13-ACETOXY-TOTARA-8,11,13-TRIEN-7-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 5cVztG6lp91 |
|---|---|
| InChI | InChI=1S/C22H30O3/c1-13(2)19-17(25-14(3)23)9-8-15-20(19)16(24)12-18-21(4,5)10-7-11-22(15,18)6/h8-9,13,18H,7,10-12H2,1-6H3/t18-,22+/m0/s1 |
| InChIKey | CMOSQRHIPYJZED-PGRDOPGGSA-N |
| Mol Weight | 342.48 g/mol |
| Molecular Formula | C22H30O3 |
| Exact Mass | 342.219495 g/mol |
| Enantiomer InChIKey | CMOSQRHIPYJZED-GCJKJVERSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
12,13-dihydroxytotara-8,11,13-trien-7-one
14-HYDROXY-13-METHOXY-8,11,13-PODOCARPATRIENE-3,7-DIONE
14-acetyl-12-[2'-(trimethylsilyl)ethoxymethoxy]podocarpa-8,11,13-trien-7-one
1-BETA,14-DIHYDROXY-13-METHOXY-8,11,13-PODOCARPATRIEN-7-ONE
14-acetyl-12-methoxypodocarpa-8,11,13-trien-7-one
8-acetyl-6-methoxy-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
UXGFDGDPHNRIBO-OXJNMPFZSA-N
Methyl RO15 - 7 - oxo - dehydroabietate
13-ACETOXY-TOTARA-8,11,13-TRIEN-6-ALPHA-OL
| Title | Journal or Book | Year |
|---|---|---|
| The synthesis and antibacterial activity of totarol derivatives. part 3: modification of ring-B | Bioorganic & Medicinal Chemistry | 2000 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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