2-Butylamino-6-chloro-4-(2,4,4-trimethylpentan-2-ylamino)-1,3,5-triazine
β Scribed by Wen, Rui-Zhi ;Li, Shui-Fang ;Li, Jiao-Juan
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 732 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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β¦ Synopsis
The crystal structure of the title compound, C 15 H 28 ClN 5 , is stabilized by intermolecular N-HΓ Γ ΓN hydrogen bonds, forming zigzag chains running along the c axis.
Related literature
For general background, see: Borzatta & Carrozza (1991). For related structures, see: Deng et al. (2006). For related literature, see: Kaiser & Thurston (1951).
π SIMILAR VOLUMES
The title compound, (I), is an important intermediate in the preparation of hindered light stabilizers (Borzatta & Carrozza, 1991;Deng et al., 2006). There are four molecules of (I) in the asymmetic unit, with simplar conformations, although two of the molecules show disorder of their tert-butyl gr
In the title compound, C 20 H 37 ClN 6 , the piperidine ring adopts a chair conformation. In the crystal structure, N-HΓ Γ ΓN hydrogen bonds link the molecules into chains along b.
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-HΓ Γ ΓN hydrogen bonds link two molecules, related by a twofold axis of symmetry, into dimers.
In the title compound, C 19 H 34 N 6 O 2 , both morpholine rings adopt chair conformations. In the crystal structure, N-HΓ Γ ΓN hydrogen bonds link the molecules into chains along c.
In the title compound, C 10 H 10 N 4 O 4 , the triazine ring is nearly planar. The 1,3-dioxane-4,6-dione ring exhibits a half-chair conformation. The molecule is disordered and the structure has been refined using a split model.