LBF12000BC17: Difference between revisions

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|IR Spectra=C=CH2: 10.54<FONT FACE="Symbol">m</FONT> [[Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859}}]]
|IR Spectra=C=CH2: 10.54<FONT FACE="Symbol">m</FONT> [[Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859|{{RelationTable/GetFirstAuthor|Reference:Freeman_NK:,J. Am. Chem. Soc.,1953,75,1859}}]]
|Source=
|Source=
|Chemical Synthesis=2-Decyl acrylic acid was prepared from the reaction of 2-methyl dodecanoic acid with phosphor chloride, followed by hydrolysis [[Reference:Cason_J:Allinger_NL:Williams_DE:,J. Org. Chem.,1953,18,842|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Williams_DE:,J. Org. Chem.,1953,18,842}}]];>.
|Chemical Synthesis=2-Decyl acrylic acid was prepared from the reaction of 2-methyl dodecanoic acid with phosphor chloride, followed by hydrolysis [[Reference:Cason_J:Allinger_NL:Williams_DE:,J. Org. Chem.,1953,18,842|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Williams_DE:,J. Org. Chem.,1953,18,842}}]].
|Metabolism=
|Metabolism=
}}
}}


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Revision as of 11:55, 25 November 2009

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(脂肪酸)
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Upper classes: LB LBF



2-Methylenedodecanoic Acid
LBF12000BC17.png
Structural Information
2-Decyl-Acrylic Acid
  • 2-Methylenedodecanoic Acid
  • 2-Decyl-Acrylic Acid
Formula C13H24O2
Exact Mass 212.17763001199998
Average Mass 212.32845999999998
SMILES CCCCCCCCCCC(=C)C(O)=O
Physicochemical Information
33.3 - 34.2°C Izawa_M
2-Decyl acrylic acid was prepared from the reaction of 2-methyl dodecanoic acid with phosphor chloride, followed by hydrolysis Cason_J et al..
Spectral Information
Mass Spectra
UV Spectra lmax 210nm Allen_CF et al.
IR Spectra C=CH2: 10.54m Freeman_NK
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF12000BC17 See above. Cason_J et al. 1953
n.a. LBF12000BC17 See above. Freeman_NK 1953
n.a. LBF12000BC17 See above. Izawa_M 1952