## Experimental A freshly distilled solution of pivaloyl chloride (1.20 g, 10 mmol) in acetone (50 ml) was added dropwise to a suspension of potassium thiocyanate (0.97 g, 10 mmol) in acetone (30 ml) and the reaction mixture was refluxed for 30 min. After cooling to room temperature, a solution of
1-(4-Nitrophenyl)-3-pivaloylthiourea
✍ Scribed by Sultana, Sarwat ;Khawar Rauf, M. ;Ebihara, Masahiro ;Badshah, Amin
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 521 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the title compound [systematic name: 1-(2,2-dimethylpropionyl)-3-(4-nitrophenyl)thiourea], C 12 H 15 N 3 O 3 S, the molecule exists in the thione form with typical thiourea C-S and C-O bonds, as well as shortened C-N bond lengths. The planes containing the thiourea N atoms form dihedral angles of 27.12 ( 7) and 1.6 (2) , respectively, with the benzene ring. The molecule exhibits only an intramolecular N-HÁ Á ÁO hydrogen bond and no intermolecular N-HÁ Á ÁS hydrogen bonds. This
📜 SIMILAR VOLUMES
The crystal structure of the title compound, C 12 H 15 BrN 2 OS, is composed of discrete molecules with bond lengths and angles quite typical for thiourea compounds of this class. The molecule exists in the solid state in its thione form with typical thiourea C-S and C-O bonds lengths, as well as sh
The title compound, C~13~H~15~F~3~N~2~OS, shows an intramolecular N—H...O hydrogen bond and forms intermolecular N—H...S hydrogen bonds, generating a chain.
The title molecule, C 12 H 15 ClN 2 OS, shows the typical geometric parameters of a substituted thiourea derivative. There is an intramolecular N-HÁ Á ÁO hydrogen bond and the crystal packing is characterized by intermolecular N-HÁ Á ÁS hydrogen bonds.
The enone group and the benzene rings of the title compound, C 16 H 13 NO 4 , are each planar. In the crystal structure, intermolecular C-HÁ Á ÁO interactions form chains along the a axis.