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Catalog Number:
12091
CAS Number:
74578-48-6
4-(Boc-amino)-L-phenylalanine
Purity:
≥ 97% (HPLC)
Synonym(s):
L-Phe(4-NHBoc)-OH
Documents
$79.22 /100MG
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Product Information

4-(Boc-amino)-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and facilitates the selective modification of peptides. Its unique structure allows for the incorporation of phenylalanine into various peptide sequences, making it an essential building block in the development of therapeutic peptides and biologically active compounds. Researchers appreciate its role in enhancing the solubility and bioavailability of peptides, which is crucial for drug formulation and delivery.

In addition to its applications in drug development, 4-(Boc-amino)-L-phenylalanine is also employed in the synthesis of complex biomolecules and as a tool in molecular biology. Its ability to serve as a chiral building block opens avenues for the creation of enantiomerically pure compounds, which are vital in the production of pharmaceuticals. With its favorable properties and broad applicability, this compound is an invaluable resource for researchers and industry professionals seeking to innovate in the fields of biochemistry and medicinal chemistry.

Synonyms
L-Phe(4-NHBoc)-OH
CAS Number
74578-48-6
Purity
≥ 97% (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.3
MDL Number
MFCD01860650
PubChem ID
67358456
Appearance
Pale yellow solid
Conditions
Store at 0-8°C
General Information
Synonyms
L-Phe(4-NHBoc)-OH
CAS Number
74578-48-6
Purity
≥ 97% (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.3
MDL Number
MFCD01860650
PubChem ID
67358456
Appearance
Pale yellow solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(Boc-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. Its protective Boc (tert-butyloxycarbonyl) group allows for selective reactions, making it easier for chemists to construct complex peptide chains.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. Its structure can be modified to enhance bioactivity and target specificity, which is crucial in developing effective treatments.
  • Bioconjugation: The compound is useful in bioconjugation processes, where it can be attached to various biomolecules. This application is significant in creating targeted drug delivery systems, improving therapeutic efficacy.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter activity due to its structural similarity to amino acids involved in brain function, aiding in the understanding of neurological disorders.
  • Protein Engineering: The compound is also applied in protein engineering, allowing researchers to introduce specific amino acid residues into proteins, which can enhance their stability and functionality in various applications.

Citations