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Catalog Number:
33596
CAS Number:
1056934-68-9
Boc-2-cloro-4-fluoro-D-fenilalanina
Synonym(s):
Boc-D-Fe(2-Cl,4-F)-OH, (Ácido R -Boc-2-amino-2-cloro-4-fluorofenilpropiónico
Documents
$58.39 /100 mg
Tamaño
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Product Information

Boc-2-chloro-4-fluoro-D-phenylalanine is a valuable amino acid derivative widely utilized in pharmaceutical and biochemical research. This compound features a unique combination of a Boc (tert-butyloxycarbonyl) protecting group and a chloro-fluoro substitution on the phenyl ring, enhancing its reactivity and selectivity in various synthetic pathways. Researchers often employ Boc-2-chloro-4-fluoro-D-phenylalanine in the development of peptide-based therapeutics, particularly in the synthesis of bioactive peptides and drug candidates. Its ability to facilitate the introduction of fluorinated residues into peptides makes it an essential tool for medicinal chemists aiming to improve the pharmacokinetic properties of their compounds.

The compound's distinctive properties, including its stability under standard laboratory conditions and compatibility with various coupling reagents, make it an ideal choice for peptide synthesis. Additionally, its fluorinated structure can enhance the binding affinity and selectivity of peptides for their biological targets, providing a significant advantage over non-fluorinated analogs. With its practical applications in drug discovery and development, Boc-2-chloro-4-fluoro-D-phenylalanine stands out as a crucial component for researchers looking to innovate in the field of medicinal chemistry.

Synonyms
Boc-D-Fe(2-Cl,4-F)-OH, (Ácido R -Boc-2-amino-2-cloro-4-fluorofenilpropiónico
CAS Number
1056934-68-9
Molecular Formula
C14H17ClFNO4
Molecular Weight
317.74
MDL Number
MFCD12198163
PubChem ID
53398085
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Boc-D-Fe(2-Cl,4-F)-OH, (Ácido R -Boc-2-amino-2-cloro-4-fluorofenilpropiónico
CAS Number
1056934-68-9
Molecular Formula
C14H17ClFNO4
Molecular Weight
317.74
MDL Number
MFCD12198163
PubChem ID
53398085
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-chloro-4-fluoro-D-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 therapeutic agents targeting specific biological pathways.
  • Drug Development: It is instrumental in the design of novel pharmaceuticals, especially in creating inhibitors for enzymes or receptors, enhancing the efficacy of drug candidates.
  • Biochemical Research: Researchers use this compound to study protein interactions and functions, providing insights into cellular mechanisms and disease pathways.
  • Fluorinated Amino Acids: Its unique fluorine substitution allows for enhanced imaging in biochemistry, making it useful in tracking metabolic processes in vivo.
  • Custom Synthesis: The compound is often employed in custom synthesis projects, catering to specific research needs in academic and industrial laboratories.

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