Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
05014
CAS Number:
177966-63-1
Fmoc-4-nitro-D-phénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Phe(4-NO2)-OH, Fmoc- p -nitro-D-Phe-OH
Documents
$29.34 /1G
Taille
Request Bulk Quote
Product Information

Fmoc-4-nitro-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its nitro group enhances the compound's reactivity, making it an attractive choice for researchers focused on developing novel therapeutics. Fmoc-4-nitro-D-phenylalanine is particularly valuable in the field of medicinal chemistry, where it serves as a building block for the synthesis of bioactive peptides and pharmaceuticals.

In addition to its applications in peptide synthesis, this compound is also used in the development of targeted drug delivery systems and in the study of protein interactions. Its unique properties allow for precise modifications, enabling researchers to explore structure-activity relationships effectively. With its robust profile, Fmoc-4-nitro-D-phenylalanine stands out as a key component in advancing research and innovation in biochemistry and pharmaceutical sciences.

Synonyms
Fmoc-D-Phe(4-NO2)-OH, Fmoc- p -nitro-D-Phe-OH
CAS Number
177966-63-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C24H20N2O6
Molecular Weight
432.4
MDL Number
MFCD00237029
PubChem ID
4278442
Melting Point
213-217 ?C
Optical Rotation
[a] D 20 = +37 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-D-Phe(4-NO2)-OH, Fmoc- p -nitro-D-Phe-OH
CAS Number
177966-63-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C24H20N2O6
Molecular Weight
432.4
MDL Number
MFCD00237029
PubChem ID
4278442
Melting Point
213-217 ?C
Optical Rotation
[a] D 20 = +37 ± 2º (C = 1 dans DMF)
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-4-nitro-D-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups.
  • Drug Development: Its unique properties make it valuable in the design of peptide-based therapeutics, particularly in targeting specific biological pathways.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted drug delivery systems and diagnostic tools.
  • Fluorescent Probes: Fmoc-4-nitro-D-phenylalanine can be incorporated into fluorescent probes for imaging applications in biological research, enhancing visualization of cellular processes.
  • Research in Chemical Biology: It plays a role in studying protein interactions and functions, contributing to advancements in understanding complex biological systems.

Citations