N-[(2R)-1-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-BIS-(PROPAN-2-YL)-SILYL]-OXY]-PENT-4-EN-2-YL]-2-NITROBENZENE-1-SULFONAMIDE
Compound with spectra: 1 NMR
![N-[(2R)-1-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-BIS-(PROPAN-2-YL)-SILYL]-OXY]-PENT-4-EN-2-YL]-2-NITROBENZENE-1-SULFONAMIDE](/api/compound/2G3KhyTQu3E.png?ph=true&h=300&w=458 "N-[(2R)-1-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-BIS-(PROPAN-2-YL)-SILYL]-OXY]-PENT-4-EN-2-YL]-2-NITROBENZENE-1-SULFONAMIDE")
| SpectraBase Compound ID | 2G3KhyTQu3E |
|---|---|
| InChI | InChI=1S/C27H31F17N2O5SSi/c1-6-9-17(45-52(49,50)19-11-8-7-10-18(19)46(47)48)14-51-53(15(2)3,16(4)5)13-12-20(28,29)21(30,31)22(32,33)23(34,35)24(36,37)25(38,39)26(40,41)27(42,43)44/h6-8,10-11,15-17,45H,1,9,12-14H2,2-5H3/t17-/m1/s1 |
| InChIKey | AQJACBMCAVPGGC-QGZVFWFLSA-N |
| Mol Weight | 846.67 g/mol |
| Molecular Formula | C27H31F17N2O5SSi |
| Exact Mass | 846.145149 g/mol |
| Enantiomer InChIKey | AQJACBMCAVPGGC-KRWDZBQOSA-N |
| Racemate InChIKey | AQJACBMCAVPGGC-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
#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
(4-{Tris[2-(perfluorohexyl)ethyl]silyl}benzyl) 2-{[(Furfuryl)amino]carbonyl}phenylcarbamate
2-{2-Methoxy-6-(3',3',4',4',5',5',6',6',7',7',8',8',8'-tridecafluorooctyl)phenyl}pyridine
4-[(Heptadecafluorodecyl)dimethylsilyl]-benzenemethanol
5-TRIDECAFLUOROHEXYL-5-METHOXY-2-METHYLISOXAZOLIDINE
5-(6-Chloro-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-hexyl)-3-methyl-2-isoxazolin-5-ol
3-Benzoyl-4-(2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptyl)oxazolidin-2-one
ZDKGSVFCDFTLNR-PTZVLDCSSA-N
1-FLUOROSULPHONYL-1,1,2,2,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-EICOSAFLUORO-13-IODOHEPTADECANE
cis and trans-Diethyl 4-(tridecafluoroheptyl)-3-benzylcyclopentane-1,1-dicarboxylate
| 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 |