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Catalog Number:
03949
CAS Number:
114346-31-5
Boc-4-(Fmoc-amino)-L-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Phe(4-NH-Fmoc)-OH, Boc- p- (Fmoc-amino)-L-Phe-OH, ( Acide S -Boc-2-amino-3-(4-Fmoc-aminophényl)propionoïque
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Product Information

Boc-4-(Fmoc-amino)-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Boc (tert-butyloxycarbonyl) group and an Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitate selective deprotection during the synthesis of complex peptides. Its unique structure allows for enhanced stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Boc-4-(Fmoc-amino)-L-phenylalanine is commonly used in the synthesis of bioactive peptides, which can serve as potential therapeutics or research tools. Its ability to provide a stable platform for peptide assembly enables the production of high-purity compounds, essential for drug discovery and development. Additionally, its compatibility with various coupling reagents and methods further enhances its utility in peptide synthesis, making it a preferred choice among professionals in pharmaceutical and academic laboratories.

Synonyms
Boc-L-Phe(4-NH-Fmoc)-OH, Boc- p- (Fmoc-amino)-L-Phe-OH, ( Acide S -Boc-2-amino-3-(4-Fmoc-aminophényl)propionoïque
CAS Number
114346-31-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C29H30N2O6
Molecular Weight
502.56
MDL Number
MFCD00151889
PubChem ID
4712502
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-Phe(4-NH-Fmoc)-OH, Boc- p- (Fmoc-amino)-L-Phe-OH, ( Acide S -Boc-2-amino-3-(4-Fmoc-aminophényl)propionoïque
CAS Number
114346-31-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C29H30N2O6
Molecular Weight
502.56
MDL Number
MFCD00151889
PubChem ID
4712502
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-4-(Fmoc-amino)-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: Its application in drug design helps in developing peptide-based therapeutics, particularly in oncology and immunology, where specific peptide sequences can enhance drug efficacy.
  • Bioconjugation: The chemical is used for attaching peptides to other molecules, such as antibodies or drugs, improving the targeting and delivery of therapeutic agents in various treatments.
  • Research in Protein Engineering: It aids in the modification of proteins, allowing scientists to explore structure-function relationships and develop proteins with enhanced properties for industrial applications.
  • Diagnostic Applications: The compound is utilized in the development of diagnostic tools, where peptides can be used as biomarkers for disease detection, improving accuracy and specificity in medical diagnostics.