Acta Crystallographica Section E (Sep 2012)

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

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

DOI
https://doi.org/10.1107/S1600536812036380
Journal volume & issue
Vol. 68, no. 9
pp. o2810 – o2811

Abstract

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The title compound, C13H15ClN2O6, 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.