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Catalog Number:
15613
CAS Number:
500770-85-4
Boc-(R-3-amino-3-(4-nitrophenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-β-Phe(4-NO2)-OH, (R-Boc-4-nitro-β-phenylalanine
Documents
$58.39 /100MG
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Product Information

Boc-(R)-3-amino-3-(4-nitrophenyl)propionic acid is a versatile compound widely utilized in pharmaceutical and biochemical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug development. Its unique structure, characterized by the presence of a 4-nitrophenyl group, allows for specific interactions in biological systems, facilitating the exploration of enzyme activity and receptor binding studies.

Researchers appreciate its application in the synthesis of bioactive peptides and as a building block in medicinal chemistry, where it can contribute to the development of novel therapeutics. The compound's ability to serve as a chiral building block also opens avenues for the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry. With its favorable properties and broad applicability, Boc-(R)-3-amino-3-(4-nitrophenyl)propionic acid stands out as a valuable tool for advancing research and development in various scientific fields.

Synonyms
Boc-D-β-Phe(4-NO2)-OH, (R-Boc-4-nitro-β-phenylalanine
CAS Number
500770-85-4
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.31
MDL Number
MFCD03427932
PubChem ID
3786935
Melting Point
128-134 ºC
Appearance
White solid
Optical Rotation
[a]D25 = +43.0 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-β-Phe(4-NO2)-OH, (R-Boc-4-nitro-β-phenylalanine
CAS Number
500770-85-4
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.31
MDL Number
MFCD03427932
PubChem ID
3786935
Melting Point
128-134 ºC
Appearance
White solid
Optical Rotation
[a]D25 = +43.0 ± 2º (C=1 in EtOH)
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-(R)-3-amino-3-(4-nitrophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of pharmaceuticals targeting specific biological pathways.
  • Drug Development: It plays a crucial role in the design of novel drugs, especially in the field of cancer research, where it can be used to create targeted therapies that improve efficacy and reduce side effects.
  • Bioconjugation: The compound is employed in bioconjugation techniques, allowing researchers to attach drugs or imaging agents to biomolecules, enhancing the delivery and effectiveness of therapeutic agents.
  • Research in Neuroscience: It is used in studies related to neurotransmitter systems, helping scientists understand the mechanisms of action for various neurological disorders.
  • Analytical Chemistry: The compound is utilized in developing analytical methods for detecting and quantifying amino acids in biological samples, aiding in metabolic studies and diagnostics.

Citations