In the crystals of the title compound, C 19 H 24 O 8 , the molecules adopt a conformation in which the bulky 2,6-dimethoxyphenoxy and 4-hydroxy-3,5-dimethoxyphenyl groups are distant from each other. The O(phenoxy)ÐCÐCÐC(phenyl) torsion angle between these groups is À177.27 (10) . The conformation i
erythro-2-(2,6-Dimethoxyphenoxy)-1-(3,4,5-trimethoxyphenyl)-1,3-propanediol
✍ Scribed by Langer, Vratislav ;Lundquist, Knut
- Publisher
- International Union of Crystallography
- Year
- 2001
- Tongue
- English
- Weight
- 373 KB
- Volume
- 57
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
Single-crystal X-ray study T = 183 K Mean '(C±C) = 0.001 A Ê R factor = 0.044 wR factor = 0.124 Data-to-parameter ratio = 25.9
For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 183 K Mean '(C±C) = 0.003 A Ê R factor = 0.051 wR factor = 0.123 Data-to-parameter ratio = 12.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
Single-crystal X-ray study T = 183 K Mean '(C±C) = 0.002 A Ê Disorder in main residue R factor = 0.049 wR factor = 0.144 Data-to-parameter ratio = 16.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
The title compound, C 16 H 15 N 1 O 5 , is a -ketoether derivative, closely related to natural 8.4 H -oxyneolignans, which are of interest because of their antiprotozoal activity. The nitro group is not coplanar with the aromatic ring, as is shown by a torsion angle of 49.4 (3) . The molecules are c