💛 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15581
CAS Number:
517905-87-2
Acide Fmoc-( R )-3-amino-3-(3-trifluorométhylphényl)propionique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-β-Phe(3-CF3)-OH, ( R )-Fmoc-3-trifluorométhyl-β-phénylalanine
Documents
$35.00 /100 mg
Taille
Request Bulk Quote
Product Information

Fmoc-(R)-3-amino-3-(3-trifluoromethylphenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique trifluoromethyl group, which enhances its biological activity and stability, making it an attractive choice for researchers focused on developing novel therapeutic agents. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide chains while providing excellent protection during synthesis.

In the pharmaceutical industry, this compound is particularly valuable for the design of peptide-based drugs, where its structural properties can lead to improved efficacy and selectivity. Additionally, its application in the synthesis of complex peptides enables researchers to explore new avenues in drug discovery and development. With its unique characteristics and practical applications, Fmoc-(R)-3-amino-3-(3-trifluoromethylphenyl)propionic acid stands out as a key reagent for professionals seeking to innovate in the fields of biochemistry and pharmacology.

Synonyms
Fmoc-D-β-Phe(3-CF3)-OH, ( R )-Fmoc-3-trifluorométhyl-β-phénylalanine
CAS Number
517905-87-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 20 F 3 NON 4
Molecular Weight
455.43
MDL Number
MFCD03428040
PubChem ID
24902252
Melting Point
185 - 187 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = 13 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-β-Phe(3-CF3)-OH, ( R )-Fmoc-3-trifluorométhyl-β-phénylalanine
CAS Number
517905-87-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 20 F 3 NON 4
Molecular Weight
455.43
MDL Number
MFCD03428040
PubChem ID
24902252
Melting Point
185 - 187 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = 13 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(3-trifluoromethylphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: The unique trifluoromethyl group enhances the pharmacological properties of compounds, making it valuable in the pharmaceutical industry for developing new drugs with improved efficacy and bioavailability.
  • Bioconjugation: It is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostics in biotechnology.
  • Material Science: The compound's properties make it suitable for creating advanced materials, particularly in the development of polymers that require specific chemical functionalities for applications in electronics and coatings.
  • Research in Neuroscience: Its structural characteristics allow for the exploration of neuroactive compounds, aiding researchers in studying neurological pathways and potential treatments for neurodegenerative diseases.

Citations