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Catalog Number:
33589
CAS Number:
167993-00-2
Boc-2,4-difluoro-L-fenilalanina
Synonym(s):
Boc-L-Phe(2,4-DiF)-OH, Ácido Boc-( S -2-amino-3-(2,4-difluorofenil)propiónico, Boc-Phe(2,4-DiF)-OH
Documents
$58.39 /100 mg
Tamaño
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Product Information

Boc-2,4-difluoro-L-phenylalanine is a valuable amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical research. This compound is recognized for its unique fluorinated phenyl group, which enhances the biological activity and stability of peptides, making it an essential building block in drug development. Researchers utilize Boc-2,4-difluoro-L-phenylalanine to create peptides with improved pharmacokinetic properties, potentially leading to more effective therapeutic agents. Its application extends to the synthesis of peptide-based drugs, where the incorporation of fluorine can significantly influence the compound's interaction with biological targets.

In addition to its utility in drug design, Boc-2,4-difluoro-L-phenylalanine is also employed in the development of novel materials and as a tool in chemical biology. The compound's ability to modify the properties of peptides allows for the exploration of new therapeutic avenues, particularly in the fields of oncology and neurology. With its unique characteristics, Boc-2,4-difluoro-L-phenylalanine stands out as a versatile compound for researchers seeking to innovate in peptide chemistry and drug discovery.

Synonyms
Boc-L-Phe(2,4-DiF)-OH, Ácido Boc-( S -2-amino-3-(2,4-difluorofenil)propiónico, Boc-Phe(2,4-DiF)-OH
CAS Number
167993-00-2
Molecular Formula
C14H17F2NO4
Molecular Weight
301.29
MDL Number
MFCD07371996
PubChem ID
16244018
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Boc-L-Phe(2,4-DiF)-OH, Ácido Boc-( S -2-amino-3-(2,4-difluorofenil)propiónico, Boc-Phe(2,4-DiF)-OH
CAS Number
167993-00-2
Molecular Formula
C14H17F2NO4
Molecular Weight
301.29
MDL Number
MFCD07371996
PubChem ID
16244018
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-2,4-difluoro-L-phenylalanine 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 fluorinated structure can enhance the stability and bioactivity of the resulting peptides.
  • Drug Development: The incorporation of Boc-2,4-difluoro-L-phenylalanine in drug candidates can improve their pharmacokinetic properties, making them more effective in treating various diseases, including cancer and neurological disorders.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme activities, providing insights into biological processes that can lead to new drug discoveries.
  • Fluorine Chemistry: Its fluorinated nature allows for unique applications in medicinal chemistry, where fluorine can influence the lipophilicity and metabolic stability of compounds, offering advantages over non-fluorinated analogs.
  • Material Science: The compound can also be explored in the development of advanced materials, such as polymers and coatings, where its properties can enhance performance characteristics like durability and resistance to degradation.

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