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.
Ethyl 1-(1,2,3-benzothiadiazol-7-ylcarbonyl)piperidine-4-carboxylate
✍ Scribed by Zhao, Jian-Zhuang ;Bao, Li-Li ;Fan, Zhi-Jin ;Song, Hai-Bin ;Liu, Xiu-Feng
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 98 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
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 packing.
📜 SIMILAR VOLUMES
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.
The title compound, C 16 H 11 N 5 S 2 , is a potent new plant elicitor (activator). The benzothiadiazole ring system is essentially planar and forms a dihedral angle of 15.76 (4) with the thiazole ring. An N-HÁ Á ÁN intramolecular hydrogen-bonding interaction is present.
In the title compound, C~23~H~25~NO~10~, the five-membered rings adopt envelope conformations and the dihedral angle between the two benzene rings is 67.1 (7)°. The crystal structure is stabilized by intramolecular N—H...O and intermolecular O—H...O hydrogen-bond interactions.