LBF10000BC03: Difference between revisions

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|Boiling Point=147-148°C/0.8mmHg [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Boiling Point=147-148°C/0.8mmHg [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Optical=<FONT FACE="Symbol">h</FONT>27/D=1.4450 [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Optical=<FONT FACE="Symbol">h</FONT>27/D=1.4450 [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Source=
|Chemical Synthesis=Diethyl (2-hexyloctyl)malonate was heated with ethanolic KOH, and the product was heated after acidification[[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]];>.
|Metabolism=
}}
}}


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Revision as of 22:00, 24 November 2009

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Upper classes: LB LBF



4-Hexyl Decanoic Acid
LBF10000BC03.png
Structural Information
4-Hexyl Decanoic Acid
  • 4-Hexyl Decanoic Acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCC(CCCCCC)CCC(O)=O
Physicochemical Information
147-148°C/0.8mmHg Asano_M et al.
h27/D=1.4450 AsanoMet al.
Diethyl (2-hexyloctyl)malonate was heated with ethanolic KOH, and the product was heated after acidification Asano_M et al.;>.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF10000BC03 See above. Asano_M et al. 1950