HMGVQWVMHOBHMA-FXMPGHHSSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | ILhhPOUFIQ8 |
|---|---|
| InChI | InChI=1S/C23H38O5/c1-18(28-19(2)24)12-8-4-5-9-13-20-16-17-22(25)21(20)14-10-6-7-11-15-23(26)27-3/h9,13,18,20-21H,4-8,10-12,14-17H2,1-3H3/b13-9+/t18-,20+,21-/m0/s1 |
| InChIKey | HMGVQWVMHOBHMA-FXMPGHHSSA-N |
| Mol Weight | 394.6 g/mol |
| Molecular Formula | C23H38O5 |
| Exact Mass | 394.271924 g/mol |
| Enantiomer InChIKey | HMGVQWVMHOBHMA-YOSMVYFFSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
11-DEOXYPROSTAGLANDIN PGE1
11-DEOXY-15-EPIPROSTAGLANDIN PGE1
(5-Z,13-E)-(8-R,12-R,15-S)-15-HYDROXY-9-OXO-PROSTA-5,13-DIENOIC_ACID
Prosta-10,13-dien-1-oic acid, 15-hydroxy-9-oxo-, (13E,15S)-
4-Penten-1-one, 1-bicyclo[2.2.1]hept-5-en-2-yl-, exo-
7-(2-(3-hydroxyoctyl)-3-oxo-4-cyclopentenyl)heptanoic acid
2-Butyl-3-keto-cyclopentanecarboxylic acid ethyl ester
4-Hexen-1-one, 1-bicyclo[2.2.1]hept-5-en-2-yl-5-methyl-, exo-
1-(2-oxocyclododecyl)propyl acetate
Methyl 2-(2'-cyclopentanonyl)undec-10-enoate
| Title | Journal or Book | Year |
|---|---|---|
| Hydroxylation of prostanoids by fungi. Synthesis of (−)-15-deoxy-19-(R)-hydroxy-PGE1 and (−)-15-deoxy-18-(S)-hydroxy-PGE1 | Canadian Journal of Chemistry | 1990 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.