Product Detail Minimum Order Qty. 10 Gram
Cas:123-66-0
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:123-66-0
Min.Order:0 Metric Ton
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Type:Manufacturers
inquiryProduct description: Product name Ethyl caproate CAS number 123-66-0 Assay ≥99% Appearance Colorless to yellowish liquid Capacity 500mt/year Application Flavor for food tobac
Cas:123-66-0
Min.Order:1 Kilogram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryEthyl caproate CAS RN: 123-66-0 Molecular formula: C8H16O2 Molecular weight: 144.21 Properties: Colorless transparent liquid Quality index:
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
DayangChem exported this product to many countries and regions at best price in China. If you are looking for the product’s supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product specifica
Cas:123-66-0
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
High purity CAS 123-66-0 Ethyl Hexanoate in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Fluorene,Ca
Cas:123-66-0
Min.Order:1 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryChemical Name: Ethyl hexanoate CAS No.: 123-66-0 Molecular Fomula:C8H16O2 Chemical Structure: Molecular weight: 144.21 Appearance: Colorless Transparent Liquid Assay:99.9% Appearance: Colorless Transparent Liquid Storage: Preserve
Hangzhou 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
Cas:123-66-0
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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:123-66-0
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryWe 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:123-66-0
Min.Order:1 Metric Ton
FOB Price: $5.0
Type:Lab/Research institutions
inquirySAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
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:123-66-0
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
Xiamen Luyunjia Trading Co.,Ltd Package:1kg/bag; 2898kg/drum, or as customer's request. Application:Xiamen Luyunjia Trading Co.,Ltd Transportation:DHL, EMS, FedEx, TNT, AIR, SEA Port:Beijing,Shanghai,Guangzhou ,China main port
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
Cas:123-66-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryin storeAppearance:Colorless - very pale yellow transparent liquid Package:500ml Application:Organic Chemicals
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:123-66-0
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryWhy choose us? 1. We are a professional manufacturer of power bank. 2. We can provide you with excellent quality products. 3. We can also provide you with OEM or ODM manufacture. 4. The battery cells of all products are imported from So
Cas:123-66-0
Min.Order:1 Kilogram
Negotiable
Type:Other
inquiryEthyl caproate Basic information Product Name: Ethyl caproate
Cas:123-66-0
Min.Order:100 Gram
Negotiable
Type:Trading Company
inquiryConditions | Yield |
---|---|
With Oxone at 20℃; for 18h; | 95% |
With oxygen at 100℃; under 3750.38 Torr; for 5h; Autoclave; |
Conditions | Yield |
---|---|
zirconium(IV) oxide for 5h; Heating; | 100% |
With 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride for 4h; | 93% |
With 8-hydroxyquinoline methanesulfonate at 85℃; for 3h; Temperature; Reagent/catalyst; Concentration; | 91.4% |
Conditions | Yield |
---|---|
Stage #1: penta-1,3-diene; ethanol With tris-(dibenzylideneacetone)dipalladium(0); methanesulfonic acid; 1,2-bis[di(t-butyl)phosphinomethyl]benzene In methanol for 0.25h; Sonication; Schlenk technique; Stage #2: carbon monoxide With hydrogen In methanol under 22502.3 Torr; |
Conditions | Yield |
---|---|
With D-(+)-glucose In aq. buffer at 15℃; for 16h; Overall yield = 44.3 %; | |
With glucose dehydrogenase; D-glucose; potassium chloride; NADPH In aq. buffer at 30℃; pH=8.5; Baeyer-Villiger Ketone Oxidation; Enzymatic reaction; regioselective reaction; |
ethyl 2-(pyridin-2-ylsulfonyl)hexanoate
Ethyl hexanoate
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In toluene for 1h; desulfonylation; Heating; | 91% |
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene for 36h; Heating; | 60% |
Multi-step reaction with 2 steps 1: 61 percent / m-CPBA / CHCl3; CH2Cl2 2: 12 percent / Bu3SnH; AIBN / benzene / 1 h / Heating View Scheme |
ethanol
hexan-1-amine
carbon monoxide
A
Ethyl hexanoate
B
ethyl n-valerate
C
ethyl heptanoate
D
N-hexylcarbamic acid ethyl ester
Conditions | Yield |
---|---|
With oxygen; Sulfate; zirconium(IV) oxide; palladium dichloride at 170℃; under 45003.6 Torr; for 3h; Further byproducts given. Title compound not separated from byproducts; | A n/a B n/a C n/a D 81% |
Conditions | Yield |
---|---|
With N,N,N,N,-tetramethylethylenediamine; cobalt(II) chloride; lithium iodide In tetrahydrofuran at 10℃; for 1h; | 78% |
(2E,4E)-ethyl hexa-2,4-dienoate
A
Ethyl hexanoate
B
ethyl (E)-hex-2-enoate
C
ethyl (E)-3-hexenoate
D
ethyl (3Z)-hex-3-enoate
Conditions | Yield |
---|---|
With hydrogen; silica-supported [(CH2)3-N(CH2PPh2)2][Pd(dba)] In methanol at 25℃; under 724.007 Torr; for 1h; Title compound not separated from byproducts; | A 7 % Chromat. B 86 % Chromat. C 4 % Chromat. D 3 % Chromat. |
Conditions | Yield |
---|---|
With hydrogen at 80℃; under 7500.75 Torr; for 1h; Autoclave; | 92% |
ethyl (E)-hex-2-enoate
Ethyl hexanoate
Conditions | Yield |
---|---|
With hydrogen In toluene at 150℃; under 18751.9 Torr; for 15h; Sealed tube; | |
Stage #1: ethyl (E)-hex-2-enoate With (+)-1,2-bis((2S,5S)-2,5-diphenylphospholanyl)ethane; copper diacetate at 20℃; for 24h; Inert atmosphere; Stage #2: With sodium hydrogencarbonate In water; ethyl acetate at 20℃; for 0.416667h; Inert atmosphere; Cooling with ice; |
ethyl 2-(pyrimidin-2-ylsulfonyl)hexanoate
Ethyl hexanoate
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene for 1h; desulfonylation; Heating; | 100% |
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene for 1h; Heating; |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; tert.-butylnitrite; iron(II) phthalocyanine; hydrogen In ethanol at 20℃; under 7500.75 Torr; for 3h; |
Conditions | Yield |
---|---|
With zinc chromite; hydrogen at 360℃; under 154457 Torr; und folgenden Hydrieren an Nickel; |
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In ethanol; benzene 1.) room temperature, 1.5 h, 2.) reflux, 23 h; | 84% |
Conditions | Yield |
---|---|
With hydrogen; palladium In diethyl ether at 25℃; | 99 % Chromat. |
With Pd(OAc)2 dopped triglycidyl 1-ethyl-3-methylimidazoliumacetate polyether In methanol at 20℃; for 2h; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 95 percent / NaH / dimethylformamide / 0 - 20 °C 2: 5.15 g / m-CPBA / CHCl3; CH2Cl2 / 20 h / -20 - 20 °C 3: 100 percent / Bu3SnH; AIBN / benzene / 1 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1: NaH / tetrahydrofuran; dimethylformamide 2: m-CPBA 3: 60 percent / Bu3SnH, AIBN / benzene / 36 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1: NaH / tetrahydrofuran; dimethylformamide 2: m-CPBA 3: Bu3SnH, AIBN / benzene / 1 h / Heating View Scheme |
Ethyl hexanoate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 5.07 g / m-CPBA / CHCl3; CH2Cl2 / -20 - 20 °C 2: 91 percent / Bu3SnH; AIBN / toluene / 1 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1: 5.07 g / m-CPBA / CHCl3; CH2Cl2 / -20 - 20 °C 2: 61 percent / m-CPBA / CHCl3; CH2Cl2 3: 12 percent / Bu3SnH; AIBN / benzene / 1 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: m-CPBA 2: 60 percent / Bu3SnH, AIBN / benzene / 36 h / Heating View Scheme |
ethyl (E)-3-hexenoate
Ethyl hexanoate
Conditions | Yield |
---|---|
With ethanol; lithium; nickel dichloride; 4,4'-di-tert-butylbiphenyl In tetrahydrofuran at 20℃; for 24h; | 86 % Chromat. |
2-(Pyrimidin-2-ylsulfanyl)-hexanoic acid ethyl ester
Ethyl hexanoate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 5.15 g / m-CPBA / CHCl3; CH2Cl2 / 20 h / -20 - 20 °C 2: 100 percent / Bu3SnH; AIBN / benzene / 1 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: m-CPBA 2: Bu3SnH, AIBN / benzene / 1 h / Heating View Scheme |
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate at 90 - 150℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With 2-nitrobenzeneseleninic acid; dihydrogen peroxide at 20℃; for 24h; | 76% |
diazoacetic acid ethyl ester
n-butane
A
Ethyl hexanoate
B
ethyl 3-methylpentanoate
Conditions | Yield |
---|---|
With C31H9AgBF27N6O at 0 - 40℃; under 190013 Torr; for 4h; Supercritical conditions; Sonication; Overall yield = 85 %; |
2-hydroxyhexanoic acid ethyl ester
Ethyl hexanoate
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; Trimethylacetic acid In tetrahydrofuran at 20 - 22℃; for 2h; | 89 % Chromat. |
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether at -20 - 20℃; | A n/a B 45% |
In tetrahydrofuran at -20 - 20℃; | A n/a B 42% |
Ethyl 2-fluoro-2-hexenoate
A
Ethyl hexanoate
B
2-fluoro hexane-1-oate d'ethyle
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethyl acetate Product distribution; Ambient temperature; other catalysts and other fluoroolefins; | A 1% B 99% |
Conditions | Yield |
---|---|
With iodosylbenzene; potassium bromide In water at 20℃; for 12h; | 15 % Chromat. |
methyl manganese chloride
C9H16O4
A
n-pentyl methyl ketone
B
Ethyl hexanoate
Conditions | Yield |
---|---|
In tetrahydrofuran at -20 - 20℃; | A 35% B n/a |
2-(1-oxy-pyridine-2-sulfonyl)-hexanoic acid ethyl ester
A
Ethyl hexanoate
B
ethyl 2-(pyridin-2-ylsulfonyl)hexanoate
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene for 1h; desulfonylation; Heating; | A 12% B 80% |
ethyl-2-bromooctanoate
Ethyl hexanoate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: 5.07 g / m-CPBA / CHCl3; CH2Cl2 / -20 - 20 °C 3: 91 percent / Bu3SnH; AIBN / toluene / 1 h / Heating View Scheme | |
Multi-step reaction with 4 steps 2: 5.07 g / m-CPBA / CHCl3; CH2Cl2 / -20 - 20 °C 3: 61 percent / m-CPBA / CHCl3; CH2Cl2 4: 12 percent / Bu3SnH; AIBN / benzene / 1 h / Heating View Scheme |
ethyl hex-3-enoate
isopropyl alcohol
A
Ethyl hexanoate
B
hexanoic acid isopropyl ester
Conditions | Yield |
---|---|
With 4,4'-di-tert-butylbiphenyl; lithium; nickel dichloride In tetrahydrofuran at 20 - 76℃; Inert atmosphere; chemoselective reaction; |
Conditions | Yield |
---|---|
With sodium aluminum tetrahydride In tetrahydrofuran at 0℃; for 0.5h; | 100% |
With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 15h; Glovebox; Autoclave; | 93% |
With ethanol; ruthenium(bis[2‐(ethylsulfanyl)ethyl]amine)(dichloro)(triphenylphosphine); potassium tert-butylate In toluene at 80℃; for 16h; Catalytic behavior; Reagent/catalyst; | 89% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on palladium(0 and II)-stabilized UiO-66-NH2 metal organic framework modified with lauric acid nanocatalyst In toluene at 20℃; for 8h; Time; Sealed tube; Enzymatic reaction; | 100% |
Conditions | Yield |
---|---|
Stage #1: 2-Amino-2-methyl-1-propanol With n-butyllithium; lanthanum(III) chloride In dichloromethane at 0℃; Metallation; after the reagent addition stirring for 15 min at this temperature under nitrogen, than warming to reflux; Stage #2: Ethyl hexanoate for 24h; Amidation; reflux; | 99% |
Conditions | Yield |
---|---|
With potassium tert-butylate for 0.0833333h; microwave irradiation; | 98% |
Ethyl hexanoate
1-<1,1-(2)H2>hexanol
Conditions | Yield |
---|---|
With lithium aluminium deuteride In diethyl ether 1.) 0 deg C, 15 min, 2.) 0 deg C -> room temperature, 2 h; | 97% |
With lithium aluminium deuteride In diethyl ether for 2h; Reduction; Heating; | 94% |
With lithium aluminium deuteride In diethyl ether for 1h; Heating; | 89% |
With lithium aluminium deuteride In diethyl ether at 0℃; | 83% |
Ethyl hexanoate
3-bromo-1-(trimethylsilyl)-1-propyne
1-Trimethylsilanyl-4-(3-trimethylsilanyl-prop-2-ynyl)-non-1-yn-4-ol
Conditions | Yield |
---|---|
Stage #1: 3-bromo-1-(trimethylsilyl)-1-propyne With chloro-trimethyl-silane; ethylene dibromide; zinc In tetrahydrofuran at 20℃; for 12h; Stage #2: Ethyl hexanoate In tetrahydrofuran at 20℃; Further stages.; | 96% |
Ethyl hexanoate
Aluminium tris(phenylthiolate)
S-phenyl hexanethioate
Conditions | Yield |
---|---|
In benzene at 25℃; | 95% |
Ethyl hexanoate
N-(pyridyl-3-imidoyl)guanidine
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 92% |
Conditions | Yield |
---|---|
Stage #1: morpholine With diisobutylaluminium hydride In tetrahydrofuran; hexane at 0℃; for 3h; Inert atmosphere; Stage #2: Ethyl hexanoate In tetrahydrofuran; hexane at 0℃; for 0.166667h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 91% |
Conditions | Yield |
---|---|
With potassium tert-butylate for 0.0583333h; microwave irradiation; | 91% |
Conditions | Yield |
---|---|
Stage #1: Ethyl hexanoate With morpholine; diisobutylaluminium hydride In tetrahydrofuran; hexane at 0℃; for 3.16667h; Inert atmosphere; Stage #2: n-butyllithium In tetrahydrofuran; hexane at 0℃; for 0.166667h; Inert atmosphere; | 91% |
Ethyl hexanoate
ethyl 2-(1-benzylpiperidin-4-ylidene)-2-cyanoacetate
C25H36N2O4
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran at -78℃; Michael addition; | 90% |
Stage #1: Ethyl hexanoate With lithium diisopropyl amide In tetrahydrofuran; hexane at -78℃; Cooling with acetone-dry ice; Stage #2: ethyl 2-(1-benzylpiperidin-4-ylidene)-2-cyanoacetate In tetrahydrofuran; hexane at -78℃; Cooling with acetone-dry ice; | 90% |
Ethyl hexanoate
methyl 2-(3-methylthiophenylamino)-3-pyridine carboxylate
3-(n-butyl)-4-hydroxy-1-(3-methylthiophenyl)-1,8-naphthyridin-2-(1H)-one
Conditions | Yield |
---|---|
With potassium tert-butylate 1.) 0.25 h, 2.) heating, 4 h; | 89% |
Conditions | Yield |
---|---|
With potassium tert-butylate for 0.0666667h; microwave irradiation; | 88% |
Conditions | Yield |
---|---|
With 1-(3-sulfopropyl)pyridinium phosphotungstate In neat (no solvent) at 120℃; for 0.666667h; Microwave irradiation; | 88% |
Ethyl hexanoate
N'-hydroxy-3-methylbenzimidamide
5-pentyl-3-(m-tolyl)-1,2,4-oxadiazole
Conditions | Yield |
---|---|
With potassium carbonate In neat (no solvent) for 0.133333h; Microwave irradiation; | 85% |
Ethyl hexanoate
4-chlorobenzamidoxime
3-(4-chlorophenyl)-5-pentyl-1,2,4-oxadiazole
Conditions | Yield |
---|---|
With potassium carbonate In neat (no solvent) for 0.133333h; Microwave irradiation; | 85% |
Ethyl hexanoate
methyl-3-(phenylamino)isonicotinate
3-Butyl-4-hydroxy-1-phenyl-1H-[1,7]naphthyridin-2-one
Conditions | Yield |
---|---|
With potassium tert-butylate 1.) 0.25 h, 2.) heating, 4 h; | 84% |
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