(S)-[3-[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-5,6-DIHYDROPYRIDIN-1(2H)-YL]-(MORPHOLINO)-METHANONE
Compound with spectra: 1 NMR
![(S)-[3-[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-5,6-DIHYDROPYRIDIN-1(2H)-YL]-(MORPHOLINO)-METHANONE](/api/compound/LKLErnxLq1T.png?ph=true&h=300&w=458 "(S)-[3-[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-5,6-DIHYDROPYRIDIN-1(2H)-YL]-(MORPHOLINO)-METHANONE")
| SpectraBase Compound ID | LKLErnxLq1T |
|---|---|
| InChI | InChI=1S/C22H26F3N3O5S/c23-22(24,25)34(31,32)28-14-19(12-20(28)17-5-3-16(15-29)4-6-17)18-2-1-7-27(13-18)21(30)26-8-10-33-11-9-26/h2-6,12,20,29H,1,7-11,13-15H2/t20-/m0/s1 |
| InChIKey | VKPZRDKLBGZPIW-FQEVSTJZSA-N |
| Mol Weight | 501.52 g/mol |
| Molecular Formula | C22H26F3N3O5S |
| Exact Mass | 501.154527 g/mol |
| Enantiomer InChIKey | VKPZRDKLBGZPIW-HXUWFJFHSA-N |
| Racemate InChIKey | VKPZRDKLBGZPIW-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
4-[3-chloranyl-5-(trifluoromethyl)pyridin-2-yl]oxy-6-nitro-2-phenyl-1H-indole
3,5,7-Triphenyl-1-tosyl-2,3-dihydro-1H-azepine
4-Methoxy-5-phenyl-2,5-diazabicyclo[2.2.2[octane-3,6-dione
2-keto-6-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-4-(3-nitrophenyl)-3,4-dihydro-1H-pyrimidine-5-carboxylic acid ethyl ester
2-Phenyl-3-(phenylsulfonyl)-1-tosyl-2,5-dihydro-1H-pyrrole
1H-Indole-3-acetamide, 1-[(4-chlorophenyl)methyl]-N-[4-fluoro-3-(trifluoromethyl)phenyl]-.alpha.-oxo-
4,11-Epoxyanthra[2,3-c]furan-1,3-dione, 3a,4,11,11a-tetrahydro-
6-Ethyl-4-methyldihydrofuro[2,3-h]coumarin-9-one
(S)-1-(2,4-DICHLOROBENZOYL)-3-ISOBUTYL-4-[(1'-BENZYL-4'-IMIDAZOLYL)-METHYL]-2-IMIDAZOLIDINONE
6-(5-bromo-2-fluoro-phenyl)-2-keto-3,4-dimethyl-1,6-dihydropyrimidine-5-carboxylic acid methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of skeletally diverse alkaloid-like molecules: exploitation of metathesis substrates assembled from triplets of building blocks | Beilstein Journal of Organic Chemistry | 2013 |