LBF08106SC02: Difference between revisions

Latest revision as of 07:47, 18 October 2010

Upper classes: LB LBF

trans-α-Octenoic acid

Structural Information
	trans-2-Octenoic acid
	trans-α-Octenoic acid 2E-Octenoic acid
	C8:1
Formula	C8H14O2
Exact Mass	142.09937969199999
Average Mass	142.19556
SMILES	`CCCCCC=CC(O)=O`
Physicochemical Information

	143°C at 15mmHg
	d15 4 0.945

	1.462
	Bachman_GB Knight_JA et al.

	Synthetic.




Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies	ID	Compound Name	Reference	Comment
n.a.	LBF08106SC02	See above.	Bachman_GB 1923
n.a.	LBF08106SC02	See above.	Knight_JA et al. 1959

@@ Line 1: / Line 1: @@
+{{Lipid/Header}}
 {{Hierarchy|{{PAGENAME}}}}
-{{Lipid/Header}}
 {{Metabolite
@@ Line 7: / Line 7: @@
 |LipidMaps=LMFA01030018
 |SysName=trans-2-Octenoic acid
-|Common Name=&&trans-alpha-Octenoic acid&&trans-2-Octenoic acid&&
+|Common Name=&&trans-alpha-Octenoic acid&&2E-Octenoic acid&&
 |Boiling Point=143°C at 15mmHg
-|Density=dX<sub>4</sub><sup>15</sup> 0.945
+|Density=d^{15}_4  0.945
-|Optical=1.462
+|Refractive=1.462
-|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}}]]<!--0156--><!--0289-->[[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=Synthetic.
+|Metabolism=
+|Symbol=C8:1
 }}
 {{Lipid/Footer}}