Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
29700
CAS Number:
1260640-43-4
Ácido R , S -Fmoc-2-amino-4,4-difluoro-butírico
Purity:
≥ 97 % (HPLC)
Documents
$93.14 /25 mg
Tamaño
Request Bulk Quote
Product Information

(R,S)-Fmoc-2-amino-4,4-difluoro-butyric acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique difluorobutyric acid structure that enhances its bioactivity and stability, making it an attractive choice for researchers in medicinal chemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains while providing excellent protection during synthesis. This compound is particularly valuable in the development of fluorinated peptides, which have shown promising applications in pharmaceuticals due to their enhanced metabolic stability and biological activity.

Researchers and industry professionals can leverage (R,S)-Fmoc-2-amino-4,4-difluoro-butyric acid in various applications, including the design of novel therapeutic agents and the exploration of new drug delivery systems. Its unique properties not only facilitate the synthesis of complex peptides but also open avenues for innovative research in drug discovery. With its growing relevance in the pharmaceutical industry, this compound stands out as a crucial tool for advancing peptide-based therapeutics.

CAS Number
1260640-43-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C19H17F2NO4
Molecular Weight
361.35
MDL Number
MFCD06738956
PubChem ID
21063801
Melting Point
146-150 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1260640-43-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C19H17F2NO4
Molecular Weight
361.35
MDL Number
MFCD06738956
PubChem ID
21063801
Melting Point
146-150 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-Fmoc-2-amino-4,4-difluoro-butyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex and biologically active molecules.
  • Drug Development: Its unique fluorinated structure enhances the pharmacological properties of drug candidates, making it valuable in pharmaceutical research for developing more effective therapeutic agents.
  • Bioconjugation: The Fmoc protecting group facilitates selective reactions in bioconjugation processes, which are essential for creating targeted drug delivery systems and diagnostic agents.
  • Research in Neuroscience: This compound can be utilized in studies related to neurotransmitter systems, providing insights into neurological pathways and potential treatments for neurodegenerative diseases.
  • Material Science: Its properties can be leveraged in the development of advanced materials, such as polymers with enhanced thermal and mechanical stability, suitable for various industrial applications.

Citas