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(Z)-9-FORMYL-3-(2-HYDROXYETHYL)-8-[2-(METHOXYCARBONYL)-ETHYL]-2,7-DIMETHYLDIPYRRIN-1(10H)-ONE

Compound with spectra: 1 NMR, and 1 MS (GC)

(Z)-9-FORMYL-3-(2-HYDROXYETHYL)-8-[2-(METHOXYCARBONYL)-ETHYL]-2,7-DIMETHYLDIPYRRIN-1(10H)-ONE
SpectraBase Compound ID 6tBKYb41STE
InChI InChI=1S/C18H22N2O5/c1-10-12(4-5-17(23)25-3)16(9-22)19-14(10)8-15-13(6-7-21)11(2)18(24)20-15/h8-9,19,21H,4-7H2,1-3H3,(H,20,24)/b15-8-
InChIKey VUWIDFWDBOUZQS-NVNXTCNLSA-N
Mol Weight 346.38 g/mol
Molecular Formula C18H22N2O5
Exact Mass 346.152872 g/mol

View Spectrum of (Z)-9-FORMYL-3-(2-HYDROXYETHYL)-8-[2-(METHOXYCARBONYL)-ETHYL]-2,7-DIMETHYLDIPYRRIN-1(10H)-ONE

MS (GC) Spectrum
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Source of Spectrum H-72-524-10

View Spectrum of (Z)-9-FORMYL-3-(2-HYDROXYETHYL)-8-[2-(METHOXYCARBONYL)-ETHYL]-2,7-DIMETHYLDIPYRRIN-1(10H)-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:CD3OD
  • 1H-Pyrrole-3-propanoic acid, 5-[[1,5-dihydro-3-(2-hydroxyethyl)-4-methyl-5-oxo-2H-pyrrol-2-ylidene]methyl]-2-formyl-4-methyl-, methyl ester, (Z)-
1H-Pyrrole-3-propanoic acid, 5-[(3-ethyl-1,5-dihydro-4-methyl-5-oxo-2H-pyrrol-2-ylidene)methyl]-2-formyl-4-methyl-, hexadecyl ester, (Z)-
Carbamic acid, [2-[[3-[5-[(3-ethyl-1,5-dihydro-4-methyl-5-oxo-2H-pyrrol-2-ylidene)methyl]-2-formyl-4-methyl-1H-pyrrol-3-yl]-1-oxopropyl]amino]ethyl]-, phenylmethyl ester, (Z)-
(-)-(S)-3-(4-Ethyl-3,8,10-trimethyl-2-oxo-1,11-dihydrodipyrrin-9-yl)butanoic acid
SODIUM-TAURO-BETA-METHYL-XANTHO-BILIRUBINATE
3-ETHYL-8-(PARA-ISOBUTOXYCARBONYLPHENYL)-2,7,9-TRIMETHYL-1,10-DIHYDRO-11H-DIPYRRIN-1-ONE
8-(PARA-CARBOXYPHENYL)-3-ETHYL-2,7,9-TRIMETHYL-1,10-DIHYDRO-11H-DIPYRRIN-1-ONE
8-(5-ETHOXYCARBONYPENTANOYL)-9-BUTYL-2,3-DIETHYL-DIPYRRIN-1-ONE
(Z)-[(3,5-DIMETHYL-4-(2-METHOXYCARBONYLETHYL)-1H-PYRROL-2-YL)-METHYLIDENYL]-ISOINDOLINONE
21H,23H-Porphine, 2,3,7,8,12,13,17,18-octaethyl-22,24-dihydro-21,23-dimethyl-
(Z)-3-[(3,5-DIMETHYL-4-(2-METHOXYCARBONYLETHYL)-1H-PYRROL-2-YL)-METHYLIDENYL]-INDOLIN-2-ONE
Title Journal or Book Year
Syntheses of Bile Pigments. Part 16. Synthesis of a vinyl-substituted 2,3-Dihydrobilinedione: Possible role of this new class of bile pigments in phycobilin biosynthesis Helvetica Chimica Acta 1989
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