LBF14112BC01: Difference between revisions

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|LipidBank=DFA7101
|LipidBank=DFA7101
|LipidMaps=LMFA01020133
|LipidMaps=LMFA01020133
|SysName=2,4-Dimethyl-2 (E) -Tetradecenoic Acid
|SysName=2,4-Dimethyl-trans-2-tetradecenoic acid
|Common Name=&&2,4-Dimethyl-2 (E) -Tetradecenoic Acid&&
|Common Name=&&2,4-Dimethyl-2E-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= eta 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}}]]
|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= lambda 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}}]]
|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, 15.03 mu [[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-methyl-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}}]].
|Metabolism=
|Metabolism=
}}
}}


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{{Lipid/Footer}}

Latest revision as of 02:40, 19 October 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-2E-tetradecenoic acid
LBF14112BC01.png
Structural Information
2,4-Dimethyl-trans-2-tetradecenoic acid
  • 2,4-Dimethyl-2E-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.
η 25/D = 1.4634 CasonJet al.
2,4-Dimethyl-2-(E)-tetradecenoic acid was prepared from the reation of 2-methyl-dodecanal with 2-bromo-propanoic acid ethyl, followed by dehydration and saponification Cason_J et al..
Spectral Information
Mass Spectra
UV Spectra λ max 219nm CasonJet al.
IR Spectra 10.08, 12.38, 13.33, 15.03 μ 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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