Dayangchem’s 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. DayangChem can provide different quantiti
Cas:110-83-8
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Cas:110-83-8
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inquiryProduct name Cyclohexene Synonyms Cyclohexene/Cycloheptanone;1-Cyclohexene;3,4,5,6-tetrahydrobenzene;Benzene, tetrahydro-;benzene,tetrahydro-;Cyclohex-1-ene;cykloheksen(polish);Hexanaphthylene
Cas:110-83-8
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inquiryOur Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
Cas:110-83-8
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
J&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
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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:110-83-8
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inquirySuperior quality Appearance:colourless 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:Used as Pharmaceutical Intermediates Transportation:
We are leading fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...)
Cas:110-83-8
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inquiryhigh 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
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air
good quality and cheap price Package:25kg/200kg Application:as intermediates Transportation:by courier/sea/air
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Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:110-83-8
Min.Order:1 Kilogram
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Type:Trading Company
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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Cyclohexene CAS 110-83-8 supplier Application:Cyclohexene CAS 110-83-8 supplier
low price and high purityAppearance:solid or liquid Storage:in sealed air resistant place Package:As customer require Application:Pharma;Industry;Agricultural Transportation:by sea or by airplane Port:any port in China
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Cas:110-83-8
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Cas:110-83-8
Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiry1. Product Name:Cyclohexene 2. CAS#110-83-8 3. Manufacturer , ISO9001 4. Purity: 99%min.
cyclohexa-1,3-diene
cyclohexene
Conditions | Yield |
---|---|
With samarium diiodide; N,N,N',N'',N''-pentamethylethylene triamine; water In tetrahydrofuran at 20℃; for 0.0833333h; | 100% |
With hydrogen In dichloromethane at 40℃; under 3000.3 Torr; for 0.75h; | 95% |
With 1‑cyanopropyl-3-methylimidazolium tetrafluoroborate; hydrogen; palladium dichloride at 100℃; under 34202.3 Torr; for 4h; Reactivity (does not react); | 90% |
cyclohexene sulfide
cis-2-methyl-3-phenyloxaziridine
A
(Z)-azomethane
B
N,N'-bis(methyl)sulphur di-imide
C
benzaldehyde
D
cyclohexene
Conditions | Yield |
---|---|
In chloroform Mechanism; Ambient temperature; via thionitrosomethane, CH3NS (also used: other oxaziridines and episulfides); | A n/a B 83% C 100% D 100% |
Conditions | Yield |
---|---|
With hydrogen sulfide; triphenylphosphine; methyltrioxorhenium(VII) In [D3]acetonitrile for 0.0833333h; Ambient temperature; | 100% |
With sodium In toluene at 110℃; for 7h; | 99% |
With biphenyl; lithium In 1,2-dimethoxyethane for 8h; Heating; | 73% |
Conditions | Yield |
---|---|
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride; ethylmagnesium bromide In tetrahydrofuran at 0℃; | 100% |
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride; tri-n-butyl-tin hydride In tetrahydrofuran for 0.25h; Ambient temperature; | 100% |
With sodium sulfide; cetyltributylphosphonium bromide In toluene at 25℃; for 12h; | 90% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; Product distribution; electrolysis, oth. solvent, var. cathodes; | 100% |
Conditions | Yield |
---|---|
With sodium amalgam; chiral Co(II) In tetrahydrofuran-d8 at 20℃; for 6h; deoxygenation; | 100% |
With lithium In tetrahydrofuran for 24h; Heating; | 96% |
With chloro-trimethyl-silane; sodium iodide In acetonitrile for 0.5h; Ambient temperature; | 94% |
(1R,2R)-1-Chloro-2-iodo-cyclohexane
cyclohexene
Conditions | Yield |
---|---|
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride; lithium triethylborohydride In tetrahydrofuran for 0.5h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With thiophenol In acetonitrile at 1℃; for 100h; Product distribution; Elimination; | A 105 % B 100% |
Conditions | Yield |
---|---|
With diazomethyl-trimethyl-silane; ruthenium Schiff-base In toluene at 70℃; for 1h; ring-closing metathesis; | 100% |
With diazomethyl-trimethyl-silane; ruthenium In toluene at 85℃; for 17h; Product distribution; Further Variations:; Catalysts; | 100% |
[2-((2,6-iPr2-Ph-imino)methyl)phenol][p-cymene][=CHPh]Ru2Cl3 In various solvent(s) at 70℃; for 4h; Product distribution; Further Variations:; Catalysts; Temperatures; | 100% |
A
bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]
B
cyclohexene
Conditions | Yield |
---|---|
With HCl In pentane (N2); HCl gas bubbled through complex soln.; | A 93% B 100% |
Conditions | Yield |
---|---|
With sulfuric acid at 250℃; for 0.5h; | 99% |
for 2h; Temperature; Heating; | 98% |
With Nafion/SiO2 at 200℃; under 15001.5 Torr; for 6h; | 90.3% |
bis(triphenylphosphoranylidene)ammonium bromide
B
cyclohexene
Conditions | Yield |
---|---|
In dichloromethane-d2 N2, in an NMR-tube, frozen in liquid N2, CD2Cl2 and PPNBr added, kept at-40°C for 12 h; not isolated, NMR; | A 99% B 57% |
Conditions | Yield |
---|---|
With C24H72Ba2N4Si8 In (2)H8-toluene at 120℃; for 16h; Inert atmosphere; Schlenk technique; Sealed tube; | A 99% B n/a |
cyclohexa-1,4-diene
1-Phenylcyclohexene
A
1-phenyl-1-cyclohexane
B
cyclohexene
Conditions | Yield |
---|---|
With C24H72Ba2N4Si8 In (2)H8-toluene at 120℃; for 3h; Inert atmosphere; Schlenk technique; Sealed tube; | A 99% B n/a |
norborn-2-ene
cyclohexa-1,4-diene
A
norbornene
B
cyclohexene
Conditions | Yield |
---|---|
With C24H72Ba2N4Si8 In (2)H8-toluene at 120℃; for 5h; Inert atmosphere; Schlenk technique; Sealed tube; | A 99% B n/a |
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 sodium hydroxide; 2,2,2-trifluoroethanol; tetrabutylammomium bromide In 1,2-dichloro-benzene at 73 - 75℃; for 0.5h; phase transfer conditions; | 98% |
With sodium hydroxide; 2,2,2-trifluoroethanol; tetrabutylammomium bromide In 1,2-dichloro-benzene at 73 - 75℃; for 0.5h; phase transfer conditions; | 98% |
With Amberlyst A 26; carbonate form In benzene for 5h; Heating; | 88% |
cis-2-(trimethylsilyl)cyclohexyl trifluoroacetate
A
cyclohexene
B
cyclohexanol
Conditions | Yield |
---|---|
In ethanol at 65℃; Kinetics; ΔH, ΔG, ΔS (excit.); | A 98% B n/a |
In water at 60℃; Kinetics; | A 9.2% B n/a |
Conditions | Yield |
---|---|
With HCl In pentane (N2); HCl gas bubbled through complex soln.; | A 90% B 98% |
Conditions | Yield |
---|---|
With hydrogen at 199.84℃; for 6h; Catalytic behavior; | 95.8% |
With phenylsilane; C28H16F24O8S2Si In 1,2-dichloro-benzene at 100℃; for 72h; Inert atmosphere; | 61% |
With fired clay fragments at 250 - 300℃; | |
Multi-step reaction with 3 steps 1: diethyl ether; sodium; alcohol / Reagens 4: Kaliumcarbonat 2: fuming hydrochloric acid / 100 °C 3: quinoline View Scheme | |
Multi-step reaction with 2 steps 1: PCl5 2: sodium; methanol View Scheme |
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; ytterbium at 393℃; under 22501.8 Torr; for 3h; | 95% |
With hydrogenchloride; <η6-C6Me6Ru η4-C6H8> | 92% |
With hydrogen; 2,2'-iminobis[ethanol]; zinc(II) sulfate; zirconium(IV) oxide In water at 150℃; under 37503.8 Torr; Autoclave; | 63.6% |
B
P(C6H5)3C6H11(1+)*BF4(1-) = P(C6H5)3C6H11BF4
C
fluorocyclohexane
D
cyclohexene
Conditions | Yield |
---|---|
With triphenylphosphine In dichloromethane-d2 N2, frozen in liquid N2, CD2CL2 and solid PPh3 added, slowly warmed to 0°C; not isolated, NMR, GLC; | A 95% B 24% C 24% D 30% |
ethanol
sodium thiophenolate
1,2-bis(5-thianthreniumyl)cyclohexane diperchlorate
A
2-ethoxycyclohex-1-ene
B
diphenyldisulfane
C
Thianthrene
D
cyclohexene
Conditions | Yield |
---|---|
In ethanol for 360h; Ambient temperature; | A 2% B 81% C 94% D 59% |
sodium thiophenolate
1,2-bis(5-thianthreniumyl)cyclohexane diperchlorate
A
diphenyldisulfane
B
Thianthrene
C
cyclohexene
Conditions | Yield |
---|---|
In dimethyl sulfoxide for 20h; Ambient temperature; | A 84% B 94% C 61% |
Conditions | Yield |
---|---|
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide at 20℃; for 14h; | 94% |
With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride at 0 - 20℃; Inert atmosphere; | 94% |
With potassium fluoride In N,N,N,N,N,N-hexamethylphosphoric triamide at 65℃; for 5h; | 90% |
B
cyclohexene
Conditions | Yield |
---|---|
In benzene (N2); Ir complex soln. treated with BF3*2H2O, stirred for 12 h at 20°C; C6H6 and ether added to H2O layer; | A 94% B 63% |
7,7-dimorpholino-cis-bicyclo<4.1.0>heptane
A
5-morpholino-2,3,6,7-tetrahydro-1,4-oxazepine
B
cyclohexene
Conditions | Yield |
---|---|
at 700℃; under 1E-05 Torr; | A 70% B 93% |
acetic acid
cyclohexene
rac-3-acetoxycyclohexene
Conditions | Yield |
---|---|
With palladium diacetate; N,N'-bis(salicylidene)-1,2-phenylene diaminocobalt(II); lithium acetate; oxygen; hydroquinone at 60℃; under 760 Torr; Product distribution; var. metal macrocyclic complexes, var. metal complexes concentration; | 100% |
With palladium diacetate; N,N'-bis(salicylidene)-1,2-phenylene diaminocobalt(II); lithium acetate; oxygen; hydroquinone at 60℃; under 760 Torr; for 20.2h; | 100% |
With manganese(IV) oxide; palladium diacetate; p-benzoquinone at 60℃; for 17h; | 97% |
Conditions | Yield |
---|---|
In decane; toluene at 30℃; | 100% |
With [Cu(4-methyl-1,3-bis(2-pyridylimino)isoindole)(OAc)] In water | 86% |
With pyrazolate-based cobalt(II)-containing MFU-1 metal-organic framework at 70℃; for 2h; | 11.9% |
Conditions | Yield |
---|---|
With sodium hydroxide; Sucrose-ethyleneoxide adducts In chloroform at 20℃; for 2h; Product distribution; further catalysts: PEG, DB18K6; further objects of study: phase-transfer catalysis;; | 100% |
With sodium hydroxide; Sucrose-ethyleneoxide adducts In chloroform at 20℃; for 2h; Product distribution; further catalysts: PEG, DB18K6; | 100% |
With potassium hydroxide; 18-crown-6 ether In dichloromethane at 40℃; for 6h; | 98% |
cyclohexene
diethylazodicarboxylate
Diethyl 1-(2-cyclohexen-1-yl)-1,2-hydrazinedicarboxylate
Conditions | Yield |
---|---|
With tin(IV) chloride In dichloromethane at -78℃; | 100% |
With tin(IV) chloride In dichloromethane at -60℃; for 0.0833333h; | 77% |
Conditions | Yield |
---|---|
trans-2 In acetonitrile for 4h; Ambient temperature; | 100% |
With tert.-butylhydroperoxide; C29H26CuN6O2 In acetonitrile for 4h; Inert atmosphere; Reflux; | 100% |
With tert.-butylhydroperoxide; oxygen In acetonitrile at 85℃; for 12h; Catalytic behavior; Reagent/catalyst; Solvent; Time; | 99% |
Conditions | Yield |
---|---|
With water; 4-methylmorpholine N-oxide; osmium; Cu-Al-hydrotalcite In toluene at 60℃; for 4.5h; | 100% |
With N-methyl-2-indolinone; fluorous OsO4 In water; acetone; tert-butyl alcohol at 20℃; for 36h; | 100% |
With 4-methylmorpholine N-oxide; In water; acetone Ambient temperature; | 95% |
Conditions | Yield |
---|---|
With sodium periodate; C31H29Br2N3Ru*CH2Cl2 In water; ethyl acetate; acetonitrile at 25℃; for 0.5h; Inert atmosphere; Schlenk technique; | 100% |
With 1H-imidazole; sodium periodate; MnCl-TPP-(PEO750)4 In water; acetonitrile at 20℃; for 24h; | 97% |
With 1-(3-sulfopropyl)-3-methylimidazolium periodate In water at 35℃; for 36h; Reagent/catalyst; Temperature; | 93% |
Conditions | Yield |
---|---|
With methyl cyanoformate; sodium decatungstate In acetonitrile at 8℃; for 90h; Irradiation; | 100% |
at 10℃; for 25h; Product distribution; Irradiation; | |
With phosphorus pentoxide; benzene |
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% |
cyclohexene
trans-Di(2-chlorocyclohexyl) sulfide
Conditions | Yield |
---|---|
With sulfur dichloride In dichloromethane at 0℃; for 2h; | 100% |
With thiobismorpholine; trichlorophosphate In dichloromethane at -40 - 20℃; | 61% |
With tetrachloromethane; sulfur dichloride at 70 - 80℃; | |
With sulfur tetrachloride | |
With sulfur dichloride |
cyclohexene
2-bromocyclocyclohexanol
Conditions | Yield |
---|---|
With N-Bromosuccinimide In water at 0 - 25℃; | 100% |
With N-Bromosuccinimide; water In 1,2-dimethoxyethane 1.) 0 deg C, 30 min, 2.) 20 deg C, 60 min; | 99% |
With tribromo-isocyanuric acid In acetone at 20℃; for 0.0833333h; | 91% |
Conditions | Yield |
---|---|
With bromine; thallium(I) acetate In tetrachloromethane for 0.583333h; Ambient temperature; | 100% |
With bromine In Hexadecane for 0.5h; Cooling; | 100% |
With tetra-N-butylammonium tribromide In chloroform Ambient temperature; ultrasonic irradiation; | 99% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; trioctylmethylammonium hydrogen tungstate; phenylphosphonate In 1,4-dioxane at 70℃; for 0.8h; | 100% |
With tert.-butylhydroperoxide; molybdenum(VI) oxide at 80℃; for 1h; | 100% |
With tert.-butylhydroperoxide; C15H12ClMoN3O7 In methanol; dichloromethane for 1h; Reagent/catalyst; | 100% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) In tetrachloromethane at 80℃; for 1.5h; Wohl-Ziegler allylic bromination; | 100% |
With N-Bromosuccinimide; 1,3-di-n-butyl-imidazolium tetrafluoroborate at 28 - 35℃; for 0.0833333h; | 85% |
With N-Bromosuccinimide Wohl-Ziegler Bromination; Reflux; | 84% |
Conditions | Yield |
---|---|
With dibenzoyl peroxide at 90℃; for 10h; | 100% |
at 27℃; for 22h; (γ-irradiation); | |
Irradiation; |
Conditions | Yield |
---|---|
With N-Bromosuccinimide | 100% |
With sodium bromide at 60℃; electrolysis in undivided cell, Pt-anode, Cu-Zn-cathode; | 80% |
With tert-butyl hypobromite | |
With tBuBrO |
(diethoxyphosphinothioyl)sulfenyl chloride
cyclohexene
1-chloro-2-(S-diethoxythiophosphoro)cyclohexane
Conditions | Yield |
---|---|
100% |
cyclohexene
(1R,2R)-1-Chloro-2-iodo-cyclohexane
Conditions | Yield |
---|---|
With K(1+)*Cl2I(1-) In tetrachloromethane for 0.333333h; | 100% |
With hydrogenchloride; potassium iodate; iodine In water at 5℃; for 0.5h; iodochlorination; | 98% |
With iodine; copper dichloride In pentane for 4h; Ambient temperature; | 95% |
5-Phenyl-1H-tetrazole
cyclohexene
2-cyclohexyl-5-phenyl-2H-tetrazole
Conditions | Yield |
---|---|
With sulfuric acid | 100% |
4-Phenyl-1,2,4-triazolidine-3,5-dione
cyclohexene
1-(cyclohex-2-enyl)-4-phenyl-1,2,4-triazolidine-3,5-dione
Conditions | Yield |
---|---|
In dichloromethane | 100% |
In dichloromethane Ambient temperature; | 89% |
In benzene at 25℃; Rate constant; other solvent; | |
In benzene at 25℃; Rate constant; other solvent: CH2Cl2; | |
In toluene at 25℃; under 1490400 Torr; Kinetics; Temperature; Pressure; Concentration; |
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate; iodine In acetonitrile for 5h; Heating; | 100% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide at 0℃; for 1h; | 100% |
With N-Bromosuccinimide In dichloromethane 1.) -20 deg C, 2 h, 2.) 15 deg C; | 83% |
With N-Bromosuccinimide In dichloromethane at -20 - 23℃; for 17.5h; Inert atmosphere; | 63% |
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate; iodine for 5h; Heating; | 100% |
With ammonium cerium(IV) nitrate; iodine for 10h; Mechanism; Heating; other substrate; | 80% |
With ammonium cerium(IV) nitrate; iodine for 10h; Heating; | 80% |
Conditions | Yield |
---|---|
In benzene for 1.5h; Irradiation; | 100% |
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