LBF14000OX02: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|Melting Point=69°C
|Melting Point=69°C
|Solubility=[[Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113|{{RelationTable/GetFirstAuthor|Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113}}]]
|Solubility=[[Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113|{{RelationTable/GetFirstAuthor|Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113}}]]
|Source=
|Chemical Synthesis=Synthetic, by action of ethyl sodioacetoacetate on ethyl 11-chloroundecanoate & hydrolysis of the reaction product, ethyl 2-acetylbrassylate
|Metabolism=
}}
}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

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Upper classes: LB LBF



10-Ketomyristic acid
LBF14000OX02.png
Structural Information
10-Oxotetradecanoic acid
  • 10-Ketomyristic acid
Formula C14H26O3
Exact Mass 242.188194698
Average Mass 242.35444
SMILES CCCCC(=O)CCCCCCCCC(O)=O
Physicochemical Information
69°C
ChuitPet al.
Synthetic, by action of ethyl sodioacetoacetate on ethyl 11-chloroundecanoate & hydrolysis of the reaction product, ethyl 2-acetylbrassylate
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF14000OX02 See above. Chuit_P et al. 1927