(1R,5R,6R)-6-[2-(4-FLUOROPHENYL)-ETHYL]-2,7-DIOXA-BICYCLO-[3.3.0]-OCTAN-3,8-DIONE
Compound with spectra: 1 NMR
![(1R,5R,6R)-6-[2-(4-FLUOROPHENYL)-ETHYL]-2,7-DIOXA-BICYCLO-[3.3.0]-OCTAN-3,8-DIONE](/api/compound/BawXvGgHnzQ.png?ph=true&h=300&w=458 "(1R,5R,6R)-6-[2-(4-FLUOROPHENYL)-ETHYL]-2,7-DIOXA-BICYCLO-[3.3.0]-OCTAN-3,8-DIONE")
| SpectraBase Compound ID | BawXvGgHnzQ |
|---|---|
| InChI | InChI=1S/C14H13FO4/c15-9-4-1-8(2-5-9)3-6-11-10-7-12(16)19-13(10)14(17)18-11/h1-2,4-5,10-11,13H,3,6-7H2/t10-,11-,13-/m1/s1 |
| InChIKey | WVJZOHTUQCJUSD-NQBHXWOUSA-N |
| Mol Weight | 264.25 g/mol |
| Molecular Formula | C14H13FO4 |
| Exact Mass | 264.079787 g/mol |
| Enantiomer InChIKey | WVJZOHTUQCJUSD-GVXVVHGQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,5R,6R,8S)-6-[2-(4-FLUOROPHENYL)-ETHYL]-8-HYDROXY-2,7-DIOXA-BICYCLO-[3.3.0]-OCTAN-3-ONE
(1R,5R,6R,8R)-6-[2-(4-FLUOROPHENYL)-ETHYL]-8-HYDROXY-2,7-DIOXA-BICYCLO-[3.3.0]-OCTAN-3-ONE
(3aR*,4S*,6aS*)-4-[(E)-2-Phenyl-1-ethenyl]perhydro-furo[3,4-b]furan-2,6-dione
(3aR*,4R*,6aS*)-4-[(E)-2-Phenyl-1-ethenyl]perhydro-furo[3,4-b]furan-2,6-dione
2-Oxabicyclo[3.2.1]octan-3-one, 6-hydroxy-8-(2-phenylethyl)-, (exo,anti)-
2H-Cyclohepta[b]furan-3-carboxylic acid, octahydro-8-hydroxy-2-oxo-, (3.alpha.,3a.alpha.,8.beta.,8a.alpha.)-
4A(R)-ACETOXY-1,2,3,6-TETRA-O-ACETYL-5-DEOXY-4A-CARBA-ALPHA-D-RIBO-HEXOFURANOSE
4A(R)-ACETOXY-1,2,3,6-TETRA-O-ACETYL-5-DEOXY-4A-CARBA-BETA-D-LYXO-HEXOFURANOSE
4A(R)-ACETOXY-1,2,3,6-TETRA-O-ACETYL-5-DEOXY-4A-CARBA-ALPHA-D-XYLO-HEXOFURANOSE
(+)-GARCINIA_ACID_DMETHYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and antifungal activity of halogenated aromatic bis-γ-lactones analogous to avenaciolide | Química Nova | 2012 |