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Chemical compound
Cyclohexene is a hydrocarbon with the formula (CH2)4C2H2. It is a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor
Cyclohexene
Chemical compound
Cyclohexene oxide is a cycloaliphatic epoxide. It can react in cationic polymerization to poly(cyclohexene oxide). As cyclohexene is monovalent, poly(cyclohexene
Cyclohexene_oxide
Type of molecule
1-Methyl-4-(prop-1-en-2-yl)cyclohex-1-ene Other names 1-Methyl-4-(1-methylethenyl)cyclohexene 4-Isopropenyl-1-methylcyclohexene p-Menth-1,8-diene Racemic: DL-Limonene;
Limonene
Enzyme
The products of this enzyme are 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic acid and carbon dioxide. It belongs to the transferase family
2-Succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase
2-Succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid_synthase
Chemical compound
in patients undergoing patch testing. 4-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde at Sigma-Aldrich Fahlbusch, K.-G.; Hammerschmidt, F
Hydroxymethylpentylcyclohexenecarboxaldehyde
Hydroxymethylpentylcyclohexenecarboxaldehyde
Chemical compound
is a white solid with a pungent sour odor. The molecule consists of a cyclohexene ring with a methylene bridge between carbons 3 and 6. The molecule carries
Norbornene
Rule in organic chemistry
describes the stereoselective addition of nucleophiles to cyclohexene derivatives. Cyclohexene derivatives, such as imines, epoxides, and halonium ions
Fürst–Plattner_rule
Chemical compound
Orestrate (INNTooltip International Nonproprietary Name), also known as estradiol 3-propionate 17β-(1-cyclohexenyl) ether, is an estrogen medication and
Orestrate
Chemical compound
Shikimic acid, more commonly known as its anionic form shikimate, is a cyclohexene, a cyclitol and a cyclohexanecarboxylic acid. It is an important biochemical
Shikimic_acid
Chemical compound
7833 RTECS number RN8640000 UNII 596C064IG4 Y UN number 2810 (1-VINYL-3-CYCLOHEXENE DIOXIDE) CompTox Dashboard (EPA) DTXSID0020604 InChI
Vinylcyclohexene_dioxide
Alpha-beta unsaturated cyclic ketone
5-Trimethylcyclohex-2-en-1-one Other names 3,5,5-Trimethyl-2-cyclohexene-1-one 1,1,3-Trimethyl-3-cyclohexene-5-one Isoforone Isoacetophorone IP Identifiers CAS
Isophorone
Chemical compound
1-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to the alkene group. Two other structural
1-Methylcyclohexene
Reaction in organic chemistry
are some intramolecular versions, such as 1,2-dibromohexane + 2 Na → cyclohexene + 2 NaBr. A related reaction, which combines alkyl halides with aryl
Wurtz_reaction
Organic molecule with one or more non-aromatic all-carbon rings
Monocyclic cycloalkenes are cyclopropene, cyclobutene, cyclopentene, cyclohexene, cycloheptene, cyclooctene, and so on. Bicyclic alkenes include norbornene
Alicyclic_compound
Brand name of an aerosol self-defense spray
chloroacetophenone (CN) in a solvent of 2-butanol, propylene glycol, cyclohexene, and dipropylene glycol methyl ether. Chemical Mace was originally developed
Mace_(spray)
Hydrocarbon compound (C6H6)
the right conditions, benzene can be partially-hydrogenated to give cyclohexene or cyclohexadienes. A similar reaction is the Birch reduction, which
Benzene
Acetate ester of tetrahydrocannabinol (THC)
between Δ8-THC and Δ9-THC is the location of the double bond within the cyclohexene ring system. In naming the esters of THC, the "-O-" is superfluous. THC
THC-O-acetate
Chemical compound
3-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent adjacent to the alkene group. Two other structural isomers
3-Methylcyclohexene
Chemical compound
reaction, by the action of diiodomethane and a zinc-copper couple on cyclohexene in diethyl ether. Smith, R. D.; Simmons, H. E. "Norcarane". Organic Syntheses;
Norcarane
Type of organic chemical reaction
Kelk Ingold in the 1920s. Coleman, G. H.; Johnstone, H. F. (1925). "Cyclohexene". Organic Syntheses. 5: 33. doi:10.15227/orgsyn.005.0033. March, Jerry
Elimination_reaction
Chemical compound
Complex-catalyzed Asymmetric Diels-Alder Reaction: (1R)-1,3,4-Trimethyl-3-cyclohexene-1-carboxaldehyde". Organic Syntheses; Collected Volumes, vol. 9, p. 722
P-Toluenesulfonic_acid
Chemical reaction
substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative. It is the prototypical pericyclic reaction with a concerted
Diels–Alder_reaction
Hydrocarbon compounds without aromatic rings
C4H8 1-Butene Alkene C4H10 Butane Alkane C5H12 Pentane Alkane C6H10 Cyclohexene Cycloalkene C6H12 Cyclohexane Cycloalkane C6H14 Hexane Alkane C7H14 Methylcyclohexane
Aliphatic_compound
Chemical compound
produce amine oxides. The following scheme shows the epoxidation of cyclohexene with mCPBA. The epoxidation mechanism is concerted: the cis or trans
Meta-Chloroperoxybenzoic_acid
Synthetic nucleic acid analogues
nucleic acid (PNA) Glycol nucleic acid (GNA) Morpholino nucleic acid Cyclohexene nucleic acid (CeNA) XNA monomers are prepared by chemical synthesis and
Xeno_nucleic_acid
Preference of chemical bonding or breaking in one direction over others
Fürst-Plattner rule for the addition of nucleophiles to derivatives of cyclohexene, especially epoxide derivatives. Regioselectivity in ring-closure reactions
Regioselectivity
Synthetic opioid painkiller
PMID 12819791. "Tilidin". Gelbe Liste Online. Satzinger, Gerhard (1969). "über Cyclohexene, I Synthese und Reaktionen von 4-Phenyl-3-amino-cyclohexenen-(1), einer
Tilidine
Citrus fruit
November 2021. Retrieved 6 March 2010. "(±)-1-methyl-4-(1-methylvinyl)cyclohexene". ECHA. January 2019. Archived from the original on 29 October 2020.
Orange_(fruit)
Chemical compound
compound consisting of a vinyl group attached to the 4-position of the cyclohexene ring. It is a colorless liquid. Although chiral, it is used mainly as
4-Vinylcyclohexene
Chemical compound
nortilidine is also known, as is the corresponding analogue with the cyclohexene ring replaced by cyclopentane, which have almost identical properties
Nortilidine
Chemical reaction
cycloelimination. It involves the formation of a diene and dienophile from a cyclohexene. It can be accomplished spontaneously with heat, or with acid or base
Retro-Diels–Alder_reaction
Chemical compound
benzene with cyclohexene. The process can proceed using benzene as the exclusive organic precursor. Its partial hydrogenation gives cyclohexene, which alkylates
Cyclohexylbenzene
Index of chemical compounds with the same molecular formula
g/mol) may refer to many dozens of compounds. Some well studied examples: Cyclohexene 2,3-Dimethyl-1,3-butadiene 1,2-Hexadiene 1,3-Hexadiene 1,4-Hexadiene
C6H10
Aromatic alcohol
Complex-Catalyzed Asymmetric Diels-Alder Reaction: (1R)-1,3,4-Trimethyl-3-Cyclohexene-1-Carboxaldehyde". Organic Syntheses. 72: 86; Collected Volumes, vol
Benzyl_alcohol
Chemical compound
Heating in the presence of acid catalysts converts cyclohexanol to cyclohexene. Cyclohexanol has at least two solid phases. One of them is a plastic
Cyclohexanol
Class of chemical compounds
dimer fatty acid. The structure may vary depending on the raw materials used. Characteristic is the cyclohexene ring formed by the Diels-Alder reaction.
Dimer_acid
Organic compound; 6-sided hydrocarbon ring
compounds Related cycloalkanes Cyclopentane Cycloheptane Related compounds Cyclohexene Benzene Supplementary data page Cyclohexane (data page) Except where
Cyclohexane
Phytocannabinoid discovered in 1940
Cannabidiol (CBD) is a phytocannabinoid, one of 113 identified cannabinoids in Cannabis, along with tetrahydrocannabinol (THC), and accounts for up to
Cannabidiol
Chemical compound
Canthaxanthin /ˌkænθəˈzænθɪn/ is a keto-carotenoid pigment widely distributed in nature. Carotenoids belong to a larger class of phytochemicals known as
Canthaxanthin
Chemical compound
Cassiffix Names Other names 3-Cyclohexene-1-methanol, 3(or 4)-methyl-1-(2,2,3-trimethyl-3-cyclopenten-1-yl)-, acid-isomerized Trimethylcyclopentenylm
Cassiffix
Topics referred to by the same term
dumpfile format Vocal cord dysfunction Vibrational circular dichroism Vinyl cyclohexene dioxide, also known as 4-vinylcyclohexene diepoxide Victoria River Downs
VCD_(disambiguation)
Antiviral medication used against influenza
Oseltamivir, sold under the brand name Tamiflu among others, is an antiviral medication used to treat and prevent influenza A and influenza B, viruses
Oseltamivir
Chemical compound
Basketene (IUPAC name: pentacyclo[4.4.0.02,5.03,8.04,7]dec-9-ene) is an organic compound with the formula C10H10. It is a polycyclic alkene and the dehydrogenated
Basketene
Most common species of mice
the urine. Among them, five compounds are specific to males, namely 3-cyclohexene-1-methanol, aminotriazole (3-amino-s-triazole), 4-ethyl phenol, 3-ethyl-2
House_mouse
Organic molecule with the formula C6H12
3-dimethylbut-1-ene 3,3-dimethylbut-1-ene 2-ethylbut-1-ene 2,3-dimethylbut-2-ene Cyclohexene Neohexene Hexene, Merriam-Webster Dictionary "Chapter 3: Physical Constants
Hexene
Chemical compound
melted under vacuum to remove water. In a related reaction, KSCN converts cyclohexene oxide to the corresponding episulfide and KOCN. C6H10O + KSCN → C6H10S
Potassium_thiocyanate
Chemical compound
3-Carene is a bicyclic monoterpene consisting of fused cyclohexene and cyclopropane rings. It occurs as a constituent of turpentine, with a content as
3-Carene
Chemical compound
C6H6O Molar mass 94.113 g·mol−1 Related compounds Related compounds Cyclohexene oxide Oxonane Except where otherwise noted, data are given for materials
Oxepine
Hydrocarbon compound containing one or more C=C bonds
ethylene is: H2C=CH2 + HBr → H3C−CH2Br Alkenes add to dienes to give cyclohexenes. This conversion is an example of a Diels-Alder reaction. Such reaction
Alkene
Chemical compound
Acarbose (INN) is an anti-diabetic drug used to treat diabetes mellitus type 2 and (in some countries), prediabetes. It is sold in Europe and China as
Acarbose
Chemical compound
Dehydronorketamine (DHNK), or 5,6-dehydronorketamine, is a minor metabolite of ketamine which is formed by dehydrogenation of its metabolite norketamine
Dehydronorketamine
Organic compounds with the formula (CH3)2C6H4
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Xylene
Chemical reaction in which water is produced as a byproduct
1021/ie401157c. ISSN 0888-5885. G. H. Coleman, H. F. Johnstone (1925). "Cyclohexene". Organic Syntheses. 5: 33. doi:10.15227/orgsyn.005.0033. J. Brent Friesen;
Dehydration_reaction
Medication
Venetoclax, sold under the brand names Venclexta and Venclyxto, is a medication used to treat adults with chronic lymphocytic leukemia (CLL), small lymphocytic
Venetoclax
British and Australian chemist (born 1937)
R. (1963). "The photochemistry of some charge-transfer complexes of cyclohexene". Tetrahedron Letters. 4 (9): 597–600. doi:10.1016/S0040-4039(01)90680-X
Richard_Robson_(chemist)
Chemical compound
reactions with several dienophiles, such as acrolein. One of the resulting cyclohexene derivatives is Lyral. Another fragrance compound made from myrcene is
Myrcene
Red-orange pigment of the terpenoids class
β-Carotene (beta-carotene) is an organic, strongly colored red-orange pigment abundant in fungi, plants, and fruits. It is a member of the carotenes, which
Β-Carotene
Chemical compound (CH2)4(COOH)2
CO + 2 H2O → HO2C(CH2)4CO2H Another method is oxidative cleavage of cyclohexene using hydrogen peroxide. The waste product is water. Auguste Laurent
Adipic_acid
Chemical compound
α-bromination followed by treatment with base. Hydrolysis of 3-chloro cyclohexene followed by oxidation of the cyclohexenol is yet another route. Cyclohexenone
Cyclohexenone
Covalent compound that contains two double bonds
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Diene
Chemical compound
reacts with the enolate. In other syntheses, pimelic acid is made from cyclohexene-4-carboxylic acid, and a fourth method also exists based on the 1,4 reaction
Pimelic_acid
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Spiropentane
Chemical compound
Diels–Alder reactions with several dienophiles, such as acrolein, to give cyclohexene derivatives that are also useful fragrances. Zanoli, Paola; Zavatti,
Myrcenol
German chemist (1876–1954)
work was done with Kurt Alder on the Diels–Alder reaction, a method for cyclohexene synthesis. The pair was awarded the Nobel Prize in Chemistry in 1950
Otto_Diels
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Trans-Propenylbenzene
Chemical compound
Astaxanthin /æstəˈzænθɪn/ is a keto-carotenoid within a group of chemical compounds known as carotenoids, a subclass of the broad group of phytochemicals
Astaxanthin
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
1,5-Hexadiene
Species of conifer
cuminol, eucarvone, 2-cyclopenten-1-one, 3,4-dimethyl-, 1,3-dimethyl-1-cyclohexene, calamenene, τ-muurolol, borneol, α-cadinol, β-thujaplicin. Some of these
Chamaecyparis_obtusa
Chemical compound
HU-320 (7-nor-7-carboxy-CBD-1,1-DMH) is a drug related to cannabidiol, which has strong antiinflammatory and immunosuppressive properties while demonstrating
HU-320
Chemical compound
Acarviosin is a sugar composed of cyclohexitol linked to a 4-amino-4,6-dideoxy-D-glucopyranose. Acarviosin is part of the potent α-amylase inhibitor acarbose
Acarviosin
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
N-Butylbenzene
Chemical compound
heated to around 427 °C (801 °F) it slowly decomposes to cyclohexane and cyclohexene, as the pivot bond joining the two rings is the longest and weakest one
Bicyclohexyl
Chemical compound
Zeinoxanthin is a rare carotenoid with antioxidant properties, commonly found in foods like oranges and also present in the tissues of the human eye. The
Zeinoxanthin
Chemical compound
4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group
4-Methylcyclohexene
Medication primarily used to treat severe acne
Isotretinoin, also known as 13-cis-retinoic acid and sold under the brand name Accutane among others, is a medication used to treat skin diseases like
Isotretinoin
Oily organic chemical found in plants
Pinene is a collection of unsaturated bicyclic monoterpenes. Two geometric isomers of pinene are found in nature, α-pinene and β-pinene. Both are chiral
Pinene
Chemical compound
Retinol is a hydrolytic metabolite of retinyl esters belonging to the group of vitamin A1 as an alcohol form. Retinol or other forms of vitamin A are fat-soluble
Retinol
Hydrocarbon compound (CH3–CH=CH–CH=CH2)
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Piperylene
Possible alternative biochemicals used by life forms
which uses 1,5-anhydrohexitol; GNA, which uses glycol; CeNA, which uses cyclohexene; LNA, which utilizes a form of ribose that contains an extra linkage
Hypothetical types of biochemistry
Hypothetical_types_of_biochemistry
Acetone -94.6 Liquid N2 Toluene -95.1 Liquid N2 Methanol -98 Liquid N2 Cyclohexene -104 Liquid N2 Isooctane -107 Liquid N2 Ethyl iodide -109 Liquid N2 Carbon
List_of_cooling_baths
Hydrocarbon composed of multiple aromatic rings
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Polycyclic aromatic hydrocarbon
Polycyclic_aromatic_hydrocarbon
Yellow organic pigment created by plants
Lutein (/ˈljuːtiɪn, -tiːn/; from Latin luteus meaning "yellow") is a xanthophyll and one of 600 known naturally occurring carotenoids. Lutein is synthesized
Lutein
Metabolite of vitamin A
Retinoic acid is a metabolite of vitamin A1 (all-trans-retinol) that exists in several distinct isomeric forms, including all-trans retinoic acid, 9-cis
Retinoic_acid
Chemical compound
Salinosporamide A (Marizomib) is a potent proteasome inhibitor being studied as a potential anticancer agent. It entered phase I human clinical trials
Salinosporamide_A
Chemical reaction
organocatalyzed by a protected cysteine and potassium tert-butoxide afforded a cyclohexene with 95% enantiomeric excess: In this reaction the phosphine is replaced
Rauhut–Currier_reaction
Chemical compound
studied. Pelubiprofen can be prepared by the reaction of 1-(1-piperidino)cyclohexene (1) with ethyl 2-(4-formylphenyl)propanoate (2). "Pelubiprofen - Daewon
Pelubiprofen
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Pentaphene
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
P-Xylene
Phytocannabinoid
Cannabidiorcol (CBDO, CBD-C1, O-1821) is a phytocannabinoid found naturally in Cannabis in trace concentrations. It is related to cannabidiol, with the
Cannabidiorcol
Chemical compound
Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist
Hagemann's_ester
Chemical compound
intermediate. In some cases, purified cyclohexanol, obtained by hydration of cyclohexene, is the precursor. Alternatively, cyclohexanone can be produced by the
Cyclohexanone
Chemical compound
Bornylene is an organic compound classified as a terpenoid. It is a bicyclic alkene related structurally to the more common norbornene, which lacks the
Bornylene
Chemical compound
its reaction with nitrosylsulfuric acid. It can also be oxidized to cyclohexene. Cyclohexanecarboxylic acid exhibits the reactions typical of carboxylic
Cyclohexanecarboxylic_acid
Chemical compound
Iodocyclohexane has been prepared by the addition of hydrogen iodide to cyclohexene. Alternatively, it can be prepared by the reaction of cyclohexane and
Iodocyclohexane
Paper on taxol synthesis
is assembled from three pre-assembled synthons. Two major parts are cyclohexene rings A and C that are connected by two short bridges creating an 8 membered
Nicolaou Taxol total synthesis
Nicolaou_Taxol_total_synthesis
Chemical compound
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Anthracene
Petrochemical process to break down saturated hydrocarbons in smaller molecules
Isononyne Isodecyne Cycloalkenes Cyclopropene Cyclobutene Cyclopentene Cyclohexene Cycloheptene Cyclooctene Cyclononene Cyclodecene Alkylcycloalkenes Methylcyclopropene
Steam_cracking
is the first to demonstrate the step by step conversion of benzene to cyclohexene with varying degrees of deuterium incorporation while binding to a tungsten
W._Dean_Harman
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
Bisabolol, or more formally α-(−)-bisabolol or also known as levomenol, is a natural monocyclic sesquiterpene alcohol. It is a colorless viscous oil that
Bisabolol
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CYCLOHEXENE
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