(3R,3AS,5R,6AR)-5-[(3S,3AR,6R,6AR)-6-(DODECYLOXY)-HEXAHYDROFURO-[3,2-B]-FURAN-3-YLOXY]-HEXAHYDROFURO-[3,2-B]-FURAN-3-YL-ACETATE
Compound with spectra: 1 NMR
![(3R,3AS,5R,6AR)-5-[(3S,3AR,6R,6AR)-6-(DODECYLOXY)-HEXAHYDROFURO-[3,2-B]-FURAN-3-YLOXY]-HEXAHYDROFURO-[3,2-B]-FURAN-3-YL-ACETATE](/api/compound/4y9zVh82U7U.png?ph=true&h=300&w=458 "(3R,3AS,5R,6AR)-5-[(3S,3AR,6R,6AR)-6-(DODECYLOXY)-HEXAHYDROFURO-[3,2-B]-FURAN-3-YLOXY]-HEXAHYDROFURO-[3,2-B]-FURAN-3-YL-ACETATE")
| SpectraBase Compound ID | 4y9zVh82U7U |
|---|---|
| InChI | InChI=1S/C26H44O8/c1-3-4-5-6-7-8-9-10-11-12-13-28-20-15-30-26-22(17-31-25(20)26)33-23-14-19-24(34-23)21(16-29-19)32-18(2)27/h19-26H,3-17H2,1-2H3/t19-,20-,21-,22+,23-,24+,25-,26-/m1/s1 |
| InChIKey | QGHWVCQSIHLFQI-LIUOYIQUSA-N |
| Mol Weight | 484.6 g/mol |
| Molecular Formula | C26H44O8 |
| Exact Mass | 484.303618 g/mol |
| Enantiomer InChIKey | QGHWVCQSIHLFQI-CQAXQRDVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2R,3AR,6R,6AS)-6-(BENZYLOXY)-2-[(3S,3AR,6R,6AR)-6-(DODECYLOXY)-HEXAHYDROFURO-[3,2-B]-FURAN-3-YLOXY]-HEXAHYDROFURO-[3,2-B]-FURAN
Tri-O-methyl-amylose fragment
heneicosa-o-methyl-beta-cyclodextrin
γ-Methyl-Cyclodextrin
Per-O-methyl-cyclohexaamylose
α-Methyl-Cyclodextrin W6 M1,8
alpha-D-MANNOPYRANOSIDE, METHYL-3,6-DI-O-ACETYL-2,4-DI-O-HEPTYL-
Methyl 3,6-di-O-acetyl-2,4-di-O-heptylhexopyranoside
.alpha.-D-Glucofuranose, 1,2-O-1,2-ethanediyl-, triacetate
Methyl 6,7-di-O-acetyl-2,3,4-tri-O-methylheptopyranoside
| Title | Journal or Book | Year |
|---|---|---|
| Iodoetherification of Isosorbide-Derived Glycals: Access to a Variety ofO-Alkyl orO-Aryl Isosorbide Derivatives | European Journal of Organic Chemistry | 2013 |