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.
7-Amino-1H-3,1-benzothiazine-2,4-dithione
✍ Scribed by Yu, Yun ;Zhong, Hui-Ping ;Yang, Kai-Bin ;Huang, Rong-Bin ;Zheng, Lan-Sun
- Book ID
- 104483309
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 159 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
Hydrothermal reaction of m-phenylenediamine and carbon disulfide in the molar ratio 1:2 produces the title compound, C 14 H 12 N 4 S 2 . X-ray crystal structure determination shows that the compound is chiral by virtue of restricted rotation and crystallizes in a non-centrosymmetric but achiral spac
In the title compound, C 17 H 15 N 3 O 5 SÁC 2 H 6 OS, the thiazine ring adopts a distorted half-chair conformation. The enolic H atom is involved in both intramolecular and intermolecular O-HÁ Á ÁO hydrogen bonds, the latter linking the molecules into centrosymmetric pairs. Both anthranilamide H at