#63D;(S)-[3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-5,6-DIHYDROPYRIDINE-1(2H)-YL]-(MORPHOLINO)-METHANON
Compound with spectra: 1 NMR
![#63D;(S)-[3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-5,6-DIHYDROPYRIDINE-1(2H)-YL]-(MORPHOLINO)-METHANON](/api/compound/EByZJBuWRB8.png?ph=true&h=300&w=458 "#63D;(S)-[3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-5,6-DIHYDROPYRIDINE-1(2H)-YL]-(MORPHOLINO)-METHANON")
| SpectraBase Compound ID | EByZJBuWRB8 |
|---|---|
| InChI | InChI=1S/C24H26F3N3O5S/c25-24(26,27)36(33,34)30-16-20(14-22(30)21-7-5-19(17-31)6-8-21)4-3-18-2-1-9-29(15-18)23(32)28-10-12-35-13-11-28/h2,5-8,14,22,31H,1,9-13,15-17H2/t22-/m0/s1 |
| InChIKey | OMGKNGZCKFIJAY-QFIPXVFZSA-N |
| Mol Weight | 525.54 g/mol |
| Molecular Formula | C24H26F3N3O5S |
| Exact Mass | 525.154527 g/mol |
| Enantiomer InChIKey | OMGKNGZCKFIJAY-JOCHJYFZSA-N |
| Racemate InChIKey | OMGKNGZCKFIJAY-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(E)-3-Phenyl-1-(6'-phenyl-1'-tosyl-1',2',5',6'-tetrahydropyridin-3'-yl)-prop-2-en-1-one
#56;(R)-2-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-5-[(1-TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROPYRIDIN-3
DWKZWCHKTSZXGA-UHFFFAOYSA-N
3-Methyl-3-[3-N-(phenylsulfonyl)-N-(1-methoxycarbonylethyl)amino-2-methylenepropyl]-2,3-dihydrobenzofuran
1-Phenyl-2-tosyl-1,2,3,4-tetrahydroisoquinoline
2H-pyrrol-2-one, 4-acetyl-1,5-dihydro-3-hydroxy-5-(4-hydroxyphenyl)-1-[2-(4-morpholinyl)ethyl]-
4-Acetyl-5-(4-bromo-phenyl)-1-(3-dimethylamino-propyl)-3-hydroxy-1,5-dihydro-pyrrol-2-one
nitric acid 3-(4-ketospiro[1,3-benzoxazine-2,1'-cyclohexane]-3-yl)propyl ester
NILUDIPINE
2',3'-[2-METHYL-2-(4-METHYL-3-PENTENYL)-DIHYDROPYRANE]-4,4'-DIHYDROXYCHALCONE;XANTHOANGELOL-I
| 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 |