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Cas:3391-86-4
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inquiryProduct description: Product name 1-Octen-3-ol CAS number 3391-86-4 Assay ≥99% Appearance Colorless to yellowish liquid Capacity 200mt/year Application Daily Flavor and food
Cas:3391-86-4
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inquiry3391-86-4 - Physico-chemical Properties Molecular Formula C8H16O Molar Mass 128.21 Density 0.837 g/mL at 20 °C0.83 g/mL at 25 °C (lit.) Melting Point -49°C Boling Point 84-85 &d
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
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inquiryProduct name 1-Octen-3-ol Synonyms Mushroom alcohol; 3-Octenol;Amyl Vinyl Carbinol CAS 3391-86-4 Molecular Formula C8H16O Mol
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...)
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inquiry1-Octen-3-olCAS: 3391-86-4 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 intermediates
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Product Detail Minimum Order Qty. 10 Gram
Cas:3391-86-4
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryProduct Name: 1-Octen-3-ol Synonyms: 1-OCTEN-3-OL, (AMYL VINYL CARBINOL) FCC;1-OCTYLENE-3-OL;1-OCTEN-3-OL;AMYL VINYL CARBINOL (1-OCTEN 3-OL);1-OCTEN-3-OL 98+% FCC;n-Pentylvinylcarbinol;1-Octen-3-ol,98%;octenol,1-octen-3-ol CAS: 3391-86-4 MF:
Cas:3391-86-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiry1-Octen-3-ol CAS:3391-86-4 Specification Product name 1-Octen-3-ol CAS number 3391-86-4 Assay ≥99% Appearance Colorless to yellowish liquid Capacity 200mt/year Applicatio
Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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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
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E-2,3-epoxy-1-octanyl tosylate
1-octen-3-ol
Conditions | Yield |
---|---|
With aluminum oxide; tellurium(2-) for 2.5h; | 100% |
With sodium hydroxide; tellurium; rongalite In tetrahydrofuran; water at 50℃; for 2h; | 80% |
With tellurium(2-) for 0.233333h; Product distribution; other reaction conditions, other reaction time, reagent, solvent; | |
Multi-step reaction with 2 steps 1: 97 percent / NaI / acetone / 3 h 2: 74 percent / Bu3SnAlEt2 / tetrahydrofuran / 1 h / 0 °C View Scheme |
3-(2-Methoxy-ethoxymethoxy)-oct-1-ene
1-octen-3-ol
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In tert-butyl alcohol for 3h; Heating; | 99% |
Conditions | Yield |
---|---|
With isocyanate de chlorosulfonyle; hydrogen; palladium diacetate; borohydride exchange resin In ethanol for 0.5h; | 97% |
With C16H26CuO In 2-methyl-propan-1-ol; toluene at 25℃; for 1h; | 92% |
With 2-methyl-propan-1-ol; [1,3-bis(2,6-di-iso-propylphenyl)imidazol-2-ylidene]copper(I) tert-butoxide In toluene at 25℃; for 1h; Inert atmosphere; Glovebox; chemoselective reaction; | 92% |
(E)-3-<(2-tetrahydropyranyl)oxy>-1-iodo-1-octene
1-octen-3-ol
Conditions | Yield |
---|---|
With trichloroisocyanuric acid In methanol at 20℃; for 5h; | 95% |
With water; lithium chloride In dimethyl sulfoxide at 90℃; for 6h; Hydrolysis; | 80% |
With magnesium bromide In diethyl ether for 2h; Ambient temperature; | 72% |
1-Octene, 3-(methoxymethoxy)-
1-octen-3-ol
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In tert-butyl alcohol for 3.5h; Heating; | 95% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol at 20℃; for 4h; | 93% |
With isoindoline; lithium aluminium tetrahydride In diethyl ether at -15℃; for 1.5h; |
N,N-Diethyl-O-(1-vinyl-hexyl)-hydroxylamine
1-octen-3-ol
Conditions | Yield |
---|---|
With zinc In acetic acid Ambient temperature; | 93% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0℃; | 92% |
In tetrahydrofuran for 4h; Heating; | 75% |
In tetrahydrofuran at -15 - 20℃; | 74% |
Conditions | Yield |
---|---|
Stage #1: 1-Bromopentane With magnesium In tert-butyl methyl ether for 1h; Reflux; Stage #2: acrolein In tert-butyl methyl ether at -5 - 2℃; for 1h; | 92% |
Stage #1: 1-Bromopentane With iodine; magnesium In diethyl ether at 0℃; Inert atmosphere; Stage #2: acrolein In diethyl ether for 1.5h; Inert atmosphere; | 85% |
Stage #1: 1-Bromopentane With iodine; magnesium In diethyl ether Inert atmosphere; Stage #2: acrolein In diethyl ether at 0℃; | 85% |
3-Nitrooxy-oct-1-ene
1-octen-3-ol
Conditions | Yield |
---|---|
With acetic acid; zinc | 83% |
2,3-epoxyoctanol
1-octen-3-ol
Conditions | Yield |
---|---|
With diethyltitanium dichloride; zinc(II) chloride; zinc In tetrahydrofuran | 82% |
With diethyltitanium dichloride; zinc(II) chloride; zinc In tetrahydrofuran Product distribution; Mechanism; other 2,3-epoxy alcohols; | 82% |
Multi-step reaction with 3 steps 1: 91 percent / powdered KOH / diethyl ether / -10 deg C, then 0 deg C, 30 min 2: 97 percent / NaI / acetone / 3 h 3: 74 percent / Bu3SnAlEt2 / tetrahydrofuran / 1 h / 0 °C View Scheme |
E-2,3-epoxy-1-iodooctane
1-octen-3-ol
Conditions | Yield |
---|---|
With zinc In methanol for 3h; Heating; | 80% |
With Bu3SnAlEt2 In tetrahydrofuran at 0℃; for 1h; | 74% |
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether at -15℃; for 1.5h; Inert atmosphere; | 79% |
In tetrahydrofuran at 23℃; for 1h; Inert atmosphere; Cooling; | |
In tetrahydrofuran at 0 - 20℃; |
Conditions | Yield |
---|---|
Stage #1: Ethyl hexanoate With lithium diisobutyl-tert-butoxyaluminum hydride In tetrahydrofuran; hexane at 0℃; Stage #2: vinyl magnesium bromide In tetrahydrofuran; diethyl ether; hexane at 20℃; Stage #3: With hydrogenchloride; water In tetrahydrofuran; diethyl ether; hexane | 78% |
1-octen-3-ol
Conditions | Yield |
---|---|
With indium(III) chloride; sodium tetrahydroborate In acetonitrile at 20℃; for 7h; | 77% |
epoxybutene
n-butyllithium
A
1-octen-3-ol
B
2-butyl-but-3-en-1-ol
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In diethyl ether at -105℃; for 0.5h; Ring cleavage; | A 16% B 75% |
1-octen-3-ol
Conditions | Yield |
---|---|
With 18-crown-6 ether In ethanol; water at 45℃; for 22h; Reagent/catalyst; Solvent; Temperature; Green chemistry; | 75% |
1-octen-3-ol
Conditions | Yield |
---|---|
With benzo[1,3,2]dioxaborole; Wilkinson's catalyst In tetrahydrofuran at 20℃; for 15h; | 65% |
2-octenol
1-octen-3-ol
Conditions | Yield |
---|---|
With silica-supported monomeric vanadium-oxo species In acetonitrile at 60℃; for 8h; Inert atmosphere; | 60% |
1-octen-3-ol
Conditions | Yield |
---|---|
With water; sodium hydrogencarbonate; bis-[(trifluoroacetoxy)iodo]benzene; meso-2,5-bis(methoxycarbonyl)-2,5-dimethylpyrrolidine-1-oxyl In dichloromethane at 20℃; for 2h; chemoselective reaction; | 55% |
oct-1-ene
A
octanol
B
1-octen-3-ol
C
2-octen-1-al
D
2-octenol
Conditions | Yield |
---|---|
With water; oxygen In ethanol at 75℃; for 24h; pH=3.7; | A n/a B 44% C 31% D n/a |
With water; oxygen In ethanol at 75℃; for 24h; pH=6.1; | A n/a B 32.5% C 14.9% D n/a |
Conditions | Yield |
---|---|
With potassium tert-butylate; tert-butyl alcohol for 336h; Ambient temperature; | A 40% B 10% |
ethanol
oct-1-ene
A
octanol
B
1-octen-3-ol
C
2-octen-1-al
D
n-octyl acetate
E
2-octenol
Conditions | Yield |
---|---|
With water; oxygen at 75℃; for 24h; pH=6.1; | A n/a B 31.7% C 20.8% D 6.8% E n/a |
oct-1-ene
acetonitrile
A
heptanal
B
octanol
C
1-octen-3-ol
D
2-octen-1-al
E
n-octyl acetate
F
1,2-Epoxyoctane
G
2-octenol
Conditions | Yield |
---|---|
With water; oxygen at 75℃; for 24h; | A 5.5% B n/a C 24.8% D 31.4% E 5.6% F 7.4% G n/a |
oct-1-ene
A
heptanal
B
octanol
C
1-octen-3-ol
D
2-octen-1-al
E
1,2-Epoxyoctane
F
2-octenol
Conditions | Yield |
---|---|
With water; oxygen In acetonitrile at 75℃; for 24h; | A 5.1% B n/a C 29.2% D 27.7% E 9.1% F n/a |
oct-1-ene
A
octanol
B
1-octen-3-ol
C
2-octen-1-al
D
1,2-Epoxyoctane
E
2-octenol
Conditions | Yield |
---|---|
With water; oxygen In acetonitrile at 75℃; for 24h; | A n/a B 26.2% C 26.2% D 6.9% E n/a |
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); carbon dioxide; 2,5-di-tert-butyl-p-benzoquinone; water In 1,4-dioxane at 40℃; under 30003 Torr; for 72h; Inert atmosphere; Autoclave; | 18% |
Multi-step reaction with 2 steps 1.1: (MesPDI)CoMe / neat (no solvent) / 1 h / 23 °C 2.1: 3-chloro-benzenecarboperoxoic acid; disodium hydrogenphosphate / dichloromethane / 1 h / Cooling with ice 2.2: 16 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
With meso-tetraphenylporphyrin iron(III) chloride; iodosylbenzene In dichloromethane for 0.5h; Ambient temperature; Yield given; | A 1% B n/a |
With dihydrogen peroxide In acetonitrile for 0.583333h; Ultrasonic irradiation; Reflux; | |
With dihydrogen peroxide In acetonitrile at 60℃; for 0.666667h; Ultrasonic irradiation; |
chloromethyl-(1-pentyl-allyl)-ether
A
formaldehyde-[bis-(1-pentyl-allyl)-acetal]
B
1-octen-3-ol
Conditions | Yield |
---|---|
With water | |
With sodium hydrogencarbonate |
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 cis-dichlorotetrakis(diemethylsulfoxide) ruthenium(II); sodium formate In water; toluene at 80℃; for 1h; Inert atmosphere; | 100% |
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; periodic acid In dichloromethane at 20℃; for 0.583333h; | 98% |
With chromium (VI) oxide In toluene for 0.333333h; microwave irradiation; | 98% |
Conditions | Yield |
---|---|
With glass encapsulated Rh-onium ion catalyst In toluene for 1.83333h; Heating; | 100% |
With potassium tert-butylate; trimethyl-4,6,9 hexaza-1,3,4,6,7,9 phospha-5 tricyclo<3.3.1.13,7>decane; dichloro(benzene)ruthenium(II) dimer In tetrahydrofuran at 75℃; for 0.25h; Kinetics; Product distribution; Further Variations:; Catalysts; Solvents; | 100% |
With C34H49ClFePRhS; hydrogen; sodium methylate In tetrahydrofuran at 82℃; under 22502.3 Torr; for 16h; Autoclave; Inert atmosphere; | 100% |
1-octen-3-ol
1,2-epoxy-3-octanol
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide In acetonitrile at 80℃; for 24h; Catalytic behavior; Reagent/catalyst; | 100% |
With tert.-butylhydroperoxide In chloroform for 4h; Catalytic behavior; Reflux; | 99% |
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0 - 20℃; for 18h; | 95% |
Conditions | Yield |
---|---|
at 20℃; Inert atmosphere; neat (no solvent); | 100% |
Conditions | Yield |
---|---|
With propionic acid at 150℃; for 3h; Temperature; Claisen Rearrangement; | 99.9% |
Conditions | Yield |
---|---|
With propionic acid at 125℃; for 2h; Temperature; Claisen Rearrangement; | 99.5% |
With propionic acid at 105℃; for 4.5h; | 87% |
With propionic acid at 100 - 105℃; |
Conditions | Yield |
---|---|
With C12H8N2*2CH4O3S at 50℃; for 3h; | 99% |
With dmap In dichloromethane at 20℃; for 1.5h; | 94% |
aluminium dodecatungsten phosphate at 20℃; for 0.0833333h; | 93% |
Conditions | Yield |
---|---|
With Cp*2Sm(THF)2; cyclohexanone oxime acetate In toluene for 0.1h; Ambient temperature; | 99% |
With iron(III) trifluoromethanesulfonate at 20℃; for 5h; Schlenk technique; | 92% |
1-octen-3-ol
tris-(trimethylsilyl)silane
6-[tris(trimethylsilyl)]-3-octanol
Conditions | Yield |
---|---|
With 1,1'-azobis(1-cyanocyclohexanenitrile) In water at 100℃; for 4h; | 99% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; C11H18Cl2CoN2S; hydrogen In isopropyl alcohol at 100℃; under 37503.8 Torr; for 16h; Reagent/catalyst; Solvent; Glovebox; Autoclave; | 98% |
With hydrogen In ethanol at 20℃; under 760.051 Torr; for 1h; chemoselective reaction; | 94% |
Stage #1: 1-octen-3-ol With lithium triethylborohydride; cobalt(II) bromide In tetrahydrofuran Inert atmosphere; Glovebox; Stage #2: With hydrogen In tetrahydrofuran at 20℃; under 1500.15 Torr; for 3h; | 93% |
1-octen-3-ol
propionic acid
Triethyl orthoacetate
ethyl trans-4-decenoate
Conditions | Yield |
---|---|
120 deg C, then 160 deg C, 2 h; | 98% |
Conditions | Yield |
---|---|
With n-butyllithium; tert-butylmagnesium chloride In diethyl ether; hexane | 98% |
Stage #1: 1-octen-3-ol With n-butyllithium In tetrahydrofuran; hexane Inert atmosphere; Stage #2: 1,2-dibromomethane With tert-butylmagnesium chloride In tetrahydrofuran; hexane Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With 2.9-dimethyl-1,10-phenanthroline; palladium diacetate; silver carbonate In acetonitrile at 60℃; for 24h; regioselective reaction; | 98% |
With 2.9-dimethyl-1,10-phenanthroline; palladium diacetate; copper(l) chloride In dimethyl sulfoxide at 50℃; under 760.051 Torr; for 12h; | 98% |
With oxygen; palladium diacetate; acetic acid; copper(l) chloride In dimethyl sulfoxide at 50℃; under 760.051 Torr; for 20h; regioselective reaction; | 94% |
Conditions | Yield |
---|---|
Stage #1: 1-octen-3-ol With [Ir(III)(η5-pentamethylcyclopentadienyl)(H2O)3](SO4); iodine; oxygen; sodium nitrite In 2-methyltetrahydrofuran; water under 760.051 Torr; for 24h; Sealed tube; Stage #2: Thiomorpholin In 2-methyltetrahydrofuran; water for 16h; | 98% |
1-octen-3-ol
tert-butyldimethylsilyl chloride
tert-butyl-dimethyl-(1-vinyl-hexyloxy)-silane
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 68h; | 97% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 25℃; for 0.5h; | 95% |
With zinc In benzene at 20℃; for 1h; | 53% |
With pyridine In dichloromethane at 0 - 20℃; |
1-octen-3-ol
1-iodohept-2-ene
Conditions | Yield |
---|---|
With zirconium(IV) chloride; sodium iodide In acetonitrile for 0.0833333h; Heating; | 95% |
dichloroacethyl chloride
1-octen-3-ol
1-pentyl-2-propenyl dichloroacetate
Conditions | Yield |
---|---|
With dmap In dichloromethane at 20℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With dmap In dichloromethane | 95% |
Stage #1: 1-octen-3-ol With pyridine In dichloromethane at 0℃; Inert atmosphere; Stage #2: acetyl chloride In dichloromethane at 0 - 20℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane for 12h; Inert atmosphere; Reflux; | 95% |
With N-ethyl-N,N-diisopropylamine In dichloromethane for 12h; Inert atmosphere; Reflux; | 95% |
Conditions | Yield |
---|---|
With 2.9-dimethyl-1,10-phenanthroline; palladium diacetate; copper(l) chloride In dimethyl sulfoxide at 50℃; under 760.051 Torr; for 12h; | 95% |
Conditions | Yield |
---|---|
With [O,O’-((S)-1,1´-dinaphthyl-2,2´-diyl)-N,N´-di-(S,S)-1-(2-methoxyphenyl)ethylphosphoramidite]; (S)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate; bis(dibenzylideneacetone)-palladium(0) In tetrahydrofuran at 25℃; for 12h; Inert atmosphere; Schlenk technique; enantioselective reaction; | 95% |
Conditions | Yield |
---|---|
94% |
Conditions | Yield |
---|---|
With magnesium bromide; (dppe)NiHCl In tetrahydrofuran at -50 - 20℃; for 1h; | 94% |
Conditions | Yield |
---|---|
Stage #1: 1-octen-3-ol With oxygen; palladium diacetate In N,N-dimethyl-formamide at 90℃; under 760.051 Torr; for 4h; Green chemistry; Stage #2: phenylboronic acid With 2.9-dimethyl-1,10-phenanthroline In N,N-dimethyl-formamide at 90℃; for 18h; Heck Reaction; Green chemistry; | 94% |
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