RH+[7E][CD3OD]2SBF6-
Compound with spectra: 1 NMR
![RH+[7E][CD3OD]2SBF6-](/api/compound/96Ir6LDkQNc.png?ph=true&h=300&w=458 "RH+[7E][CD3OD]2SBF6-")
| SpectraBase Compound ID | 96Ir6LDkQNc |
|---|---|
| InChI | InChI=1S/C38H22F24O2P2.2CH4O.6FH.Rh.Sb/c39-31(40,41)17-5-18(32(42,43)44)10-25(9-17)65(26-11-19(33(45,46)47)6-20(12-26)34(48,49)50)63-29-3-1-2-4-30(29)64-66(27-13-21(35(51,52)53)7-22(14-27)36(54,55)56)28-15-23(37(57,58)59)8-24(16-28)38(60,61)62;2*1-2;;;;;;;;/h5-16,29-30H,1-4H2;2*2H,1H3;6*1H;;/q;;;;;;;;;-1;+5/p-4/t29-,30-;;;;;;;;;;/m0........../s1/i;2*1D3,2D;;;;;;;; |
| InChIKey | JIWWEOGDLQFYKW-JVQFHFPQSA-J |
| Mol Weight | 1441.3 g/mol |
| Molecular Formula | C40H242H8F30O4P2RhSb |
| Exact Mass | 1439.989192 g/mol |
| Parent InChIKey | QUIMJLSEUCIDMR-QIXJFRDVSA-J |
| Enantiomer InChIKey | JIWWEOGDLQFYKW-NSGOFSJGSA-J |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD2Cl2 |
RH+[7A][CD3OD]2SBF6-
APLYSINONE-C
2-Chloro-3,4,5,6-tetrahydrocyclobuta[9,10]phenanthro[2,3-d][1,3]dioxole-1(2H)-one
5,7,4'-TRIHYDROXY-6-METHOXY-ISOFLAVONE-7-O-ALPHA-L-RHAMNOPYRANOSYL-(1->4)-O-ALPHA-L-ARABINOPYRANOSYL-4'-O-BETA-D-XYLOPYRANOSIDE
XGXYVPDICYRPFJ-XGTXGMFGSA-N
1,2,3,4-TETRAHYDRO-1-ALPHA,2-BETA,7-TRIHYDROXY-1-BETA,6-DIMETHYL-4-BETA-ISOPROPYLNAPHTHALENE-1-O-BETA-D-GLUCOPYRANOSIDE
Lycopodan-5-one, 12-hydroxy-15-methyl-, (15R)-
6-Amino-3-(5-chloro-2-thienyl)-4-(4-hydroxy-3-methoxy-phenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile
rac-1,1'-Bis[2,2-dimethyl-1,3-bis[2-(methoxycarbonyl)-2,2-dimethylethoxycarbonyl]cyclopropane]
2-[4-(4,5-dimethoxy-2-methylol-phenoxy)-3,5,6-trimethoxy-1-phenanthryl]ethyl-methyl-cyanamide
| Title | Journal or Book | Year |
|---|---|---|
| Electronic Effects in Asymmetric Catalysis: Structural Studies of Precatalysts and Intermediates in Rh-Catalyzed Hydrogenation of Dimethyl Itaconate and Acetamidocinnamic Acid Derivatives Using C2-Symmetric Diarylphosphinite Ligands | The Journal of Organic Chemistry | 1999 |