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Chemical compound
Cyclohexanone is the organic compound with the formula (CH2)5CO. The molecule consists of six-carbon cyclic molecule with a ketone functional group. This
Cyclohexanone
Chemical compound
Cyclohexanone oxime is an organic compound containing the functional group oxime. This colorless solid is an important intermediate in the production
Cyclohexanone_oxime
In enzymology, cyclohexanone dehydrogenase (EC 1.3.99.14) is an enzyme that catalyzes a redox chemical reaction of the form cyclohexanone + electron acceptor
Cyclohexanone_dehydrogenase
Organic compound; 6-sided hydrocarbon ring
cyclohexane undergoes autoxidation to give a mixture of cyclohexanone and cyclohexanol. The cyclohexanone–cyclohexanol mixture, called "KA oil", is a raw material
Cyclohexane
Class of enzymes
Cyclohexanone monooxygenase (EC 1.14.13.22, cyclohexanone 1,2-monooxygenase, cyclohexanone oxygenase, cyclohexanone:NADPH:oxygen oxidoreductase (6-hydroxylating
Cyclohexanone_monooxygenase
Chemical compound
caprolactam. It was estimated that 90% of all caprolactam is synthesised from cyclohexanone (1), which is first converted to its oxime (2). Treatment of this oxime
Caprolactam
Organic compound (C6H5OH)
alkenes, and ketones. Thus, adamantyl-1-bromide, dicyclopentadiene), and cyclohexanones give respectively 4-adamantylphenol, a bis(2-hydroxyphenyl) derivative
Phenol
Chemical compound
to both phenol and cyclohexanone. Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam
Cyclohexene
3-methylcyclohexanone, and 4-methylcyclohexanone. They can be viewed as derivative of cyclohexanone. They can be prepared by oxidation of methylcyclohexane as well as partial
Methylcyclohexanone
Organic compounds of the form >C=O
for cyclopropanone ((CH2)2CO) to the tens. Larger derivatives exist. Cyclohexanone ((CH2)5CO), a symmetrical cyclic ketone, is an important intermediate
Ketone
Chemical compound
the formation of cyclohexanone. Cyclohexanol undergoes the main reactions expected for a secondary alcohol. Oxidation gives cyclohexanone, which is converted
Cyclohexanol
Synthetic opioid
4-Dimethylamino-4-(p-tolyl)cyclohexanone (sometimes known as dimetamine) is a opioid analgesic with an arylcyclohexylamine chemical structure. It was
4-Dimethylamino-4-(p-tolyl)cyclohexanone
4-Dimethylamino-4-(p-tolyl)cyclohexanone
American chemical company
cyclohexanol and cyclohexanone made from phenol, caprolactam, as well as ammonium sulfate generated by the Beckmann rearrangement of cyclohexanone oxime. The
AdvanSix
Chemical compound
and/or tantalic acid. It is also obtained by reductive amination of cyclohexanone with ammonia or cyclohexylamine. Dicyclohexylamine may also be prepared
Dicyclohexylamine
Chemical compound
Isobutyric anhydride is a reagent in the production of the ester of cyclohexanone oxime. Isobutyric anhydride is used as an acylating agent in organic
Isobutyric_anhydride
Polymer resin widely used in packaging
carbon disulfide, chlorinated aliphatic hydrocarbons, chloroform, cyclohexanone, dioxane, ethyl acetate, ethylbenzene, MEK, NMP, THF Thermal conductivity
Polystyrene
Chemical compound (CH2)4(COOH)2
known as adipates. Adipic acid is produced by oxidation of a mixture of cyclohexanone and cyclohexanol, which is called KA oil, an abbreviation of ketone-alcohol
Adipic_acid
Class of enzymes
acetyl-CoA + cyclohexanone Hence, this enzyme has one substrate, (1-hydroxycyclohexan-1-yl)acetyl-CoA, and two products, acetyl-CoA and cyclohexanone. This enzyme
(1-hydroxycyclohexan-1-yl)acetyl-CoA lyase
(1-hydroxycyclohexan-1-yl)acetyl-CoA_lyase
Chemical reaction
synthesize tetrahydrocarbazoles by the acid-catalyzed cyclization of cyclohexanone arylhydrazones. The reaction was first described by Edmund Drechsel [de]
Borsche–Drechsel_cyclization
Substance dissolving a solute resulting in a solution
Solvent R-12 toluene 60%, butyl acetate 30%, xylene 10%. Solvent R-14 cyclohexanone 50%, toluene 50%. Solvent R-24 solvent[clarification needed] 50%, xylene
Solvent
Chemical compound
In terms of its structure, it can also be regarded as benzo-fused cyclohexanone. It is a colorless oil with a faint odor. It is used as starting material
1-Tetralone
Colourless non-flammable greenhouse gas
degradation of the nitrolic acid intermediate derived from the nitration of cyclohexanone. Microbial processes that generate nitrous oxide may be classified as
Nitrous_oxide
Industrial process
cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone. Cyclohexanone is an important precursor to some nylons. Starting with the alkylation
Cumene_process
Chemical compound
produced by a Wittig reaction or a reaction with a Tebbe's reagent from cyclohexanone. It can also be synthesized as a side product of the dehydration of
Methylenecyclohexane
Species of plant in the carrot family
γ‑terpinene, trimethylene dichloride, β-pinene, 2-(1-cyclohexenyl), cyclohexanone, β-phellandrene, 3-carene, α-thujene, and linalool. Wikibooks Cookbook
Caraway
Class of chemical compounds
industry. For example, the cobalt catalyzed oxidation of cyclohexane to cyclohexanone: C6H12 + O2 → (CH2)5C=O + H2O Drying oils, as found in many paints and
Hydroperoxide
Organic chemical reaction
Knoevenagel condensation is demonstrated in this MORE synthesis with cyclohexanone, malononitrile and 3-amino-1,2,4-triazole: The Weiss–Cook reaction consists
Knoevenagel_condensation
Chemical compound
process. On an industrial scale, the well-filtered starting materials cyclohexanone and glyoxylic acid are first transformed in an acid-catalyzed aldol
2-Coumaranone
Type of aldol condensation reaction
used in order to perform the crossed condensation between acetone and cyclohexanone. The deprotonation step using LDA is so fast that the enolate formed
Self-condensation
Organic compound ((CH3)2CO); simplest ketone
Determination of the Equilibrium Constants for Keto-Enol Tautomerism for Cyclohexanone and Acetone". Bulletin of the Chemical Society of Japan. 49 (11): 3089–3092
Acetone
Chemical compound
(C6H10OH)2O2. It is one of the peroxides derived from the reaction of cyclohexanone and hydrogen peroxide. Upon treatment with acid and additional peroxide
1,1'-Dihydroxydicyclohexyl peroxide
1,1'-Dihydroxydicyclohexyl_peroxide
Chemical group (–OSO2CF3) or anion (charge –1)
addition reaction between benzaldehyde and the silyl enol ether of cyclohexanone with an 81% chemical yield. The corresponding reaction with the yttrium
Triflate
Organic reaction
consisted of a nucleophilic aliphatic substitution of the enolate of ethyl cyclohexanone-2-carboxylate with 1,4-diiodobutane and sodium hydride followed by ring
Dowd–Beckwith ring-expansion reaction
Dowd–Beckwith_ring-expansion_reaction
Organic compound consisting entirely of hydrogen and carbon
xylenes, acetone together with phenol from cumene (isopropylbenzene), and cyclohexanone from cyclohexane. The process, which is called autoxidation, begins
Hydrocarbon
Index of chemical compounds with the same molecular formula
The molecular formula C6H11NO may refer to: Caprolactam (CPL) Cyclohexanone oxime N-Formylpiperidine Nylon 6 (repeating unit), or polycaprolactam Pentyl
C6H11NO
Chemical compound
J. Pachter, and M. L. Scheinbaum (1974). "2,2-(Trimethylenedithio)cyclohexanone". Organic Syntheses. 54: 39{{cite journal}}: CS1 maint: multiple names:
Pyrrolidine
Chemical reactions with oxygen
cyclohexane K-A process Co and Mn salts (homogeneous) cyclohexanol cyclohexanone nylon precursor ethylene Wacker process Pd and Cu salts (homogeneous)
Catalytic_oxidation
Dissociative anesthetic and anti-depressant
Ketamine is a cyclohexanone-derived general anesthetic and NMDA receptor antagonist with analgesic and hallucinogenic properties, used medically for anesthesia
Ketamine
Highly corrosive mineral acid
is produced on a large scale by oxidation of "KA oil"—a mixture of cyclohexanone and cyclohexanol—with nitric acid. Nitric acid has been used in various
Nitric_acid
Chemical compound
typically used to assist in industrially producing cyclohexanol and cyclohexanone. These compounds are then usually turned into the polymer nylon 6 (polycaprolactam)
Cyclohexyl_hydroperoxide
Class of psychoactive drugs
DR (1967). "An anaesthetic agent: 2-orthochlorophenyl, 2-methylamino cyclohexanone HCl (CI-581)". Anesthesiology. 28 (5): 823–33. doi:10.1097/00000542-196709000-00008
Dissociative
Chemical compound
cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone: C6H5−C6H10OOH → C6H5OH + OC6H10 Cyclohexanone is an important precursor to some nylons. Быков
Cyclohexylbenzene
Chemical rearrangement
aptitude. The archetypal Beckmann rearrangement is the conversion of cyclohexanone to caprolactam via the oxime. Caprolactam is the feedstock in the production
Beckmann_rearrangement
Chemical compound
catalysts, such as the Henbest Catalyst for transfer hydrogenation of cyclohexanones. PubChem. "Iridium tetrachloride". pubchem.ncbi.nlm.nih.gov. Retrieved
Iridium_tetrachloride
Pharmaceutical drug
[citation needed] The compound is synthesized by reacting acetylene with cyclohexanone to form 1-ethynylcyclohexanol. This intermediate is then converted into
Ethinamate
Chemical compound
and Speed of Sound in the Binary Mixtures of Ethyl Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol at (298.15, 303
Bromobenzene
Pyrophoric liquid
selectively than in its absence. For example, the enolate from treating cyclohexanone with potassium hydride produces 2-allylcyclohexanone in 90% yield when
Triethylborane
Industrial accident in North Lincolnshire, England (1974)
used in the manufacture of nylon 6. The caprolactam was produced from cyclohexanone. This was originally produced by hydrogenation of phenol, but in 1972
Flixborough_disaster
and Speed of Sound in the Binary Mixtures of Ethyl Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol at (298.15, 303
List_of_viscosities
Composite material
methyl ethyl ketone peroxide (MEKP), acetyl acetone peroxide (AAP) or cyclohexanone peroxide (CHP). Vinyl ester resin is used under high impact stress.
Pre-preg
Chemical compound
polycarbonate plastics. It is prepared by the condensation of phenol and cyclohexanone: Clinofibrate Helmut Fiege; Heinz-Werner Voges; Toshikazu Hamamoto;
Bisphenol_Z
Chemical compound
in the UK in March 2012. 1-Ethynylcyclohexanol can be prepared from cyclohexanone by reacting it with sodium acetylide in liquid ammonia, followed by
1-Ethynylcyclohexanol
Saturated alicyclic hydrocarbon
using cobalt catalysts: 2 C6H12 + O2 → 2 C6H11OH This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock
Cycloalkane
Class of chemical compounds
129188-99-4 Phenol 3,3,5-Trimethylcyclohexanone Bisphenol Z 843-55-0 Phenol Cyclohexanone Dinitrobisphenol A 5329-21-5 Bisphenol A Nitric acid Tetrabromobisphenol
Bisphenol
Chemical compound
Jansen, A. B. A.; Walker, T. (1952), "A synthesis of vitamin a from cyclohexanone", J. Chem. Soc.: 1094–1111, doi:10.1039/JR9520001094. Paquette, Leo
Manganese_dioxide
Organic reaction
David P.; Massey, Vincent (1 September 2001). "Mechanistic Studies of Cyclohexanone Monooxygenase: Chemical Properties of Intermediates Involved in Catalysis"
Baeyer–Villiger_oxidation
Organometallic networks in chemistry
of [(ZnI2)3(TPT)2] crystalline sponges. The guest compounds, such as cyclohexanone, cinnamaldehyde were dropped onto the pre-made single crystal of crystalline
Crystalline_sponges
Chemical reaction in organic chemistry
reaction. Robinson and Rapson found in 1935 that the interaction between cyclohexanone and α,β-unsaturated ketone afforded the desired cyclohexenone. It remains
Robinson_annulation
Chemical compound
or cerium oxide. Cycloheptanone is also produced by the reaction of cyclohexanone with sodium ethoxide and nitromethane. The resulting sodium salt of
Cycloheptanone
Chemical compound
as dioxolanes are known. For example, consider the compound methyl cyclohexanone-4-carboxylate, where lithium aluminium hydride reduction will produce
Dioxolane
Chemical compound
a commercial fire retardant. It can be prepared by condensation of cyclohexanone to give cyclohexenylcyclohexanone. The latter undergoes dehydrogenation
2-Phenylphenol
Chemical compound
(acetaldehyde trimer) with SeO2 gives glyoxal and the oxidation of cyclohexanone gives 1,2-cyclohexanedione. The selenium starting material is reduced
Selenium_dioxide
Chemical compound
caprolactone. Many other methods exist. Pimelic acid has been synthesized from cyclohexanone and from salicylic acid. In the former route, the additional carbon
Pimelic_acid
Environmental pollutant reference values
carbofuran - 0.017 9 ng/L 100 VII Other substances asbestos - 100 - - cyclohexanone - 150 0.5 15,000 dimethyl phthalate - 82 - - diethyl phthalate - 53
Dutch_pollutant_standards
Cyclic amide
form from cyclic ketones and hydrazoic acid in the Schmidt reaction. Cyclohexanone with hydrazoic acid, forms ε - Caprolactam, which upon treatment with
Lactam
Chemical element with atomic number 41 (Nb)
extraction of the fluorides from aqueous solution by organic solvents like cyclohexanone. The complex niobium and tantalum fluorides are extracted separately
Niobium
Chemical compound
3-Fluorodeschloroketamine Identifiers IUPAC name 2-(3-Fluorophenyl)-2-methylamino-cyclohexanone CAS Number 2657761-23-2 PubChem CID 156538475 CompTox Dashboard (EPA)
3-Fluorodeschloroketamine
Burning within well-defined lower and upper bounds
Book Published by McGraw-Hill Professional, 2001 pg. 216 "ICSC 0425 - CYCLOHEXANONE". www.inchem.org. Retrieved 18 March 2018. "MSDS Cyclopentadiene". ox
Flammability_limit
salt to ice. Dry ice Acetonitrile -41 Dry ice Pyridine -42 Dry ice Cyclohexanone -46 Dry ice m-Xylene -47 Dry ice Diethyl carbitol -52 Dry ice n-Octane
List_of_cooling_baths
Predictive model in organic chemistry
from one side. In the simplest model, a conformationally constrained cyclohexanone is reduced to the corresponding alcohol. Reducing agents add a hydride
Cieplak_effect
Index of chemical compounds with the same molecular formula
The molecular formula C6H10O may refer to: Cyclohexanone Cyclohexene oxide cis-3-Hexenal Mesityl oxide 3-Methyl-3-penten-2-one Methylpentynol Methylene
C6H10O
Chemical compound
reduction of anisole followed by acid hydrolysis. It can be obtained from cyclohexanone by α-bromination followed by treatment with base. Hydrolysis of 3-chloro
Cyclohexenone
Acid that is insoluble in the reaction medium
ethylene to give ethylbenzene. Another application is the rearrangement of cyclohexanone oxime to caprolactam. Many alkylamines are prepared by amination of
Solid_acid
Organometallic compound (Pb(C2H3O2)4)
doi:10.1016/j.tetlet.2006.07.020. Conversion of 1-allylcyclohexanol to cyclohexanone, in the proposed reaction mechanism the allyl group is first converted
Lead(IV)_acetate
Species of plant
the pennyroyal plant is pennyroyal oil. The oil contains pulegone (a cyclohexanone), the molecule found in the highest concentration (80-92%) in the pennyroyal
Mentha_pulegium
Chemical compound
which then further decompose. HNO is generated via organic oxidation of cyclohexanone oxime with lead tetraacetate to form 1-nitrosocyclohexyl acetate: This
Nitroxyl
Chemical reaction
benzaldehyde from toluene, acrolein from propylene, acetone from cumene, cyclohexanone from cyclohexanol. In teaching laboratories and small scale operations
Alcohol_oxidation
Inorganic compound
rearrangement Approximately 95% of hydroxylamine is used in the synthesis of cyclohexanone oxime, a precursor to Nylon 6. The treatment of this oxime with acid
Hydroxylamine
3-dihydro-1-methyl-7-nitro-2H-1, 4-benzodiazepin-2-one) Ketamine (Cyclohexanone, 2-(2-chlorophenyl)-2-(methylamino)) Mazindol (5-(p-Chlorophenyl)-2
Psychotropic Substances Act (Thailand)
Psychotropic_Substances_Act_(Thailand)
Organic reaction
series of ketones are in the orders Cl3CCOCH3 > CH3COCH3 > C6H5COCH3 and cyclohexanone > cyclopentanone > cycloheptanone > cyclooctanone. These orders of reactivity
Büchner–Curtius–Schlotterbeck reaction
Büchner–Curtius–Schlotterbeck_reaction
Chemical reaction
Williams, D. R.; Druelinger, M. (1976). "Enantioselective alkylation of cyclohexanone via chiral lithio-chelated enamines". Journal of the American Chemical
Enders SAMP/RAMP hydrazone-alkylation reaction
Enders_SAMP/RAMP_hydrazone-alkylation_reaction
Common odor found in new cars
cars included the carcinogen benzene, two other possible carcinogens cyclohexanone and styrene, and several other toxic chemicals. A more recent study
New_car_smell
Class of chemical compounds
I. J. Pachter, M. L. Scheinbaum (1974). "2,2- (Trimethylenedithio)cyclohexanone". Organic Syntheses. 54: 39. doi:10.15227/orgsyn.054.0039{{cite journal}}:
Enamine
Chemical compound
cyclohexanone oxime hydrochloride. This process exploits the tendency of NOCl to undergo photodissociation into NO and Cl radicals. The cyclohexanone
Nitrosyl_chloride
8-hydroxyquinoline Coronene Coumarin m-Cresidine Cyclamates Cyclochlorotine Cyclohexanone 4H-Cyclopenta[def]chrysene 5,6-Cyclopenteno-1,2-benzanthracene D & C
IARC_group_3
pentylenetetrazol 54-95-5 C6H10O acetylcyclobutane 3019-25-8 C6H10O cyclohexanone 108-94-1 C6H10O cyclohexene oxide 286-20-4 C6H10O hexenal 1335-39-3
List of compounds with carbon number 6
List_of_compounds_with_carbon_number_6
Organic reaction
methylamine to cyclohexen-2-one gives the compound 3-(N-methylamino)-cyclohexanone. Conjugated carbonyls react with hydrogen cyanide to 1,4-keto-nitriles
Nucleophilic conjugate addition
Nucleophilic_conjugate_addition
Chemical used in plastics, xenoestrogen
Formaldehyde Bisphenol S 80-09-1 Phenol Sulfur trioxide Bisphenol Z 843-55-0 Phenol Cyclohexanone Tetramethyl bisphenol F 5384-21-4 2,6-xylenol Formaldehyde
Bisphenol_A
Organic reaction
1979. It is a metal-mediated rearrangement of enol ether pyrans to cyclohexanones. Typically, this reaction is catalyzed by mercury salts, specifically
Ferrier_carbocyclization
Canadian federal drug regulation act
and analogues, including: Ketamine (2-(2-chlorophenyl)-2-(methylamino)cyclohexanone) Piritramide (1-(3-cyano-3,3-diphenylpropyl)-4-(1-piperidino)piperidine-4-carboxylic
Controlled Drugs and Substances Act
Controlled_Drugs_and_Substances_Act
3D printing process that melts thermoplastic material from a spool of filament
ethylbenzene, formaldehyde, acetaldehyde, nonanal, tetrahydrofuran, cyclohexanone, butanone, crotonaldehyde, acrylic acid, hydroxyethyl acrylate and methyl
Fused_filament_fabrication
Chemical reaction that removes a carboxyl group and releases carbon dioxide
strategy is the decarboxylative cross-coupling reaction. Upon heating in cyclohexanone, amino acids decarboxylate. In the related Hammick reaction, uncatalyzed
Decarboxylation
Species of bacteria
phthalate, phenylalanine, trans-cinnamate, benzamide, salicylate, cyclohexanone, cyclohexanol and cyclohexane-2-carboxylate. Ramana, Ch. V. (1 September
Rubrivivax_benzoatilyticus
Chemical process intended to reverse the polarity of a molecular functional group
halides such as benzyl bromide, with other carbonyl compounds such as cyclohexanone or oxiranes such as phenyl-epoxyethane, shown below. After hydrolysis
Umpolung
Medication
hours Identifiers IUPAC name (S)-2-(2-chlorophenyl)-2-(methylamino)cyclohexanone CAS Number 33643-46-8 Y HCl: 33643-47-9 Y PubChem CID 182137 IUPHAR/BPS
Esketamine
Chemical element with atomic number 73 (Ta)
H2[NbOF7]. liquid-liquid extraction into organic solvents, such as cyclohexanone, octanol, and methyl isobutyl ketone. This simple procedure allows the
Tantalum
Organic compounds of the form >C=N–OH
caprolactam, a precursor to Nylon 6. About half of the world's supply of cyclohexanone, more than a million tonnes annually, is converted to the oxime. In
Oxime
include diacetyl, acetoin, 2,3-pentanedione (buttery), camphor and cyclohexanone (minty), benzaldehyde (cherry or almond), cinnamaldehyde (cinnamon)
Health effects of electronic cigarettes
Health_effects_of_electronic_cigarettes
Chemical compound
Reagents to a,b-Ethylenic Ketones\: 2-(1,1-Dimethylpentyl)-5-methyl-cyclohexanone from Pulegone". Organic Syntheses. 72: 135. doi:10.15227/orgsyn.072
Manganese(II)_chloride
Chemical compound (H2SO4)
industry. For example, it is the usual acid catalyst for the conversion of cyclohexanone oxime to caprolactam, used for making nylon. It is used for making hydrochloric
Sulfuric_acid
CYCLOHEXANONE
CYCLOHEXANONE
CYCLOHEXANONE
CYCLOHEXANONE
Male
English
English name derived from Latin Damianus, DAMIAN means "to tame, to subdue" and euphemistically "to kill."Â
Surname or Lastname
English (West Midlands)
English (West Midlands) : from a medieval personal name, a pet form of Hay 3, formed with the Middle English hypocoristic suffix -cok (see Cocke).
Surname or Lastname
English
English : variant spelling of Hewitt 1.German (Hütt) : status name for someone living in a hut or owning a small shop, Middle High German hütte, or a habitational name from any of several places called Hütt or Hütte.
Boy/Male
Shakespearean
Antony and Cleopatra'. Attendant on Cleopatra.
Boy/Male
Muslim/Islamic
Greatest
Girl/Female
Assamese, Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit, Sindhi, Telugu
Goddess Lakshmi; Fortunate
Surname or Lastname
English and Irish
English and Irish : variant spelling of Farren.
Boy/Male
Muslim
Rising, Standing, Existing
Girl/Female
Arabic, Islamic, Muslim, Pakistani, Urdu
Happy; Pretty; Nice
Boy/Male
Arabic, Indian, Muslim
Worth; Worth Live
CYCLOHEXANONE
CYCLOHEXANONE
CYCLOHEXANONE
CYCLOHEXANONE
CYCLOHEXANONE