LBF10105BC01: Difference between revisions
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|Optical=<FONT FACE="Symbol">h</FONT>20/D = 1.4562 [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]] | |Optical=<FONT FACE="Symbol">h</FONT>20/D = 1.4562 [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]] | ||
|Source= | |Source= | ||
|Chemical Synthesis=6-Isopentyl-9-methyl-5-decenoic acid is prepared from the reaction of 9-methyl-6-oxo-decanoic acid ethyl with isopentylmagnesium bromide, followed by saponification with KOH [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]] | |Chemical Synthesis=6-Isopentyl-9-methyl-5-decenoic acid is prepared from the reaction of 9-methyl-6-oxo-decanoic acid ethyl with isopentylmagnesium bromide, followed by saponification with KOH [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]. | ||
|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 | DFA7110 |
| LipidMaps | LMFA01020142 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF10105BC01 |
| 6-Isopentyl-9-Methyl-5-Decenoic Acid | |
|---|---|
| |
| Structural Information | |
| 6-Isopentyl-9-Methyl-5-Decenoic Acid | |
| |
| Formula | C16H30O2 |
| Exact Mass | 254.22458020399998 |
| Average Mass | 254.4082 |
| SMILES | CC(C)CCC=C(CCCC(O)=O)CCC(C)C |
| Physicochemical Information | |
| 142 - 145°C/0.2mmHg Asano_M et al. | |
| h20/D = 1.4562 AsanoMet al. | |
| 6-Isopentyl-9-methyl-5-decenoic acid is prepared from the reaction of 9-methyl-6-oxo-decanoic acid ethyl with isopentylmagnesium bromide, followed by saponification with KOH Asano_M et al.. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | ||||||||||
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