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Cas:110-82-7
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Cas:110-82-7
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Cas:110-82-7
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inquiryCyclohexane Basic information Product Name: Cyclohexane Synonyms: NAPHTHENE;Benzene, hexahydro-;benzenehexahydride;Cicloesano;Cyclohesan;cyclohexaan;cyclohexan;Cyclohexan(FormI)
Cas:110-82-7
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryProduct Description Product name Cyclohexane CAS 110-82-7 Assay 99% Appearance Colorless liquid
Alias: Hexahydrobenzene CAS No.: 110-82-7 EINECS No.: 203-806-2 Molecular formula: C6H12 Molecular weight: 84.16 Properties:
Cas:110-82-7
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Cas:110-82-7
Min.Order:1 Kilogram
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:110-82-7
Min.Order:10 Gram
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inquirySuperior quality Appearance:colorless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Suitable for HPLC, spectrophotometry, environmental t
Product name: Cyclohexane CAS No.:110-82-7 Molecule Formula:C6H12 Molecule Weight:84.16 Purity: 99.0% Package: 200kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
We are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
Cas:110-82-7
Min.Order:1 Gram
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inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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Hangzhou Dingyan Chem is a leading manufacturer and supplier of chemicals in China.We develop,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals. We could give you: 1.Best qualit
Product nameCyclohexane CAS 110-82-7 MF C6H12 MW 84.16 Product nameCyclohexaneCAS 110-82-7 MF C6H12 MW 84.16mp4-7°C(lit.)bp…
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:110-82-7
Min.Order:1 Kilogram
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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cyclohexaneAppearance:liquid Storage:store in a cool dry place and keep away from strong Package:Aluminum foil bag/as requirements Application:in research Transportation:by air or by sea
Supply CyclohexaneAppearance:As specifications Storage:Store in dry, dark and ventilated place Package:As requirement Application:industrial,pharmaceutical, research Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. B
cyclohexa-1,3-diene
cyclohexane
Conditions | Yield |
---|---|
With Pd/C; hydrogen In chloroform at 20℃; under 760.051 Torr; for 2h; Catalytic behavior; | 100% |
With hydrogen; HRh(CO)3 at 79.9℃; under 3750.3 Torr; for 1.66667h; | 63% |
With hydrogen In tetrahydrofuran at 20℃; under 760.051 Torr; for 10h; | 50% |
Conditions | Yield |
---|---|
With hydrogen; mer-Os(PPh3)3HBr(CO) at 150℃; under 3800 Torr; for 1h; Product distribution; | 100% |
With hydrogen; decacarbonyldirhenium(0) at 230℃; under 37503 Torr; for 0.25h; | 100% |
With {(η6-C6H6)Ru(NCCH3)3}{BF4}2; water; hydrogen In benzene at 90℃; under 30400 Torr; for 4h; | 100% |
Conditions | Yield |
---|---|
With hydrogen; [(norbornadiene)rhodium(I)chloride]2; polydiacetylene In n-heptane at 30℃; under 60800 Torr; for 0.9h; Product distribution; various aromatic compounds and other catalyst also investigated; | 100% |
With hydrogen; Ni-Tc on γ-Al2O3 at 175 - 250℃; under 760 Torr; Product distribution; dependence of catalytic activity on the reduction temperature; enhanced activity of bimetallic catalysts; | 100% |
With hydrogen; decacarbonyldirhenium(0) at 230℃; under 75005.9 Torr; for 0.25h; | 100% |
Conditions | Yield |
---|---|
With 9-borabicyclo[3.3.1]nonane dimer; triphenylstannane In toluene at 0℃; | 100% |
With triethylsilane; aluminium trichloride In dichloromethane at 18 - 20℃; for 0.25h; | 95% |
With water; sodium iodide; nickel dichloride; zinc; sonication In N,N,N,N,N,N-hexamethylphosphoric triamide at 60℃; for 1h; Product distribution; | 82% |
Conditions | Yield |
---|---|
With hydrogen; Leuna-Kontakt 6525 at 150℃; Product distribution; other halogen organic compounds, var. catalysts; | 100% |
With hydrogen; platinum at 120℃; under 16501.7 Torr; for 1.66667h; Autoclave; Inert atmosphere; | 12.8% |
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; hydrogen; triethylamine In isopropyl alcohol at 75℃; under 31028.9 Torr; for 4h; other chloroaromatics; var. reaction time; catalytic hydrodechlorination; |
Conditions | Yield |
---|---|
With C53H82ClN3P2Ru In dichloromethane-d2 at 50℃; under 3040.2 Torr; for 3h; Reagent/catalyst; Time; | 100% |
at 25℃; Catalytic behavior; | |
With ReH(NO)2(P(CH(CH3)2)3)2; Dimethylphenylsilane; tris(pentafluorophenyl)borate at 100℃; under 30003 Torr; for 1h; Catalytic behavior; Autoclave; | |
With [ReH(NO)2(P(C6H11)3)2]; Dimethylphenylsilane; tris(pentafluorophenyl)borate at 100℃; under 30003 Torr; for 1h; Catalytic behavior; Autoclave; | |
at 80℃; under 30003 Torr; for 24h; |
Conditions | Yield |
---|---|
With isopropyl alcohol at 150℃; under 7500.75 Torr; for 12h; Inert atmosphere; Autoclave; | A 25.1% B 100% C 74.9% |
With isopropyl alcohol at 160℃; for 15h; Autoclave; Inert atmosphere; | |
With isopropyl alcohol at 150℃; for 10h; Catalytic behavior; Reagent/catalyst; Temperature; Sealed tube; | A 24.6 %Chromat. B 47.8 %Chromat. C 24.3 %Chromat. |
With isopropyl alcohol at 150℃; for 6h; Temperature; Sealed tube; | A 15.2 %Chromat. B 17.7 %Chromat. C 5.8 %Chromat. |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 8h; | 99.9% |
bei der katalytischen Hyrierung; | |
With phosphoric acid; 5% Pd(II)/C(eggshell); hydrogen In water at 249.84℃; under 37503.8 Torr; for 0.5h; Autoclave; | 87 %Chromat. |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 2h; | 99.9% |
With rhodium contaminated with carbon; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 120℃; under 30003 Torr; for 6h; Autoclave; | 91.5% |
With carbon nanotubes-supported ruthenium; hydrogen In dodecane; water at 220℃; under 37503.8 Torr; for 3h; Autoclave; | 64 %Chromat. |
With hydrogen at 130℃; under 15001.5 Torr; for 6h; Ionic liquid; Autoclave; Schlenk technique; | 99.4 %Chromat. |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 12h; | 99.9% |
Multi-step reaction with 2 steps 1: hydrogen / water / 8 h / 200 °C / 30003 Torr / Autoclave 2: hydrogen / water / 4 h / 200 °C / 30003 Torr View Scheme | |
With palladium on activated charcoal; hydrogen In water at 150℃; under 30003 Torr; for 4h; Reagent/catalyst; Autoclave; |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 2h; | 99.6% |
With rhodium contaminated with carbon; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 120℃; under 30003 Torr; for 6h; Autoclave; | 93.5% |
With Ni-doped silica; hydrogen In decalin at 140℃; under 22502.3 Torr; for 5h; Reagent/catalyst; Autoclave; | 91.7% |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 300℃; under 45004.5 Torr; for 1h; Autoclave; | 99.3% |
With hafnium tetrakis(trifluoromethanesulfonate); Ru/Al2O3; hydrogen In octane at 250℃; under 30003 Torr; for 2h; Sealed tube; | 94.3% |
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 2h; | 92% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 180℃; | 99% |
With platinum on activated charcoal; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 120℃; under 30003 Torr; for 2h; Autoclave; | 93.5% |
at 300℃; Leiten ueber Aktivkohle; |
Conditions | Yield |
---|---|
With tris-(trimethylsilyl)silane; 2,2'-azobis(isobutyronitrile) In toluene at 80℃; for 0.666667h; | 99% |
Conditions | Yield |
---|---|
With bis(acetylacetonate)nickel(II); cetyltrimethylammonim bromide; lithium tri-t-butoxyaluminum hydride; sodium t-butanolate; tricyclohexylphosphine In toluene at 70℃; for 5h; Micellar solution; | A 99% B 99% |
With Ru0.6Ni0.4; hydrogen In water at 95℃; under 760.051 Torr; for 16h; Reagent/catalyst; | A 92% B 96% |
With hydrogen In water at 110℃; under 7500.75 Torr; for 1h; Autoclave; |
Conditions | Yield |
---|---|
With gold on titanium oxide In decane at 299.84℃; under 22502.3 Torr; for 12h; Temperature; High pressure; Inert atmosphere; Autoclave; | 98.7% |
With hydrogen In water at 200℃; under 37503.8 Torr; for 2h; Autoclave; Green chemistry; | |
With hydrogen In dodecane at 224.84℃; under 30003 Torr; for 2h; Autoclave; | |
With carbon nanotubes-supported ruthenium; hydrogen In dodecane; water at 220℃; under 37503.8 Torr; for 3h; Autoclave; | 90 %Chromat. |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 8h; | 98.6% |
With dihydrogen hexachloroplatinate; hydrogen; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide at 60℃; under 7500.75 Torr; for 15h; Autoclave; |
aniline
A
cyclohexane
B
cyclohexylamine
C
N-cyclohexyl-cyclohexanamine
D
cyclohexene
Conditions | Yield |
---|---|
With ammonia; hydrogen at 180 - 200℃; | A n/a B 98.4% C 0.08% D n/a |
With hydrogen at 160 - 200℃; under 150015 Torr; | A n/a B 95.9% C 0.45% D n/a |
Conditions | Yield |
---|---|
With gold on titanium oxide In decane at 299.84℃; under 22502.3 Torr; for 12h; Time; High pressure; Inert atmosphere; Autoclave; | 98.2% |
Conditions | Yield |
---|---|
With hydrogen In water at 130℃; for 20h; Reagent/catalyst; Inert atmosphere; Autoclave; Heating; stereoselective reaction; | 97.9% |
With rhodium contaminated with carbon; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 120℃; under 30003 Torr; for 24h; Reagent/catalyst; Autoclave; | 97.3% |
With hydrogen In water at 249.84℃; under 30003 Torr; | 93.7% |
Conditions | Yield |
---|---|
With hydrogen In neat (no solvent) at 200℃; under 37503.8 Torr; for 24h; Autoclave; | 97% |
With hydrogen; aluminum oxide; nickel at 190℃; | 90% |
With hydrogen; K-10 montmorillonite; platinum In diethylene glycol dimethyl ether under 37503 Torr; for 30h; Reduction; | 82% |
Conditions | Yield |
---|---|
With hydrogen; palladium dichloride In N,N-dimethyl-formamide under 18751.5 Torr; for 0.333333h; Product distribution; Ambient temperature; various time; | A 0.05% B 95.6% |
With ammonium acetate In methanol Electrochemical reaction; | A 88% B 12% |
With hydrogen; (η3-C3H5)Co[P(OMe)3]3 for 24h; Ambient temperature; | A 7.6% B 48.3% |
Conditions | Yield |
---|---|
With hydrogen In decalin at 20 - 220℃; under 37503.8 - 45004.5 Torr; Reagent/catalyst; Inert atmosphere; Autoclave; | 95% |
With ruthenium-carbon composite; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 150℃; under 7500.75 Torr; for 6h; Autoclave; | 91.2% |
With hydrogen; platinum unter geringem Ueberdruck; |
triethylsilane
fluorocyclohexane
A
triethylsilyl fluoride
B
cyclohexane
Conditions | Yield |
---|---|
With C21H16N3P(2+) In dichloromethane at 25℃; for 4h; Reagent/catalyst; | A 95% B n/a |
With [(SIMes)PFMe2][B(C6F5)4]2 In dichloromethane-d2 for 1h; Catalytic behavior; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 2h; | 95% |
Conditions | Yield |
---|---|
With tris-(trimethylsilyl)silane; 2,2'-azobis(isobutyronitrile) at 70℃; | A 4.1% B 93% C 2% |
With tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile) at 70℃; | A 15% B 83% C 1.2% |
With 9-borabicyclo[3.3.1]nonane dimer; tribenzyltin hydride In toluene at 0℃; Product distribution; variation of reagent; | A 29% B 68% C 3% |
Conditions | Yield |
---|---|
With rhodium contaminated with carbon; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 150℃; under 7500.75 Torr; for 6h; Autoclave; | 92.3% |
With hydrogen In dodecane at 224.84℃; under 30003 Torr; for 2h; Autoclave; |
1-methoxy-3-phenoxybenzene
A
3-methoxycyclohexan-1-ol
B
cyclohexane
Conditions | Yield |
---|---|
With bis(acetylacetonate)nickel(II); cetyltrimethylammonim bromide; lithium tri-t-butoxyaluminum hydride; sodium t-butanolate; tricyclohexylphosphine In toluene at 70℃; for 5h; Micellar solution; | A 92% B 89% |
Conditions | Yield |
---|---|
With palladium on activated charcoal; N-methyldiethanolamine trifluoromethanesulfonate; hydrogen at 150℃; under 7500.75 Torr; for 6h; Autoclave; | A 91.5% B 90.3% |
With carbon nanotubes-supported ruthenium; hydrogen In dodecane; water at 220℃; under 37503.8 Torr; for 3h; Autoclave; | A 95 %Chromat. B 44 %Chromat. |
With hydrogen at 130℃; under 15001.5 Torr; for 6h; Ionic liquid; Autoclave; Schlenk technique; |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 300℃; under 45004.5 Torr; for 1h; Autoclave; | A 6.08% B 90.52% |
With hydrogen at 320℃; under 127513 Torr; for 1h; Reagent/catalyst; Autoclave; | A 6.8 %Chromat. B 67 %Chromat. |
Conditions | Yield |
---|---|
With bromine; aluminum tri-bromide; Acetyl bromide In dichloromethane at -20℃; for 3h; | 100% |
With bromine; sodium t-butanolate In cyclohexane at 40℃; for 15h; | 100% |
With manganese(IV) oxide; bromine at 80℃; for 0.166667h; Product distribution; Further Variations:; Reagents; reagent ratios, reaction time; | 99% |
Conditions | Yield |
---|---|
cobalt (III) fluoride at 360℃; for 3h; | 100% |
With fluorine Product distribution; Irradiation; | 30% |
With lead(IV) fluoride at 200℃; zuletzt bei 400grad; |
Conditions | Yield |
---|---|
With Fe2(4,4″-dioxido-[1,1′:4′,1″-terphenyl]-3,3″-dicarboxylate); 1-(tert-butylsulfonyl)-2-iodosylbenzene In [D3]acetonitrile at 20℃; for 1.5h; | A 100% B 100% |
With 3-chloro-benzenecarboperoxoic acid; [Ni2(L2H2)(OAc)2] at 20℃; for 1h; | A 7% B 93% |
With 3-chloro-benzenecarboperoxoic acid; (5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato)iron(III) chloride In dichloromethane; acetonitrile for 1h; Product distribution; Ambient temperature; other catalysts; kinetic isotope effect; | A 2% B 89% |
Conditions | Yield |
---|---|
With 4-tert-butylpyridine; hydrogen sulfide; oxygen; iron(II) chloride In acetonitrile for 4h; Ambient temperature; | 100% |
With 4-tert-butylpyridine; 2-Picolinic acid; dihydrogen peroxide; triphenylphosphine; iron(II) chloride In acetonitrile at 0℃; | 99% |
With di-tert-butyl peroxide at 120℃; for 18h; Reagent/catalyst; | 96% |
cyclohexane
N,O-bistrimethylsilyl-N-(ethoxycarbonyl)hydroxylamine
A
Hexamethyldisiloxane
B
ethyl N-cyclohexylcarbamate
C
urethane
Conditions | Yield |
---|---|
at 100℃; for 25h; | A 100% B 80% C 8% |
at 45℃; for 58h; Irradiation; | A 75% B 45% C 55% |
cyclohexane
perpentene-4 oate de tertiobutyle
A
cyclohexylcyclohexane
B
butylcyclohexane
C
cyclohexyl-5 pentanolide-4
D
acetone
E
5-methyl-dihydro-furan-2-one
F
tert-butyl alcohol
Conditions | Yield |
---|---|
at 120℃; for 4h; Product distribution; Mechanism; different ratios of reactant, reactants, reaction times and temperatures; | A 5% B 5% C 35% D n/a E 1% F 100% |
cyclohexane
1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindol-2-yloxoyl radical
2-(t-butylazo)prop-2-yl hydroperoxide
A
2-cyclohexyloxy-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole
B
2-tert-butoxy-1,1,3,3-tetramethylisoindoline
C
acetone
D
isobutene
Conditions | Yield |
---|---|
at 70℃; for 17h; Mechanism; Rate constant; Thermodynamic data; var. of nitroxide, solvent, temp., EA, ΔH(excit.), ΔS(excit.); | A 96% B 82% C 100% D 15% |
Conditions | Yield |
---|---|
cobalt (III) fluoride at 360℃; for 3h; Product distribution; | A n/a B 100% |
Conditions | Yield |
---|---|
With 4-tert-butylpyridine; hydrogen sulfide; oxygen; iron(II) chloride In acetonitrile for 4h; Ambient temperature; | 100% |
cyclohexane
2,2,2-trichloroethyl sulfamate
Conditions | Yield |
---|---|
With [bis(acetoxy)iodo]benzene; C32H44ClN4O4Rh2*3CH2Cl2 at 20℃; for 3h; Inert atmosphere; | 100% |
With bis(tertbutylcarbonyloxy)iodobenzene; Rh2(esp)2 In benzene at 23℃; | 95% |
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; [bis(acetoxy)iodo]benzene In water at 4℃; for 24h; | 64% |
With [p-(trifluoromethyl)phenyl](diacetoxy)-λ3-bromane at 0 - 15℃; for 3h; Inert atmosphere; | 18% |
Conditions | Yield |
---|---|
In gas reaction in a mass spectrometer; total pressure: 4E-6 Torr; | A 100% B 100% |
nonafluoro-tert-butanesulfenyl chloride
cyclohexane
A
nonafluoro-tert-butanethiol
B
cyclohexyl chloride
Conditions | Yield |
---|---|
A 100% B 100% | |
A 100% B 100% |
Conditions | Yield |
---|---|
In benzene at 80℃; for 4h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With MCM-41 silicate; hydrogen; di(rhodium)tetracarbonyl dichloride at 100℃; under 21001.7 Torr; for 20h; | 99.4% |
With Rh; benzaldehyde In benzene Mechanism; Irradiation; other d8 metal carbonyls, other aromatic ketones and aldehydes; relative quantum yields; |
Conditions | Yield |
---|---|
With C28H6Ag2Au2F24N2 In cyclohexane for 12h; Inert atmosphere; | 99% |
With C56H82Cl2Cu2N4O2P2; sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate In dichloromethane at 20℃; for 12h; Inert atmosphere; Schlenk technique; | 98% |
With C4H11B22Br12IN2(2-)*2Li(1+); copper dichloride In tetrahydrofuran at 90℃; for 3h; Reagent/catalyst; Inert atmosphere; Reflux; | 92.6% |
Conditions | Yield |
---|---|
With nitric acid; trifluoroacetic acid; N-hydroxy-5-carboxy-phthalimide at 23℃; for 18h; Reagent/catalyst; | 99% |
With 2-pyrazylcarboxylic acid; FeCl2(κ3-HC(C3H3N2)3); ozone at 20℃; for 6h; Catalytic behavior; Time; Reagent/catalyst; Schlenk technique; Green chemistry; | 96% |
In acetic acid at 115℃; under 22502.3 Torr; for 5h; Reagent/catalyst; Pressure; | 95% |
Conditions | Yield |
---|---|
With dibenzoyl peroxide for 14h; Product distribution; Heating; further educts and peroxides; | 99% |
With dilauryl peroxide for 14h; Heating; | 99% |
With dibenzoyl peroxide at 80℃; Yield given; |
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