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CAS 142186-36-5

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(S)-N-BOC-4-Fluorophenylglycine

Description:
(S)-N-BOC-4-Fluorophenylglycine is an amino acid derivative characterized by the presence of a fluorine atom on the para position of the phenyl ring and a tert-butyloxycarbonyl (BOC) protecting group on the amine. This compound is typically used in organic synthesis and pharmaceutical research due to its role as a building block for peptide synthesis and its potential biological activity. The BOC group serves to protect the amino group during chemical reactions, allowing for selective modifications of other functional groups. The fluorine substitution can enhance the compound's lipophilicity and influence its interaction with biological targets. As a chiral molecule, it exists in two enantiomeric forms, with the (S)-configuration often being of particular interest in medicinal chemistry for its potential therapeutic effects. The compound is generally stable under standard laboratory conditions but should be handled with care due to the presence of reactive functional groups.
Formula:C13H15FNO4
InChI:InChI=1/C13H16FNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-4-6-9(14)7-5-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17)/p-1/t10-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](c1ccc(cc1)F)C(=O)[O-])O
Synonyms:
  • (L)-N-tert-Butoxycarbonyl-alpha-(4-fluorophenyl)acetic acid
  • (2S)-[(tert-butoxycarbonyl)amino](4-fluorophenyl)ethanoate
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