LBF10000BC04: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidBank=DFA7141
|LipidBank=DFA7141
|LipidMaps=LMFA01020173
|LipidMaps=LMFA01020173
|SysName=2-Ethyl-2-Butyl Decanoic Acid
|SysName=2-Ethyl-2-butyl decanoic acid
|Common Name=&&2-Ethyl-2-Butyl Decanoic Acid&&
|Common Name=&&2-Ethyl-2-butyl decanoic acid&&
|Boiling Point=138-139°C/0.4mmHg [[Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837|{{RelationTable/GetFirstAuthor|Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837}}]]
|Boiling Point=138-139°C/0.4mmHg [[Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837|{{RelationTable/GetFirstAuthor|Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837}}]]
|Optical=<FONT FACE="Symbol">h</FONT>25/D=1.4500 [[Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837|{{RelationTable/GetFirstAuthor|Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837}}]]
|Refractive= eta 25/D=1.4500 [[Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837|{{RelationTable/GetFirstAuthor|Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837}}]]
|Source=
|Chemical Synthesis=2-Ethylhexanate(1,1-diethylpropyl)ester was treated with potassium amide in liquid ammonia, and further treated with octyl bromide. Then the product was heated in a mixture of hydrochloric acid/dioxane[[Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837|{{RelationTable/GetFirstAuthor|Reference:Hauser_CR:Chambers_WJ:,J. Am. Chem. Soc.,1956,78,3837}}]].
|Metabolism=
}}
}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

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Upper classes: LB LBF



2-Ethyl-2-butyl decanoic acid
LBF10000BC04.png
Structural Information
2-Ethyl-2-butyl decanoic acid
  • 2-Ethyl-2-butyl decanoic acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCCCC(CC)(CCCC)C(O)=O
Physicochemical Information
138-139°C/0.4mmHg Hauser_CR et al.
η 25/D=1.4500 Hauser_CR et al.
2-Ethylhexanate(1,1-diethylpropyl)ester was treated with potassium amide in liquid ammonia, and further treated with octyl bromide. Then the product was heated in a mixture of hydrochloric acid/dioxane Hauser_CR 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. LBF10000BC04 See above. Hauser_CR et al. 1956