3-(4-nitrophenyl)-L-alanine ethyl ester hydrochloride
Supplier: BACHEM AMERICAS INC
Synonyms:
H-Phe(4-NO2)-OEt.HCl
, H-4-Nitro-Phe-OEt·HCl
, H-Phe(4-NO2)-OEt·HCl
Sequence: H-4-Nitro-Phe-OEt · HCl
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).
Formula:
C₁₁H₁₄N₂O₄·HCl MW: 274.701 g/mol Storage Temperature: Refrigerator |
MDL Number:
MFCD08275409 CAS Number: 58816-66-3 EINECS: 261-455-0 |
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