N-Acetyl-5-chloro-3-nitro-L-tyrosine ethyl ester

Teresa T. Mutahi, Benson J. Edagwa, Frank R. Fronczek, Rao M. Uppu

Research output: Contribution to journalArticle

Abstract

The title compound, C13H15ClN2O 6, was synthesized by hypochlorous acid-mediated chlorination of N-acetyl-3-nitro-l-tyrosine ethyl ester. The OH group forms an intramolecular O - H⋯O hydrogen bond to the nitro group and the N - H group forms an Intermolecular N - H⋯O hydrogen bonds to an amide O atom, linking the molecules into chains along [100]. The crystal studied was a non-merohedral twin, with a 0.907 (4):0.093 (4) domain ratio.

Original languageEnglish (US)
Pages (from-to)o2810-o2811
JournalActa Crystallographica Section E: Structure Reports Online
Volume68
Issue number9
DOIs
StatePublished - Sep 2012

ASJC Scopus subject areas

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

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