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CAS 41153-30-4

:

(S)-N-BOC-4-Fluorophenylalanine

Description:
(S)-N-BOC-4-Fluorophenylalanine is a derivative of the amino acid phenylalanine, modified to include a tert-butyloxycarbonyl (BOC) protecting group and a fluorine atom at the para position of the phenyl ring. This compound is characterized by its chiral nature, with the (S) configuration indicating the specific spatial arrangement of its atoms. The BOC group serves as a protective moiety, commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. The presence of the fluorine atom can enhance the compound's biological activity and lipophilicity, making it of interest in medicinal chemistry and drug design. This amino acid derivative is typically utilized in the synthesis of peptides and proteins, particularly in studies involving structure-activity relationships. Additionally, its unique properties may contribute to the development of novel therapeutics, especially in targeting specific biological pathways. As with many chemical substances, proper handling and storage are essential to maintain its stability and efficacy.
Formula:C14H18FNO4
InChI:InChI=1/C14H18FNO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc(cc1)F)C(=O)O)O
Synonyms:
  • Boc-L-4-Fluorophenylalanine
  • Boc-4-Fluoro-L-Phe-OH
  • Boc-4-Fluoro-L-phenylalanine
  • Boc-L-4-Fluorophe
  • Boc-Phe(4-F)-OH
  • BOC-P-FLUORO-PHENYLALANINE
  • N-TERT-BUTOXYCARBONYL-4-FLUOROPHENYL-L-ALANINE
  • BOC-4-FLUORO-L-PHE
  • BOC-4-FLUORO PHENYLALANINE
  • BOC-L-PHE(4-F)-OH
  • See more synonyms
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