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Catalog Number:
15564
CAS Number:
507472-17-5
Fmoc-(S-3-amino-3-(2-bromophenyl)propionic acid
Synonym(s):
Fmoc-L-β-Phe(2-Br)-OH, (S-Fmoc-2-bromo-β-phenylalanine
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Product Information

Fmoc-(S)-3-amino-3-(2-bromophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which allows for selective deprotection during the synthesis process, making it an invaluable tool for researchers focused on developing complex peptides and proteins. Its specific structure, characterized by the presence of a bromophenyl group, enhances its reactivity and compatibility with various coupling reactions, facilitating the creation of diverse peptide sequences.

In addition to its role in peptide synthesis, Fmoc-(S)-3-amino-3-(2-bromophenyl)propionic acid has potential applications in drug discovery and development, particularly in the design of bioactive compounds. Researchers can leverage its unique properties to explore novel therapeutic agents targeting various biological pathways. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, making it a preferred choice for professionals seeking reliable and efficient reagents for their projects.

Synonyms
Fmoc-L-β-Phe(2-Br)-OH, (S-Fmoc-2-bromo-β-phenylalanine
CAS Number
507472-17-5
Molecular Formula
C24H20BrNO4
Molecular Weight
466.33
MDL Number
MFCD03427999
PubChem ID
22831636
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(2-Br)-OH, (S-Fmoc-2-bromo-β-phenylalanine
CAS Number
507472-17-5
Molecular Formula
C24H20BrNO4
Molecular Weight
466.33
MDL Number
MFCD03427999
PubChem ID
22831636
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(2-bromophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide structures efficiently.
  • Drug Development: Its unique structure makes it valuable in medicinal chemistry for developing new pharmaceuticals, especially those targeting specific biological pathways.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems and diagnostics.
  • Research in Neuroscience: It serves as a tool in studying neurotransmitter systems due to its ability to mimic certain amino acids, aiding in the understanding of neurological functions.
  • Material Science: This chemical can be incorporated into polymers and materials for creating specialized coatings or films, improving their properties for various industrial applications.

Citations