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Catalog Number:
33605
CAS Number:
1038828-38-4
4-Fluoro-2-méthyl-L-phénylalanine
Synonym(s):
L-Phe(4-F,2-CH3)-OH, ( Acide S -2-amino-4-fluoro-2-méthylphénylpropionique, H-Phe(4-F,2-CH3)-OH
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$79.22 /100 mg
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Product Information

4-Fluoro-2-methyl-L-phenylalanine is a specialized amino acid derivative that has garnered attention in pharmaceutical and biochemical research. This compound is recognized for its unique structural features, which include a fluorine atom that enhances its biological activity and stability. Researchers have utilized 4-Fluoro-2-methyl-L-phenylalanine in the development of novel therapeutics, particularly in the fields of neuropharmacology and cancer treatment. Its ability to mimic natural amino acids while providing distinct advantages makes it a valuable tool for studying protein interactions and enzyme mechanisms.

In addition to its applications in drug discovery, this compound is also being explored for its potential in synthesizing peptide-based drugs, where its incorporation can lead to improved efficacy and reduced side effects. The presence of the fluorine atom not only contributes to its unique properties but also allows for better tracking in biological systems, making it an ideal candidate for advanced research applications. Overall, 4-Fluoro-2-methyl-L-phenylalanine stands out as a promising compound for researchers looking to innovate in the realms of medicinal chemistry and biochemistry.

Synonyms
L-Phe(4-F,2-CH3)-OH, ( Acide S -2-amino-4-fluoro-2-méthylphénylpropionique, H-Phe(4-F,2-CH3)-OH
CAS Number
1038828-38-4
Molecular Formula
C 10 H 12 FNO 2
Molecular Weight
197.21
MDL Number
MFCD12198172
PubChem ID
3542838
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
L-Phe(4-F,2-CH3)-OH, ( Acide S -2-amino-4-fluoro-2-méthylphénylpropionique, H-Phe(4-F,2-CH3)-OH
CAS Number
1038828-38-4
Molecular Formula
C 10 H 12 FNO 2
Molecular Weight
197.21
MDL Number
MFCD12198172
PubChem ID
3542838
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Fluoro-2-methyl-L-phenylalanine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key building block in the synthesis of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Protein Engineering: It is employed in the modification of proteins to study the effects of fluorinated amino acids on protein structure and function, aiding in the design of more effective therapeutics.
  • Biochemical Research: Researchers use it to explore metabolic pathways and enzyme activities, providing insights into how modifications can affect biological processes.
  • Drug Design: The compound's unique properties allow for the creation of more selective and potent drug candidates, enhancing efficacy while minimizing side effects.
  • Material Science: It is also applied in the development of new materials, particularly those requiring specific interactions at the molecular level, such as in sensors or drug delivery systems.

Citations