LBF15000HO02: Difference between revisions

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|Melting Point=63.5-64°C
|Melting Point=63.5-64°C
|Boiling Point=166°C at 2 mm Hg
|Boiling Point=166°C at 2 mm Hg
|Solubility=soluble in ethyl alcohol, chloroform and ether[[Reference:Davies_LA:Adams_R:,J. Am. Chem. Soc.,1928,50,1749|{{RelationTable/GetFirstAuthor|Reference:Davies_LA:Adams_R:,J. Am. Chem. Soc.,1928,50,1749}}]]
|Solubility=soluble in ethyl alcohol, chloroform and ether[[Reference:Davies_LA:Adams_R:,J. Am. Chem. Soc.,1928,50,1749|{{RelationTable/GetFirstAuthor|Reference:Davies_LA:Adams_R:,J. Am. Chem. Soc.,1928,50,1749}}]]<!--0476-->
|Source=
|Source=
|Chemical Synthesis=Synthetic, by reaction of n-butylmagnesium bromide and methyl 11-aldoundecanoate / by partial reduction of pentadecanedioic acid demethyl ester
|Chemical Synthesis=Synthetic, by reaction of n-butylmagnesium bromide and methyl 11-aldoundecanoate / by partial reduction of pentadecanedioic acid demethyl ester

Revision as of 16:30, 26 January 2010

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Upper classes: LB LBF



Convolvulinolic acid
LBF15000HO02.png
Structural Information
11-Hydroxypentadecanoic acid
  • Convolvulinolic acid
  • 11-Hydroxypentadecanoic acid
Formula C15H30O3
Exact Mass 258.21949482599996
Average Mass 258.3969
SMILES CCCCC(O)CCCCCCCCCC(O)=O
Physicochemical Information
63.5-64°C
166°C at 2 mm Hg
soluble in ethyl alcohol, chloroform and ether Davies_LA et al.
Synthetic, by reaction of n-butylmagnesium bromide and methyl 11-aldoundecanoate / by partial reduction of pentadecanedioic acid demethyl ester
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF15000HO02 See above. Davies_LA et al. 1928