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CAS 517905-85-0

:

Fmoc-D-3-Amino-3-(3-bromophenyl)-propionic acid

Description:
Fmoc-D-3-Amino-3-(3-bromophenyl)-propionic acid is a synthetic amino acid derivative commonly used in peptide synthesis and drug development. It features a fluorene-9-methoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under mild acidic conditions. The compound contains a D-amino acid configuration, which can impart unique properties to peptides, such as increased resistance to enzymatic degradation. The presence of a 3-bromophenyl group enhances its hydrophobic character and can influence the biological activity of the resulting peptides. This compound is typically used in research settings for the development of novel peptides with specific functionalities, including potential therapeutic applications. Its molecular structure allows for various modifications, making it a versatile building block in medicinal chemistry. As with many synthetic compounds, handling should be done with care, following appropriate safety protocols due to potential hazards associated with brominated compounds.
Formula:C24H20BrNO4
InChI:InChI=1/C24H20BrNO4/c25-16-7-5-6-15(12-16)22(13-23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m1/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@H](CC(=O)O)c1cccc(c1)Br)O
Synonyms:
  • (3R)-3-(3-Bromophenyl)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
  • benzenepropanoic acid, 3-bromo-beta-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (betaR)-
  • Fmoc-(R)-3-Amino-3-(3-bromophenyl)-propionic acid
  • Fmoc-(R)-3-Amino-3-(3-Bromo-Phenyl)-Propionic Acid
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