LBF14112BC01: Difference between revisions
No edit summary |
No edit summary |
||
| Line 13: | Line 13: | ||
|IR Spectra=10.08, 12.38, 13.33, 15.03<FONT FACE="Symbol">m</FONT>[[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]] | |IR Spectra=10.08, 12.38, 13.33, 15.03<FONT FACE="Symbol">m</FONT>[[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]] | ||
|Source= | |Source= | ||
|Chemical Synthesis=2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-mrthyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]] | |Chemical Synthesis=2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-mrthyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]. | ||
|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 | DFA7101 |
| LipidMaps | LMFA01020133 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF14112BC01 |
| 2,4-Dimethyl-2 (E) -Tetradecenoic Acid | |
|---|---|
| |
| Structural Information | |
| 2,4-Dimethyl-2 (E) -Tetradecenoic Acid | |
| |
| Formula | C16H30O2 |
| Exact Mass | 254.22458020399998 |
| Average Mass | 254.4082 |
| SMILES | CCCCCCCCCCC(C)C=C(C)C(O)=O |
| Physicochemical Information | |
| 176 - 177°C/1.5mmHg Cason_J et al. | |
| h25/D = 1.4634 CasonJet al. | |
| 2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-mrthyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification Cason_J et al.. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | lmax 219nm CasonJet al. |
| IR Spectra | 10.08, 12.38, 13.33, 15.03m CasonJet al. |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
|
