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.
2,4-Dichloro-1,3,5-triazine
✍ Scribed by Hechenbleikner, I.
- Book ID
- 120297097
- Publisher
- American Chemical Society
- Year
- 1954
- Tongue
- English
- Weight
- 143 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0002-7863
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📜 SIMILAR VOLUMES
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.
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 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.
## 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