14). Another example of IUPAC organic nomenclature is cyclohexanol: The substituent name for a ring compound is cyclo. The indication (substituent
International Union of Pure and Applied Chemistry
International_Union_of_Pure_and_Applied_Chemistry
Spontaneous oxidation by oxygen at normal temperature
diisopropylbenzene as a substrate. the autoxidation of cyclohexane yields cyclohexanol and cyclohexanone. p-xylene undergoes auoxidation to terephthalic acid
Autoxidation
Organic reduction of any carbonyl group by a reducing agent
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Carbonyl_reduction
Organic reaction
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Nucleophilic conjugate addition
Nucleophilic_conjugate_addition
Chemical compound
Kifunensine is an alkaloid originally isolated from Kitasatosporia kifunense, an actinobacterium (formerly called an actinomycete). It is a neutral, stable
Kifunensine
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Threitol
Free radical species
1-Adamantyl Calcium Halides and Their Addition to Ketones: 1-(1-Adamantyl)cyclohexanol". Org. Synth. 72: 147. doi:10.15227/orgsyn.072.0147. Castillo, Maximiliano;
Radical_anion
Organic reaction
peroxide often promotes side-reactions. Oxygen can be used to convert cyclohexanol to caprolactone, but the process generates hydrogen peroxide in situ:
Baeyer–Villiger_oxidation
Group specially prepared, highly reactive metal powder
1-Adamantyl Calcium Halides and Their Addition to Ketones: 1-(1-Adamantyl)cyclohexanol"". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors
Rieke_metal
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
1-Docosanol
Primary alcohol with 17 carbons
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
1-Heptadecanol
Organic compound ethane-1,2-diol
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Ethylene_glycol
Chemical compound
Ramesh Krishnamurti; G. K. Surya Prakash (1995). "1-Trifluoromethyl-1-cyclohexanol". Org. Synth. 72: 232. doi:10.15227/orgsyn.072.0232. George. A. Olah;
Trifluoromethyltrimethylsilane
Trifluoromethyltrimethylsilane
American chemist (1938–2024)
Catalytic conversion of cyclohexylhydroperoxide to cyclohexanone and cyclohexanol, Journal of Molecular Catalysis (1988), 48(1), 129–48 John W. Collette
Chadwick_A._Tolman
Chemical compound
Lyster (1979). "Cleavage of Methyl Ethers with Iodotrimethylsilane: Cyclohexanol from Cyclohexyl Methyl Ether". Organic Syntheses. 59: 35. doi:10.15227/orgsyn
Hexamethyldisiloxane
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
1-Octen-3-ol
Semi-synthetic opioid
Dihydrocodeine, sold under the brand name Dicodin among others, is a semi-synthetic opioid analgesic prescribed for pain or severe dyspnea, or as an antitussive
Dihydrocodeine
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
Mannitol
Chemical compound
3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol
2-Heptanol
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL
CYCLOHEXANOL