In the title compound, C 18 H 23 NS 2 , the bond lengths and angles are unexceptional. The butyl chain is in a fully extended conformation. The dihedral angle between the thiazole and phenyl rings is 87.21 (2) . The crystal structure is stabilized by one weak intramolecular C-HÁ Á ÁS hydrogen bond.
3-(1-Methyl-1-phenylethoxy)-1,3-thiazole-2(3H)-thione: a tertiary thiohydroxamic acid O-ester
✍ Scribed by Hartung, Jens ;Schneiders, Nina ;Bergsträsser, Uwe
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 156 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The steric demand of a tertiary alkyl substituent attached to the thiohydroxamate O atom in the title compound, C 13 H 15 NOS 2 , is reflected in a widening of the associated N-O-C angle [116.4 (2) ]. Close contacts along [100] indicate C-HÁ Á ÁS interactions in the crystal structure.
📜 SIMILAR VOLUMES
The cyclohexyl ring of the title compound, C 20 H 25 NS 2 , has a chair conformation. The dihedral angle between the thiazole and phenyl rings is 89.70 (2) . The crystal structure involves two weak intramolecular C-HÁ Á ÁS hydrogen-bond contacts.
In the title compound, C 26 H 18 Cl 2 N 4 O 2 S, the two spiro junctions link a planar 2-oxindole ring, a pyrrolidine ring in an envelope conformation and a planar benzo [4,5]imidazo[2,1-b]thiazol-3-one ring. Molecules form dimers connected by NÐHÁ Á ÁN hydrogen bonds.
The title compound, C 9 H 7 N 3 OS 2 , is essentially planar and features an intramolecular OÐHÁ Á ÁN interaction. Centrosymmetrically related molecules associate via NÐHÁ Á ÁS contacts.