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

Catalog Number:
15382
CAS Number:
270065-80-0
Boc-4-trifluoromethyl-L-ॆ-homophenylalanine
Purity:
≥ 98%
Synonym(s):
Boc-L-β-HomoPhe(4-CF3)-OH, Boc-(S-3-amino-4-(4-trifluoromethylphenyl)butyric acid
Documents
$106.96 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-4-trifluoromethyl-L-b-homophenylalanine is a specialized amino acid derivative that has garnered attention in the fields of medicinal chemistry and peptide synthesis. This compound is characterized by its unique trifluoromethyl group, which enhances its lipophilicity and metabolic stability, making it an attractive building block for the development of novel pharmaceuticals. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection during peptide synthesis, facilitating the incorporation of this amino acid into complex peptide structures.

Researchers and industry professionals utilize Boc-4-trifluoromethyl-L-b-homophenylalanine in the design of peptide-based therapeutics, particularly in the development of inhibitors targeting specific biological pathways. Its distinctive properties enable the creation of more potent and selective compounds, which can lead to improved therapeutic outcomes. Additionally, the trifluoromethyl moiety can enhance the binding affinity of peptides to their targets, making this compound a valuable asset in drug discovery and development.

Synonyms
Boc-L-β-HomoPhe(4-CF3)-OH, Boc-(S-3-amino-4-(4-trifluoromethylphenyl)butyric acid
CAS Number
270065-80-0
Purity
≥ 98%
Molecular Formula
C16H20F3NO4
Molecular Weight
347.33
MDL Number
MFCD01861070
PubChem ID
53397970
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-HomoPhe(4-CF3)-OH, Boc-(S-3-amino-4-(4-trifluoromethylphenyl)butyric acid
CAS Number
270065-80-0
Purity
≥ 98%
Molecular Formula
C16H20F3NO4
Molecular Weight
347.33
MDL Number
MFCD01861070
PubChem ID
53397970
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-4-trifluoromethyl-L-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its unique structure allows for the introduction of trifluoromethyl groups, enhancing the biological activity of the resulting peptides.
  • Drug Discovery: Researchers leverage this chemical in the design of novel pharmaceuticals. The trifluoromethyl group can improve the metabolic stability and bioavailability of drug candidates, making them more effective in treating various diseases.
  • Bioconjugation: It is used in bioconjugation processes to create targeted drug delivery systems. By attaching this compound to antibodies or other biomolecules, scientists can enhance the specificity and efficacy of treatments for conditions like cancer.
  • Material Science: The compound finds applications in the development of advanced materials, particularly in coatings and polymers that require enhanced chemical resistance and durability due to the presence of the trifluoromethyl group.
  • Analytical Chemistry: This chemical is also utilized in analytical methods, such as chromatography, to separate and identify complex mixtures. Its distinct properties help improve the resolution and sensitivity of analytical techniques.

Citations