LBF14112BC01: Difference between revisions

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|Common Name=&&2,4-Dimethyl-2 (E) -Tetradecenoic Acid&&
|Common Name=&&2,4-Dimethyl-2 (E) -Tetradecenoic Acid&&
|Boiling Point=176 - 177°C/1.5mmHg [[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=176 - 177°C/1.5mmHg [[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 = 1.4634 [[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=eta25/D = 1.4634 [[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=<FONT FACE="Symbol">l</FONT>max 219nm [[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=lambdamax 219nm [[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}}]]
|IR Spectra=10.08, 12.38, 13.33, 15.03<FONT FACE="Symbol">m</FONT>[[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}}]]
|IR Spectra=10.08, 12.38, 13.33, 15.03mu[[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=
|Chemical Synthesis=2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-mrthyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification [[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}}]].
|Chemical Synthesis=2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-mrthyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification [[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}}]].

Revision as of 14:00, 19 February 2010

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Upper classes: LB LBF



IDs and Links
LipidBank DFA7101
LipidMaps LMFA01020133
CAS
KEGG {{{KEGG}}}
KNApSAcK {{{KNApSAcK}}}
mol LBF14112BC01
2,4-Dimethyl-2 (E) -Tetradecenoic Acid
LBF14112BC01.png
Structural Information
2,4-Dimethyl-2 (E) -Tetradecenoic Acid
  • 2,4-Dimethyl-2 (E) -Tetradecenoic Acid
Formula C16H30O2
Exact Mass 254.22458020399998
Average Mass 254.4082
SMILES CCCCCCCCCCC(C)C=C(C)C(O)=O
Physicochemical Information
176 - 177°C/1.5mmHg Cason_J et al.
η25/D = 1.4634 CasonJet al.
2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-mrthyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification Cason_J et al..
Spectral Information
Mass Spectra
UV Spectra lambdamax 219nm CasonJet al.
IR Spectra 10.08, 12.38, 13.33, 15.03μ CasonJet al.
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF14112BC01 See above. Cason_J et al. 1955


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