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Catalog Number:
03951
CAS Number:
55533-25-0
Boc-L-Phe(4-NHZ)-OH
Purity:
≥ 98% (Chiral HPLC, HPLC)
Synonym(s):
Boc-4-(Z-amino)-L-phenylalanine, Boc-p-(Z-amino)-L-Phe-OH, (S-Boc-2-amino-3-(4-Z-aminophenyl)propionoic acid
Documents
$72.31 /1G
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Product Information

Boc-L-Phe(4-NHZ)-OH is a valuable compound in the field of peptide synthesis and pharmaceutical research. This amino acid derivative, known for its protective Boc (tert-butyloxycarbonyl) group, is particularly useful in the synthesis of peptides where selective deprotection is required. Its unique structure allows for the introduction of a phenyl group, enhancing the compound's stability and solubility, making it an ideal choice for researchers focused on developing novel therapeutic agents.

In practical applications, Boc-L-Phe(4-NHZ)-OH serves as a key building block in the production of bioactive peptides, which can be utilized in drug development, particularly in oncology and immunology. Its ability to facilitate the formation of complex peptide structures while maintaining high purity levels makes it a preferred choice among professionals in the pharmaceutical industry. The compound's versatility and efficiency in peptide coupling reactions further underscore its significance in advancing research and development in medicinal chemistry.

Synonyms
Boc-4-(Z-amino)-L-phenylalanine, Boc-p-(Z-amino)-L-Phe-OH, (S-Boc-2-amino-3-(4-Z-aminophenyl)propionoic acid
CAS Number
55533-25-0
Purity
≥ 98% (Chiral HPLC, HPLC)
Molecular Formula
C22H26N2O6
Molecular Weight
414.44
MDL Number
MFCD00038751
PubChem ID
4712501
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-4-(Z-amino)-L-phenylalanine, Boc-p-(Z-amino)-L-Phe-OH, (S-Boc-2-amino-3-(4-Z-aminophenyl)propionoic acid
CAS Number
55533-25-0
Purity
≥ 98% (Chiral HPLC, HPLC)
Molecular Formula
C22H26N2O6
Molecular Weight
414.44
MDL Number
MFCD00038751
PubChem ID
4712501
Appearance
White to off-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-L-Phe(4-NHZ)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic proteins and biologics.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for creating novel drug candidates, especially in targeting specific diseases through peptide-based therapies.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach drugs or imaging agents to biomolecules, enhancing their efficacy and specificity.
  • Research in Cancer Therapeutics: It is explored in cancer research for developing targeted therapies that can selectively attack cancer cells, minimizing damage to healthy tissues.
  • Protein Engineering: This chemical aids in protein engineering efforts, enabling scientists to modify proteins for improved stability and functionality in various applications.

Citations