LBF14000BC08: Difference between revisions

Latest revision as of 12:04, 25 May 2010

Upper classes: LB LBF

6-Ethyltetradecanoic acid

Structural Information
	6-Ethyltetradecanoic acid
	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

Biospecies	ID	Compound Name	Reference	Comment
n.a.	LBF14000BC08	See above.	Asano_M et al. 1950

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+{{Lipid/Header}}
 {{Hierarchy|{{PAGENAME}}}}
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 |LipidBank=DFA7137
 |LipidMaps=LMFA01020169
-|SysName=6-Ethyl Tetradecanoic Acid
+|SysName=6-Ethyltetradecanoic acid
+|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}}]]
+|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}}