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Catalog Number:
04993
CAS Number:
171820-74-9
Nα-Boc-Nδ-allyloxycarbonyl-L-ornithine
Purity:
≥ 97% (HPLC)
Synonym(s):
Boc-L-Orn(Aloc)-OH
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Product Information

Na-Boc-Nd-allyloxycarbonyl-L-ornithine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a Boc (tert-butoxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure allows for selective reactions, facilitating the incorporation of L-ornithine into peptides, which can be crucial for developing therapeutics targeting various biological pathways.

The practical applications of Na-Boc-Nd-allyloxycarbonyl-L-ornithine extend to the synthesis of bioactive peptides and the exploration of novel drug candidates. Its ability to serve as a building block in peptide synthesis positions it as a valuable tool for researchers aiming to create compounds with specific biological activities. Additionally, its compatibility with various coupling reactions makes it a preferred choice for professionals looking to streamline their synthetic processes. With its unique properties and potential for diverse applications, this compound is an essential asset for any laboratory focused on peptide chemistry and drug discovery.

Synonyms
Boc-L-Orn(Aloc)-OH
CAS Number
171820-74-9
Purity
≥ 97% (HPLC)
Molecular Formula
C14H24N2O6
Molecular Weight
316.4
MDL Number
MFCD00800349
PubChem ID
5047479
Melting Point
124-129 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -8 ± 1º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Orn(Aloc)-OH
CAS Number
171820-74-9
Purity
≥ 97% (HPLC)
Molecular Formula
C14H24N2O6
Molecular Weight
316.4
MDL Number
MFCD00800349
PubChem ID
5047479
Melting Point
124-129 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -8 ± 1º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-Nd-allyloxycarbonyl-L-ornithine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential for developing new drugs and therapeutic agents.
  • Drug Development: Its unique structure allows for the creation of novel drug candidates, particularly in the field of cancer therapy, where targeted delivery is crucial.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to drugs or imaging agents, enhancing the efficacy of treatments.
  • Research in Neuroscience: It plays a role in studying neurotransmitter pathways, helping researchers understand neurological disorders and potential treatments.
  • Material Science: The compound is also explored in the development of smart materials that respond to environmental stimuli, which can be applied in various industrial applications.

Citations