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Catalog Number:
15425
CAS Number:
270596-51-5
Boc-3-fluoro-L-β-homophénylalanine
Purity:
≥ 98%
Synonym(s):
Boc-L-β-HomoPhe(3-F)-OH, Acide boc-( S -3-amino-4-(3-fluorophényl)butyrique)
Documents
$86.23 /250 mg
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Product Information

Boc-3-fluoro-L-b-homophenylalanine is a valuable amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound is particularly recognized for its unique fluorine substitution, which enhances the biological activity and stability of peptides. Researchers utilize Boc-3-fluoro-L-b-homophenylalanine in the development of novel therapeutics, especially in the design of peptide-based drugs targeting various diseases. Its ability to improve binding affinity and selectivity makes it an essential building block in the pharmaceutical industry.

In addition to its applications in drug development, Boc-3-fluoro-L-b-homophenylalanine is also employed in the synthesis of complex biomolecules and as a tool in biochemical research. The compound's stability under various conditions allows for versatile use in laboratory settings, making it a preferred choice for chemists and biochemists alike. With its unique properties and practical applications, Boc-3-fluoro-L-b-homophenylalanine stands out as a crucial component in advancing research and innovation in the field of biochemistry.

Synonyms
Boc-L-β-HomoPhe(3-F)-OH, Acide boc-( S -3-amino-4-(3-fluorophényl)butyrique)
CAS Number
270596-51-5
Purity
≥ 98%
Molecular Formula
C 15 H 20 FNO 4
Molecular Weight
297.33
MDL Number
MFCD01861011
PubChem ID
53398010
Melting Point
119-125 °C
Appearance
Poudre blanche
Optical Rotation
[α] D 21 = -16 ± 2º (C=1, dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-β-HomoPhe(3-F)-OH, Acide boc-( S -3-amino-4-(3-fluorophényl)butyrique)
CAS Number
270596-51-5
Purity
≥ 98%
Molecular Formula
C 15 H 20 FNO 4
Molecular Weight
297.33
MDL Number
MFCD01861011
PubChem ID
53398010
Melting Point
119-125 °C
Appearance
Poudre blanche
Optical Rotation
[α] D 21 = -16 ± 2º (C=1, dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-3-fluoro-L-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of novel therapeutic agents. Its unique structure allows for the incorporation of fluorine, enhancing the biological activity of the resulting peptides.
  • Drug Development: Researchers leverage this chemical in the design of new drugs targeting specific receptors. The fluorine substitution can improve the pharmacokinetic properties of drug candidates, making them more effective.
  • Biochemical Research: It is used in studies examining protein interactions and enzyme activity, providing insights into metabolic pathways and disease mechanisms. This can lead to breakthroughs in understanding various health conditions.
  • Material Science: The compound finds applications in creating advanced materials with tailored properties, such as improved thermal stability and mechanical strength, which are essential in various industrial applications.
  • Diagnostic Tools: Boc-3-fluoro-L-b-homophenylalanine is also explored in the development of diagnostic agents, particularly in imaging techniques that utilize fluorine for enhanced contrast in medical imaging.

Citations