1,3,5-TRIMETHOXY-2-[(1R,2S,3S,4R,5S)-2,3,4-TRI-O-BENZYL-2,3,4,5-TETRAHYDROXYCYCLOHEXYL]-BENZENE
Compound with spectra: 1 NMR
![1,3,5-TRIMETHOXY-2-[(1R,2S,3S,4R,5S)-2,3,4-TRI-O-BENZYL-2,3,4,5-TETRAHYDROXYCYCLOHEXYL]-BENZENE](/api/compound/2l0BRbdEbCT.png?ph=true&h=300&w=458 "1,3,5-TRIMETHOXY-2-[(1R,2S,3S,4R,5S)-2,3,4-TRI-O-BENZYL-2,3,4,5-TETRAHYDROXYCYCLOHEXYL]-BENZENE")
| SpectraBase Compound ID | 2l0BRbdEbCT |
|---|---|
| InChI | InChI=1S/C36H40O7/c1-38-28-19-31(39-2)33(32(20-28)40-3)29-21-30(37)35(42-23-26-15-9-5-10-16-26)36(43-24-27-17-11-6-12-18-27)34(29)41-22-25-13-7-4-8-14-25/h4-20,29-30,34-37H,21-24H2,1-3H3/t29-,30-,34-,35+,36+/m1/s1 |
| InChIKey | IGZMJNWFULFHAP-QXJSLAGPSA-N |
| Mol Weight | 584.7 g/mol |
| Molecular Formula | C36H40O7 |
| Exact Mass | 584.277404 g/mol |
| Enantiomer InChIKey | IGZMJNWFULFHAP-VEHVIUBUSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
4-ACETYL-1,3,5-TRIHYDROXY-2-C-(BETA-D-MANNOPYRANOSYL)-BENZENE
phenyl 2-(4-methylphenylsulfide)-3,4,6-tri-O-benzyl-b-C-glucoside
RAC-(1R,4AR,9BS)-7,9-DIMETHOXY-1-(1-METHYLETHYL)-1,2,3,4,4A,9B-HEXAHYDRODIBENZOFURAN-4-ONE
(1R,4aR,9bS)-1-isopropyl-7,9-dimethoxy-2,3,4a,9b-tetrahydro-1H-dibenzofuran-4-one
SECUNDIFLOROL-H;5,7,3'-TRIHYDROXY-2',4'-DIMETHOXY-ISOFLAVANONE
.alpha.-D-xylo-Hexodialdo-1,4-furanose, 5-deoxy-1,2-O-(1-methylethylidene)-6-C-phenyl-3-O-(phenylmethyl)-
(1R)-2,6-ANHYDRO-1-PHENYL-1-O-[2-(TRIMETHYLSILYL)-ETHOXYMETHYL]-4-O-METHYL-5,7-O-BENZYLIDENE-ALPHA-D-ALTRO-HEPTITOL
BENZYL-2,4-DI-O-ACETYL-3-O-(2,3,4,6-TETRA-O-BENZYL-BETA-D-GLUCOPYRANOSYL)-BETA-D-RIBOPYRANOSIDE
RAC-(5AR,9R,9AS)-1,3-DIMETHOXY-9-(1-METHYLETHYL)-6-METHYLIDENE-5A,6,7,7,9,9A-HEXAHYDRODIBENZOFURAN
| Title | Journal or Book | Year |
|---|---|---|
| Triisobutylaluminium (TIBAL) Promoted Rearrangement of C-glycosides | Molecules | 2005 |