[(4bS,8aS)-2,4b,8,8-tetramethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]methanol
Compound with spectra: 1 NMR
![[(4bS,8aS)-2,4b,8,8-tetramethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]methanol](/api/compound/3FfuyCMQrID.png?ph=true&h=300&w=458 "[(4bS,8aS)-2,4b,8,8-tetramethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]methanol")
| SpectraBase Compound ID | 3FfuyCMQrID |
|---|---|
| InChI | InChI=1S/C19H28O/c1-13-10-14-6-7-17-18(2,3)8-5-9-19(17,4)16(14)11-15(13)12-20/h10-11,17,20H,5-9,12H2,1-4H3/t17-,19+/m0/s1 |
| InChIKey | KKNKPNWCLXGIJP-PKOBYXMFSA-N |
| Mol Weight | 272.43 g/mol |
| Molecular Formula | C19H28O |
| Exact Mass | 272.214016 g/mol |
| Enantiomer InChIKey | KKNKPNWCLXGIJP-MJGOQNOKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(4bS,8aS)-2,4b,8,8-tetramethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3-carbaldehyde
(4bS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol
12-HYDROXY-13-FORMYL-PODOCARPA-8,11,13-TRIENE
13-HYDROXY-12-METHOXY-8,11,13-PODOCARPATRIENE
12-METHOXY-13-HYDROXY-PODOCARPA-8,11,13-TRIENE
13-BROMO-12-METHOXYPODOCARPA-8,11,13-TRIENE
12-HYDROXY-13-METHOXY-8,11,13-PODOCARPATRIENE
12-N,N-diethylcarbamoyloxypodocarpa-8,11,13-triene
CYICURFSCPGZJS-NRRUETGQSA-N
15,16-Didehydro-dehydro-abietol
| Title | Journal or Book | Year |
|---|---|---|
| Facile access to optically active ring C aromatic diterpene derivatives from manool. Highly efficient syntheses of (+)-12-methyl-7-oxo-podocarpa-8,11,13-triene-13-carboxylic acid, (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12-carboxylic acid and (+)-nimbiol | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |