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CAS 104504-43-0

:

4-Benzoyl-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine

Description:
4-Benzoyl-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine, with CAS number 104504-43-0, is a synthetic organic compound that belongs to the class of amino acids and derivatives. This substance features a phenylalanine backbone, which is an essential amino acid, modified with a benzoyl group and a tert-butoxycarbonyl (Boc) protecting group. The presence of the benzoyl moiety contributes to its potential applications in organic synthesis and medicinal chemistry, particularly in the development of peptide-based drugs. The tert-butoxycarbonyl group serves as a protective group for the amino functionality, facilitating selective reactions during peptide synthesis. This compound is typically characterized by its solid state at room temperature, and it is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide. Its stability and reactivity make it a valuable intermediate in the synthesis of more complex molecules. As with many organic compounds, handling should be done with care, following appropriate safety protocols to mitigate any potential hazards.
Formula:C21H23NO5
InChI:InChI=1S/C21H23NO5/c1-21(2,3)27-20(26)22-17(19(24)25)13-14-9-11-16(12-10-14)18(23)15-7-5-4-6-8-15/h4-12,17H,13H2,1-3H3,(H,22,26)(H,24,25)/t17-/m0/s1
InChI key:InChIKey=HIQJNYPOWPXYIC-KRWDZBQOSA-N
SMILES:C(=O)(C1=CC=C(C[C@H](NC(OC(C)(C)C)=O)C(O)=O)C=C1)C2=CC=CC=C2
Synonyms:
  • 4-Benzoyl-N-[(1,1-dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-phenylalanine
  • <span class="text-smallcaps">L</span>-Phenylalanine, 4-benzoyl-N-[(1,1-dimethylethoxy)carbonyl]-
  • Boc-4-Benzoyl-L-phenylalanine
  • Boc-L-4-Benzoylalanine
  • Boc-L-4-Benzoylphenylalanine
  • Boc-L-Bpa-Oh
  • Boc-L-P-Benzoylphenylalanine
  • Boc-P-Bz-Phe-Oh
  • Boc-P-Bz-Phenylalanine
  • Boc-Phe(4-Bz)-Oh
  • See more synonyms
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