Methyl 11-hydroxy-14-methoxy-7-oxopodocarpa-8,11,13-trien-19-oate
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 95vYveaXXIx |
|---|---|
| InChI | InChI=1S/C19H24O5/c1-18-8-5-9-19(2,17(22)24-4)14(18)10-12(21)15-13(23-3)7-6-11(20)16(15)18/h6-7,14,20H,5,8-10H2,1-4H3/t14?,18-,19-/m0/s1 |
| InChIKey | MBZTZRIPWDMECO-SQJZIBIZSA-N |
| Mol Weight | 332.4 g/mol |
| Molecular Formula | C19H24O5 |
| Exact Mass | 332.162374 g/mol |
| Enantiomer InChIKey | MBZTZRIPWDMECO-JDBFWQQPSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | B-51-1171-15 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
7-OXO-11,14-DIMETHOXY-ABIETA-8,11,13-TRIENE
(1S,4aS,10aR)-6-methoxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid methyl ester
METHYL-13-ISOPROPYL-12-METHOXY-7-OXOPODOCARPA-8,11,13-TRIEN-19-OATE
INUROYLEANOL
Methyl 7-oxo-13-acetyl-12-hydroxypodocarpa-8,11,13-trien-15-oate
> methyl 13 - acetyl - 12 - hydroxy - 7 - oxo - podocarpa - 8,11,13 - trien - 15 - oate
1-Phenanthrenecarboxylic acid, 7-(diethoxyphosphinyl)-1,2,3,4,4a,9,10,10a-octahydro-6-methoxy-1,4a-d imethyl-, methyl ester, [1S-(1.alpha.,4a.alpha.,10a.beta.)]-
METHYL-13-(4',4'-DIMETHYL-4',5'-DIHYDROOXAZOL-2'-YL)-12-METHOXY-PODOCARPA-8,11,13-TRIEN-19-OATE
Methyl 13-(4',4'-Dimethyl-4',5'-dihydroxazol-2'-yl)-12-methoxypodocarpa-8,11,13-trien-19-oate
METHYL-12-HYDROXY-13-(4-BETA-METHOXYCARBONYL-19-NORPODOCARPA-8,11,13-TRIEN-12-YLOXY)-PODOCARPA-8,11,13-TRI
| Title | Journal or Book | Year |
|---|---|---|
| Acid-Promoted Fries Rearrangements of Benzannulated Lactones | Australian Journal of Chemistry | 1998 |
Wiley Registry of Mass Spectral Data 12th Edition
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.