LBF10000BC04: Difference between revisions
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|LipidBank=DFA7141 | |LipidBank=DFA7141 | ||
|LipidMaps=LMFA01020173 | |LipidMaps=LMFA01020173 | ||
|SysName=2-Ethyl-2- | |SysName=2-Ethyl-2-butyl decanoic acid | ||
|Common Name=&&2-Ethyl-2- | |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}}]] | ||
| | |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}} | {{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) |
Journals (雑誌一覧) |
How to edit (ページの書き方) |
IDs and Links | |
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LipidBank | DFA7141 |
LipidMaps | LMFA01020173 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF10000BC04 |
2-Ethyl-2-butyl decanoic acid | |
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Structural Information | |
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 | ||||||||||
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