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Catalog Number:
04118
CAS Number:
249648-08-6
D-3,4-Difluorophenylalanine
Purity:
≥ 99% (Assay)
Synonym(s):
D-Phe(3,4-DiF)-OH, H-3,4-difluoro-D-Phe-OH, H-D-Phe(3,4-DiF)-OH
Documents
$79.22 /1G
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Product Information

D-3,4-Difluorophenylalanine is a specialized amino acid derivative that has garnered attention in the fields of biochemistry and pharmaceutical research. This compound is recognized for its unique fluorinated structure, which enhances its stability and bioactivity compared to non-fluorinated analogs. Researchers often utilize D-3,4-Difluorophenylalanine in the development of novel therapeutics, particularly in the study of protein interactions and enzyme mechanisms. Its ability to mimic natural amino acids while providing distinct properties makes it an invaluable tool in drug design and development.

In addition to its applications in drug discovery, D-3,4-Difluorophenylalanine is also employed in the synthesis of peptide-based compounds, where it can influence the conformation and activity of peptides. This versatility allows scientists to explore new pathways in medicinal chemistry and develop targeted therapies for various diseases. With its unique characteristics, D-3,4-Difluorophenylalanine stands out as a promising compound for advancing research in pharmacology and biochemistry.

Synonyms
D-Phe(3,4-DiF)-OH, H-3,4-difluoro-D-Phe-OH, H-D-Phe(3,4-DiF)-OH
CAS Number
249648-08-6
Purity
≥ 99% (Assay)
Molecular Formula
C9H9F2NO2
Molecular Weight
201.2
MDL Number
MFCD01631986
PubChem ID
2737044
Melting Point
215-223º C
Appearance
Almost white powder
Optical Rotation
+17.0±1º
Conditions
Store at 0-8°C
General Information
Synonyms
D-Phe(3,4-DiF)-OH, H-3,4-difluoro-D-Phe-OH, H-D-Phe(3,4-DiF)-OH
CAS Number
249648-08-6
Purity
≥ 99% (Assay)
Molecular Formula
C9H9F2NO2
Molecular Weight
201.2
MDL Number
MFCD01631986
PubChem ID
2737044
Melting Point
215-223º C
Appearance
Almost white powder
Optical Rotation
+17.0±1º
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

D-3,4-Difluorophenylalanine is widely utilized in research focused on:

  • Drug Development: This compound serves as a valuable building block in the synthesis of novel pharmaceuticals, particularly in the development of targeted therapies for cancer treatment.
  • Biochemical Research: It is used in studies investigating protein structure and function, helping researchers understand how modifications can affect enzyme activity and stability.
  • Neuroscience: The compound is applied in the exploration of neurotransmitter pathways, aiding in the development of treatments for neurological disorders by mimicking natural amino acids.
  • Fluorinated Amino Acids: Its unique fluorine substitutions enhance the properties of peptides, making them more resistant to enzymatic degradation, which is beneficial in drug formulation.
  • Material Science: D-3,4-Difluorophenylalanine is explored for its potential in creating new materials with specific properties, such as improved thermal stability and mechanical strength.

Citations