METHYL-(2'R,3'R,4'R,5'R)-2-[2'-(3-CHLOROPHENYL)-ETHYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE
Compound with spectra: 1 NMR
![METHYL-(2'R,3'R,4'R,5'R)-2-[2'-(3-CHLOROPHENYL)-ETHYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE](/api/compound/A0NXBVMsVZV.png?ph=true&h=300&w=458 "METHYL-(2'R,3'R,4'R,5'R)-2-[2'-(3-CHLOROPHENYL)-ETHYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE")
| SpectraBase Compound ID | A0NXBVMsVZV |
|---|---|
| InChI | InChI=1S/C18H23ClO5/c1-18(2)23-16-13(10-15(20)21-3)14(22-17(16)24-18)8-7-11-5-4-6-12(19)9-11/h4-6,9,13-14,16-17H,7-8,10H2,1-3H3/t13-,14-,16-,17-/m1/s1 |
| InChIKey | ABSLOEVEQLYBPQ-MUIFIZLQSA-N |
| Mol Weight | 354.83 g/mol |
| Molecular Formula | C18H23ClO5 |
| Exact Mass | 354.123402 g/mol |
| Enantiomer InChIKey | ABSLOEVEQLYBPQ-OTRWWLKZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6-Bromo-3,6-dideoxy-3-C-(methoxycarbonylmethyl)-1,2-O-isopropylidene-.alpha.-D-allofuranose
METHYL-(2'R,3'R,4'R,5'R)-2-[(Z)-2'-(3-CHLOROPHENYL)-VINYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE
6-O-Benzyl-3-deoxy-1,2-O-isopropylidene-3-C-[2-(4-methoxybenzyloxy)ethyl]-.beta.-L-talofuranose
.alpha.-D-Allofuranose, 3-deoxy-3-[[(4-methoxyphenyl)methoxy]methyl]-1,2-O-(1-methylethylidene)-6-O-(phenylmethyl)-
.alpha.-D-Allofuranose, 5,6-anhydro-3-deoxy-3-[[(4-methoxyphenyl)methoxy]methyl]-1,2-O-(1-methylethylidene)-
2,3-(Isopropylidenedioxy)-4-methyl-6-hydroxycyclopenta[b]tetrahydrofuran isomer
YKSFARWYNBQERF-FOVGZEBNSA-N
YKSFARWYNBQERF-WJYNVNEKSA-N
2,3-(Isopropylidenedioxy)-5-methyl-7-hydroxy-1-oxabicyclo[3.3.0]octane
Ethyl 5,6-Dideoxy-1,2-O-isopropylidene-3-O-(S-methylthiocarbonate)-.alpha.,D-xylo-heptofuranuronate
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and antifungal activity of halogenated aromatic bis-γ-lactones analogous to avenaciolide | Química Nova | 2012 |