LBF20118BC02: Difference between revisions

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|Melting Point=66.3 - 67.6°C [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]]
|Melting Point=66.3 - 67.6°C [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]]
|Boiling Point=203 - 205°C/2.5mmHg(Me ESTER) [[Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836}}]]
|Boiling Point=203 - 205°C/2.5mmHg(Me ESTER) [[Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836}}]]
|UV Spectra=<FONT FACE="Symbol">l</FONT>max 217nm (<FONT FACE="Symbol">e</FONT>max 13,490) [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]]
|UV Spectra=lambdamax 217nm (epsilonmax 13,490) [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]]
|IR Spectra=C=C: 12.60<FONT FACE="Symbol">m</FONT>, 13.52<FONT FACE="Symbol">m</FONT>, 15.50<FONT FACE="Symbol">m</FONT> [[Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836}}]]
|IR Spectra=C=C: 12.60mu, 13.52mu, 15.50mu [[Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Kalm_MJ:,J. Org. Chem.,1954,19,1836}}]]
|Source=
|Source=
|Chemical Synthesis=2-Metyl-2-icosenoic acid was prepared from 2-methyl-2-icosenoic acid methyl [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]].
|Chemical Synthesis=2-Metyl-2-icosenoic acid was prepared from 2-methyl-2-icosenoic acid methyl [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,608}}]].

Revision as of 14:00, 19 February 2010

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Upper classes: LB LBF



2-Methyl-2-Icosenoic Acid
LBF20118BC02.png
Structural Information
2-Methyl-2-Icosenoic Acid
  • 2-Methyl-2-Icosenoic Acid
Formula C21H40O2
Exact Mass 324.302830524
Average Mass 324.5411
SMILES C(CCCCCCCCCCCCCC=C(C)C(O)=O)CCC
Physicochemical Information
66.3 - 67.6°C Allen_CF et al.
203 - 205°C/2.5mmHg(Me ESTER) Cason_J et al.
2-Metyl-2-icosenoic acid was prepared from 2-methyl-2-icosenoic acid methyl Allen_CF et al..
Spectral Information
Mass Spectra
UV Spectra lambdamax 217nm (epsilonmax 13,490) Allen_CF et al.
IR Spectra C=C: 12.60μ, 13.52μ, 15.50μ CasonJet al.
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20118BC02 See above. Allen_CF et al. 1963
n.a. LBF20118BC02 See above. Cason_J et al. 1954