Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide

Bohari Mohd. Yamin, Monica Lulo Rodis, Dayang N B A Chee

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

In the title compound, C10H19N3S, the cyclohexyl group adopts a chair conformation and adopts a position approximately syn to the thione S atom. The CN2S thiourea moiety makes dihedral angle of 13.13(10)° with the propan-2-ylideneamino group. An intramolecular N-H⋯N hydrogen bond is noted. In the crystal, inversion dimers linked by pairs of N-H⋯S hydrogen bonds generate R2 2(8) loops.

Original languageEnglish
Pages (from-to)o1109
JournalActa Crystallographica Section E: Structure Reports Online
Volume70
Issue number10
DOIs
Publication statusPublished - 1 Oct 2014

Fingerprint

Hydrogen bonds
Crystal structure
hydrogen bonds
Thiones
Thiourea
crystal structure
Thioureas
thioureas
Dihedral angle
Dimers
seats
Conformations
dihedral angle
dimers
inversions
Atoms
Crystals
crystals
atoms
thiosemicarbazide

Keywords

  • biological activity
  • crystal structure
  • hydrogen bonding
  • thiosemicarbazide
  • thiourea

ASJC Scopus subject areas

  • Condensed Matter Physics
  • Materials Science(all)
  • Chemistry(all)

Cite this

Crystal structure of 4-cyclohexyl-1-(propan-2-ylidene)thiosemicarbazide. / Mohd. Yamin, Bohari; Rodis, Monica Lulo; Chee, Dayang N B A.

In: Acta Crystallographica Section E: Structure Reports Online, Vol. 70, No. 10, 01.10.2014, p. o1109.

Research output: Contribution to journalArticle

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