LBF20118BC02: Difference between revisions
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|UV Spectra=<FONT FACE="Symbol">l</FONT>max 217nm (<FONT FACE="Symbol">e</FONT>max 13,490) [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]] | |UV Spectra=<FONT FACE="Symbol">l</FONT>max 217nm (<FONT FACE="Symbol">e</FONT>max 13,490) [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]] | ||
|IR Spectra=C=C: 12.60<FONT FACE="Symbol">m</FONT>, 13.52<FONT FACE="Symbol">m</FONT>, 15.50<FONT FACE="Symbol">m</FONT> [[Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836}}]] | |IR Spectra=C=C: 12.60<FONT FACE="Symbol">m</FONT>, 13.52<FONT FACE="Symbol">m</FONT>, 15.50<FONT FACE="Symbol">m</FONT> [[Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836}}]] | ||
|Source= | |||
|Chemical Synthesis=2-Metyl-2-icosenoic acid was prepared from 2-methyl-2-icosenoic acid methyl [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]];>. | |||
|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 | DFA7104 |
| LipidMaps | LMFA01020136 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20118BC02 |
| 2-Methyl-2-Icosenoic Acid | |
|---|---|
| |
| Structural Information | |
| 2-Methyl-2-Icosenoic Acid | |
| |
| Formula | C21H40O2 |
| Exact Mass | 324.302830524 |
| Average Mass | 324.5411 |
| SMILES | C(CCCCCCCCCCCCCC=C(C)C(O)=O)CCC |
| Physicochemical Information | |
| 66.3 - 67.6°C Allen_CF et al. | |
| 203 - 205°C/2.5mmHg(Me ESTER) Cason_J et al. | |
| 2-Metyl-2-icosenoic acid was prepared from 2-methyl-2-icosenoic acid methyl Allen_CF et al.;>. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | lmax 217nm (emax 13,490) Allen_CF et al. |
| IR Spectra | C=C: 12.60m, 13.52m, 15.50m CasonJet al. |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | |||||||||||||||
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