LBF15113SC01: Difference between revisions

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|Solubility=[[Reference:Chuit_P_et_al:,J. Am. Chem. Soc.,1941,63,1153|{{RelationTable/GetFirstAuthor|Reference:Chuit_P_et_al:,J. Am. Chem. Soc.,1941,63,1153}}]]
|Solubility=[[Reference:Chuit_P_et_al:,J. Am. Chem. Soc.,1941,63,1153|{{RelationTable/GetFirstAuthor|Reference:Chuit_P_et_al:,J. Am. Chem. Soc.,1941,63,1153}}]]
|Source=
|Source=
|Chemical Synthesis= Synthetic, by conversion of myristic acid, to <FONT FACE="Symbol">a</FONT>-hydroxymyristic acid, then, by the action of Pb tetraacetate, to tridecanoldehyde which is then condensed with malonic acid in presence of pyridine.
|Chemical Synthesis= Synthetic, by conversion of myristic acid, to alpha -hydroxymyristic acid, then, by the action of Pb tetraacetate, to tridecanoldehyde which is then condensed with malonic acid in presence of pyridine.
|Metabolism=
|Metabolism=
|Symbol=C15:1
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 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)
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(雑誌一覧)
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Upper classes: LB LBF



2-Pentadecenoic acid
LBF15113SC01.png
Structural Information
2-Pentadecenoic acid
  • 2-Pentadecenoic acid
C15:1
Formula C15H28O2
Exact Mass 240.20893013999998
Average Mass 240.38162
SMILES CCCCCCCCCCCCC=CC(O)=O
Physicochemical Information
4.5°C
Chuit_P_et_al
Synthetic, by conversion of myristic acid, to alpha -hydroxymyristic acid, then, by the action of Pb tetraacetate, to tridecanoldehyde which is then condensed with malonic acid in presence of pyridine.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF15113SC01 See above. Chuit_P et al. 1941
n.a. LBF15113SC01 See above. Chuit_P_et_al 1941