LBF18000BC11: Difference between revisions

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|Chemical Synthesis=Diethyl ester of (3-methyl tetradecyl) malonate was heated with ethanolic KOH. After acidification the product was obtained by distillation under deminished pressure.
|Chemical Synthesis=Diethyl ester of (3-methyl tetradecyl) malonate was heated with ethanolic KOH. After acidification the product was obtained by distillation under deminished pressure.
|Metabolism=
|Metabolism=
|Biological Activity=[[Reference:Freeman_NK:,J. Am. Chem. Soc.,1952,74,2523|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1952,74,2523}}]][[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
}}
}}


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Revision as of 21:00, 6 January 2010

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(脂肪酸)
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Upper classes: LB LBF



5-Methyl Octadecanoic Acid
LBF18000BC11.png
Structural Information
5-Methyl Octadecanoic Acid
  • 5-Methyl Octadecanoic Acid
Formula C19H38O2
Exact Mass 298.28718046
Average Mass 298.50382
SMILES CCCCCCCCCCCCCC(C)CCCC(O)=O
Physicochemical Information
44.5-45°C Cason_J et al.
174°C/0.1mmHg
Diethyl ester of (3-methyl tetradecyl) malonate was heated with ethanolic KOH. After acidification the product was obtained by distillation under deminished pressure.
Freeman_NK Cason_J et al.
Spectral Information
Mass Spectra
UV Spectra 209nm CasonJet al.
IR Spectra 7.76m, 8.25m(CS2) Freeman_NK
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18000BC11 See above. Cason_J et al. 1951
n.a. LBF18000BC11 See above. Cason_J et al. 1950
n.a. LBF18000BC11 See above. Freeman_NK 1952