(8R(*),12R(*),13E)-15-hydroxy-9-oxo-10-oxaprost-14-en-5-ynoic acid
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 8F7Cv6M8k0C |
|---|---|
| InChI | InChI=1S/C19H28O5/c1-2-3-6-9-16(20)13-12-15-14-24-19(23)17(15)10-7-4-5-8-11-18(21)22/h12-13,15-17,20H,2-3,5-6,8-11,14H2,1H3,(H,21,22)/b13-12+/t15-,16?,17+/m1/s1 |
| InChIKey | GLYWTDYAPNKXOM-FHTCIYEWSA-N |
| Mol Weight | 336.43 g/mol |
| Molecular Formula | C19H28O5 |
| Exact Mass | 336.193674 g/mol |
| Enantiomer InChIKey | GLYWTDYAPNKXOM-OFNVMITKSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | B-40-1264-24 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
4-Hydroxybutyl bicyclo[2.2.1]hept-2-ene-5-carboxylate
Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 2-methoxyethyl ester
Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 2-ethoxyethyl ester
(4AR,7R,8AS)-3,4,4A,7,8,8A-HEXAHYDRO-7-METHYL-1H-2-BENZOPYRAN-1-ONE
(1R,2R,4R)-BICYCLO-[2.2.1]-HEPT-5-ENE-2-CARBOXYLIC-ACID-2,2,2-TRIFLUORO-ETHYLESTER
5-bicyclo[2.2.1]hept-2-enecarboxylic acid tert-butyl ester
5-EXO-METHOXYCARBONYLBICYCLO-[2.2.2]-OCT-2-ENE
Methyl O-deuteroprostaglandin A1
9R-PHYTOPROSTANE-F1-TYPE-II-METHYLESTER
ENT-9R-PHYTOPROSTANE-F1-TYPE-II-METHYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| The Preparation of 9-Oxo-10-Oxaprostanoids by the Conjugate Addition of (E)-1-(Phenylthio)Oct-2-Enyllithium to γ-Crotonolactone and the Direct Alkylation of the Derived Enolate With Methyl 7-Bromohept-5-ynoate and Related Electrophiles | Australian Journal of Chemistry | 1987 |
This compound is available in the following databases:
Wiley Registry of Mass Spectral Data 2023
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.