DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:2548-87-0
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:2548-87-0
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inquiryThe 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
Shanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
Cas:2548-87-0
Min.Order:1 Kilogram
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inquiryHigh quality and low price of (E)-2-Octenal from Henan Tianfu Chemical: Henan Tianfu Chemical Co.,LTD 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 establis
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Cas:2548-87-0
Min.Order:1 Gram
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Min.Order:1 Kilogram
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Min.Order:10 Gram
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Cas:2548-87-0
Min.Order:500 Kilogram
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Type:Lab/Research institutions
inquiry(E)-2-Octenal CAS: 2548-87-0 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediat
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Min.Order:1 Gram
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Type:Lab/Research institutions
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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
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Min.Order:0 Metric Ton
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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
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
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Min.Order:10 Gram
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Type:Lab/Research institutions
inquirysuperior quality moderate price & quick delivery 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 to make o
Product name: Trans-2-Octenal CAS No.:2548-87-0 Molecule Formula:C8H14O Molecule Weight:126.19 Purity: 98.0% Package: 25kg/drum Description:Colorless to pale yellow liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryzhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed produc
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryShandong Mopai Biotechnology 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 chemicals. W
1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
SAGECHEM 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
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
Lower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the 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
AN ISO 9001, ISO 14001, ISO 22024 CERTIFIED FACTORY,HALAL 、KOSHER、FCC AND FDA CERTIFICATE ARE AVAILABLE. Storage:1000KG Package:5 or 25 KG per drum Application:Daily flavor, food additives Transportation:by air /by sea or by courier like DHL or Fedex
Cas:2548-87-0
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Type:Manufacturers
inquiry(E)-oct-2-en-1-ol
(E)-2-Octenal
Conditions | Yield |
---|---|
With dmap; tetrakis(actonitrile)copper(I) hexafluorophosphate; N,N'-di-tert-butylethylenediamine; oxygen In dichloromethane at 20℃; under 760.051 Torr; for 1h; Schlenk technique; Molecular sieve; Sealed tube; | 99% |
With 1-methyl-1H-imidazole; [2,2]bipyridinyl; 2,2,6,6-tetramethyl-piperidine-N-oxyl; TPGS-750-M; copper(I) bromide In water at 20℃; for 9h; | 93% |
With potassium osmate(VI) dihydrate; potassium carbonate; potassium hexacyanoferrate(III) In water; acetonitrile at 60℃; for 14h; chemoselective reaction; | 88% |
cis-2-octene
trans-2-Octene
A
(E)-2-Octenal
B
cis-2-octene oxide
Conditions | Yield |
---|---|
With (5,10,15,20-tetramesitylporphyrinato)manganese(III) chloride; 3-chloro-benzenecarboperoxoic acid In water; acetonitrile at 20℃; for 0.166667h; Reagent/catalyst; Concentration; Solvent; Inert atmosphere; | A 7% B 91% |
1,1-Diethoxy 2(E)-octene
(E)-2-Octenal
Conditions | Yield |
---|---|
With water for 0.133333h; Microwave irradiation; | 84% |
Conditions | Yield |
---|---|
tris(triphenylphosphine)ruthenium(II) chloride; tris(1-methylethyl)phosphine In toluene for 36h; Heating; | A 82% B n/a |
Conditions | Yield |
---|---|
With water; potassium carbonate In tetrahydrofuran; diethyl ether for 17h; Ambient temperature; | 81% |
With potassium carbonate In tetrahydrofuran; diethyl ether; water at 25℃; | 81% |
(E)-2-Octenal
Conditions | Yield |
---|---|
With carbon tetrabromide; triphenylphosphine In dichloromethane for 140h; Ambient temperature; | 80% |
With water; toluene-4-sulfonic acid for 4h; Ambient temperature; |
cis-2-octene oxide
(E)-2-Octenal
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In chloroform Heating; | 75% |
1,1-diethoxy-3-octanol
(E)-2-Octenal
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran; water for 4h; Heating; | 75% |
(Z)-1-tert-Butylsulfanyl-oct-1-en-3-ol
A
di-tert-butyl disulfide
B
(E)-2-Octenal
Conditions | Yield |
---|---|
With copper(II) oxide In water; acetone for 1h; Ambient temperature; | A 33% B 74% |
(Z)-oct-2-en-1-ol
(E)-2-Octenal
Conditions | Yield |
---|---|
With pyridinium chlorochromate In dichloromethane for 3h; low temperature; | 66% |
Conditions | Yield |
---|---|
With chromium (VI) oxide; air In chloroform for 4h; Hydrolysis; Oxidation; Heating; | A 60% B 40% |
triphenylarsonium salt of bromoacetaldehyde
hexanal
A
(E)-2-Octenal
B
2,4-trans,trans-decadienal
Conditions | Yield |
---|---|
With potassium carbonate In tetrahydrofuran; diethyl ether; water at 40℃; for 17h; | A 48% B 46% |
oct-1-ene
A
oct-1-en-3-one
B
(E)-2-Octenal
C
hexyl-methyl-ketone
Conditions | Yield |
---|---|
With oxygen; palladium(II) trifluoroacetate In acetonitrile for 22h; Irradiation; Yields of byproduct given; | A n/a B n/a C 10% |
With oxygen; palladium(II) trifluoroacetate In acetonitrile for 22h; Irradiation; Yield given. Yields of byproduct given; | A n/a B n/a C 10% |
With oxygen; palladium(II) trifluoroacetate In acetonitrile Irradiation; |
1,1-diethoxy-oct-2c-ene
(E)-2-Octenal
Conditions | Yield |
---|---|
With sulfuric acid | |
Multi-step reaction with 2 steps 1: p-C6H4-SO3H / acetone; H2O / 0.25 h / 0 °C 2: 75 percent / p-CH3-C6H4-SO3H / CHCl3 / Heating View Scheme |
(E)-2-Octenal
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether und Behandeln des Reaktionsprodukts mit wss.Schwefelsaeure; |
Conditions | Yield |
---|---|
With boron fluoride ether und Erhitzen des Reaktionsprodukts mit wss.Essigsaeure; |
hept-1-en-t-yl-trimethyl-silane
Dichloromethyl methyl ether
(E)-2-Octenal
Conditions | Yield |
---|---|
(i) TiCl4, CH2Cl2, (ii) aq. MeOH; Multistep reaction; |
1t-phenylsulfanyl-oct-1-en-3-ol
(E)-2-Octenal
Conditions | Yield |
---|---|
With mercury dichloride In water; acetonitrile |
dimethyl-dithiocarbamic acid oct-2t-enyl ester
(E)-2-Octenal
Conditions | Yield |
---|---|
(i) LDA, (ii) Me2S2, (iii) Hg2+, aq. MeCN; Multistep reaction; |
Conditions | Yield |
---|---|
Multistep reaction; |
1t,3-bis-methylsulfanyl-oct-1-ene
(E)-2-Octenal
Conditions | Yield |
---|---|
With mercury dichloride In tetrahydrofuran; acetonitrile |
1-dimethylcarbamoylsulfanyl-1-methylsulfanyl-oct-2-ene
(E)-2-Octenal
Conditions | Yield |
---|---|
With water; calcium carbonate; mercury dichloride |
trans-2-benzenesulfinyl-3-hexyl-oxirane
(E)-2-Octenal
Conditions | Yield |
---|---|
In xylene Heating; |
Conditions | Yield |
---|---|
With p-C6H4-SO3H In water; acetone at 0℃; for 0.25h; Yield given. Title compound not separated from byproducts; |
oct-1-ene
A
oct-1-en-3-one
B
(E)-2-Octenal
C
(E)-oct-2-en-1-ol
D
1-octen-3-ol
E
1,2-Epoxyoctane
Conditions | Yield |
---|---|
With oxygen; bis(acetylacetonato)dioxidomolybdenum(VI); cobalt(III) acetylacetonate In 1,2-dichloro-benzene at 110℃; for 5.3h; Product distribution; other temperatures, catalysts, times, olefins; | A n/a B n/a C n/a D n/a E 61 % Chromat. |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In water; acetone at 0℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
cis-2-(1'-hexyl)-1-(trimethylsilyl)oxirane
(E)-2-Octenal
Conditions | Yield |
---|---|
With trimethyl ester of coenzyme PQQ; oxygen; palladium diacetate In N,N-dimethyl-formamide at 70℃; for 7h; | |
With palladium diacetate In N,N-dimethyl-formamide at 60℃; for 7h; | 80 % Chromat. |
Conditions | Yield |
---|---|
With benzaldehyde In diethyl ether for 5h; Yield given. Yields of byproduct given; | |
With benzaldehyde In diethyl ether for 5h; Product distribution; |
α,α-bis(trimethylsilyl)-tert-butylacetaldehyde imine
hexanal
(E)-2-Octenal
Conditions | Yield |
---|---|
With zinc(II) chloride; zinc dibromide 1) THF, RT, 6 h, 2) ether, water, RT, 1 h; Yield given. Multistep reaction; |
1,1-dimethoxy-oct-2t-ene
(E)-2-Octenal
Conditions | Yield |
---|---|
With water; toluene-4-sulfonic acid for 4h; Ambient temperature; |
Conditions | Yield |
---|---|
With (S)-hydroxynitrile lyase from Hevea brasiliensis Addition; Enzymatic reaction; | 100% |
With hydroxynitrile lyase from Hevea brasiliensis In water at 15℃; for 0.25h; pH 5.5; | 96% |
Conditions | Yield |
---|---|
With lithium chloride In tetrahydrofuran at 22℃; for 22h; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 17h; | 98% |
Conditions | Yield |
---|---|
With triethylamine In chloroform at 110℃; for 1h; Michael Addition; Inert atmosphere; Microwave irradiation; | 98% |
Conditions | Yield |
---|---|
Stage #1: (E)-2-Octenal With boron trifluoride diethyl etherate In diethyl ether at -30℃; for 0.5h; Inert atmosphere; Stage #2: 1-ethoxyacetylene In diethyl ether; hexane at -30℃; for 1.5h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
Stage #1: 1-Heptyne With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.25h; Stage #2: (E)-2-Octenal In tetrahydrofuran; hexane at -78℃; for 30h; | 97% |
Conditions | Yield |
---|---|
With acetamide; toluene-4-sulfonic acid for 0.166667h; Beller reaction; microwave irradiation; | 96% |
Conditions | Yield |
---|---|
Stage #1: potassium cyanide; (E)-2-Octenal In diethyl ether; water at -10℃; for 0.166667h; Stage #2: With hydrogenchloride In diethyl ether; water at -10 - 20℃; | 96% |
(E)-2-Octenal
(E)-oct-2-en-1-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol for 3h; | 95% |
With sodium bis(2-methoxyethoxy)aluminium dihydride In diethyl ether at 0 - 20℃; for 3.5h; | 84.4% |
With formic acid; 4-methoxy-N-(1-(naphthalen-2-yl)ethylidene)aniline; sodium formate In water at 80℃; for 6h; pH=4.5; Inert atmosphere; chemoselective reaction; | 78% |
(E)-2-Octenal
L-Phenylalaninol
(S,2E)-2-((E)-oct-2-enylideneamino)-3-phenylpropan-1-ol
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 0.333333h; | 95% |
Conditions | Yield |
---|---|
With ammonium chloride; zinc In tetrahydrofuran; water at 0 - 25℃; for 4h; Barbier Coupling Reaction; | 95% |
Conditions | Yield |
---|---|
With phosphate buffer; D-glucose; Synechococcus sp. PCC 7942; Triton X-100 In water at 25℃; for 72h; pH=7.0; Irradiation; | A 94% B 5% |
(E)-2-Octenal
(E)-oct-3-en-2-ol
Conditions | Yield |
---|---|
With 1-Phenylethanol In toluene at 120℃; for 12h; Inert atmosphere; chemoselective reaction; | 94% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; lithium chloride In acetonitrile for 3h; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
With piperidine In tetrahydrofuran for 144h; Ambient temperature; | 90% |
(E)-2-Octenal
7-chlorobicyclo<2.2.1>hepta-2,5-diene
7-(1'-hydroxyoct-2'-enyl)bicyclo[2.2.1]hepta-2,5-diene
Conditions | Yield |
---|---|
Stage #1: 7-chlorobicyclo<2.2.1>hepta-2,5-diene With 4,4'-di-tert-butylbiphenyl; lithium In tetrahydrofuran at -78℃; for 0.5h; Stage #2: (E)-2-Octenal In tetrahydrofuran at -78 - 20℃; for 1h; | 90% |
(E)-2-Octenal
Acetic acid 2-methoxy-4-[3-oxo-4-(triphenyl-λ5-phosphanylidene)-butyl]-phenyl ester
Conditions | Yield |
---|---|
In benzene Heating; | 89% |
Conditions | Yield |
---|---|
With samarium(III) trifluoromethanesulfonate at 20℃; for 0.0833333h; Etherification; | 89% |
(E)-2-Octenal
2,3-epoxyoctanal
Conditions | Yield |
---|---|
With dihydrogen peroxide; sodium hydroxide In water for 2h; pH=8 - 8.5; | 88% |
With dihydrogen peroxide; sodium carbonate; alpha cyclodextrin In water at 0℃; for 3h; | 76 % Turnov. |
With oxone; 1,1,1-trifluoro-2-propanone; edetate disodium; sodium hydrogencarbonate In water; acetonitrile for 3h; |
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane; water at 0℃; for 21h; | 88% |
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran at -78℃; for 1h; | 88% |
Conditions | Yield |
---|---|
Stage #1: (E)-2-Octenal; L-proline tert-butyl ester hydrochloride In dichloromethane at 20℃; for 0.166667h; Inert atmosphere; Stage #2: With sodium tris(acetoxy)borohydride In dichloromethane at 20℃; for 3h; Inert atmosphere; | 88% |
(E)-2-Octenal
(carbethoxyethylidene)triphenylphosphorane
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 18h; | 87% |
(E)-2-Octenal
N-benzyl-N-trimethylsilanylethynyl-4-methylbenzenesulphonamide
Conditions | Yield |
---|---|
Stage #1: N-benzyl-N-trimethylsilanylethynyl-4-methylbenzenesulphonamide With titanium(IV) isopropylate; isopropylmagnesium chloride Stage #2: (E)-2-Octenal Stage #3: With hydrogen cation Acid hydrolysis; Further stages.; | 87% |
(E)-2-Octenal
(trimethylsilyl)methylmagnesium chloride
Conditions | Yield |
---|---|
In diethyl ether for 2h; Ambient temperature; | 86% |
Conditions | Yield |
---|---|
With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; [Rh(OAc)(C2H4)2]2 In methanol at 40℃; for 24h; optical yield given as %ee; enantioselective reaction; | 86% |
(E)-2-Octenal
methylmagnesium bromide
(E)-non-3-en-2-ol
Conditions | Yield |
---|---|
In diethyl ether at 0℃; for 0.133333h; | 85% |
In tetrahydrofuran at 0 - 20℃; for 2.33h; Inert atmosphere; |
(E)-2-Octenal
dimethyl 1-(1-diazo-2-oxopropyl)phosphonate
malononitrile
(E)-dimethyl 3-cyano-4-(hept-1-enyl)-1H-pyrazol-5-ylphosphonate
Conditions | Yield |
---|---|
With potassium hydroxide In methanol at 20℃; for 1h; Molecular sieve; regioselective reaction; | 85% |
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