Date published: 2026-4-24

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N-delta-Boc-L-Ornithine (CAS 13650-49-2)

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CAS Number:
13650-49-2
Molecular Weight:
232.28
Molecular Formula:
C10H20N2O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-delta-Boc-L-Ornithine is a derivative of the amino acid ornithine, which has been studied for its broad range of applications. As a carboxylic acid derivative, N-delta-Boc-L-Ornithine serves as a precursor for various biochemical processes. Its versatility makes it a reagent for synthesizing diverse compounds, and it also functions as a catalyst in numerous biochemical reactions. N-delta-Boc-L-Ornithine has garnered significant attention due to its wide range of applications. It serves as a precursor for synthesizing an array of compounds, including peptides, peptidomimetics, and other bioactive molecules. It acts as a catalyst in various biochemical processes, such as polyamine synthesis, amino acid synthesis, and nucleotide synthesis. H-Orn(Boc)-OH serves as an intermediate in synthesizing other compounds. In reactions involving electrophiles, H-Orn(Boc)-OH acts as a nucleophile, enabling its interaction with an assortment of molecules, including peptides, peptidomimetics, and other bioactive compounds. Various enzymes, such as transaminases, dehydrogenases, and kinases, catalyze these reactions.


N-delta-Boc-L-Ornithine (CAS 13650-49-2) References

  1. Synthesis of a hydroxyethylene isostere of the tripeptide Arg-Gly-Leu via a convergent acyl-like radical addition strategy.  |  Jensen, CM., et al. 2005. J Org Chem. 70: 7512-9. PMID: 16149778
  2. Theranostic Gallium Siderophore Ciprofloxacin Conjugate with Broad Spectrum Antibiotic Potency.  |  Pandey, A., et al. 2019. J Med Chem. 62: 9947-9960. PMID: 31580658

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-delta-Boc-L-Ornithine, 1 g

sc-263826
1 g
$51.00

N-delta-Boc-L-Ornithine, 5 g

sc-263826A
5 g
$92.00