LBF10000BC04: Difference between revisions
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|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}}]] | |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}}]] | ||
|Source= | |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}}]] | |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= | |Metabolism= | ||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} | ||
Revision as of 11:55, 25 November 2009
| 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 | |
|---|---|
| LipidBank | DFA7141 |
| LipidMaps | LMFA01020173 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF10000BC04 |
| 2-Ethyl-2-Butyl Decanoic Acid | |
|---|---|
| |
| 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. | |
| h25/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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