(S)-N-[1-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-ALLYL]-2-NITROBENZENE-SULFONAMIDE
Compound with spectra: 1 NMR
![(S)-N-[1-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-ALLYL]-2-NITROBENZENE-SULFONAMIDE](/api/compound/DedNHzFxqek.png?ph=true&h=300&w=458 "(S)-N-[1-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-ALLYL]-2-NITROBENZENE-SULFONAMIDE")
| SpectraBase Compound ID | DedNHzFxqek |
|---|---|
| InChI | InChI=1S/C32H33F17N2O5SSi/c1-6-22(50-57(54,55)24-10-8-7-9-23(24)51(52)53)21-13-11-20(12-14-21)17-56-58(18(2)3,19(4)5)16-15-25(33,34)26(35,36)27(37,38)28(39,40)29(41,42)30(43,44)31(45,46)32(47,48)49/h6-14,18-19,22,50H,1,15-17H2,2-5H3/t22-/m0/s1 |
| InChIKey | RLWZMBYXQKYGRA-QFIPXVFZSA-N |
| Mol Weight | 908.7 g/mol |
| Molecular Formula | C32H33F17N2O5SSi |
| Exact Mass | 908.160799 g/mol |
| Enantiomer InChIKey | RLWZMBYXQKYGRA-JOCHJYFZSA-N |
| Racemate InChIKey | RLWZMBYXQKYGRA-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-Benzyl-2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxoethyl]carbamic acid 4-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)benzyl ester
(+)-2-(2',4'-DIMETHOXYPHENYL)-2-(2''-NITROBENZENE)-SULFONYLAMINOPROPIONALDEHYDE
4-{6-[Ethyl(1H,1H,2H,2H-perfluorooctyl)amino]benzofuran-2-yl}benzoic acid ethyl ester
AAVJEMVFNGPUQG-UHFFFAOYSA-N
2,2,3,3,4,4,6,6,7,7,8,8,9,9-Tetradecafluoro-1-oxaspiro[4.4]nonane
(Z)-1-[4-(tert-Butyl)-2-(1H,1H,2H-perfluorodec-2-en-1-yl)phenyl]-1H-pyrazole
3-[(undecafluorocyclohexyl)methoxy]-1-adamantyl methacrylate
1-TRIFLUOROMETHYL-2-METHOXYPERFLUOROCYCLOHEXANE (ISOMER 1)
UKHWOBYXCRHCDL-JPMGXVIASA-N
2-[allyl-(2-nitrophenyl)sulfonyl-amino]-N-[2-(3,4-dimethoxyphenyl)ethyl]butyramide
| 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 |