In the title compound, C 15 H 19 NO 2 , inversion-related molecules are linked into dimers by interactions between the hydroxyl groups and the nitrile groups. C-HÁ Á ÁO hydrogen bonds join the dimers into an infinite ladder-like chain.
1-Cyclohexylmethoxymethyl-5-[2-hydroxy-1-(hydroxymethyl)ethylamino]cyclohexane-1,2,3,4-tetraol
✍ Scribed by Zhang, Hong ;Li, Wei-Fen ;Wang, Kui-Wu ;Pan, Yuan Jiang
- Publisher
- International Union of Crystallography
- Year
- 2004
- Tongue
- English
- Weight
- 440 KB
- Volume
- 60
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
The title compound, C 17 H 33 NO 7 , contains two six-membered rings which adopt chair conformations. The molecular packing is governed by intermolecular OÐHÁ Á ÁO hydrogen bonding.
📜 SIMILAR VOLUMES
In the molecule of the title compound, C~28~H~42~O~2~, the two cyclohexane rings adopt chair conformations. The olefinic bond and carbonyl group are approximately coplanar.
The title compound, C 19 H 23 N 3 O 5 , adopts the keto±amine tautomeric form and the con®guration around the ÐN NÐ double bond is trans. There is an intramolecular NÐHÁ Á ÁO hydrogen bond and intermolecular OÐHÁ Á ÁO interactions, forming a three-dimensional network.
Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.005 A Ê Disorder in main residue R factor = 0.047 wR factor = 0.124 Data-to-parameter ratio = 15.9 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.