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Catalog Number:
15569
CAS Number:
507472-18-6
Fmoc-(S-3-amino-3-(3-bromophenyl)propionic acid
Synonym(s):
Fmoc-L-β-Phe(3-Br)-OH, (S-Fmoc-3-bromo-β-phenylalanine
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Product Information

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

In addition to its role in peptide synthesis, this compound has shown potential in the development of bioactive molecules, particularly in the design of inhibitors and therapeutic agents. Its ability to form stable interactions with biological targets makes it a valuable asset in pharmaceutical research. Researchers can leverage Fmoc-(S)-3-amino-3-(3-bromophenyl)propionic acid to streamline their synthesis processes while ensuring high yields and purity of their final products, ultimately accelerating the path from concept to application.

Synonyms
Fmoc-L-β-Phe(3-Br)-OH, (S-Fmoc-3-bromo-β-phenylalanine
CAS Number
507472-18-6
Molecular Formula
C24H20BrNO4
Molecular Weight
466.33
MDL Number
MFCD03428000
PubChem ID
22831639
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(3-Br)-OH, (S-Fmoc-3-bromo-β-phenylalanine
CAS Number
507472-18-6
Molecular Formula
C24H20BrNO4
Molecular Weight
466.33
MDL Number
MFCD03428000
PubChem ID
22831639
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-(3-bromophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as 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 properties make it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors or pathways due to its bromophenyl group.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to enhance drug delivery systems or create targeted therapies, improving treatment efficacy.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter activity, helping researchers understand the mechanisms of action for various neurological disorders.
  • Material Science: The compound's properties make it suitable for creating functional materials, such as sensors or drug delivery systems, that respond to environmental stimuli.

Citations