4,4,6-Trimethyl-1-phenyl-3,4-dihydropyrimidine-2(1H)-thione

Bohari Mohd. Yamin, Noor Azilah M Kasim, Noraini Hamzah

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The reaction of cinnamoyl isothiocyanate and aniline gave a the title cyclized thiourea, C13H16N2S. There are two molecules in the asymmetric unit. The pyrimidine-2-thione moiety in each molecule is almost perpendicular to the phenyl group. The molecules are linked by two intermolecular N-H⋯S hydrogen bonds to form a dimer.

Original languageEnglish
JournalActa Crystallographica Section E: Structure Reports Online
Volume61
Issue number1
DOIs
Publication statusPublished - Jan 2005

Fingerprint

Thiones
Thiourea
Hydrogen
Molecules
molecules
Thioureas
thioureas
pyrimidines
Aniline
aniline
Dimers
Hydrogen bonds
dimers
hydrogen bonds
pyrimidine
isothiocyanic acid

ASJC Scopus subject areas

  • Condensed Matter Physics
  • Structural Biology

Cite this

4,4,6-Trimethyl-1-phenyl-3,4-dihydropyrimidine-2(1H)-thione. / Mohd. Yamin, Bohari; Kasim, Noor Azilah M; Hamzah, Noraini.

In: Acta Crystallographica Section E: Structure Reports Online, Vol. 61, No. 1, 01.2005.

Research output: Contribution to journalArticle

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