🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
07384
CAS Number:
142995-31-1
Boc-3-trifluorometil-L-fenilalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Fe(3-CF3)-OH, Boc-L-Phe(3-trifluorometil)-OH, Boc-Fe(3-CF3)-OH
Documents
$117.78 /1G
Tamaño
Request Bulk Quote
Product Information

Boc-3-trifluoromethyl-L-phenylalanine is a valuable amino acid derivative widely utilized in the fields of medicinal chemistry and peptide synthesis. This compound features a unique trifluoromethyl group, which enhances its biological activity and stability, making it an excellent candidate for drug development and research applications. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides and biologically active compounds. Researchers have successfully employed Boc-3-trifluoromethyl-L-phenylalanine in the design of novel therapeutics, particularly in the development of inhibitors targeting specific enzymes and receptors.

The compound's distinctive properties, such as its lipophilicity and ability to influence molecular interactions, provide significant advantages over similar amino acid derivatives. This makes it an essential tool for chemists and biochemists looking to optimize the pharmacological profiles of their compounds. Whether in academic research or pharmaceutical development, Boc-3-trifluoromethyl-L-phenylalanine stands out as a versatile building block that can enhance the efficacy of peptide-based drugs.

Synonyms
Boc-L-Fe(3-CF3)-OH, Boc-L-Phe(3-trifluorometil)-OH, Boc-Fe(3-CF3)-OH
CAS Number
142995-31-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD00672524
PubChem ID
4678092
Melting Point
135 - 139 °C
Appearance
Polvo blanco
Optical Rotation
[a] 25 D = 7,7 ± 1 ° (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Fe(3-CF3)-OH, Boc-L-Phe(3-trifluorometil)-OH, Boc-Fe(3-CF3)-OH
CAS Number
142995-31-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD00672524
PubChem ID
4678092
Melting Point
135 - 139 °C
Appearance
Polvo blanco
Optical Rotation
[a] 25 D = 7,7 ± 1 ° (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-3-trifluoromethyl-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it helps create compounds with enhanced biological activity.
  • Drug Development: Its unique trifluoromethyl group can improve the pharmacokinetic properties of drug candidates, making it valuable in the development of new therapeutics.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to drugs or imaging agents, enhancing their efficacy and specificity.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter systems, helping scientists understand the role of amino acids in brain function and disorders.
  • Fluorinated Compound Studies: The presence of fluorine in its structure allows it to be a subject of interest in studies exploring the effects of fluorinated compounds in medicinal chemistry.

Citas