LBF14000BC08: Difference between revisions
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|LipidBank=DFA7137 | |LipidBank=DFA7137 | ||
|LipidMaps=LMFA01020169 | |LipidMaps=LMFA01020169 | ||
|SysName=6- | |SysName=6-Ethyltetradecanoic acid | ||
|Common Name=&&6- | |Common Name=&&6-Ethyltetradecanoic acid&& | ||
|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= | |||
|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= | |||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} |
Latest revision as of 12:04, 25 May 2010
LipidBank Top (トップ) |
Fatty acid (脂肪酸) |
Glycerolipid (グリセロ脂質) |
Sphingolipid (スフィンゴ脂質) |
Journals (雑誌一覧) |
How to edit (ページの書き方) |
IDs and Links | |
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LipidBank | DFA7137 |
LipidMaps | LMFA01020169 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF14000BC08 |
6-Ethyltetradecanoic acid | |
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Structural Information | |
6-Ethyltetradecanoic 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 | ||||||||||
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