LBF17115BC01: Difference between revisions
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|Optical=<FONT FACE="Symbol">h</FONT>25/D = 1.4662 [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]] | |Optical=<FONT FACE="Symbol">h</FONT>25/D = 1.4662 [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]] | ||
|UV Spectra=<FONT FACE="Symbol">l</FONT>max 218.5nm [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]] | |UV Spectra=<FONT FACE="Symbol">l</FONT>max 218.5nm [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]] | ||
|Source= | |||
|Chemical Synthesis=2,5-Dimethyl-2-heptadecenoic acid was prepared from 2,5-dimethyl-2-heptadecenoic acid methyl [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]];>. | |||
|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 | DFA7107 |
| LipidMaps | LMFA01020139 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF17115BC01 |
| 2,5-Dimethyl-2-Heptadecenoic Acid | |
|---|---|
| |
| Structural Information | |
| 2,5-Dimethyl-2-Heptadecenoic Acid | |
| |
| Formula | C19H36O2 |
| Exact Mass | 296.271530396 |
| Average Mass | 296.48794000000004 |
| SMILES | CCCCCCCCCCCCC(C)CC=C(C)C(O)=O |
| Physicochemical Information | |
| 170°C/0.1mmHg Cason_J et al. | |
| h25/D = 1.4662 CasonJet al. | |
| 2,5-Dimethyl-2-heptadecenoic acid was prepared from 2,5-dimethyl-2-heptadecenoic acid methyl Cason_J et al.;>. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | lmax 218.5nm CasonJet al. |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | ||||||||||
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