2,4-Dichloro-6-(piperidin-1-yl)-1,3,5-triazine
✍ Scribed by Deng, Yi ;Wang, Xiao-Ji ;Wen, Fei ;Wang, Lei ;Zhang, Yan
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 117 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the crystal structure of the title compound, C 8 H 10 Cl 2 N 4 ,stacking interactions are observed between the triazine rings. These interactions link the molecules into a dimer, packing along the a axis. The piperidine ring adopts a chair conformation.
📜 SIMILAR VOLUMES
This paper reports the synthesis of the title compound, C 7 H 8 Cl 2 N 4 O, and its crystal structure. The molecule possesses a mirror plane and the morpholine ring adopts a chair conformation.
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 16 H 28 ClN 5 , the piperidine ring has a classical chair conformation. In the crystal structure, weak intermolecular N-HÁ Á ÁN hydrogen bonds link two molecules, related by a twofold axis of symmetry, into dimers.
The title compound, C~21~H~30~Cl~2~N~4~O, contains a sterically hindered phenol group. The dihedral angle between the two rings is 72.3 (1)°. The propyl chain is disordered over two orientations.