Z-ISOMER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | HT3ecPjViA7 |
|---|---|
| InChI | InChI=1S/C24H36O10/c1-21(2)27-13-11(25-19-17(15(13)29-21)31-23(5,6)33-19)9-10-12-14-16(30-22(3,4)28-14)18-20(26-12)34-24(7,8)32-18/h9-20H,1-8H3/b10-9-/t11-,12-,13+,14+,15+,16+,17-,18-,19-,20-/m1/s1 |
| InChIKey | OGBLHAKLBXMXBO-FIIGPGBASA-N |
| Mol Weight | 484.5 g/mol |
| Molecular Formula | C24H36O10 |
| Exact Mass | 484.230847 g/mol |
| Enantiomer InChIKey | OGBLHAKLBXMXBO-MWZXHBMQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
.alpha.-D-Galactopyranose, 6-deoxy-6-[(2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)imino]-1,2:3,4-bis-O-(1-methylethylidene)-
Ethyl (Z)-6,7-dideoxy-[1,2:3,4]-di-O-isopropylidene-6.alpha.-D-galacto-octeno-pyrannuronate
Ethyl (E)-6,7-dideoxy-[1,2:3,4]-di-O-isopropylidene-6.alpha.-D-galacto-octeno-pyrannuronate
6,7,9-TRIDEOXY-8-HYDROXYIMINO-1,2:3,4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTO-NON-6-(E)-ENPYRANOSE
(E)-7-Benzoyl-6,7-dideoxy-1,2:3,4-di-O-isopropylidene-6.alpha.-D-galacto-hepteno-1,5-pyrannose
D-glycero-.alpha.-D-galacto-Oct-7-enopyranose, 8-bromo-7,8-dideoxy-1,2:3,4-bis-O-(1-methylethylidene)-, (E)-
BETA-D-GALACTO-PYRANOSE-(1->6)-1,2:3,4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOSE
YLYWSJMFJUTLDG-ATIFRJIPSA-N
6-0-(ALPHA-D-RIBOPYRANOSYL)-1,2:3,4-DI-O-ISOPROPYLIDEN-ALPHA-D-GALACTOPYRANOSE
O-ISOPROPYL-S-(1,2:3,4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOS-6-YL)-DITHIOCARBONATE
| Title | Journal or Book | Year |
|---|---|---|
| Extended Alkenyl Glycosides by Ruthenium-Catalyzed Cross-Metathesis Reaction and Application toward Novel C-Linked Pseudodisaccharides | The Journal of Organic Chemistry | 1999 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.