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Catalog Number:
15606
CAS Number:
507472-25-5
Ácido Fmoc-( S )-3-amino-3-(2-nitrofenil)propiónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-L-β-Phe(2-NO2)-OH, ( S )-Fmoc-2-nitro-β-fenilalanina
Documents
$38.06 /100 mg
Tamaño
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Product Information

Fmoc-(S)-3-amino-3-(2-nitrophenyl)propionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. 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 nitrophenyl group, enhances its reactivity and allows for the introduction of various functional groups, making it an essential building block in the design of bioactive peptides and pharmaceuticals.

Researchers and industry professionals appreciate the compound's stability and compatibility with various coupling reagents, facilitating efficient peptide assembly. Its applications extend to the development of therapeutic peptides, where precise control over amino acid sequences is critical. Additionally, the nitrophenyl moiety can be exploited for further modifications, enabling the creation of targeted drug delivery systems. With its unique properties and practical applications, Fmoc-(S)-3-amino-3-(2-nitrophenyl)propionic acid stands out as a valuable tool in modern chemical research and development.

Synonyms
Fmoc-L-β-Phe(2-NO2)-OH, ( S )-Fmoc-2-nitro-β-fenilalanina
CAS Number
507472-25-5
Purity
≥ 95 % (HPLC)
Molecular Formula
C24H20N2O6
Molecular Weight
432.43
MDL Number
MFCD03428007
PubChem ID
6915691
Appearance
Sólido de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-β-Phe(2-NO2)-OH, ( S )-Fmoc-2-nitro-β-fenilalanina
CAS Number
507472-25-5
Purity
≥ 95 % (HPLC)
Molecular Formula
C24H20N2O6
Molecular Weight
432.43
MDL Number
MFCD03428007
PubChem ID
6915691
Appearance
Sólido 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

Fmoc-(S)-3-amino-3-(2-nitrophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in developing targeted therapies for various diseases.
  • Bioconjugation: The chemical's reactive groups facilitate the attachment of biomolecules, enhancing the development of bioconjugates for drug delivery systems.
  • Fluorescent Probes: Used in the creation of fluorescent probes, it helps in imaging and tracking biological processes in live cells, providing insights into cellular functions.
  • Research in Neuroscience: This compound's properties make it valuable in studying neurotransmitter systems, contributing to advancements in understanding neurological disorders.

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