2-(1,3-Dithian-2-yl)benzaldehyde and N-{2-[2-(1,3-dioxan-2-yl)phenoxy]ethyl}phthalimide

Paul G. Jene, James A. Ibers

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

The crystal structures of two elaborated-porphyrin precursors have been determined. In the crystalline state, 2-(1,3-dithian-2-yl)benzaldehyde, C11H12OS2, has its dithiane ring in a slightly distorted chair conformation. The molecules pack in anti-parallel chains. N-{2-[2-(1,3-Dioxan-2-yl)phenoxy]ethyl}-phthalimide, C20H19NO5, is in a folded conformation. The dihedral angle between the phthalimide and phenyl planes is 80.07 (3)°. In the crystalline states, molecules stack on top of one another.

Original languageEnglish (US)
Pages (from-to)705-707
Number of pages3
JournalActa Crystallographica, Section C: Crystal Structure Communications
Volume56
Issue number6
DOIs
StatePublished - Jun 2000

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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