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Catalog Number:
03948
CAS Number:
164332-89-2
Boc-4-amino-D-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-D-Phe(4-NH2)-OH, Boc-p-amino-D-Phe-OH
Documents
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Product Information

Boc-4-amino-D-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 solubility, making it an ideal building block for the development of bioactive peptides. Its unique structure allows for selective modifications, facilitating the design of peptides with specific biological activities. Researchers often employ Boc-4-amino-D-phenylalanine in the synthesis of peptide-based drugs, particularly in the fields of oncology and neurology, where targeted therapies are crucial.

Additionally, this compound serves as a valuable tool in the study of protein interactions and enzyme mechanisms, providing insights into the structure-activity relationships of various biomolecules. Its ability to mimic natural amino acids while offering enhanced stability makes it a preferred choice for scientists looking to explore new therapeutic avenues. With its broad applicability in drug development and biochemical research, Boc-4-amino-D-phenylalanine stands out as a key component for advancing innovative solutions in the pharmaceutical industry.

Synonyms
Boc-D-Phe(4-NH2)-OH, Boc-p-amino-D-Phe-OH
CAS Number
164332-89-2
Purity
≥ 98% (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.3
MDL Number
MFCD00236818
PubChem ID
571496
Melting Point
125-130 ºC
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -23 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-Phe(4-NH2)-OH, Boc-p-amino-D-Phe-OH
CAS Number
164332-89-2
Purity
≥ 98% (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.3
MDL Number
MFCD00236818
PubChem ID
571496
Melting Point
125-130 ºC
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -23 ± 2º (C=1 in MeOH)
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-4-amino-D-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 the development of therapeutic proteins and biologically active peptides.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for designing and optimizing drugs that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: Researchers use it for bioconjugation processes, linking drugs to antibodies or other biomolecules, which improves targeted delivery in cancer therapies.
  • Research in Neuroscience: This compound is valuable in studies related to neurotransmitter functions, aiding in the understanding of neurological disorders and potential treatments.
  • Custom Synthesis: It is often employed in custom synthesis projects, allowing researchers to tailor compounds for specific applications, thus meeting unique research needs.

Citations