The title compound, C 15 H 17 N 3 O 3 S, a potent new plant elicitor, was synthesized by reaction between 1,2,3-benzothiadiazole-7carbonyl chloride and ethyl piperidine-4-carboxylate. The piperidine ring adopts a chair conformation. Weak intermolecular C-HÁ Á ÁO hydrogen bonds stabilize the crystal
Ethyl 2,1,3-benzothiadiazole-5-carboxylate
✍ Scribed by Li, Xue-Mei ;Du, Li-Ping ;Yang, Jun ;Zhang, Shu-Sheng
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 92 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
In the essentially planar molecule of the title compound, C 9 H 8 N 2 O 2 S, the dihedral angle between the benzene and thiadiaole rings is 0.44 (7) . In the crystal structure, molecules are stabilized byinteractions and van der Waals forces.
📜 SIMILAR VOLUMES
In the title compound, C 23 H 20 N 3 O 2 PS, the molecules form a supramolecular structure via intermolecular C-HÁ Á ÁO and C-HÁ Á ÁN hydrogen bonds.
The crystal structure of the title compound, C 12 H 13 NO 3 S, is stabilized by intermolecular N-HÁ Á ÁO hydrogen bonds, which are formed between the NH groups and the sulfoxide O atoms.