2,6-Bis(imidazol-1-ylmethyl)-4-methylphenol monohydrate
✍ Scribed by Zhou, Yun-Shu ;Shen, Hong ;Xu, Gang ;Huang, Wei ;Gou, Shao-Hua
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 316 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the title compound, C 15 H 16 N 4 OÁH 2 O, the two imidazole rings adopt a trans conformation with respect to the phenol plane. A hydrogen-bonded two-dimensional supramolecular network exists in the crystal structure.
📜 SIMILAR VOLUMES
In the title compound, C 18 H 16 N 4 , the two imidazole rings are twisted away from the central naphthalene ring system by 81.4 (1) and 88.4 (1) . The crystal packing is stabilized by C-HÁ Á ÁN hydrogen bonds
The title compound, C 13 H 13 N 5 Á1.5H 2 O, was synthesized by the reaction of 2,6-bis(bromomethyl)pyridine with imidazole. The asymmetric unit contains two crystallographically independent 2,6-bis(1H-imidazol-1-ylmethyl)pyridine molecules and three water molecules. The crystal packing is stabilize
In the title compound, C 12 H 15 Cl 2 NO, the piperidine ring adopts a chair conformation. An intramolecular O-HÁ Á ÁN hydrogen bond is observed. The packing of the molecules in the crystal structure is stabilized byinteractions and ClÁ Á ÁCl contacts.
In the title compound, C 9 H 12 N 4 , the asymmetric unit contains one half-molecule. The C atom of the bridging methylene group lies on a twofold rotation axis. The dihedral angle between the symmetry-related imidazole rings is 88.1 (2) .