LBF09107BC01: Difference between revisions

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|LipidBank=DFA7096
|LipidBank=DFA7096
|LipidMaps=LMFA01020128
|LipidMaps=LMFA01020128
|SysName=3-Methyl-2-Nonenoic Acid
|SysName=3-Methyl-2-nonenoic acid
|Common Name=&&3-Methyl-2-Nonenoic Acid&&
|Common Name=&&3-Methyl-2-nonenoic acid&&
|Boiling Point=113 - 114°C/1mmHg [[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
|Boiling Point=113 - 114°C/1mmHg [[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
|Refractive=<FONT FACE="Symbol">h</FONT>25/D = 1.4648 [[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
|Refractive= eta 25/D = 1.4648 [[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
|UV Spectra=<FONT FACE="Symbol">l</FONT>max 219m<FONT FACE="Symbol">m</FONT> [[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
|UV Spectra= lambda max 219m mu  [[Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Sumrell_G:,J. Org. Chem.,1951,16,1177}}]]
|IR Spectra=5.90(C=O), 6.10(C=C) [[Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859}}]]
|IR Spectra=5.90(C=O), 6.10(C=C) [[Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859}}]]
|Source=
|Source=

Latest revision as of 21:00, 14 April 2010

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Upper classes: LB LBF



3-Methyl-2-nonenoic acid
LBF09107BC01.png
Structural Information
3-Methyl-2-nonenoic acid
  • 3-Methyl-2-nonenoic acid
Formula C10H18O2
Exact Mass 170.13067981999998
Average Mass 170.24872
SMILES CCCCCCC(C)=CC(O)=O
Physicochemical Information
113 - 114°C/1mmHg Cason_J et al.
η 25/D = 1.4648 CasonJet al.
3-Methyl-2-nonenoic acid is prepared from 3-hydroxy-3-methyl-pelargonic acid and acetanhydride Fieser_LF_et_al .
Spectral Information
Mass Spectra
UV Spectra λ max 219m μ CasonJet al.
IR Spectra 5.90(C=O), 6.10(C=C) Freeman_NK
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF09107BC01 See above. Cason_J et al. 1951
n.a. LBF09107BC01 See above. Fieser_LF_et_al 1948
n.a. LBF09107BC01 See above. Freeman_NK 1953