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CAS 112229-51-3

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Z-D-Orn-OH

Description:
Z-D-Orn-OH, also known as Z-D-ornithine, is a synthetic amino acid derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the amino group of D-ornithine. This compound is typically used in peptide synthesis and research due to its ability to serve as a building block for the formation of peptides. The Z group protects the amino functionality, allowing for selective reactions at other sites on the molecule. Z-D-Orn-OH is generally soluble in polar solvents, which facilitates its use in various chemical reactions. Its structure includes a primary amine and a carboxylic acid functional group, making it an amino acid. The D-configuration indicates that it is a non-natural isomer, which can be important in studies of biological activity and interactions. As with many amino acid derivatives, Z-D-Orn-OH may exhibit specific biological properties, making it of interest in pharmacological and biochemical research. Proper handling and storage conditions are essential to maintain its stability and reactivity.
Formula:C13H18N2O4
InChI:InChI=1S/C13H18N2O4/c14-8-4-7-11(12(16)17)15-13(18)19-9-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9,14H2,(H,15,18)(H,16,17)/t11-/m1/s1
InChI key:ZYGRWJVRLNJIMR-LLVKDONJSA-N
SMILES:C1=CC=C(C=C1)COC(=O)N[C@H](CCCN)C(=O)O
Synonyms:
  • (2R)-5-amino-2-(phenylmethoxycarbonylamino)pentanoic acid
  • (R)-5-Amino-2-(((benzyloxy)carbonyl)amino)pentanoic acid
  • N2-benzyloxycarbonyl-L-ornithine
  • Nα-Z-D-ornithine≥ 99% (Titration)
  • Nα-Z-D-ornithine
  • N2-[(Phenylmethoxy)carbonyl]-D-ornithine
  • (2R)-5-amino-2-{[(benzyloxy)carbonyl]amino}pentanoic acid
  • N2-Benzyloxycarbonyl-D-ornithine
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