Z-p-fluoro-Phe-OH, also known as Z-4-fluorophenylalanine, is an amino acid derivative characterized by the presence of a fluorine atom on the para position of the phenyl ring of phenylalanine. This compound typically features a Z (or cis) configuration in its peptide bond, which influences its conformational properties. The fluorine substitution can enhance the compound's hydrophobicity and alter its interaction with biological systems, making it of interest in medicinal chemistry and biochemistry. Z-p-fluoro-Phe-OH is often utilized in the synthesis of peptides and proteins, particularly in studies involving structure-activity relationships and the design of novel therapeutics. Its unique properties may also affect its stability and reactivity compared to its non-fluorinated counterparts. As with many fluorinated compounds, it may exhibit distinct pharmacokinetic and pharmacodynamic profiles, making it a valuable tool in drug development and research. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.

Z-p-fluoro-Phe-OH

17543-58-7: Z-p-fluoro-Phe-OH, also known as Z-4-fluorophenylalanine, is an amino acid derivative characterized by the presence of a fluorine atom on the para position of the phenyl ring of phenylalanine. This compound typically features a Z (or cis) configuration in its peptide bond, which influences its conformational properties. The fluorine substitution can enhance the compound's hydrophobicity and alter its interaction with biological systems, making it of interest in medicinal chemistry and biochemistry. Z-p-fluoro-Phe-OH is often utilized in the synthesis of peptides and proteins, particularly in studies involving structure-activity relationships and the design of novel therapeutics. Its unique properties may also affect its stability and reactivity compared to its non-fluorinated counterparts. As with many fluorinated compounds, it may exhibit distinct pharmacokinetic and pharmacodynamic profiles, making it a valuable tool in drug development and research. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.

CAS 17543-58-7

Z-p-fluoro-Phe-OH

Z-P-Fluoro-Phe-OH

Ref: IN-DA0020ZC

(2S)-Cbz-3-(4-fluorophenyl)propanoic acid

Ref: 54-PC99602

Z-4-Fluoro-Phe-OH

Ref: 7W-GM8719

Z-4-Fluoro-phenylalanine

Ref: 10-M03203