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Catalog Number:
24171
CAS Number:
33787-05-2
2,6-Difluoro-l-phénylalanine
Purity:
≥ 99 % (HPLC chirale)
Synonym(s):
Acide ( S )-2-amino-3-(2,6-difluorophényl)propionique
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$110.57 /1G
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Product Information

2,6-Difluoro-l-phenylalanine is a unique amino acid derivative known for its distinctive fluorinated phenyl group, which enhances its biochemical properties. This compound is particularly valuable in pharmaceutical research and development, where it serves as a building block for the synthesis of novel peptides and proteins. Its fluorine substituents can significantly alter the pharmacokinetic and pharmacodynamic profiles of therapeutic agents, making it an essential component in the design of drugs with improved efficacy and reduced side effects. Researchers have utilized 2,6-Difluoro-l-phenylalanine in studies aimed at understanding protein folding and stability, as well as in the development of targeted therapies for various diseases, including cancer.

The compound's unique structure allows for enhanced interactions with biological targets, making it a promising candidate for drug discovery and development. Its application extends to the synthesis of fluorinated compounds that can be used in imaging techniques, providing researchers with tools for better visualization of biological processes. With its ability to modify the properties of peptides, 2,6-Difluoro-l-phenylalanine stands out as a versatile compound in the toolkit of chemists and biochemists alike, facilitating advancements in medicinal chemistry and related fields.

Synonyms
Acide ( S )-2-amino-3-(2,6-difluorophényl)propionique
CAS Number
33787-05-2
Purity
≥ 99 % (HPLC chirale)
Molecular Formula
C 9 H 9 F 2 NON 2
Molecular Weight
201.17
MDL Number
MFCD00236245
PubChem ID
2737043
Appearance
Blanc cassé uni
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acide ( S )-2-amino-3-(2,6-difluorophényl)propionique
CAS Number
33787-05-2
Purity
≥ 99 % (HPLC chirale)
Molecular Formula
C 9 H 9 F 2 NON 2
Molecular Weight
201.17
MDL Number
MFCD00236245
PubChem ID
2737043
Appearance
Blanc cassé uni
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

2,6-Difluoro-l-phenylalanine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is used in the synthesis of novel drugs, particularly in the development of treatments for neurological disorders due to its ability to influence neurotransmitter activity.
  • Biochemical Research: It serves as a valuable tool in studying protein structures and functions, helping researchers understand enzyme mechanisms and interactions within biological systems.
  • Neuroscience Studies: The compound is employed in research aimed at understanding the role of amino acids in brain function, potentially leading to breakthroughs in mental health therapies.
  • Peptide Synthesis: It is utilized in the creation of peptides with enhanced properties, offering advantages in stability and efficacy compared to traditional amino acids.
  • Drug Design: The unique fluorine substitutions allow for modifications that can improve the pharmacokinetic profiles of compounds, making it a key player in rational drug design strategies.

Citations