LBF08106BC02: Difference between revisions

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|Common Name=&&4-Ethyl-2-Methyl-2-Octenoic Acid&&
|Common Name=&&4-Ethyl-2-Methyl-2-Octenoic Acid&&
|Boiling Point=141 - 142°C/4.6mmHg [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]
|Boiling Point=141 - 142°C/4.6mmHg [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]
|Optical=<FONT FACE="Symbol">h</FONT>25/D = 1.4628 [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]
|Refractive=<FONT FACE="Symbol">h</FONT>25/D = 1.4628 [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]
|UV Spectra=200 - 270nm [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]
|UV Spectra=200 - 270nm [[Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Rinehart_KL_Jr:,J. Org. Chem.,1955,20,1591}}]]
|Source=
|Source=

Revision as of 21:00, 6 January 2010

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Upper classes: LB LBF



4-Ethyl-2-Methyl-2-Octenoic Acid
LBF08106BC02.png
Structural Information
4-Ethyl-2-Methyl-2-Octenoic Acid
  • 4-Ethyl-2-Methyl-2-Octenoic Acid
Formula C11H20O2
Exact Mass 184.14632988399998
Average Mass 184.2753
SMILES CCCCC(CC)C=C(C)C(O)=O
Physicochemical Information
141 - 142°C/4.6mmHg Cason_J et al.
h25/D = 1.4628 CasonJet al.
4-Ethyl-2-methyl-2-octenoic acid was prepared from the reaction of 4-ethyl-3-hydroxy-2-methyl-octanoic acid ethyl and phosphoryl chloride, followed by heating with sulfuric acid Cason_J et al..
Spectral Information
Mass Spectra
UV Spectra 200 - 270nm CasonJet al.
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF08106BC02 See above. Cason_J et al. 1955