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

Catalog Number:
14042
CAS Number:
167993-21-7
Boc-L-Phe(2-trifluoromethyl)-OH
Purity:
≥ 99% (ee)
Synonym(s):
Boc-L-Phe(2-CF3)-OH, Boc-o-trifluoromethyl-L-phenylalanine, (S-Boc-2-amino-3-(2-trifluoromethyl-phenyl)propionicacid
Documents
$120.88 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-L-Phe(2-trifluoromethyl)-OH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the pharmaceutical industry for its ability to enhance the stability and bioavailability of peptides. The presence of the trifluoromethyl group not only contributes to its unique chemical properties but also allows for increased lipophilicity, making it an excellent candidate for applications in medicinal chemistry. Researchers often utilize this compound in the design of novel therapeutics, especially in the development of targeted drug delivery systems and in the synthesis of biologically active peptides.

In addition to its applications in drug development, Boc-L-Phe(2-trifluoromethyl)-OH is also employed in various research settings, including studies focused on protein interactions and enzyme activity. Its ability to serve as a building block in the synthesis of complex molecules makes it an invaluable tool for chemists and biochemists alike. The compound's unique features, such as its enhanced stability and reactivity, provide significant advantages over similar compounds, making it a preferred choice for professionals seeking reliable and effective solutions in their research and development endeavors.

Synonyms
Boc-L-Phe(2-CF3)-OH, Boc-o-trifluoromethyl-L-phenylalanine, (S-Boc-2-amino-3-(2-trifluoromethyl-phenyl)propionicacid
CAS Number
167993-21-7
Purity
≥ 99% (ee)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD01862946
PubChem ID
4444636
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Phe(2-CF3)-OH, Boc-o-trifluoromethyl-L-phenylalanine, (S-Boc-2-amino-3-(2-trifluoromethyl-phenyl)propionicacid
CAS Number
167993-21-7
Purity
≥ 99% (ee)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD01862946
PubChem ID
4444636
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-L-Phe(2-trifluoromethyl)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in creating modified amino acids that enhance the stability and activity of therapeutic peptides.
  • Drug Development: Its unique trifluoromethyl group contributes to the development of novel pharmaceuticals, offering improved bioavailability and metabolic stability compared to similar compounds.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Medicinal Chemistry: It plays a significant role in medicinal chemistry studies, helping scientists explore structure-activity relationships and optimize drug candidates.
  • Fluorine Chemistry Applications: The incorporation of fluorine in the compound allows for enhanced interactions in biological systems, making it valuable in various fields like agrochemicals and materials science.

Citations