The ring itself has a somewhat flattened twist-boat conformation. C-HÁ Á ÁO interactions join the molecules into a twodimensional network running parallel to the (101) plane.
(3S)-3-Benzyloxymethyl-1,4-dioxane-2,5-dione
✍ Scribed by Kooijman, Huub ;Leemhuis, Mark ;Nostrum, Cornelus F. van ;Hennink, Wim E. ;Spek, Anthony L.
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 195 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The lactide ring in the title compound, C 12 H 12 O 5 , adopts a screw-boat conformation. C-HÁ Á ÁO interactions link the molecules into a chain in the [100] direction.
📜 SIMILAR VOLUMES
The ring itself has a boat conformation. C-HÁ Á ÁO interactions link the molecules into a chain in the [010] direction.
Single-crystal X-ray study T = 297 K Mean (C-C) = 0.004 A Disorder in main residue R factor = 0.076 wR factor = 0.204 Data-to-parameter ratio = 12.9 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
In the title compound, C 10 H 10 N 4 O 4 , the triazine ring is nearly planar. The 1,3-dioxane-4,6-dione ring exhibits a half-chair conformation. The molecule is disordered and the structure has been refined using a split model.
In the title compound C 7 H 9 NO 4 , the 1,3-dioxane-4,6-dione ring exhibits an envelope conformation. Intermolecular hydrogen bonds connect the molecules into chains. One intramolecular N-HÁ Á ÁO hydrogen bond to a carbonyl O atom is also observed, forming a six-membered ring.