#63C;(S)-3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-N-(PYRIDIN-3-YL)-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI
Compound with spectra: 1 NMR
![#63C;(S)-3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-N-(PYRIDIN-3-YL)-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI](/api/compound/ByHlLflJ8cD.png?ph=true&h=300&w=458 "#63C;(S)-3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-N-(PYRIDIN-3-YL)-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI")
| SpectraBase Compound ID | ByHlLflJ8cD |
|---|---|
| InChI | InChI=1S/C25H23F3N4O4S/c26-25(27,28)37(35,36)32-16-20(13-23(32)21-9-7-19(17-33)8-10-21)6-5-18-3-2-12-31(15-18)24(34)30-22-4-1-11-29-14-22/h1,3-4,7-11,13-14,23,33H,2,12,15-17H2,(H,30,34)/t23-/m0/s1 |
| InChIKey | MFMFYWLLAUKITK-QHCPKHFHSA-N |
| Mol Weight | 532.54 g/mol |
| Molecular Formula | C25H23F3N4O4S |
| Exact Mass | 532.139211 g/mol |
| Enantiomer InChIKey | MFMFYWLLAUKITK-HSZRJFAPSA-N |
| Racemate InChIKey | MFMFYWLLAUKITK-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(S)-6-[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-3,4-DIHYDRO-1H-AZEPIN-2(7H)-ONE
(E)-3-(p-Chlorophenyl)-1-(6'-(p'-chlorophenyl)-1'-tosyl-1',2',5',6'-tetrahydropyridin-3'-yl)-prop-2-en-1-one
BALIBALOSIDE
(E)-3-(p-Fluorophenyl)-1-(6'-(p'-fluorophenyl)-1'-tosyl-1',2',5',6'-tetrahydropyridin-3'-yl)-prop-2-en-1-one
4H-pyran-3-carboxylic acid, 6-amino-5-cyano-2-methyl-4-[4-(trifluoromethyl)phenyl]-, ethyl ester
5-(3-methoxyphenyl)-1-(4-methylphenyl)-3-(4-toluidino)-1,5-dihydro-2H-pyrrol-2-one
N-(2,4,6-Trimethylbenzenesulfonyl)-2-(2,2-dimethyl-1-oxopropyl)-3-(4-methylphenyl)aziridine
4-acetyl-1-(2-ethylhexyl)-5-(4-ethylphenyl)-3-hydroxy-1,5-dihydro-2H-pyrrol-2-one
4-(4H-pyrrolo[1,2-a]indol-4-yl)morpholine
Dimethyl 1,2,6-trimethyl-4-(2-thienyl)-1,4-dihydro-3,5-pyridinedicarboxylate
| 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 |