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Catalog Number:
16841
CAS Number:
1217818-53-5
Ácido Fmoc- (R) -3-amino-4-(2,4,5-trifluorofenil)-butírico
Purity:
≥ 98 % (HPLC)
Documents
$99.85 /25 mg
Tamaño
Request Bulk Quote
Product Information

Fmoc-(R)-3-amino-4-(2,4,5-trifluorophenyl)butyric is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorinated aromatic ring, enhancing its bioactivity and stability, making it particularly valuable in pharmaceutical research. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with precision. Researchers utilize this compound in the development of peptide-based therapeutics, especially in targeting specific biological pathways due to its unique structural properties.

The trifluorophenyl group contributes to the compound's lipophilicity, improving membrane permeability and enhancing the efficacy of drug candidates. Its application extends to the synthesis of peptide ligands and inhibitors, which are essential in the fields of biochemistry and medicinal chemistry. By incorporating Fmoc-(R)-3-amino-4-(2,4,5-trifluorophenyl)butyric into their research, scientists can explore innovative therapeutic strategies and develop next-generation pharmaceuticals with improved performance.

CAS Number
1217818-53-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H20F3NO4
Molecular Weight
455.43
MDL Number
MFCD06659148
PubChem ID
53398431
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1217818-53-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H20F3NO4
Molecular Weight
455.43
MDL Number
MFCD06659148
PubChem ID
53398431
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

Fmoc-(R)-3-amino-4-(2,4,5-trifluorophenyl)butyric is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and improving the efficiency of complex peptide assembly.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in targeting specific biological pathways due to its fluorinated phenyl group.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to various surfaces, which is crucial in developing targeted drug delivery systems.
  • Research in Neurobiology: It aids in the study of neuroactive compounds, contributing to the understanding of neurological disorders by enabling the synthesis of compounds that interact with neurotransmitter systems.
  • Material Science: The compound finds applications in the development of advanced materials, particularly those that require specific chemical functionalities for enhanced performance in electronic or optical devices.

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