🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15615
CAS Number:
507472-26-6
Acide Fmoc-( R -3-amino-3-(4-nitrophényl)propionique
Synonym(s):
Fmoc-D-β-Phe(4-NO2)-OH, ( R -Fmoc-4-nitro-β-phénylalanine
Documents
$206.60 /1G
Taille
Request Bulk Quote
Product Information

Fmoc-(R)-3-amino-3-(4-nitrophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of a 4-nitrophenyl moiety, enhances its reactivity and allows for the development of complex peptide sequences with improved biological activity. Researchers and industry professionals appreciate its role in facilitating the synthesis of bioactive peptides, which can be applied in drug discovery, therapeutic development, and various biochemical applications.

The compound's stability under standard reaction conditions, coupled with its ease of deprotection, makes it an ideal choice for those engaged in peptide chemistry. Its specific properties enable the creation of peptides with tailored functionalities, paving the way for innovations in pharmaceuticals and biotechnology. With its proven efficacy in enhancing peptide synthesis, Fmoc-(R)-3-amino-3-(4-nitrophenyl)propionic acid stands out as a valuable asset for researchers aiming to explore new therapeutic avenues.

Synonyms
Fmoc-D-β-Phe(4-NO2)-OH, ( R -Fmoc-4-nitro-β-phénylalanine
CAS Number
507472-26-6
Molecular Formula
C24H20N2O6
Molecular Weight
432.43
MDL Number
MFCD03428008
PubChem ID
2759202
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(4-NO2)-OH, ( R -Fmoc-4-nitro-β-phénylalanine
CAS Number
507472-26-6
Molecular Formula
C24H20N2O6
Molecular Weight
432.43
MDL Number
MFCD03428008
PubChem ID
2759202
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(4-nitrophenyl)propionic acid 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 (SPPS), allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, as its derivatives can mimic amino acids involved in neurotransmission, aiding in the understanding of neurological pathways.
  • Fluorescent Labeling: The nitrophenyl group allows for fluorescent labeling in various assays, making it useful in biological imaging and diagnostics, providing clear visualization of cellular processes.

Citations