LBF12000BC15: Difference between revisions

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|Boiling Point=131-132°C/1mmHg [[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]]
|Boiling Point=131-132°C/1mmHg [[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]]
|Source=
|Source=
|Chemical Synthesis=Barium 6-oxododecanate was treated with ethyl magnesium iodide in Ether, then the hydrolysate was heated with iodine at 180°C, followed by hydrogenation with Pt in methyl alchol[[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]].
|Chemical Synthesis=Barium 6-oxododecanate was treated with ethyl magnesium iodide in ether, then the hydrolysate was heated with iodine at 180°C, followed by hydrogenation with Pt in methyl alcohol[[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]].
|Metabolism=
|Metabolism=
}}
}}


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Revision as of 05:25, 23 March 2010

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Upper classes: LB LBF



6-Ethyldodecanoic Acid
LBF12000BC15.png
Structural Information
6-Ethyldodecanoic Acid
  • 6-Ethyldodecanoic Acid
Formula C14H28O2
Exact Mass 228.20893013999998
Average Mass 228.37091999999998
SMILES CCCCCCC(CC)CCCCC(O)=O
Physicochemical Information
131-132°C/1mmHg Asano_M et al.
Barium 6-oxododecanate was treated with ethyl magnesium iodide in ether, then the hydrolysate was heated with iodine at 180°C, followed by hydrogenation with Pt in methyl alcohol Asano_M et al..
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF12000BC15 See above. Asano_M et al. 1950