[(1R,4aR,4bS,8aS,10aR)-2,4b,8,8,10a-pentamethyl-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthren-1-yl]methanol
Compound with spectra: 1 NMR, and 1 MS (GC)
![[(1R,4aR,4bS,8aS,10aR)-2,4b,8,8,10a-pentamethyl-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthren-1-yl]methanol](/api/compound/DYwYr3GVeY3.png?ph=true&h=300&w=458 "[(1R,4aR,4bS,8aS,10aR)-2,4b,8,8,10a-pentamethyl-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthren-1-yl]methanol")
| SpectraBase Compound ID | DYwYr3GVeY3 |
|---|---|
| InChI | InChI=1S/C20H34O/c1-14-7-8-17-19(4,15(14)13-21)12-9-16-18(2,3)10-6-11-20(16,17)5/h7,15-17,21H,6,8-13H2,1-5H3/t15-,16+,17+,19+,20+/m1/s1 |
| InChIKey | URRUSDHNWZECKY-ORZNMBHWSA-N |
| Mol Weight | 290.5 g/mol |
| Molecular Formula | C20H34O |
| Exact Mass | 290.260966 g/mol |
| Enantiomer InChIKey | URRUSDHNWZECKY-AZNNDXHDSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | KC-1983-138-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1S,4aS,4bR,8aR,10aS)-1-(iodanylmethyl)-2,4b,8,8,10a-pentamethyl-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthrene
isocopal-12-ene-15-carbonitrile
Isocopal-12-en-15-propionitroile
(14R)-ENT-ISOCOPAL-13(16)-EN-15-OL
17,18,19,25-Tetranor-cheilanth-13(24)-en-16-al
13-[1'-Methylene-5',9',13'-trimethyltetradeca-4',8',12-trienyl]-4,4,8,10-tetramethyl(perhydro)naphthaleno[8,9-a]cyclopentane
13.alpha.-H-Marabaricatriene
(7S,8R,8aR,10S,10aS)-8-(4,8-Dimethyl-nona-3,7-dienyl)-1,1,4a,8a-tetramethyl-7-methylene-tetradecahydro-phenanthrene
(1.alpha.,4a.beta.,4b.alpha.,8a.beta.,10a.alpha.)]- tetradecahydro-4b,8,8,10a-tetramethyl-1-phenanthrene-carboxylic acid, methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Chemical simulation of polycyclic diterpenoid biosynthesis using mercury(II) triflate/N,N-dimethylaniline complex: mechanistic aspects of a biomimetic olefin cyclization | The Journal of Organic Chemistry | 1986 |