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Catalog Number:
15438
CAS Number:
374791-01-2
Fmoc-(S)-3-amino-3-(3-nitrophenyl)propionic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-L-β-Phe(3-NO2)-OH, (S)-Fmoc-3-nitro-β-phenylalanine
Documents
$72.31 /100MG
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Product Information

Fmoc-(S)-3-amino-3-(3-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 essential 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 functionalities, making it an invaluable tool for researchers in medicinal chemistry and biochemistry.

This compound is particularly beneficial in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of bioactive peptides, which can serve as potential drugs or research tools in various fields, including cancer research and neurobiology. The stability of the Fmoc group under standard conditions, combined with the compound's ability to facilitate the formation of complex peptide structures, positions Fmoc-(S)-3-amino-3-(3-nitrophenyl)propionic acid as a preferred choice for professionals seeking reliable and efficient solutions in peptide synthesis.

Synonyms
Fmoc-L-β-Phe(3-NO2)-OH, (S)-Fmoc-3-nitro-β-phenylalanine
CAS Number
374791-01-2
Purity
≥ 97% (HPLC)
Molecular Formula
C24H20N2O6
Molecular Weight
432.43
MDL Number
MFCD01631072
PubChem ID
17830545
Appearance
White to off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-β-Phe(3-NO2)-OH, (S)-Fmoc-3-nitro-β-phenylalanine
CAS Number
374791-01-2
Purity
≥ 97% (HPLC)
Molecular Formula
C24H20N2O6
Molecular Weight
432.43
MDL Number
MFCD01631072
PubChem ID
17830545
Appearance
White to off-white solid
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

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

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), enhancing the efficiency and yield of desired peptide sequences.
  • Drug Development: Its unique structure allows for the incorporation of specific functionalities into peptide-based drugs, making it valuable in pharmaceutical research aimed at developing targeted therapies.
  • Bioconjugation: The compound can be used to create bioconjugates, linking peptides to other biomolecules or drugs, which is essential in creating more effective therapeutic agents.
  • Research in Neuroscience: Due to its nitrophenyl group, it can be utilized in studies related to neurotransmitter activity, aiding in the development of neuroactive compounds.
  • Fluorescent Labeling: The chemical can be modified for use in fluorescent labeling techniques, helping researchers visualize and track peptides in biological systems.

Citations