N-Methyl-3-(4-bromo-1H-pyrrole-2-carbonyl)aminopropionitrile
✍ Scribed by Zeng, Xiang-Chao ;Li, Yu-Xia ;Xu, Shi-Hai ;Liu, Po-Run
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 340 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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The title compound, C 23 H 26 BrN 5 O 2 , was synthesized by the reaction of 4- [(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine and 3-(3-nitrophenyl)-5-chloromethyl-1,2,4-oxadiazole. There are intramolecular C-HÁ Á ÁN and intermolecular N-HÁ Á ÁO and C-HÁ Á ÁO hydrogen bonds in the crystal struc
The title compound, C 23 H 26 ClN 5 O 2 , was synthesized by the reaction of 4- [(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine and 5-chloromethyl-3-(2-chlorophenyl)-1,2,4oxadiazole. In the structure, there are intramolecular C-HÁ Á ÁN, N-HÁ Á ÁN and C-HÁ Á ÁO hydrogen bonds, and intermolecular
The title compound, C 42 H 44 N 2 O 8 S 2 , features a molecular thread. The molecules have crystallographic C i symmetry. The crystal packing shows staples stabilized by weak C-HÁ Á ÁO interactions.
Molecules of the title compound, C 24 H 26 N 4 , are linked by C-HÁ Á ÁN hydrogen bonds, forming a C(5) chain along the [010] direction. Neighboring chains are connected by four C-HÁ Á Á interactions, resulting in the formation of a threedimensional network.