(2Z,4S,5S,6S,15R)-4,5-EPOXY-6-HYDROXYHEXADEC-2-EN-15-OLIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 4J7yVH8bCFo |
|---|---|
| InChI | InChI=1S/C16H26O4/c1-12-8-6-4-2-3-5-7-9-13(17)16-14(20-16)10-11-15(18)19-12/h10-14,16-17H,2-9H2,1H3/b11-10-/t12-,13+,14-,16+/m1/s1 |
| InChIKey | IZGOODGYUHMELK-RGIWVCTASA-N |
| Mol Weight | 282.38 g/mol |
| Molecular Formula | C16H26O4 |
| Exact Mass | 282.183109 g/mol |
| Enantiomer InChIKey | IZGOODGYUHMELK-WHPTYWQGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1,4,9-Trioxaspiro[4.15]eicos-6-en-8-one, 10-methyl-, (E)-
TETRADENOLIDE;5,6-DIHYDRO-6-(1,2-DIHYDROXYHEXYL)-2-PYRONE
11,12-Dihydroxy-6,14-dimethyl-1,7-dioxacyclotetradeca-3,9-diene-2,8-dione
DG-4
DG-3
9-O-DI-[10-HYDROXY-HEPTACOSADI-7(Z),26-ENYL]-ETHER
DYSIDEOLIDE-B;(4S,5R)-4,5-DIHYDROXY-3-METHYLDODEC-2-EN-1,5-OLIDE
| Title | Journal or Book | Year |
|---|---|---|
| Synthese des Makrolid-Antibiotikums (−)-A26771B mit Photolactonisierung als Schlüsselreaktion und Computersimulation als effektive Optimierungshilfe | Helvetica Chimica Acta | 1991 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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