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Catalog Number:
31661
CAS Number:
114290-82-3
Boc-Phe-y(CH2NH)-Phe-OH
Purity:
≥ 99.0% (HPLC)
Documents
$86.23 /25MG
Pack Size Availability Price
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Product Information

Boc-Phe-?(CH2NH)-Phe-OH is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected amino acid derivative features a Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Researchers often employ Boc-Phe-?(CH2NH)-Phe-OH in the development of peptide-based therapeutics, where its unique structure allows for the introduction of phenylalanine residues, crucial for maintaining the biological activity of peptides.

In addition to its role in peptide synthesis, this compound is valuable in the study of protein interactions and drug design, providing insights into molecular recognition processes. Its ability to facilitate the formation of complex structures makes it a preferred choice among researchers focused on developing novel therapeutic agents. With its favorable properties and practical applications, Boc-Phe-?(CH2NH)-Phe-OH stands out as a key building block in the field of medicinal chemistry and biochemistry.

CAS Number
114290-82-3
Purity
≥ 99.0% (HPLC)
Molecular Formula
C23H30N2O4
Molecular Weight
398.5
MDL Number
MFCD00237441
PubChem ID
4712526
Melting Point
198-205 °C
Appearance
White amorphous powder
Conditions
Store at 0-8 °C
General Information
CAS Number
114290-82-3
Purity
≥ 99.0% (HPLC)
Molecular Formula
C23H30N2O4
Molecular Weight
398.5
MDL Number
MFCD00237441
PubChem ID
4712526
Melting Point
198-205 °C
Appearance
White amorphous 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-Phe-?(CH2NH)-Phe-OH 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. This is crucial for researchers developing new pharmaceuticals.
  • Drug Development: It plays a role in the design of peptide-based drugs, particularly in oncology and immunology, where peptides can mimic natural processes to target specific diseases.
  • Bioconjugation: The compound is used in bioconjugation techniques, linking peptides to other biomolecules, enhancing the efficacy of therapeutic agents in targeted drug delivery systems.
  • Research in Neuroscience: It aids in the study of neuropeptides, which are vital for understanding signaling pathways in the nervous system, potentially leading to treatments for neurological disorders.
  • Custom Peptide Libraries: Researchers utilize this compound to create diverse peptide libraries for high-throughput screening, facilitating the discovery of new bioactive compounds.

Citations