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Catalog Number:
07183
CAS Number:
138109-65-6, 34702-59-5
Pentafluoro-L-fenilalanina
Purity:
≥ 99 % (HPLC ChiraL)
Synonym(s):
L-Fe(F)5-OH, H-Pentafluoro-L-Phe-OH
Documents
$55.00 /100 mg
Tamaño
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Product Information

Pentafluoro-L-phenylalanine is a unique amino acid derivative characterized by its five fluorine atoms attached to the phenyl ring, which significantly enhances its chemical stability and lipophilicity. This compound is particularly valuable in the field of medicinal chemistry and drug design, where it serves as a building block for the synthesis of fluorinated peptides and proteins. Its distinctive properties allow researchers to explore novel therapeutic agents with improved pharmacokinetic profiles. Additionally, Pentafluoro-L-phenylalanine can be utilized in the development of advanced materials and as a tool in bioconjugation techniques, offering potential applications in targeted drug delivery systems and imaging agents.

The incorporation of fluorinated amino acids like Pentafluoro-L-phenylalanine into peptide sequences can lead to enhanced biological activity and selectivity, making it a vital component in the design of next-generation pharmaceuticals. Its unique structure not only aids in the stabilization of peptide conformations but also provides insights into protein folding and interactions. Researchers and industry professionals can leverage this compound to push the boundaries of current therapeutic strategies, making it an essential addition to any chemical toolkit.

Synonyms
L-Fe(F)5-OH, H-Pentafluoro-L-Phe-OH
CAS Number
138109-65-6, 34702-59-5
Purity
≥ 99 % (HPLC ChiraL)
Molecular Formula
C9H6NO2F5
Molecular Weight
255.12
MDL Number
MFCD01860881
PubChem ID
2735935
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
L-Fe(F)5-OH, H-Pentafluoro-L-Phe-OH
CAS Number
138109-65-6, 34702-59-5
Purity
≥ 99 % (HPLC ChiraL)
Molecular Formula
C9H6NO2F5
Molecular Weight
255.12
MDL Number
MFCD01860881
PubChem ID
2735935
Appearance
Sólido blanco
Conditions
Conservar entre 0 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

Pentafluoro-L-phenylalanine is widely utilized in research focused on:

  • Drug Development: This compound is valuable in designing new pharmaceuticals, particularly in the field of cancer treatment, due to its unique fluorinated structure that can enhance drug efficacy and selectivity.
  • Protein Engineering: Researchers use it to create modified proteins with altered properties, which can lead to improved enzyme activity or stability in biotechnological applications.
  • Fluorinated Amino Acids in Biochemistry: Its incorporation into peptides allows scientists to study protein folding and interactions, providing insights into biological processes and disease mechanisms.
  • Material Science: The compound's unique properties make it suitable for developing advanced materials, such as coatings or polymers, that require enhanced chemical resistance and durability.
  • Analytical Chemistry: It serves as a standard in various analytical techniques, helping researchers accurately measure and analyze other compounds in complex mixtures.

Citas