4-Nitro-L-phenylalanine
Supplier: BACHEM AMERICAS INC
Synonyms:
H-Phe(4-NO2)-OH, (S)-4-Nitrophenylalanine, (S)-2-Amino-3-(4-nitrophenyl)propanoic acid
Sequence: H-p-Nitro-Phe-OH
Bachem offers a considerable choice of ring-substituted phenylalanines, protected derivatives of: p-Aminophenylalanine p-Azidophenylalanine p-Benzoylphenylalanine p-Biphenylalanine p-Bromophenylalanine p-t-Butylphenylalanine p-Carboxyphenylalanine p-Chlorophenylalanine p-Cyanophenylalanine 3,4-Dichlorophenylalanine Fluorophenylalanines p-Iodophenylalanine p-Methylphenylalanine p-Nitrophenylalanine p-Phosphonophenylalanine. p-Methoxy- and p-ethoxyphenylalanine derivatives are listed in the Tyr family, whereas β,β-diphenylalanine derivatives can be found in the "β-Substituted Alanines" family.
p-Nitrophenylalanine (4-Nph, Phe(4-NO₂)) is incorporated into peptides as a chromophore. In FRET substrates, it acts as quencher. Bachem also offers resin-bound Fmoc-Nph (Fmoc-p-nitro-Phe-Wang resin, D-1135).
Intermediate in the synthesis of (S)-6-nitroindoline-2-carboxylic acid.
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Formula:
C₉H₁₀N₂O₄ MW: 210.19 g/mol Storage Temperature: Ambient |
MDL Number:
MFCD00051221 CAS Number: 949-99-5 EINECS: 213-446-8 |
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