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CAS 164332-89-2

:

4-Amino-N-[(1,1-dimethylethoxy)carbonyl]-D-phenylalanine

Description:
4-Amino-N-[(1,1-dimethylethoxy)carbonyl]-D-phenylalanine, with the CAS number 164332-89-2, is a synthetic amino acid derivative that features a phenylalanine backbone modified with an amino group and a tert-butoxycarbonyl (Boc) protecting group. This compound is characterized by its chiral center, which contributes to its potential use in peptide synthesis and pharmaceutical applications. The presence of the Boc group enhances its stability and solubility in organic solvents, making it suitable for various chemical reactions, particularly in the context of peptide coupling. The amino group allows for further functionalization, enabling the synthesis of more complex molecules. Additionally, the compound's structure suggests potential interactions with biological systems, which may be explored in drug development or biochemical research. Its unique properties, including its solubility and reactivity, make it a valuable intermediate in organic synthesis and a subject of interest in medicinal chemistry.
Formula:C14H20N2O4
InChI:InChI=1S/C14H20N2O4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-4-6-10(15)7-5-9/h4-7,11H,8,15H2,1-3H3,(H,16,19)(H,17,18)/t11-/m1/s1
InChI key:InChIKey=NDMVQEZKACRLDP-LLVKDONJSA-N
SMILES:C([C@@H](NC(OC(C)(C)C)=O)C(O)=O)C1=CC=C(N)C=C1
Synonyms:
  • (2R)-3-(4-Aminophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • (R)-3-(4-Aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoicacid
  • 4-Amino-N-[(1,1-dimethylethoxy)carbonyl]-<span class="text-smallcaps">D</span>-phenylalanine
  • 4-amino-N-(tert-butoxycarbonyl)-D-phenylalanine
  • 4-amino-N-(tert-butoxycarbonyl)-L-phenylalanine
  • <span class="text-smallcaps">D</span>-Phenylalanine, 4-amino-N-[(1,1-dimethylethoxy)carbonyl]-
  • Boc-4-Amino-D-phenylalanine
  • Boc-D-4-Aminophenylalanine
  • Boc-D-4-aminophe
  • Boc-D-Phe(4-NH2)-OH
  • See more synonyms
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