(1R,6S,7S,8S,9S)-8-CYCLOHEXYL-9-METHYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE
Compound with spectra: 1 NMR
![(1R,6S,7S,8S,9S)-8-CYCLOHEXYL-9-METHYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE](/api/compound/6binmR1a5uj.png?ph=true&h=300&w=458 "(1R,6S,7S,8S,9S)-8-CYCLOHEXYL-9-METHYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE")
| SpectraBase Compound ID | 6binmR1a5uj |
|---|---|
| InChI | InChI=1S/C26H37NO3/c1-26-20-16-22(24(26)19-12-6-3-7-13-19)25(30-27(26)28-17-20)29-23-15-9-8-14-21(23)18-10-4-2-5-11-18/h2,4-5,10-11,19-25H,3,6-9,12-17H2,1H3/t20-,21+,22-,23-,24-,25-,26+/m1/s1 |
| InChIKey | VBASXKFNCNJXCE-PMZIORBOSA-N |
| Mol Weight | 411.6 g/mol |
| Molecular Formula | C26H37NO3 |
| Exact Mass | 411.277344 g/mol |
| Enantiomer InChIKey | VBASXKFNCNJXCE-LWBJWRMRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C6D6 |
Pyrrolo[2,1-a]isoquinoline, 5,6-dihydro-3-(2-thienyl)-1-(2-thienylmethyl)-
Estra-1,3,5(10)-trien-16-one, 3-methoxy-17-[(trimethylsilyl)oxy]-, O-methyloxime, (17.beta.)-
benzoic acid, 3-[[1-oxo-3-(2,4,8,10-tetramethylpyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidin-3-yl)propyl]amino]-, ethyl ester
2-PHENYL-3,3-DIFLUORO-5-TRIISOPROPYLSILYL-7,7-DICARBOETHOXY-BICYCLO-[4.2.0]-OCTA-1,4-DIENE
FERRUGINYL-NAPROXENATE
(rel-14b.alpha.,8a.alpha.,14a.beta.)-(+-)-8,8a,9,10,11,12,13,14,14a,14b-Decahydro-8-phenylcycloocta[3,4]pyrazolo[5,1-a]isoquinoline
Isoxazolo[2,3-b][1,2]benzoxazine-2-carboxylic acid, decahydro-4-phenyl-8a-[(trimethylsilyl)oxy]-, methyl ester
endo-3,9-Dibromo-9-deuterio-4-(bromodeuteriomethyl)camphor
| Title | Journal or Book | Year |
|---|---|---|
| Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process | The Journal of Organic Chemistry | 1998 |