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CAS No.: | 14727-68-5 |
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Name: | (Z)-N,N-dimethyl-9-octadecenylamine |
Article Data: | 5 |
Molecular Structure: | |
Formula: | C20H41 N |
Molecular Weight: | 295.552 |
Synonyms: | 9-Octadecen-1-amine,N,N-dimethyl-, (Z)-; 9-Octadecenylamine, N,N-dimethyl-, (Z)- (8CI);9-Octadecenylamine, N,N-dimethyl-, cis- (7CI); Armeen DMOD;N,N-Dimethyloleylamine; Oleyldimethylamine |
Density: | 0.822g/cm3 |
Boiling Point: | 376.5°Cat760mmHg |
Flash Point: | 163.1°C |
PSA: | 3.24000 |
LogP: | 6.58550 |
N,N-dimethyl oleamide
N,N-dimethyl-N-oleylamine
Conditions | Yield |
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With lithium aluminium tetrahydride In diethyl ether for 6h; Heating; | 36.9% |
(Z)-1-bromo-9-octadecene
dimethyl amine
N,N-dimethyl-N-oleylamine
Conditions | Yield |
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In isopropyl alcohol |
(Z)-9-octadecenoyl chloride
N,N-dimethyl-N-oleylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 100 percent / benzene / 1 h / Ambient temperature 2: 36.9 percent / LiAlH4 / diethyl ether / 6 h / Heating View Scheme |
oleoyl alcohol
N,N-dimethyl-N-oleylamine
Conditions | Yield |
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Multi-step reaction with 2 steps 1: (i) TsCl, Py, H2O, (ii) LiBr, MeCOEt 2: propan-2-ol View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: LiAlH4 / diethyl ether 2: (i) TsCl, Py, H2O, (ii) LiBr, MeCOEt 3: propan-2-ol View Scheme |
cis-9-octadecenoamide
N,N-dimethyl-(12S,13R)-epoxy-cis-9-octadecenyl amide
Palmitamide
stearamide
A
N,N-dimethylhexadecylamine
B
N,N-dimethyl-n-octadecylamine
C
N,N-dimethyl-(12S,13R)-epoxy-cis-9-octadecenyl amine
D
N,N-dimethyl-N-oleylamine
Conditions | Yield |
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With lithium aluminium tetrahydride In diethyl ether for 0.5h; Reflux; |
trivernolin
N,N-dimethyl-N-oleylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: sodium methylate / methanol; hexane 2.1: sodium methylate / methanol / 2 h / Reflux 2.2: 24.25 h / 0 °C 3.1: lithium aluminium tetrahydride / diethyl ether / 0.5 h / Reflux View Scheme |
methyl (9Z,12S,13R)-12,13-epoxy-9-octadecenoate
N,N-dimethyl-N-oleylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium methylate / methanol / 2 h / Reflux 1.2: 24.25 h / 0 °C 2.1: lithium aluminium tetrahydride / diethyl ether / 0.5 h / Reflux View Scheme |
Conditions | Yield |
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With [Ru(2-(6-methoxypyridin-2-yl)-1,10-phenanthroline)(MeCN)2Cl]Cl; sodium methylate at 110℃; for 12h; Green chemistry; | 78 %Spectr. |
Conditions | Yield |
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With ethanol; sodium In hexane at 0℃; for 0.333333h; Inert atmosphere; Overall yield = 83 %; Overall yield = 70.7 mg; chemoselective reaction; |