LBF12000BC17: Difference between revisions
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{{Lipid/Header}} | |||
{{Hierarchy|{{PAGENAME}}}} | {{Hierarchy|{{PAGENAME}}}} | ||
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|LipidBank=DFA7111 | |LipidBank=DFA7111 | ||
|LipidMaps=LMFA01020143 | |LipidMaps=LMFA01020143 | ||
|SysName=2- | |SysName=2-Methylenedodecanoic acid | ||
|Common Name=&&2- | |Common Name=&&2-Decylacrylic acid&&2-Methylenelauric acid&& | ||
|Melting Point=33.3 - 34.2°C [[Reference:Izawa_M:,Bull. Chem. Soc. Jpn.,1952,25,182|{{RelationTable/GetFirstAuthor|Reference:Izawa_M:,Bull. Chem. Soc. Jpn.,1952,25,182}}]] | |Melting Point=33.3 - 34.2°C [[Reference:Izawa_M:,Bull. Chem. Soc. Jpn.,1952,25,182|{{RelationTable/GetFirstAuthor|Reference:Izawa_M:,Bull. Chem. Soc. Jpn.,1952,25,182}}]] | ||
|UV Spectra= | |UV Spectra= lambda 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 | |IR Spectra=C=CH2: 10.54 mu [[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= | |||
}} | }} | ||
{{Lipid/Footer}} | |||
Latest revision as of 21:00, 14 April 2010
| LipidBank Top (トップ) |
Fatty acid (脂肪酸) |
Glycerolipid (グリセロ脂質) |
Sphingolipid (スフィンゴ脂質) |
Journals (雑誌一覧) |
How to edit (ページの書き方) |
| IDs and Links | |
|---|---|
| LipidBank | DFA7111 |
| LipidMaps | LMFA01020143 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF12000BC17 |
| 2-Decylacrylic acid | |
|---|---|
| |
| Structural Information | |
| 2-Methylenedodecanoic 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 | λ max 210nm Allen_CF et al. |
| IR Spectra | C=CH2: 10.54 μ Freeman_NK |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | ||||||||||||||||||||
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