In the title compound, C 22 H 28 N 2 O 2 S, the carbonyl group closer to the thiol group is almost perpendicular to the attached benzene ring. The crystal packing is stabilized by intermolecular N-HÁ Á ÁO and C-HÁ Á ÁO hydrogen bonds.
1-tert-Butyl-2-(tert-butoxysulfanyl)-1-(3,5-dimethylbenzoyl)-2-(4-ethylbenzoyl)hydrazine
✍ Scribed by Shang, Jian ;Wang, Qing-Min ;Huang, Run-Qiu ;Chen, Li ;Guo, Jian-Hua
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 130 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the title compound, C 26 H 36 N 2 O 3 S, the amide bearing the N-S bond has an s-cis conformation, whereas that bearing the N-tert-butyl group has an s-trans conformation, the N-N-C O torsion angles being À15.1 (2) and À174.3 (2) , respectively. The steric size of the N-tert-butyl group causes the 3,5-dimethylphenyl group to be directed away from it.
📜 SIMILAR VOLUMES
The crystal structure of the title compound, C 38 H 42 N 4 O 4 S, an insect-growth regulator, has been determined. The two tertbutyl groups are in different environments and this is reflected in the 1 H NMR spectrum.
Overall Enantioselective a-Alkylation of Aspartic and Glutamic Acid through Dilithium Enolatocarboxylates of 2-~3-Benzoyl-2-(~erf-butyl)-l-methyl-5-oxoimidazolidin-4-yl~acetic and 3-[3-Benzoyl-2-(~er~-bntyl)-1-methyl-5-oxoimidazolidin-4-yl~propionic Acid, respectively The pure methyl esters 10 of t