LBF18000BC10: Difference between revisions

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|Melting Point=40.9-42.4°C [[Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695}}]]
|Melting Point=40.9-42.4°C [[Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695}}]]
|Boiling Point=183°C/0.4mmHg<!--7073-->
|Boiling Point=183°C/0.4mmHg<!--7073-->
|IR Spectra=7.78<FONT FACE="Symbol">m</FONT>, 8.10<FONT FACE="Symbol">m</FONT>, 13.5<FONT FACE="Symbol">m</FONT>(CS2) [[Reference:Freeman_NK:,J. Am. Chem. Soc.,1952,74,2523|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1952,74,2523}}]]
|IR Spectra=7.78mu, 8.10mu, 13.5mu(CS2) [[Reference:Freeman_NK:,J. Am. Chem. Soc.,1952,74,2523|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1952,74,2523}}]]
|Source=
|Source=
|Chemical Synthesis=Ethylester of 15-methyl-12-oxooctadecanate was heated at 200°C with hydrazine hydrate, sodium hydroxide and diethylene glycol[[Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695}}]].
|Chemical Synthesis=Ethylester of 15-methyl-12-oxooctadecanate was heated at 200°C with hydrazine hydrate, sodium hydroxide and diethylene glycol[[Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Coad_RA:,J. Am. Chem. Soc.,1950,72,4695}}]].

Revision as of 14:00, 19 February 2010

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Upper classes: LB LBF



15-Methyl Octadecanoic Acid
LBF18000BC10.png
Structural Information
15-Methyl Octadecanoic Acid
  • 15-Methyl Octadecanoic Acid
Formula C19H38O2
Exact Mass 298.28718046
Average Mass 298.50382
SMILES CCCC(C)CCCCCCCCCCCCCC(O)=O
Physicochemical Information
40.9-42.4°C Cason_J et al.
183°C/0.4mmHg
Ethylester of 15-methyl-12-oxooctadecanate was heated at 200°C with hydrazine hydrate, sodium hydroxide and diethylene glycol Cason_J et al..
Freeman_NK
Spectral Information
Mass Spectra
UV Spectra
IR Spectra 7.78μ, 8.10μ, 13.5μ(CS2) Freeman_NK
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18000BC10 See above. Cason_J et al. 1950
n.a. LBF18000BC10 See above. Freeman_NK 1952