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.
2,4-Dichloro-6-morpholino-1,3,5-triazine
✍ Scribed by Dong, Chuan-Ming ;Chen, Li-Gong ;Duan, Xue-Min ;Shu, Xue-Gui ;Zeng, Tao ;Yan, Xi-Long
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 122 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
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.
📜 SIMILAR VOLUMES
The title compound, C 13 H 14 ClN 5 O, was synthesized from 2,4dichloro-6-morpholino-1,3,5-triazine and aniline. In the crystal structure, there are intermolecular N-HÁ Á ÁO hydrogen bonds which propagate infinite chains parallel to the c axis. The morpholine ring adopts a chair conformation.
## Abstract The hydrolysis of the 2‐substituted 4,6‐dichloro‐1,3,5‐triazines was investigated in a mixture of water and acetone. The reaction constant of the hydrolysis of the first chlorine atom was determined, and is discussed in relation to the structure of the triazine derivatives.
In the title compound, C 10 H 8 Cl 2 N 4 O, the dihedral angle between the benzene and triazine rings is 29.57 (8) . The crystal structure is stabilized by weak N-HÁ Á ÁN interactions.
## Abstract An improved synthesis of 4,6‐dichloro‐2‐phenoxy‐1,3,5,‐triazine from cyanuric chloride and phenol in the presence of collidine (2,4,6‐trimethyl‐pyridine) induced us to investigate the scope and limitation of the substitution of one chlorine atom in cyanuric chloride and the influence of