LBF08106SC01: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidMaps=LMFA01030017
|LipidMaps=LMFA01030017
|SysName=cis-2-Octenoic acid
|SysName=cis-2-Octenoic acid
|Common Name=&&3-n-Amylacrylic acid&&cis-alpha-octenoic acid&&cis-2-Octenoic acid&&
|Common Name=&&cis-alpha-Octenoic acid&&2Z-Octenoic acid&&3-n-Amylacrylic acid&&
|Boiling Point=154°C at 22mmHg
|Boiling Point=154°C at 22mmHg
|Density=dX<sub>4</sub><sup>20</sup> 0.9807
|Density=d^{20}_4  0.9807
|Optical=1.4587 at 20°C
|Refractive=1.4587 at 20°C
|Solubility=[[Reference:Bachman_GB:,J. Am. Chem. Soc.,1923,55,4279|{{RelationTable/GetFirstAuthor|Reference:Bachman_GB:,J. Am. Chem. Soc.,1923,55,4279}}]][[Reference:Knight_JA:Diamond_JH:,J. Org. Chem.,1959,24,400|{{RelationTable/GetFirstAuthor|Reference:Knight_JA:Diamond_JH:,J. Org. Chem.,1959,24,400}}]]
|Solubility=[[Reference:Bachman_GB:,J. Am. Chem. Soc.,1923,55,4279|{{RelationTable/GetFirstAuthor|Reference:Bachman_GB:,J. Am. Chem. Soc.,1923,55,4279}}]]<!--0157-->[[Reference:Knight_JA:Diamond_JH:,J. Org. Chem.,1959,24,400|{{RelationTable/GetFirstAuthor|Reference:Knight_JA:Diamond_JH:,J. Org. Chem.,1959,24,400}}]]
|Source=
|Chemical Synthesis=Synthesized by condensation of caprylic aldehyde with malonic acid in the presence of pyridine.
|Metabolism=
|Symbol=C8:1
}}
}}
{{Lipid/Footer}}

Latest revision as of 08:58, 4 October 2010

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(脂肪酸)
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Upper classes: LB LBF



cis-α-Octenoic acid
LBF08106SC01.png
Structural Information
cis-2-Octenoic acid
  • cis-α-Octenoic acid
  • 2Z-Octenoic acid
  • 3-n-Amylacrylic acid
C8:1
Formula C8H14O2
Exact Mass 142.09937969199999
Average Mass 142.19556
SMILES CCCCCC=CC(O)=O
Physicochemical Information
154°C at 22mmHg
d20
4
   0.9807
1.4587 at 20°C
Bachman_GB Knight_JA et al.
Synthesized by condensation of caprylic aldehyde with malonic acid in the presence of pyridine.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF08106SC01 See above. Bachman_GB 1923
n.a. LBF08106SC01 See above. Knight_JA et al. 1959