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CAS 121695-40-7

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L-PHENYL-D5-ALANINE-N-T-BOC

Description:
L-Phenyl-D5-alanine-N-T-BOC, with the CAS number 121695-40-7, is a synthetic amino acid derivative characterized by its incorporation of deuterium isotopes, which are denoted by the "D5" in its name. This compound features a phenyl group attached to the alpha carbon of the alanine backbone, contributing to its hydrophobic properties. The N-T-BOC (tert-butyloxycarbonyl) group serves as a protective group for the amino function, facilitating its use in peptide synthesis and other organic reactions by preventing unwanted side reactions. The presence of deuterium enhances its utility in studies involving mass spectrometry and NMR spectroscopy, as it provides distinct isotopic signatures. L-Phenyl-D5-alanine-N-T-BOC is typically utilized in research and pharmaceutical applications, particularly in the development of peptide-based drugs and in the study of protein interactions. Its stability and reactivity are influenced by the protective BOC group, making it a valuable intermediate in organic synthesis.
Formula:C14H14D5NO4
InChI:InChI=1/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m0/s1/i4D,5D,6D,7D,8D
SMILES:CC(C)(C)OC(=N[C@@H](Cc1c(c(c(c(c1[2H])[2H])[2H])[2H])[2H])C(=O)O)O
Synonyms:
  • L-Phenyl-D5-Alanine, N-T-Boc Derivative
  • Boc-Phe-Oh-(Ring-D5)
  • (2S)-2-((tert-Butoxycarbonyl)amino)-3-phenyl-d5-propionic Acid
  • N-[(1,1-Dimethylethoxy)carbonyl]-L-phenyl-d5-alanine
  • N-Boc-L-phenyl-d5-alanine
  • tert-Butoxycarbonyl-L-phenyl-d5-alanine
  • Boc-Phe-OH-phenyl-d5
  • N-(tert-butoxycarbonyl)-L-(2,3,4,5,6-2H5)phenylalanine
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