LBF13000BC05: Difference between revisions
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|Boiling Point=154°C/2mmHg [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]] | |Boiling Point=154°C/2mmHg [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]] | ||
|Optical=<FONT FACE="Symbol">h</FONT> 25/D = 1.4462 [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]] | |Optical=<FONT FACE="Symbol">h</FONT> 25/D = 1.4462 [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]] | ||
|Source= | |||
|Chemical Synthesis=9-Hydroxy-9-methyltridecanitril was warmed with ethanolic KOH. The product was heated with a small amount of iodine at 200°C, followed by hydrogenation with Pt in ethanol[[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]];>. | |||
|Metabolism= | |||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} | ||
Revision as of 22:00, 24 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 | DFA7127 |
| LipidMaps | LMFA01020159 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF13000BC05 |
| 9-Methyltridecanoic Acid | |
|---|---|
| |
| Structural Information | |
| 9-Methyltridecanoic Acid | |
| |
| Formula | C14H28O2 |
| Exact Mass | 228.20893013999998 |
| Average Mass | 228.37091999999998 |
| SMILES | CCCCC(C)CCCCCCCC(O)=O |
| Physicochemical Information | |
| 154°C/2mmHg Rapport_H et al. | |
| h 25/D = 1.4462 RapportHet al. | |
| 9-Hydroxy-9-methyltridecanitril was warmed with ethanolic KOH. The product was heated with a small amount of iodine at 200°C, followed by hydrogenation with Pt in ethanol Rapport_H et al.;>. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | ||||||||||
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