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Catalog Number:
33696
CAS Number:
486460-00-8
Acide boc-( R -3-amino-4-(2,4,5-trifluorophényl)butyrique
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$100.05 /25 mg
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Product Information

Boc-(R)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, making it an essential intermediate in the synthesis of various bioactive molecules. Its unique trifluorophenyl moiety enhances its biological activity, making it a valuable candidate for drug discovery, particularly in the development of therapeutics targeting neurological disorders and metabolic diseases. Researchers appreciate its stability and ease of handling, which facilitate efficient synthesis and purification processes.

In addition to its applications in medicinal chemistry, Boc-(R)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid can be employed in peptide synthesis and as a building block for more complex organic compounds. Its ability to selectively modify biological pathways positions it as a promising tool for advancing research in pharmacology and biochemistry. The compound's favorable properties, including its solubility and reactivity, further enhance its appeal to professionals in the field, ensuring it meets the rigorous demands of modern scientific inquiry.

CAS Number
486460-00-8
Molecular Formula
C 15 H 18 F 3 NON 4
Molecular Weight
333.3
MDL Number
MFCD06659147
PubChem ID
21911205
Conditions
Conserver entre 2 et 8 °C
General Information
CAS Number
486460-00-8
Molecular Formula
C 15 H 18 F 3 NON 4
Molecular Weight
333.3
MDL Number
MFCD06659147
PubChem ID
21911205
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

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

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders. Its unique structure allows for the development of drugs with improved efficacy and reduced side effects.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, where the Boc protecting group helps in the selective formation of peptide bonds. This application is crucial in creating therapeutic peptides for various medical applications.
  • Research in Medicinal Chemistry: Researchers leverage its properties to explore new drug candidates. The trifluorophenyl group enhances the compound's bioactivity, making it a valuable tool in medicinal chemistry studies.
  • Biochemical Assays: This chemical is utilized in biochemical assays to study enzyme interactions and protein binding, providing insights into biological processes and potential therapeutic targets.
  • Material Science: Its unique chemical properties allow for applications in developing advanced materials, including polymers that can be used in drug delivery systems, enhancing the effectiveness of treatments.

Citations