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CAS 57292-45-2

:

(2R)-2-(tert-Butoxycarbonylamino)-3-(4-fluorophenyl)propanoic acid

Description:
(2R)-2-(tert-Butoxycarbonylamino)-3-(4-fluorophenyl)propanoic acid, commonly referred to as a derivative of amino acids, exhibits several notable characteristics. This compound features a chiral center, which contributes to its stereochemistry, specifically the (2R) configuration. The presence of the tert-butoxycarbonyl (Boc) group indicates that it is likely used as a protecting group in peptide synthesis, enhancing its utility in organic chemistry. The 4-fluorophenyl moiety introduces a fluorine atom, which can influence the compound's electronic properties and biological activity. As a propanoic acid derivative, it possesses both acidic and basic functional groups, allowing for potential interactions in various chemical environments. The compound's solubility, stability, and reactivity can vary based on pH and solvent conditions, making it versatile for applications in pharmaceuticals and biochemistry. Overall, this compound is significant in synthetic organic chemistry, particularly in the development of peptide-based therapeutics.
Formula:C14H18FNO4
InChI:InChI=1S/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-/m1/s1
InChI key:InChIKey=RCXSXRAUMLKRRL-LLVKDONJSA-N
SMILES:C([C@@H](NC(OC(C)(C)C)=O)C(O)=O)C1=CC=C(F)C=C1
Synonyms:
  • (2R)-2-(tert-Butoxycarbonylamino)-3-(4-fluorophenyl)propanoic acid
  • (2R)-3-(4-Fluorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • <span class="text-smallcaps">D</span>-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-fluoro-
  • Boc-4-Fluoro-D-Phe-OH
  • Boc-4-Fluoro-D-phenylalanine
  • Boc-D-4-Fluorophe
  • Boc-D-4-Fluorophenylalanine
  • Boc-D-Phe(4-F)-OH
  • N-[(1,1-Dimethylethoxy)carbonyl]-4-fluoro-<span class="text-smallcaps">D</span>-phenylalanine
  • N-[(1,1-Dimethylethoxy)carbonyl]-4-fluoro-D-phenylalanine
  • D-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-fluoro-
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