💛 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15575
CAS Number:
517905-86-1
Fmoc-(R)-3-amino-3-(2-trifluoromethylphenyl)propionic acid
Synonym(s):
Fmoc-D-β-Phe(2-CF3)-OH, (R-Fmoc-2-trifluoromethyl-β-phenylalanine
Documents
$206.60 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-(R)-3-amino-3-(2-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 therapeutics. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide chains while facilitating selective deprotection, streamlining the synthesis process.

In the pharmaceutical industry, this compound is particularly valuable for the design of peptide-based drugs, where its structural properties can significantly influence the pharmacokinetics and pharmacodynamics of the resulting peptides. Researchers have successfully employed Fmoc-(R)-3-amino-3-(2-trifluoromethylphenyl)propionic acid in the development of compounds targeting various biological pathways, showcasing its potential in advancing drug discovery and development. Its unique characteristics and practical applications make it an essential tool for professionals in the fields of organic chemistry and biochemistry.

Synonyms
Fmoc-D-β-Phe(2-CF3)-OH, (R-Fmoc-2-trifluoromethyl-β-phenylalanine
CAS Number
517905-86-1
Molecular Formula
C25H20F3NO4
Molecular Weight
455.43
MDL Number
MFCD03428039
PubChem ID
24902251
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(2-CF3)-OH, (R-Fmoc-2-trifluoromethyl-β-phenylalanine
CAS Number
517905-86-1
Molecular Formula
C25H20F3NO4
Molecular Weight
455.43
MDL Number
MFCD03428039
PubChem ID
24902251
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(2-trifluoromethylphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in targeting specific biological pathways due to its trifluoromethyl group.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostic agents.
  • Research in Neuroscience: It plays a role in the development of compounds that can modulate neurotransmitter systems, providing insights into neurological disorders.
  • Analytical Chemistry: This chemical is useful in the development of analytical methods for detecting and quantifying amino acids and peptides in various samples.

Citations