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CAS 135944-09-1

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N-fmoc-D-homophenylalanine

Description:
N-Fmoc-D-homophenylalanine is a derivative of the amino acid homophenylalanine, characterized by the presence of a 9-fluorenylmethoxycarbonyl (Fmoc) protective group. This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where the Fmoc group serves as a temporary protecting group for the amino group, allowing for selective coupling reactions. The D-configuration of the amino acid indicates that it is a stereoisomer, which can influence the biological activity and properties of the resulting peptides. N-Fmoc-D-homophenylalanine is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Its molecular structure includes a phenyl group, which contributes to its hydrophobic characteristics, making it useful in the design of peptides with specific interactions. As with many synthetic amino acids, it is important to handle N-Fmoc-D-homophenylalanine with care, following appropriate safety protocols in a laboratory setting.
Formula:C25H23NO4
Synonyms:
  • fmoc-D-homophenylalanine
  • Fmoc-D-Homophe-OH
  • Fmoc-D-Hfe-OH
  • Fmoc-D-Homophe
  • Benzenebutanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(αR)-
  • Fmoc-D-HoPhe-OH
  • FMOC-(R)-2-AMINO-4-PHENYLBUTYRIC ACID
  • N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-(-)-ALPHA-4-PHENYLBUTYRIC ACID
  • N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-HOMOPHENYLALANINE
  • N-FMOC-D-HOMOPHE-OH
  • See more synonyms
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