LBF12000BC13: Difference between revisions

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|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=<FONT FACE="Symbol">h</FONT>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}}]]
|Refractive=eta25/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.

Revision as of 14:00, 19 February 2010

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Upper classes: LB LBF



(S)-4-Methyl-Dodecanoic Acid
LBF12000BC13.png
Structural Information
(S)-4-Methyl-Dodecanoic Acid
  • (S)-4-Methyl-Dodecanoic Acid
  • (S)-4-Methyl-Dodecanoic 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.
η25/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
Biospecies ID Compound Name Reference Comment
n.a. LBF12000BC13 See above. Cason_J et al. 1953