LBF13000BC07: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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{{Metabolite
{{Metabolite
|LipidBank=DFA7135
|LipidBank=DFA7135
|LipidMaps=LMFA01020167
|LipidMaps=LMFA01020167
|SysName=3-Ethyl-3-Methyltridecanoic Acid
|SysName=3-Ethyl-3-methyltridecanoic acid
|Common Name=&&3-Ethyl-3-Methyltridecanoic Acid&&
|Common Name=&&3-Ethyl-3-methyltridecanoic acid&&
|Boiling Point=168-171°C/1mmHg [[Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359|{{RelationTable/GetFirstAuthor|Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359}}]]
|Boiling Point=168-171°C/1mmHg [[Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359|{{RelationTable/GetFirstAuthor|Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359}}]]
|Optical=<FONT FACE="Symbol">h</FONT> 25/D = 1.4515 [[Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359|{{RelationTable/GetFirstAuthor|Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359}}]]
|Refractive= eta  25/D = 1.4515 [[Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359|{{RelationTable/GetFirstAuthor|Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359}}]]
|Source=
|Chemical Synthesis=A mixture of 3-ethyl-3-methylglutarate monomethyl, decanoic acid, methylalcohol and small amount of sodium was electrolysed, followed by treatment with aq. potassium hydroxide[[Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359|{{RelationTable/GetFirstAuthor|Reference:Rabjohn_N:Farmer_HH:,J. Org. Chem.,1959,24,359}}]].
|Metabolism=
}}
}}


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

Latest revision as of 21:00, 14 April 2010

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Upper classes: LB LBF



3-Ethyl-3-methyltridecanoic acid
LBF13000BC07.png
Structural Information
3-Ethyl-3-methyltridecanoic acid
  • 3-Ethyl-3-methyltridecanoic acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCCCCCC(C)(CC)CC(O)=O
Physicochemical Information
168-171°C/1mmHg Rabjohn_N et al.
η 25/D = 1.4515 RabjohnNet al.
A mixture of 3-ethyl-3-methylglutarate monomethyl, decanoic acid, methylalcohol and small amount of sodium was electrolysed, followed by treatment with aq. potassium hydroxide Rabjohn_N et al..
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF13000BC07 See above. Rabjohn_N et al. 1959