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1-Methyl-3-phenyl-thio-urea.


ABSTRACT: The title compound, C8H10N2S, was prepared by reaction of methyl-amine solution, KOH and phenyl-iso-thio-cyanate in ethanol. It adopts a syn-Me and anti-Ph conformation relative to the C=S double bond. The dihedral angle between the N-C(=S)-N thio-urea and phenyl planes is 67.83?(6)°. In the crystal, the mol-ecules centrosymmetrical dimers by pairs of N(Ph)-H?S hydrogen bonds. The dimers are linked by N(Me)-H?S hydrogen bonds into layers parallel to (100).

SUBMITTER: Su HX 

PROVIDER: S-EPMC4011236 | biostudies-literature | 2014 May

REPOSITORIES: biostudies-literature

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1-Methyl-3-phenyl-thio-urea.

Su Hou-Xiang HX  

Acta crystallographica. Section E, Structure reports online 20140409 Pt 5


The title compound, C8H10N2S, was prepared by reaction of methyl-amine solution, KOH and phenyl-iso-thio-cyanate in ethanol. It adopts a syn-Me and anti-Ph conformation relative to the C=S double bond. The dihedral angle between the N-C(=S)-N thio-urea and phenyl planes is 67.83 (6)°. In the crystal, the mol-ecules centrosymmetrical dimers by pairs of N(Ph)-H⋯S hydrogen bonds. The dimers are linked by N(Me)-H⋯S hydrogen bonds into layers parallel to (100). ...[more]

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