http://metabolomics.jp/mediawiki/index.php?title=LBF21406CV08&feed=atom&action=history
LBF21406CV08 - Revision history
2024-03-28T21:56:41Z
Revision history for this page on the wiki
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http://metabolomics.jp/mediawiki/index.php?title=LBF21406CV08&diff=107741&oldid=prev
Editor at 00:00, 1 October 2008
2008-10-01T00:00:00Z
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<td colspan='2' style="background-color: white; color:black;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black;">Revision as of 00:00, 1 October 2008</td>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;">{{Hierarchy|{{PAGENAME}}}}</ins></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>{{Metabolite</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>{{Metabolite</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>|LipidBank=XPR8008</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>|LipidBank=XPR8008</div></td></tr>
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http://metabolomics.jp/mediawiki/index.php?title=LBF21406CV08&diff=107740&oldid=prev
Editor at 00:00, 30 September 2008
2008-09-30T00:00:00Z
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<p><b>New page</b></p><div>{{Metabolite<br />
|LipidBank=XPR8008<br />
|LipidMaps=LMFA03120008<br />
|SysName=methyl (5Z,7E) -7- [ (R) -4-chloro-2-hydroxy-2- [ (Z) -2-octenyl ] -5-oxo-3-cyclopentenylidene ] -5-heptenoate<br />
|Common Name=&&chlorovulone I <<8025/8026>>&&<br />
|Reflactive=[<FONT FACE="Symbol">a</FONT>]<SUB><FONT SIZE=-1>D</FONT></SUB> -1.2°(C 0.17, CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<<8025>><br />
|Solubility=Chlorovulones are soluble in MeOH, EtOH, CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>, or hexane.<br />
|UV Spectra=<FONT FACE="Symbol">l</FONT><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB>(EtOH) 243 nm(<FONT FACE="Symbol">e</FONT>14600),315 nm(<FONT FACE="Symbol">e</FONT>15100)<<8025>><br />
|IR Spectra=<FONT FACE="Symbol">n</FONT><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB>(CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>)1705cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP><<8025>><br />
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(400MHz,CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<FONT FACE="Symbol">d</FONT>ppm0.88(3H,t,J=7.2Hz),1.30(6H,m),1.80(2H,quint.,J=7.4Hz),1.97(2H,brq,J=7.0Hz),2.35(2H,t,J=7.4Hz),2.42(2H,m),2.67(1H,ddd,J=0.5,7.8,14.2Hz),2.82(1H,ddd,J=0.5,7.5,14.2Hz),3.68(3H,s),5.22(1H,ttd,J=1.5,7.7,10.9Hz),5.54(1H,ttd,J=1.4,8.7,10.9Hz),6.11(1H,tdd,J=7.9,0.9,10.9Hz),6.77(1H,tdd,J=1.5,10.9,12.6Hz),7.21(1H,d,J=0.6Hz),7.33(1H,brd,J=12.6Hz).<<8025>><SUP><FONT SIZE=-1>1</FONT></SUP><SUP><FONT SIZE=-1>3</FONT></SUP>C-NMR(100MHz,CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<FONT FACE="Symbol">d</FONT>ppm13.9(q),22.4(t),24.3(t),27.1(t),27.3(t),29.0(t),31.4(t),33.2(t),33.6(t),51.6(q),77.7(s),121.7(d),123.8(d),127.9(d),134.8(d),136.4(s),137.9(s),143.6(d),154.0(d),173.6(s),187.7(s).<<8025>><br />
|NOTE Spectra=CD<FONT FACE="Symbol">l</FONT><SUB><FONT SIZE=-1>e</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB><SUB><FONT SIZE=-1>t</FONT></SUB>(EtOH)(<FONT FACE="Symbol">D</FONT><FONT FACE="Symbol">e</FONT>)nm 232(+7.6),265(-6.1),360(+3.1).<<8028>><br />
}}</div>
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