LBF12000BC17: Difference between revisions

Revision as of 22:00, 24 November 2009

Upper classes: LB LBF

2-Methylenedodecanoic Acid

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
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

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 |UV Spectra=<FONT FACE="Symbol">l</FONT>max 210nm [[Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,616|{{RelationTable/GetFirstAuthor|Reference:Allen_CF:Kalm_MJ:,Org. Synth.,1963,4,616}}]]
 |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=
+|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=
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