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Catalog Number:
15568
CAS Number:
517905-85-0
Acide Fmoc-( R -3-amino-3-(3-bromophényl)propionique
Synonym(s):
Fmoc-D-β-Phe(3-Br)-OH, ( R -Fmoc-3-bromo-β-phénylalanine
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Product Information

Fmoc-(R)-3-amino-3-(3-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 facilitates the selective protection of amino groups during the synthesis of peptides. Its chiral center enhances its utility in creating enantiomerically pure compounds, making it particularly valuable in pharmaceutical research where stereochemistry is crucial.

Researchers and industry professionals can leverage this compound in the development of bioactive peptides and drug candidates, especially in the fields of oncology and neurology, where specific molecular interactions are essential. The presence of the bromophenyl group can also enhance the compound's binding affinity and selectivity, potentially leading to more effective therapeutic agents. With its robust profile, Fmoc-(R)-3-amino-3-(3-bromophenyl)propionic acid stands out as a key reagent for advancing peptide-based research and drug development.

Synonyms
Fmoc-D-β-Phe(3-Br)-OH, ( R -Fmoc-3-bromo-β-phénylalanine
CAS Number
517905-85-0
Molecular Formula
C24H20BrNO4
Molecular Weight
466.33
MDL Number
MFCD03428038
PubChem ID
22831639
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(3-Br)-OH, ( R -Fmoc-3-bromo-β-phénylalanine
CAS Number
517905-85-0
Molecular Formula
C24H20BrNO4
Molecular Weight
466.33
MDL Number
MFCD03428038
PubChem ID
22831639
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R)-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, allowing researchers to create complex structures with specific amino acid sequences. Its Fmoc protecting group facilitates easy removal during the synthesis process.
  • Drug Development: The unique properties of this compound make it valuable in the pharmaceutical industry for developing new drugs, particularly in targeting specific receptors or pathways in diseases.
  • Bioconjugation: It is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and therapeutics.
  • Research in Neuroscience: The bromophenyl group can be utilized in studies related to neurobiology, potentially aiding in the development of compounds that interact with neurotransmitter systems.
  • Material Science: Its properties can be leveraged in the creation of novel materials, such as polymers or nanomaterials, which have applications in electronics and nanotechnology.

Citations