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Catalog Number:
07309
CAS Number:
269078-76-4
Acide Fmoc-( R , S -3-amino-3-(4-bromophényl)propionique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-DL-β-Phe(4-Br)-OH, Fmoc-( R , S -4-bromo-β-phénylalanine
Documents
$113.87 /250 mg
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Product Information

Fmoc-(R,S)3-amino-3-(4-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 structure, characterized by the presence of a bromophenyl moiety, enhances its reactivity and allows for diverse modifications, making it an essential tool for researchers in drug development and protein engineering.

In practical applications, Fmoc-(R,S)3-amino-3-(4-bromophenyl)propionic acid is particularly valuable in the design of bioactive peptides and pharmaceuticals, where precise control over amino acid sequences is critical. Its ability to undergo various coupling reactions enables the creation of complex peptide structures, which can lead to the discovery of new therapeutic agents. Additionally, the compound's stability and compatibility with standard peptide synthesis protocols make it a preferred choice for both academic and industrial laboratories focused on peptide-based research.

Synonyms
Fmoc-DL-β-Phe(4-Br)-OH, Fmoc-( R , S -4-bromo-β-phénylalanine
CAS Number
269078-76-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C24H20BrNO4
Molecular Weight
466.35
MDL Number
MFCD01863199
PubChem ID
2759183
Melting Point
191-197 °C
Appearance
Poudre amorphe blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-DL-β-Phe(4-Br)-OH, Fmoc-( R , S -4-bromo-β-phénylalanine
CAS Number
269078-76-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C24H20BrNO4
Molecular Weight
466.35
MDL Number
MFCD01863199
PubChem ID
2759183
Melting Point
191-197 °C
Appearance
Poudre amorphe blanche
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,S)3-amino-3-(4-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, enhancing the efficiency and yield of complex peptide sequences.
  • Drug Development: Its unique structure allows for the design of novel pharmaceutical compounds, especially in developing targeted therapies for various diseases, including cancer.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted drug delivery systems, improving the specificity and efficacy of therapeutic agents.
  • Research in Neuroscience: It is applied in the synthesis of neuroactive peptides, facilitating research into neurological disorders and potential treatments.
  • Analytical Chemistry: This chemical is valuable in the development of analytical methods for detecting and quantifying peptides in biological samples, aiding in biomarker discovery and validation.

Citations