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Catalog Number:
15100
CAS Number:
158741-21-0
Boc-3-nitro-D-phenylalanine
Purity:
≥ 97% (HPLC)
Synonym(s):
Boc-D-Phe(3-NO2)-OH, Boc-3-nitro-D-Phe-OH
Documents
$72.31 /1G
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Product Information

Boc-3-nitro-D-phenylalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique nitro group provides additional functionality, allowing for the incorporation of specific properties into peptides, which can be beneficial in various therapeutic applications, including cancer treatment and antimicrobial agents.

In the pharmaceutical industry, Boc-3-nitro-D-phenylalanine is utilized as a building block for the synthesis of bioactive peptides, enabling the design of novel compounds with enhanced efficacy and selectivity. Its ability to facilitate the introduction of nitro groups into peptide chains opens up new avenues for research in medicinal chemistry. Researchers appreciate its ease of use and compatibility with standard coupling reagents, making it a preferred choice for those looking to streamline their synthesis processes while achieving high yields.

Synonyms
Boc-D-Phe(3-NO2)-OH, Boc-3-nitro-D-Phe-OH
CAS Number
158741-21-0
Purity
≥ 97% (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.3
MDL Number
MFCD01317702
PubChem ID
6915692
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Phe(3-NO2)-OH, Boc-3-nitro-D-Phe-OH
CAS Number
158741-21-0
Purity
≥ 97% (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.3
MDL Number
MFCD01317702
PubChem ID
6915692
Appearance
White powder
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

Boc-3-nitro-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create analogs of bioactive peptides, aiding in the development of new therapeutic agents. Its unique properties can enhance the efficacy of drug candidates.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This application is crucial in the fields of diagnostics and targeted drug delivery.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter pathways, particularly in understanding the role of modified amino acids in brain function and behavior.
  • Material Science: Boc-3-nitro-D-phenylalanine finds applications in the development of functional materials, such as hydrogels, which can be used in drug delivery systems or tissue engineering.

Citations