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Catalog Number:
15604
CAS Number:
500770-83-2
Ácido Boc-( S -3-amino-3-(2-nitrofenil)propiónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Boc-L-β-Fe(2-NO2)-OH, ( S -Boc-2-nitro-β-fenilalanina
Documents
$65.40 /250 mg
Tamaño
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Product Information

Boc-(S)-3-amino-3-(2-nitrophenyl)propionic acid is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and facilitates its use in peptide synthesis. Its unique structure, characterized by the presence of a nitrophenyl group, allows for specific interactions in biological systems, making it an ideal candidate for the development of novel therapeutics and drug delivery systems. Researchers have found it particularly useful in the synthesis of bioactive peptides, where it can serve as a building block due to its ability to undergo selective reactions while maintaining the integrity of the peptide chain.

In addition to its applications in peptide synthesis, Boc-(S)-3-amino-3-(2-nitrophenyl)propionic acid has shown promise in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor ligands. Its ability to modulate biological activity through structural modifications makes it a valuable tool for researchers aiming to explore new therapeutic avenues. With its favorable properties and versatility, this compound stands out as a key ingredient in the development of innovative solutions in drug discovery and development.

Synonyms
Boc-L-β-Fe(2-NO2)-OH, ( S -Boc-2-nitro-β-fenilalanina
CAS Number
500770-83-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.31
MDL Number
MFCD03427931
PubChem ID
6915690
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-β-Fe(2-NO2)-OH, ( S -Boc-2-nitro-β-fenilalanina
CAS Number
500770-83-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.31
MDL Number
MFCD03427931
PubChem ID
6915690
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 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-(S)-3-amino-3-(2-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 biologically active molecules. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: Researchers leverage this compound in the design of new pharmaceuticals, especially in the field of neuropharmacology. Its structural features can lead to the creation of compounds with improved efficacy and selectivity for specific biological targets.
  • Bioconjugation: The compound can be used in bioconjugation processes, where it helps in attaching drugs or imaging agents to biomolecules. This application is crucial in developing targeted therapies and diagnostic tools in medicine.
  • Research in Neuroscience: Its unique properties make it suitable for studying neurotransmitter systems and developing potential treatments for neurological disorders, providing insights into synaptic functions and signaling pathways.
  • Analytical Chemistry: The compound can be employed in analytical methods to detect and quantify amino acids and related compounds, aiding researchers in various fields, including food science and environmental analysis.