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Cas:3661-77-6
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Type:Lab/Research institutions
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CYCLOHEPTADECANONE CAS:3661-77-6 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 interme
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Min.Order:1 Gram
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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 Metric Ton
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Type:Trading Company
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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
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Type:Lab/Research institutions
inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
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2-hydroxy-cycloheptadecanone
cycloheptadecanone
Conditions | Yield |
---|---|
With hydrogenchloride; zinc In 1,4-dioxane; water at 95 - 100℃; for 17h; | 80% |
With hydrogenchloride; zinc In 1,4-dioxane | |
Multi-step reaction with 2 steps 1: N2H4, NaOH / bis-(2-hydroxy-ethyl) ether / 210 °C 2: CrO3, aq. H2SO4 View Scheme |
cycloheptadec-9-en-1-one
cycloheptadecanone
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen In ethanol at 20℃; | 60% |
With palladium on activated charcoal; hydrogen In ethyl acetate at 20℃; under 760.051 Torr; for 16h; Schlenk technique; Glovebox; | 52% |
With ethanol; colloid; palladium Hydrogenation; | |
Multi-step reaction with 2 steps 1: platinum black; glacial acetic acid / Hydrogenation 2: benzene; Cr2O3-H2SO4 View Scheme | |
Multi-step reaction with 3 steps 1: sodium; alcohol 2: platinum black; glacial acetic acid / Hydrogenation 3: benzene; Cr2O3-H2SO4 View Scheme |
Conditions | Yield |
---|---|
With etheric solution; lithium N-ethyl-N-phenylamide Erhitzen des Reaktionsprodukts mit 70prozentig. wss. Schwefelsaeure; |
Conditions | Yield |
---|---|
With thionyl chloride; benzene anschl. mit Triaethylamin in Benzol bei 40grad; |
Conditions | Yield |
---|---|
With ethanol; platinum | |
With acetic acid; platinum | |
With diethyl ether; platinum Hydrogenation; |
Conditions | Yield |
---|---|
With chromium(III) oxide; sulfuric acid; benzene | |
With chromium(VI) oxide; sulfuric acid |
Conditions | Yield |
---|---|
With diethyl ether; platinum Hydrogenation; | |
With ethanol; platinum | |
With acetic acid; platinum |
Conditions | Yield |
---|---|
und Kochen des Reaktionsprodukts mit 70prozentiger H2SO4; |
cycloheptadecanone
Conditions | Yield |
---|---|
With sulfuric acid |
cycloheptadecanone
Conditions | Yield |
---|---|
at 350 - 400℃; under 30 - 40 Torr; Thermolysis; | |
With iron at 350 - 400℃; under 30 - 40 Torr; Thermolysis; | |
With copper at 350 - 400℃; under 30 - 40 Torr; Thermolysis; |
Conditions | Yield |
---|---|
Hydrogenation; |
A
cycloheptadecanone
Conditions | Yield |
---|---|
at 300 - 400℃; | |
at 300 - 400℃; |
1-vinyl-cyclopentadecanol
cycloheptadecanone
Conditions | Yield |
---|---|
at 650℃; under 0.75006 - 3.00024 Torr; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 67 percent / sodium methoxide / methanol / 28 °C / Electrolysis 2: sodium / xylene / 2.5 h / Heating 3: 80 percent / zink; hydrogen chloride / dioxane; H2O / 17 h / 95 - 100 °C View Scheme |
diethyl heptadecanedioate
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium / xylene / 2.5 h / Heating 2: 80 percent / zink; hydrogen chloride / dioxane; H2O / 17 h / 95 - 100 °C View Scheme | |
Multi-step reaction with 2 steps 1: Na / xylene 2: Zn, HCl / dioxane View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 1.2: tetrahydrofuran / 0.5 h / 25 °C 2.1: 65 percent / 650 °C / 0.75 - 3 Torr 3.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 3.2: tetrahydrofuran / 0.5 h / 25 °C 4.1: 650 °C / 0.75 - 3 Torr 5.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 5.2: tetrahydrofuran / 0.5 h / 25 °C 6.1: 650 °C / 0.75 - 3 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 1.2: tetrahydrofuran / 0.5 h / 25 °C 2.1: 650 °C / 0.75 - 3 Torr View Scheme |
(2E)-cyclopentadec-2-en-1-one
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: 100 percent / H2 / Pd/C 2.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 2.2: tetrahydrofuran / 0.5 h / 25 °C 3.1: 650 °C / 0.75 - 3 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 1.2: tetrahydrofuran / 0.5 h / 25 °C 2.1: 650 °C / 0.75 - 3 Torr 3.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 3.2: tetrahydrofuran / 0.5 h / 25 °C 4.1: 650 °C / 0.75 - 3 Torr View Scheme |
1-Vinyl-cycloundecanol
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 65 percent / 650 °C / 0.75 - 3 Torr 2.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 2.2: tetrahydrofuran / 0.5 h / 25 °C 3.1: 650 °C / 0.75 - 3 Torr 4.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 4.2: tetrahydrofuran / 0.5 h / 25 °C 5.1: 650 °C / 0.75 - 3 Torr View Scheme |
1-vinyl-cyclotridecanol
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: 650 °C / 0.75 - 3 Torr 2.1: CeCl3 / tetrahydrofuran / 0.5 h / 20 °C 2.2: tetrahydrofuran / 0.5 h / 25 °C 3.1: 650 °C / 0.75 - 3 Torr View Scheme |
(E)-2-methoxycarbonyl-9-cycloheptadecenoate
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: KOH; aqueous methanol 2: ethanol; platinum View Scheme |
E-cycloheptadec-9-enol
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: platinum black; glacial acetic acid / Hydrogenation 2: benzene; Cr2O3-H2SO4 View Scheme | |
Multi-step reaction with 3 steps 1: diluted Cr2O3-H2SO4 2: platinum black; glacial acetic acid / Hydrogenation 3: benzene; Cr2O3-H2SO4 View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: (i) HBr, AcOH, (ii) /BRN= 1718733/, H2SO4, (iii) Zn, EtOH, HBr 2: (i), (ii) aq. KOH 3: (esterification) 4: (hydrogenation) 5: Na / xylene 6: Zn, HCl / dioxane View Scheme |
heptadec-8-enedioic acid
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: (esterification) 2: (hydrogenation) 3: Na / xylene 4: Zn, HCl / dioxane View Scheme |
trans-16-Brom-hexadecen-(9)-saeure-ethylester
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: (i), (ii) aq. KOH 2: (esterification) 3: (hydrogenation) 4: Na / xylene 5: Zn, HCl / dioxane View Scheme |
trans-1,15-Bisethoxycarbonyl-pentadecen-(7)
cycloheptadecanone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: (hydrogenation) 2: Na / xylene 3: Zn, HCl / dioxane View Scheme |
cycloheptadecanone
trimethylsulfoxonium iodide
1-oxaspiro[2.16]nonadecane
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol at 50℃; | 91% |
methanol
cycloheptadecanone
methyl (1Z)-cyclohexadec-1-ene-1-carboxylate
Conditions | Yield |
---|---|
With iodine; potassium hydroxide at -5 - 0℃; Favorskii rearrangement; stereospecific reaction; | 50% |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With piperidine anschliessend Behandeln mit 90prozentig. wss. Schwefelsaeure; |
cycloheptadecanone
sodium cyanide
1,3-diaza-spiro[4.16]heneicosane-2,4-dione
Conditions | Yield |
---|---|
With ammonium carbonate |
cycloheptadecanone
nitromalondialdehyde sodium salt
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With potassium peroxomonosulphate; sulfuric acid; Petroleum ether at 30 - 50℃; |
cycloheptadecanone
dihydrocivetone
Conditions | Yield |
---|---|
With hydrogen azide; sulfuric acid; benzene unter Kuehlung; |
Conditions | Yield |
---|---|
With chromium(VI) oxide; acetic acid |
Conditions | Yield |
---|---|
With ethanol; nickel at 120℃; under 58840.6 Torr; Hydrogenation; | |
With lithium aluminium tetrahydride; diethyl ether |
cycloheptadecanone
2-methyl-cycloheptadecanone
Conditions | Yield |
---|---|
With diethyl ether; sodium amide; benzene nachfolgend Kochen mit Methyljodid; |
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With diethyl ether; sodium amide |
cycloheptadecanone
chloroacetic acid ethyl ester
cycloheptadecanecarbaldehyde
Conditions | Yield |
---|---|
With diethyl ether; sodium amide Behandeln der bei 143-150grad/0,03 Torr siedenden Fraktion des Reaktionsprodukts mit aethanol. KOH und Erhitzen der gebildeten Saeure unter vermindertem Druck; |
cycloheptadecanone
(2,4-dinitro-phenyl)-hydrazine
cycloheptadecanone-(2,4-dinitro-phenylhydrazone)
cycloheptadecanone
Dimethyl phosphite
1-Hydroxy-cycloheptadecanyl-(1)-phosphonsaeure-dimethylester
Conditions | Yield |
---|---|
With sodium methylate In methanol Ambient temperature; |
acetal-aminal of β-dimethylaminoacrolein
cycloheptadecanone
2-((E)-1,3-Bis-dimethylamino-allyl)-cycloheptadecanone
Conditions | Yield |
---|---|
at 90 - 95℃; for 3h; | 0.4 g |
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