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CAS 218609-00-8

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Boc-(R)-3-amino-4-(4-fluoro-phenyl)-butyric acid

Description:
Boc-(R)-3-amino-4-(4-fluoro-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group, an amino group, and a fluorinated phenyl moiety. This compound is typically used in peptide synthesis and medicinal chemistry due to its ability to serve as a building block for more complex molecules. The presence of the Boc group allows for the protection of the amino functionality during synthetic procedures, facilitating selective reactions. The (R) configuration at the chiral center indicates its specific stereochemistry, which can significantly influence the biological activity of the resulting compounds. The 4-fluorophenyl group enhances the lipophilicity and potentially the binding affinity of the compound to biological targets. Overall, Boc-(R)-3-amino-4-(4-fluoro-phenyl)-butyric acid is notable for its utility in drug development and its role in the synthesis of various pharmaceutical agents.
Formula:C15H20FNO4
InChI:InChI=1/C15H20FNO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-4-6-11(16)7-5-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1ccc(cc1)F)CC(=O)O)O
Synonyms:
  • Boc-L-3-Amino-4-(4-fluorophenyl)-butyric acid
  • (3R)-3-[(tert-butoxycarbonyl)amino]-4-(4-fluorophenyl)butanoic acid
  • Boc-β-HoPhe(4-F)-OH
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