LBF12000BC13: Difference between revisions
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|LipidBank=DFA7125 | |LipidBank=DFA7125 | ||
|LipidMaps=LMFA01020157 | |LipidMaps=LMFA01020157 | ||
|SysName= | |SysName=4S-Methyldodecanoic acid | ||
|Common Name=&&(S)-4- | |Common Name=&&(S)-4-Methyllauric acid&& | ||
|Boiling Point=162-164°C/5.5mmHg [[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}}]] | |Boiling Point=162-164°C/5.5mmHg [[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}}]] | ||
|Density=D25/ =0.888 [[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}}]] | |Density=D25/ =0.888 [[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}}]] | ||
| | |Refractive= eta 25/D=1.4424 [[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= | |Source= | ||
|Chemical Synthesis=1-Bromo-3-methyl undecane was incubated with potassium cyanide in ethanol, followed by heating in aq. Potassium hydroxide. | |Chemical Synthesis=1-Bromo-3-methyl undecane was incubated with potassium cyanide in ethanol, followed by heating in aq. Potassium hydroxide. |
Latest revision as of 06:31, 22 June 2010
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 | |
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LipidBank | DFA7125 |
LipidMaps | LMFA01020157 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF12000BC13 |
(S)-4-Methyllauric acid | |
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Structural Information | |
4S-Methyldodecanoic acid | |
| |
Formula | C13H26O2 |
Exact Mass | 214.19328007599998 |
Average Mass | 214.34433999999996 |
SMILES | CCCCCCCCC(C)CCC(O)=O |
Physicochemical Information | |
162-164°C/5.5mmHg Cason_J et al. | |
D25/ =0.888 CasonJet al. | |
η 25/D=1.4424 CasonJet al. | |
1-Bromo-3-methyl undecane was incubated with potassium cyanide in ethanol, followed by heating in aq. Potassium hydroxide. | |
Spectral Information | |
Mass Spectra | |
UV Spectra | |
IR Spectra | |
NMR Spectra | |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | ||||||||||
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