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 23:00, 19 February 2010

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Upper classes: LB LBF



(S)-4-Methyl-Dodecanoic Acid
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
[hide]Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF12000BC13 See above. Cason_J et al. 1953