As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis
Cas:100-41-4
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryHebei yanxi chemical co. LTD. has expanded a compositive entity from initially only as a small manufacturer. The company dedicated to the development, production and marketing of chemicals. After many years of efforts, we have established stable
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so
Cas:100-41-4
Min.Order:1 Metric Ton
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Type:Lab/Research institutions
inquiryProduct name Ethylbenzene CAS No. 100-41-4 EINECS 202-710-8 Molecular formula C
Minimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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
Superior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediat
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,
Cas:100-41-4
Min.Order:1 Kilogram
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inquiryWe 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:100-41-4
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryHangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical,
Cas:100-41-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city?in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api,?intermediat
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:100-41-4
Min.Order:1 Kilogram
FOB Price: $112.0
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
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
Manufacturer supply Ethylbenzene Application:Manufacturer supply Ethylbenzene
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
Manufacturer supply EthylbenzeneAppearance:Off-White powder Storage:Dry and cool Package:aluminium foil bag,drum Application:standard anti-malarial API Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport
Cas:100-41-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryEthylenzene Basic information Product Name: Ethylenzene Synonyms: ET2O;ETHER;ETHOXYETHANE;ETHYL ETHER 1000;ethylenzene;ETHYLBENZENE;ETHYL OXIDE;DIETHYL ETHER 300 CAS:
Changzhou Xuanming Chemical Co., Ltd. is dedicated to the technology development, manufacturing, import and export chemicals, which are specialized in pharmaceutical intermediates, pesticide intermediate, industry of fine chemicals and custom synt
Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers. Our advantages: 1, High quality with competitive price: 1) Standard:BP/USP/EP/Enterprise standard 2) All Purity&ge
Cas:100-41-4
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquirystyrene
ethylbenzene
Conditions | Yield |
---|---|
With hydrogen; p In methanol for 0.316667h; other substrates; | 100% |
With polymeric thiol; hydrogen; palladium on activated charcoal for 1h; Product distribution; var. catalysts, further thiol; poisoning effect of thiols; | 100% |
With hydrogen; Pd-1percent Ho In neat (no solvent) at 90℃; for 0.00583333h; Product distribution; selective hydrogenation; variation of temperature and contact time; | 100% |
Conditions | Yield |
---|---|
With n-butyllithium; potassium 2-methylbutan-2-olate Mechanism; 1) r.t., 17 h, 2) reflux, 7 h; further reagent: D2O; | 100% |
at 400℃; Leiten ueber Chrom(III)-oxyd; | |
at 300 - 320℃; Leiten ueber Nickel-Aluminiumoxyd; |
1-Phenylethanol
ethylbenzene
Conditions | Yield |
---|---|
With formic acid; ammonium formate; 5%-palladium/activated carbon In ethanol; water at 80℃; Product distribution / selectivity; | 100% |
With palladium dichloride In methanol at 40℃; for 18h; Inert atmosphere; Green chemistry; chemoselective reaction; | 99% |
With hydrogen; palladium diacetate; sodium dioctyl sulfosuccinate In tetrahydrofuran at 25℃; under 760.051 Torr; for 24h; | 99% |
Conditions | Yield |
---|---|
With hydrogen; palladium on C60 In methanol under 760 Torr; for 0.216667h; Ambient temperature; other substrates: cyclohexene, hex-1-ene, other catalysts: palladium on activated charcoal, C60, other reaction time; | 100% |
silver tetrafluoroborate; (Ph2PCH2PPh2CHC(O)Ph)>I In dichloromethane at 65℃; for 18h; Pressure (range begins): 120 ; | 100% |
With hydrogen; N,N′-bis(salicylidene)-ethylenediamino‑palladium In methanol for 0.85h; | 100% |
Conditions | Yield |
---|---|
With hydrogen at 80℃; under 37503.8 Torr; for 0.5h; Autoclave; chemoselective reaction; | 100% |
With hydrogen In ethanol at 39.84℃; under 760.051 Torr; for 5h; | 100% |
With Pd/C; hydrogen In chloroform at 20℃; under 760.051 Torr; for 8h; Catalytic behavior; | 100% |
Conditions | Yield |
---|---|
With C52H46ClN3P2Ru In dichloromethane-d2 at 50℃; under 3040.2 Torr; for 16h; Reagent/catalyst; Time; | 100% |
With [Ir(6-Neo)(COD)Cl] In ethanol under 3750.38 Torr; for 1h; Solvent; | 100 %Spectr. |
at 80℃; under 30003 Torr; for 24h; Reagent/catalyst; |
Conditions | Yield |
---|---|
With C61H98ClN3P2Ru In dichloromethane-d2 at 50℃; under 3040.2 Torr; for 14h; | 100% |
styrene
Dimethylphenylsilane
A
ethylbenzene
B
dimethyl(phenyl)(2-phenylethenyl)silane
Conditions | Yield |
---|---|
With C11H14FeO4Si2 In toluene at 50℃; for 24h; Kinetics; Reagent/catalyst; Temperature; Inert atmosphere; Schlenk technique; | A n/a B 100% |
Conditions | Yield |
---|---|
With hydrogen at 240 - 400℃; under 15001.5 Torr; Reagent/catalyst; Temperature; | 99.5% |
Conditions | Yield |
---|---|
Product distribution; Heating; synthesis by chemorectification; | 99% |
mesoporous ZSM-5 Si/Al=120 at 310 - 370℃; under 1875.19 - 3750.38 Torr; Product distribution / selectivity; | 75% |
boron trifluoride at 180℃; under 22501.8 Torr; Product distribution; other temperatures, other volumetric rates; | 59.9% |
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine)palladium dichloride In benzene at 80℃; for 3h; | 99% |
Conditions | Yield |
---|---|
With hydrogen; 5% rhodium-on-charcoal; tris(acetylacetonato)cobalt In tetrahydrofuran at 20℃; for 16h; | A 99% B 89% |
With hydrogen; 5% rhodium-on-charcoal; iron(II) acetate In tetrahydrofuran at 20℃; for 16h; | A 98% B 80% |
With hydrogen; 5% rhodium-on-charcoal In tetrahydrofuran at 20℃; for 16h; Product distribution / selectivity; | A 93% B 31% |
With hydrogen at 110℃; under 4560.31 Torr; for 24h; Autoclave; chemoselective reaction; |
Conditions | Yield |
---|---|
1,1'-bis-(diphenylphosphino)ferrocene; [1,1'-bis(diphenylphosphino)ferrocene]nickel(II) chloride; potassium iodide In diethyl ether; toluene at 80℃; for 10h; | 99% |
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; triisopropyl phosphite; chlorotriisopropylsilane In ethyl-cyclohexane at 160℃; for 15h; Inert atmosphere; | 99% |
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; triisopropyl phosphite; chlorotriisopropylsilane In ethylcyclohexane at 160℃; for 15h; Inert atmosphere; | 99 %Chromat. |
With bis(acetylacetonate)nickel(II); 1,1,3,3-Tetramethyldisiloxane; trimethylaluminum; tricyclohexylphosphine In toluene at 130℃; for 24h; Inert atmosphere; | 67 %Chromat. |
With bis(1,5-cyclooctadiene)nickel (0); hydrogen; trimethylaluminum; tricyclohexylphosphine In toluene at 130℃; under 750.075 Torr; for 24h; Schlenk technique; | 79 %Chromat. |
With lithium borohydride; C30H21F6N2NiO2P In tetrahydrofuran at 70℃; for 3h; Schlenk technique; Inert atmosphere; | 7 %Chromat. |
Conditions | Yield |
---|---|
With 3% Au/meso-CeO2; potassium formate In water at 25℃; chemoselective reaction; | A 7% B 99% |
With gold supported on mesoporous ceria; hydrogen In isopropyl alcohol at 100℃; under 7500.75 Torr; for 1h; | |
With tetrakis[3,5-bis(trifluoromethyl)phenyl]boric acid bis(diethyl ether) complex; C32H63CoNP2Si; hydrogen In tetrahydrofuran at 25℃; under 760.051 Torr; for 24h; | A 16 %Chromat. B 99 %Chromat. |
With hydrogen In isopropyl alcohol at 130℃; under 11400.8 Torr; for 5h; Reagent/catalyst; |
Conditions | Yield |
---|---|
With formic acid In water at 120℃; for 3h; Green chemistry; | A 98% B 99% |
With Cu/Al2O3; hydrogen In ethyl acetate at 150℃; under 18751.9 Torr; for 21h; Inert atmosphere; Autoclave; | A 19.1% B 21.7% |
With nickel-molybdenum sulfide; hydrogen; potassium hydroxide In methanol at 180℃; under 7500.75 Torr; for 1h; | A 46 %Chromat. B 54 %Chromat. |
2-phenethoxybenzene
A
ethyl-cyclohexane
B
ethylbenzene
C
cyclohexanol
Conditions | Yield |
---|---|
With hydrogen; lanthanum(lll) triflate In isopropyl alcohol at 120℃; for 2h; | A 33% B 66% C 99% |
With hydrogen In n-heptane at 160℃; under 750.075 Torr; for 6h; Catalytic behavior; Temperature; | A 8 %Chromat. B 92 %Chromat. C 100 %Chromat. |
With isopropyl alcohol at 170℃; under 7500.75 Torr; Inert atmosphere; Autoclave; |
Conditions | Yield |
---|---|
With phosphonic Acid; iodine In benzene at 100℃; for 36h; Inert atmosphere; | 98% |
With sodium tetrahydroborate; cetyltributylphosphonium bromide In water; toluene at 80℃; for 3h; Product distribution; | 85% |
With sodium tetrahydroborate; water In methanol at 20℃; for 0.5h; | 81% |
Conditions | Yield |
---|---|
In benzene-d6 under Ar; 90°C, 6 h; | A 98% B 63% C 4% |
Conditions | Yield |
---|---|
With hydrogen In hexane at 30℃; under 760.051 Torr; for 6h; | A 97% B 3% |
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics; | A 95% B n/a |
With hydrogen In ethyl acetate at 20℃; under 760.051 Torr; for 0.5h; | A 9% B 91% |
3-Phenyl-propionic acid 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl ester
ethylbenzene
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In toluene for 3h; Heating; decarboxylation was investigated; | 97% |
1-phenylethyl acetate
ethylbenzene
Conditions | Yield |
---|---|
With hafnium(IV) trifluoromethanesulfonate; palladium 10% on activated carbon; hydrogen In neat (no solvent) at 25℃; under 750.075 Torr; for 18h; Time; | 97% |
With triethylsilane; indium tribromide In chloroform at 60℃; for 1h; Inert atmosphere; | 76% |
With pyrrolidine; samarium diiodide; water In tetrahydrofuran; decane at 20℃; | 73 %Chromat. |
Conditions | Yield |
---|---|
With Ni0.85Rh0.15; hydrogen In water at 95℃; under 760.051 Torr; for 16h; Reagent/catalyst; | A 96% B 27% C 59% |
With Ni0.85Ru0.15; hydrogen In water at 95℃; under 760.051 Torr; for 16h; Reagent/catalyst; | A 76% B 69% C 26% |
With 57 wt. % Ni/SiO2 In water at 120℃; under 4500.45 Torr; for 1.5h; Activation energy; Catalytic behavior; Temperature; Pressure; Autoclave; |
(1-bromoethyl)benzne
ethylbenzene
Conditions | Yield |
---|---|
With phosphonic Acid; iodine In 1,2-dichloro-ethane at 120℃; for 36h; Inert atmosphere; | 95% |
With zinc-modified cyanoborohydride In diethyl ether for 3h; Ambient temperature; | 91% |
With zinc(II) tetrahydroborate In diethyl ether for 1h; Ambient temperature; | 91% |
Conditions | Yield |
---|---|
In benzene-d6 Irradiation (UV/VIS); under Ar; room temp., 7 h; not isolated; NMR; | A 95% B 86% |
Conditions | Yield |
---|---|
With 1,2-dimethoxy-4-methylbenzene In tetrahydrofuran at 60℃; for 0.0833333h; | 95% |
styrene
1,1-Diphenylethylene
A
1,1'-ethylidenebis-benzene
B
ethylbenzene
Conditions | Yield |
---|---|
With C28H18Co(1-)*K(1+)*2C4H10O2; hydrogen at 20℃; under 1500.15 Torr; for 3h; | A 18% B 95% |
C16H18O
ethylbenzene
Conditions | Yield |
---|---|
With palladium on activated charcoal In 1,4-dioxane at 160℃; for 8h; Thermodynamic data; | 95% |
Conditions | Yield |
---|---|
With hydrogen In ethanol at 20℃; under 760.051 Torr; for 5h; | A 6% B 94% |
With carbon dioxide; 5%-palladium/activated carbon; hydrogen In water at 49.84℃; under 15001.5 Torr; for 13h; Autoclave; Green chemistry; | A 93% B 7% |
With hydrogen In ethanol at 39.84℃; under 760.051 Torr; for 4h; | A 92% B 8% |
Conditions | Yield |
---|---|
With hydrogen at 150℃; under 2280.15 Torr; for 0.166667h; Kinetics; Reagent/catalyst; Temperature; | 100% |
With Ti8O8(14+)*6C8H4O4(2-)*4O(2-)*3.3Li(1+)*0.7Co(2+)*0.7C4H8O*0.7H(1-); hydrogen In neat (no solvent) at 120℃; under 37503.8 Torr; for 18h; | 89% |
With octylated silica; hydrogen; sodium 4-dodecylbenzenesulfonate; {[(CH3)(C8H17)3N](+)[RhCl4](-)} at 80℃; under 10343 Torr; for 24h; | 63% |
ethylbenzene
1-Phenylethanol
Conditions | Yield |
---|---|
With cerium(IV) triflate; water In acetonitrile at 20℃; for 20h; | 100% |
With C20H26B10Cl2FeN6; dihydrogen peroxide In methanol at 20℃; for 6h; | 91% |
With perchloric acid; C13H30N4*Fe(3+)*CF3O3S(1-)*C2H2F3O(1-)*C6H5IO In 2,2,2-trifluoroethanol; acetone at -40℃; for 0.166667h; Kinetics; Inert atmosphere; Schlenk technique; Further stages; | 39% |
ethylbenzene
(1-bromoethyl)benzne
Conditions | Yield |
---|---|
With manganese(IV) oxide; bromine In dichloromethane at 20℃; for 0.166667h; | 100% |
With bromine In tetrachloromethane Solvent; | 100% |
With carbon tetrabromide; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate In dichloromethane at 20℃; for 36h; Solvent; Reagent/catalyst; Schlenk technique; Inert atmosphere; Irradiation; | 99% |
Conditions | Yield |
---|---|
With potassium permanganate; iron(III) chloride In acetone at -78 - 20℃; for 16h; | 100% |
With potassium bromate; cerium(IV) oxide In 1,4-dioxane; water; acetic acid at 95℃; for 1h; | 100% |
With cerium(IV) triflate; water In acetonitrile at 20℃; for 19.5h; | 99.7% |
ethylbenzene
10-methylacridinium perchlorate
Conditions | Yield |
---|---|
In water; acetonitrile Irradiation; | 100% |
In acetonitrile at 24.9℃; Rate constant; Quantum yield; Irradiation; also in MeOH; |
ethylbenzene
2,2,2-trichloroethyl sulfamate
Conditions | Yield |
---|---|
With [bis(acetoxy)iodo]benzene; C32H44ClN4O4Rh2*3CH2Cl2 at 20℃; for 3h; Inert atmosphere; | 100% |
With [bis(acetoxy)iodo]benzene; bis[rhodium(α,α,α',α'-tetramethyl-1,3-benzenedipropionic acid)]; sodium hydrogencarbonate | 90% |
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; [bis(acetoxy)iodo]benzene In water at 4℃; for 24h; | 86% |
ethylbenzene
A
4-Ethylphenol
B
1-Phenylethanol
C
2-phenylethanol
Conditions | Yield |
---|---|
With rabbit liver microsomal cytochrome P-450 In water at 25℃; for 12h; | A 0.13% B 99.8% C 0.08% |
chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer
ethylbenzene
[(η5-pentamethylcyclopentadienyl)Ru(η6-ethylbenzene)]Cl
Conditions | Yield |
---|---|
In water other Radiation; (N2); using Schlenk techniques; combining of ethylbenzene (8 equiv.), ((C5Me5)RuCl)4 (1 equiv.) and H2O in glass microwave reaction vessel with stir bar; sealing; microwave irradn. at 50 W (ca. 130°C for 10 min); evapn. of solvent under reduced pressure, extn., trituration with hexane; drying; | 99% |
In tetrahydrofuran; water other Radiation; (N2); using Schlenk techniques; combining of ethylbenzene (1 equiv.), ((C5Me5)RuCl)4 (1 equiv.), H2O and THF (2:1); microwave irradn. for 15 minat 130°C; cooling to room temp., removal of solvent under reduced pressure, trituration with toluene; drying; | 99% |
In water Sonication; (N2); using Schlenk techniques; combining of benzene (8 equiv.), ((C5Me5)RuCl)4 (1 equiv.) and H2O in Schlenk tube with stir bar; sealing; heating in oil bath (ca. 115.degre.C) with intermittent sonication for 1-3 ds; cooling to ca. 25°C; evapn. of solvent under reduced pressure, extn./trituration with toluene; drying; |
ethylbenzene
5-bromo-2-chloro-benzoyl chloride
(5-bromo-2-chlorophenyl)(4-ethylphenyl)methanone
Conditions | Yield |
---|---|
Stage #1: ethylbenzene; 5-bromo-2-chloro-benzoyl chloride With aluminum (III) chloride at 10℃; for 0.5h; Stage #2: With sodium hydroxide In water at 15 - 20℃; for 5h; | 99% |
Stage #1: ethylbenzene; 5-bromo-2-chloro-benzoyl chloride With aluminum (III) chloride In chloroform at 5℃; Friedel Crafts acylation; Cooling; Stage #2: With water In chloroform Cooling with ice; |
N-tert-butoxycarbonyl-L-leucine
ethylbenzene
1-phenylethyl N-(tert-butoxycarbonyl)-L-leucinate
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water at 80℃; for 8h; | 99% |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water at 80℃; for 3h; | 99% |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water at 80℃; for 8h; | 99% |
With di-tert-butyl peroxide; C11H23N2(1+)*Br4Fe(1-) at 110℃; for 16h; | 84% |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water at 80℃; for 8h; | 99% |
With di-tert-butyl peroxide; C11H23N2(1+)*Br4Fe(1-) at 110℃; for 24h; | 88% |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water at 80℃; for 8h; | 99% |
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