Quick Details CAS No.: 112-41-4 Other Names: Dodecene MF: C12H24 EINECS No.: 203-968-4 Place of Origin:
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inquiryProduct Name: Dodecyl aldehyde CAS: 112-54-9 MF: C12H24O MW: 184.32 EINECS: 203-983-6 Mol File: 112-54-9.mol Dodecyl aldehyde Structure Dodecyl aldehyde Chemical Properties Melting point 12 °C Boiling point 185 °C/
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inquiryChemical Name: Dodecyl aldehyde CAS No.: 112-54-9 Molecular Fomula: C12H24O Molecular weight: 184.32 Appearance: Colorless to light yellow oily liquid Assay:99%min Appearance:Colorless Clear Liquid Storage:Preserve in well-closed, light-resistant
factory?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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Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical at 20℃; for 0.5h; electrolysis; | 100% |
Stage #1: 1-dodecyl alcohol With oxalyl dichloride; dimethyl sulfoxide In dichloromethane at -78℃; for 0.25h; Oxidation; Stage #2: With triethylamine at -78 - 20℃; for 0.166667h; | 100% |
With iodosylbenzene; Cl-CH2-PS supported 5-amino-1,10-phenanthroline-Ru In acetonitrile at 60℃; for 6h; | 100% |
Conditions | Yield |
---|---|
Stage #1: 2-undecanyl-1,3-dioxolane With 2,4,6-trimethyl-pyridine; 2-methyl-2-octyl-[1,3]dioxolane; triethylsilyl trifluoromethyl sulfonate In dichloromethane at 0℃; for 1h; Stage #2: With water In dichloromethane for 0.1h; | 100% |
Stage #1: 2-undecanyl-1,3-dioxolane With triethylsilyl trifluoromethyl sulfonate; tris-(o-tolyl)phosphine In dichloromethane at -5℃; for 0.5h; Schlenk technique; Inert atmosphere; Stage #2: With 2,6-di-tert-butyl-pyridine; water In dichloromethane at 20℃; for 1.5h; Schlenk technique; | 95% |
With 2,6-dimethylpyridine; triethylsilyl trifluoromethyl sulfonate In dichloromethane at 0℃; for 1h; | 82% |
Conditions | Yield |
---|---|
Stage #1: ethyl laurate With morpholine; diisobutylaluminium hydride In tetrahydrofuran; hexane at 0℃; for 3.16667h; Inert atmosphere; Stage #2: With lithium diisobutylmethoxy aluminum hydride In tetrahydrofuran; hexane at 0℃; for 0.166667h; Inert atmosphere; | 99% |
With chromite at 375℃; under 735.5 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With sodium hypochlorite; sodium hydrogencarbonate; potassium bromide; [4-(TEMPO-4-yloxymethyl)-1H-[1,2,3]triazol-1-ylmethyl]-PS In dichloromethane at 0℃; for 0.5h; | A n/a B 99% |
With C30H24N2O7W; dihydrogen peroxide In water; acetonitrile for 22h; Reflux; | A 1% B 82% |
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxone; potassium bromide; methyltrioxorhenium(VII) In acetonitrile at 0℃; for 4h; | A 6% B 53% |
1-dodecene sulfate
Dodecanal
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane 1.) -78 deg C, 2 h, 2.) -78 deg C, 1 h; r.t., 14 h; | 99% |
Dodecanal
Conditions | Yield |
---|---|
With chloral hydrate; Py(HF)x In acetonitrile at 20℃; for 5h; Product distribution; | 97% |
With 6C72H112O8*8H2O In chloroform-d1; water for 1h; Inert atmosphere; |
Conditions | Yield |
---|---|
With ammonium hydroxide; formic acid In diethyl ether; chloroform for 0.416667h; Ambient temperature; | 96% |
With polymer(resin Amberlyst A-26)-supported tetracarbonylhydridoferrate anion In tetrahydrofuran for 2h; Heating; | 94% |
With pumice stone; platinum at 200 - 205℃; under 50 Torr; Hydrogenation; | |
With piperidine; diethyldihydroaluminate 1.) THF, RT, 30 min, 2.) THF, toluene, RT, 1 h; Multistep reaction; |
1,1-dimethoxy-dodecane
Dodecanal
Conditions | Yield |
---|---|
Stage #1: 1,1-dimethoxy-dodecane With triethylsilyl trifluoromethyl sulfonate; tris-(o-tolyl)phosphine In dichloromethane at -5℃; for 0.5h; Inert atmosphere; Stage #2: With water In dichloromethane at 20℃; for 1h; Inert atmosphere; | 95% |
With copper(II) sulfate; sodium iodide In acetone at 56℃; for 0.333333h; | 93% |
With chloral hydrate; Py(HF)x In acetonitrile at 20℃; for 1h; Product distribution; | 90% |
Conditions | Yield |
---|---|
With chloro(cyclopentadienyl)[bis(diphenylphosphino)methane]ruthenium; water In isopropyl alcohol at 100℃; for 12h; | 94% |
With dihydrogen peroxide; sodium acetate; benzo[1,3,2]dioxaborole 1.) C6H6, 80 deg C, 12 h, 2.) C6H6; Yield given. Multistep reaction; | |
With N,N-dimethyl acetamide; benzo[1,3,2]dioxaborole 1.) CH2Cl2, room temperature, 1 h; other reagent: catecholborane; Yield given. Multistep reaction; |
Dodecanal
Conditions | Yield |
---|---|
With silica gel | 93% |
1-(1,2,3,4,5-pentamethyl-2,4-cyclopentadienyl)-1-dodecanol
A
Dodecanal
B
1,2,3,4,5-pentamethylcyclopentadiene
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In toluene at 110℃; for 12h; | A 92% B n/a |
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; 1,1,3,3-Tetramethyldisiloxane In methyl cyclohexane at 20℃; for 48h; Inert atmosphere; | 90% |
1,1-dodecanediol diacetate
Dodecanal
Conditions | Yield |
---|---|
zeolite HSZ-360 for 0.333333h; Irradiation; | 88% |
Dodecanal
Conditions | Yield |
---|---|
With aluminium trichloride; 1-benzyl-1-aza-4-azoniabicyclo<2.2.2>octane periodate at 20℃; for 0.583333h; | 88% |
With cetyl(trimethyl)-ammonium tribromide In dichloromethane at 0 - 5℃; for 0.5h; | 85% |
Stage #1: 1,1-bis-ethylsulfanyl-dodecane With acetyl chloride; sodium nitrite In dichloromethane at 0 - 5℃; for 0.25h; Stage #2: With water In dichloromethane at 0 - 20℃; for 0.916667h; | 82% |
With dihydrogen peroxide; vanadia; ammonium bromide In dichloromethane; water at 0 - 5℃; for 1.75h; | 80% |
With ammonium heptamolybdate; dihydrogen peroxide; ammonium bromide; perchloric acid In dichloromethane; water at 0 - 5℃; for 0.5h; | 60% |
1,1-bis(phenyltelluro)dodecane
Dodecanal
Conditions | Yield |
---|---|
With iodine; sodium iodide | 86% |
Dodecanal
Conditions | Yield |
---|---|
In tetrahydrofuran; water for 2.5h; | 86% |
In tetrahydrofuran; water for 2.5h; Product distribution; Mechanism; acid-catalyzed solvolysis of polyenol ethers under var. conditions; | 86% |
Conditions | Yield |
---|---|
In tetrahydrofuran; water for 4h; | A 36% B 85% |
n-dodecanaldoxime
Dodecanal
Conditions | Yield |
---|---|
With manganese(IV) oxide; acrylic acid methyl ester In dichloromethane at 20℃; for 18h; Oxidation; | 85% |
With manganese(IV) oxide In hexane for 0.25h; | 78% |
2-Undecyl-[1,3]dithiane
Dodecanal
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; 1-n-butyl-3-methylimidazolim bromide at 60 - 70℃; for 0.366667h; | 84% |
With antimonypentachloride In dichloromethane at 0℃; for 0.166667h; | 81% |
With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile for 1h; Ambient temperature; | 71% |
With oxygen; 2,4,6-tris(p-chlorophenyl)pyrylium perchlorate In dichloromethane for 5h; Irradiation; | 14% |
Dodecanal
Conditions | Yield |
---|---|
Stage #1: 2-Undecyl-1,3-oxathiolane With acetyl chloride; sodium nitrite In dichloromethane at 0 - 5℃; for 0.25h; Stage #2: With water In dichloromethane at 0 - 20℃; for 0.166667h; | 84% |
With perchloric acid; dihydrogen peroxide; ammonium bromide; molybdic acid In dichloromethane at 0 - 5℃; for 1.5h; | 76% |
With ammonium bromide; dihydrogen peroxide; vanadia In dichloromethane at 0 - 5℃; for 1.5h; | 76% |
Conditions | Yield |
---|---|
With trimethylamine-N-oxide In dimethyl sulfoxide for 5h; Ambient temperature; other halides; | 83% |
With trimethylamine-N-oxide In dimethyl sulfoxide for 5h; Ambient temperature; | 83% |
With sodium hydrogencarbonate; dimethyl sulfoxide; sodium iodide at 115℃; for 2h; | 76 % Chromat. |
With 4-methylmorpholine N-oxide; potassium iodide In neat (no solvent) at 80℃; for 1h; Sonication; Green chemistry; |
Conditions | Yield |
---|---|
With potassium hydrogensulfate; ammonium iron(III) sulfate; acetic acid for 3h; Heating; | A 16 mg B 82% |
Conditions | Yield |
---|---|
With potassium hydrogensulfate; ammonium iron(III) sulfate for 3h; Heating; | A 16 mg B 82% |
Conditions | Yield |
---|---|
With sodium tris(diethylamino)aluminum hydride In tetrahydrofuran; dodecane at 0℃; for 3h; | 82% |
Multi-step reaction with 2 steps 1: chlorobis(cyclooctene)-iridium(I) dimer / dichloromethane / 2 h / 23 °C / Inert atmosphere 2: hydrogenchloride / water; tetrahydrofuran / 1 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In tetrahydrofuran; N,N-dimethyl-formamide at -70℃; for 0.0333333h; | A 81% B n/a |
With pyridine; sodium tetrahydroborate In tetrahydrofuran; N,N-dimethyl-formamide at 0℃; for 0.0166667h; Product distribution; |
2-undecyl-1,3-dithiolane
Dodecanal
Conditions | Yield |
---|---|
With nitric acid; arsenic(III) trioxide In dichloromethane at 0 - 5℃; | 81% |
With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile for 1h; Ambient temperature; | 21% |
Conditions | Yield |
---|---|
manganese(II) iodide In tetrahydrofuran at 70℃; for 2h; | A 80% B 3% C n/a |
Dodecanal
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate In various solvent(s) | 78% |
Dodecanal
Conditions | Yield |
---|---|
In tetrahydrofuran; water for 3h; | 75% |
n-dodecanal diisopropyl acetal
Dodecanal
Conditions | Yield |
---|---|
Stage #1: n-dodecanal diisopropyl acetal With triethylsilyl trifluoromethyl sulfonate; tris-(o-tolyl)phosphine In dichloromethane at -5℃; for 4h; Stage #2: With water In dichloromethane at 20℃; for 0.5h; | 72% |
Multi-step reaction with 2 steps 1: dichloromethane / 0.5 h / -5 °C / Schlenk technique; Inert atmosphere 2: water / dichloromethane / 0.5 h / 20 °C / Schlenk technique View Scheme |
Dodecanal
(2R*,3S*)-N-hydroxy-3-(trimethylsilyl)-4-penten-2-amine
(2R*,3S*)-(Z)-N-undecylidene-3-(trimethylsilyl)-4-penten-2-amine N-oxide
Conditions | Yield |
---|---|
With calcium chloride In diethyl ether at -20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
ytterbium (III) tris-[tris-(nonafluorobutanesulfonyl)methide] In ethanol for 48h; Heating / reflux; | 100% |
With hydrogenchloride In ethanol; water at -10 - 90℃; for 20.1667h; | 82% |
With hydrogenchloride In ethanol at 20 - 90℃; for 17h; | 76% |
Conditions | Yield |
---|---|
Stage #1: Methoxyallene With n-butyllithium In diethyl ether; hexane at -40℃; for 0.166667h; Inert atmosphere; Stage #2: Dodecanal In diethyl ether; hexane at -40℃; Inert atmosphere; | 100% |
Stage #1: Methoxyallene With n-butyllithium In diethyl ether; hexane at -40℃; Stage #2: Dodecanal In diethyl ether; hexane at -78℃; Further stages.; | |
Stage #1: Methoxyallene With n-butyllithium In diethyl ether; hexane at -40℃; for 0.5h; Inert atmosphere; Stage #2: Dodecanal In diethyl ether; hexane at -78℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With N-chloro-succinimide; thiourea at 23℃; for 0.75h; | 99% |
With Br(1-)*C19H14Br3O3PS*Na(1+) at 20℃; | 92% |
With Zr-MOF-808 at 45℃; for 22h; Irradiation; | 7% |
Conditions | Yield |
---|---|
With aluminium trichloride; diphenylstibane In tetrahydrofuran for 3h; Ambient temperature; | 99% |
Stage #1: Dodecanal With phenylsilane; potassium tert-butylate In toluene at 20℃; for 0.5h; Inert atmosphere; Stage #2: With water; sodium hydroxide In toluene at 0 - 20℃; | 99% |
With LaNi5 hydride In tetrahydrofuran; methanol 1) 0 deg C, 4 h, 2) r.t., 14 h; | 98% |
Dodecanal
dimethyl lithiomethylphosphonate
dimethyl 2-hydroxytridecylphosphonate
Conditions | Yield |
---|---|
99% |
Conditions | Yield |
---|---|
With iron oxide; oxygen; ethyl acetoacetate at 75 - 80℃; under 760.051 Torr; for 24h; Green chemistry; | 99% |
With oxygen; copper(II) acetate monohydrate; cobalt(II) diacetate tetrahydrate In water at 40℃; under 760.051 Torr; for 3h; | 97% |
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 25℃; for 12h; | 94% |
Dodecanal
dimethyl methane phosphonate
dimethyl 2-hydroxytridecylphosphonate
Conditions | Yield |
---|---|
Stage #1: dimethyl methane phosphonate With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.0833333h; Metallation; Stage #2: Dodecanal In tetrahydrofuran; hexane at -78℃; for 0.0833333h; Addition; | 99% |
Dodecanal
sodium glutamate
Conditions | Yield |
---|---|
In methanol at 20℃; | 99% |
Dodecanal
Conditions | Yield |
---|---|
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen; 18O-labeled water In 1,2-dichloro-ethane at 25℃; for 12h; | 99% |
With Iron(III) nitrate nonahydrate; oxygen; 18O-labeled water In acetonitrile at 25℃; under 760.051 Torr; for 12h; Schlenk technique; | 89% |
Dodecanal
(carbethoxyethylidene)triphenylphosphorane
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 18h; | 98% |
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; sodium iodide In acetonitrile for 1.46667h; Heating; | 98% |
With hydroxylamine hydrochloride In dimethyl sulfoxide at 100℃; for 0.5h; | 96% |
With hydroxylamine hydrochloride In o-xylene at 133℃; under 760.051 Torr; for 5h; | 89% |
Dodecanal
benzamide
β-naphthol
N-(1-(2-hydroxynaphthalen-1-yl)dodecyl)benzamide
Conditions | Yield |
---|---|
With zirconyl triflate In neat (no solvent) at 80℃; for 0.0333333h; | 98% |
With dodecylphosphonic acid at 90℃; for 0.5h; Neat (no solvent); | 70% |
Dodecanal
ethyl (4-methoxyphenylimino)acetate
Conditions | Yield |
---|---|
Stage #1: Dodecanal With 1-(3,5-bis(trifluoromethyl)phenyl)-3-((R)-(6-methoxyquinolin-4-yl)((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methyl)thiourea; L-proline In neat (no solvent) at 25℃; for 0.166667h; Stage #2: ethyl (4-methoxyphenylimino)acetate In neat (no solvent) at 25℃; for 0.0833333h; Catalytic behavior; Reagent/catalyst; Solvent; Time; Concentration; stereoselective reaction; | 98% |
Conditions | Yield |
---|---|
zeolite HSZ-360 for 4h; Ambient temperature; | 97% |
With boron trifluoride diethyl etherate at 20℃; Esterification; salt-ice cooling; | 75% |
With boron trifluoride Addition; | 75% |
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 2h; | 97% |
Dodecanal
ethyl (triphenylphosphoranylidene)acetate
(E)-ethyl tetradec-2-enoate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 15h; Wittib reaction; | 97% |
In benzene at 0 - 20℃; for 6h; Wittig reaction; | 84% |
In dichloromethane at 20℃; Wittig Olefination; | 45% |
Conditions | Yield |
---|---|
With copper(II) acetate monohydrate In ethyl acetate at 20℃; for 12h; | 97% |
With zinc(II) acetate dihydrate In acetonitrile at 20℃; for 18h; | 93% |
Dodecanal
methyl 2-acetylamino-2-(dimethoxyphosphinyl)acetate
Conditions | Yield |
---|---|
Stage #1: methyl 2-acetylamino-2-(dimethoxyphosphinyl)acetate With N,N,N',N'-tetramethylguanidine In tetrahydrofuran at -78℃; Horner-Wadsworth-Emmons Olefination; Stage #2: Dodecanal In tetrahydrofuran at -78 - 25℃; for 4h; Horner-Wadsworth-Emmons Olefination; | 97% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; for 1.75h; | 96.8% |
In tetrahydrofuran; diethyl ether at -50 - 20℃; |
Conditions | Yield |
---|---|
With phenyltellurotrimethylsilane; zinc(II) iodide In benzene for 3h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
In diethyl ether for 1.5h; Heating; | 96% |
Conditions | Yield |
---|---|
With triethylsilane; tris(pentafluorophenyl)borate In dichloromethane at 20℃; for 20h; | 96% |
Stage #1: Dodecanal With triethylsilane; tris(pentafluorophenyl)borate In dichloromethane at 20℃; for 20h; Stage #2: In ethanol for 7h; Heating; Further stages.; | 96% |
With hydrogen In neat (no solvent) at 180℃; under 6000.6 Torr; for 1h; Autoclave; | 71% |
Multi-step reaction with 2 steps 1: methanol / 60 °C / Inert atmosphere 2: potassium carbonate; methanol; hydrogen; palladium 10% on activated carbon / 24 h / 65 °C / 760.05 Torr View Scheme | |
With hydrogen In neat (no solvent) at 180℃; under 6000.6 Torr; Catalytic behavior; Autoclave; High pressure; |