Cholest-5-en-3β-yl 3-(4-ethoxyphenyl)prop-2-enoate

Bernhard Bugenhagen, Ariane Munk, Volkmar Vill, Yosef Al-Jasem, Thies Thiemann

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

In the asymmetric unit of the title compound, C38H 56O3, there are two symmetry-independent molecules that differ in the rotation angle along the C - O bond between the 3-(4-ethoxyphenyl)prop-2-enoate and cholest-5-en-3β-yl groups by 169.3 (3)°. In both molecules, steroid ring B adopts a half-chair conformation, rings A and C adopt a chair conformation and ring D exists in an envelope form. The two symmetry-independent molecules pack in the crystal into separate layers parallel to (1̄02) with their long axis parallel to the [201] direction. Short intermolecular C - H⋯O and C - H⋯π contacts are observed.

Original languageEnglish
Pages (from-to)o2064
JournalActa Crystallographica Section E: Structure Reports Online
Volume68
Issue number7
DOIs
Publication statusPublished - Jul 2012

ASJC Scopus subject areas

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

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