LBF14000BC08: Difference between revisions

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|Boiling Point=140-142°C/0.01mmHg [[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=140-142°C/0.01mmHg [[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-oxotetradecanate was treated with ethyl magnesium iodide in ether, followed by treatment with hydrochloric acid. Then the product was heated with iodine at 180°C. The product isolated was hydrogenated with Pt in methyl alcohol to give 6-etHYL TETRADECANOIC ACID[[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-oxotetradecanate was treated with ethyl magnesium iodide in ether, followed by treatment with hydrochloric acid. Then the product was heated with iodine at 180°C. The product isolated was hydrogenated with Pt in methyl alcohol to give 6-ethyl tetradecanoic acid[[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 08:39, 23 March 2010

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Upper classes: LB LBF



6-Ethyl Tetradecanoic Acid
LBF14000BC08.png
Structural Information
6-Ethyl Tetradecanoic Acid
  • 6-Ethyl Tetradecanoic Acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCCCC(CC)CCCCC(O)=O
Physicochemical Information
140-142°C/0.01mmHg Asano_M et al.
Barium 6-oxotetradecanate was treated with ethyl magnesium iodide in ether, followed by treatment with hydrochloric acid. Then the product was heated with iodine at 180°C. The product isolated was hydrogenated with Pt in methyl alcohol to give 6-ethyl tetradecanoic acid 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. LBF14000BC08 See above. Asano_M et al. 1950