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Catalog Number:
15586
CAS Number:
500770-79-6
Acide boc-( S -3-amino-3-(4-trifluorométhylphényl)propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-β-Phe(4-CF3)-OH, ( S -Boc-4-trifluorométhyl-β-phénylalanine
Documents
$65.40 /250 mg
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Product Information

Boc-(S)-3-amino-3-(4-trifluoromethylphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug formulation. Its unique trifluoromethyl group contributes to its lipophilicity, allowing for improved membrane permeability and bioavailability in drug delivery systems.

Researchers and industry professionals can leverage this compound in the synthesis of bioactive peptides and as a building block in the development of novel therapeutic agents. Its specific structural characteristics enable the exploration of new pharmacological profiles, particularly in the fields of medicinal chemistry and drug discovery. The compound's ability to facilitate the creation of complex molecular architectures makes it a valuable tool for advancing research in various therapeutic areas, including oncology and neurology.

Synonyms
Boc-L-β-Phe(4-CF3)-OH, ( S -Boc-4-trifluorométhyl-β-phénylalanine
CAS Number
500770-79-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 18 F 3 NON 4
Molecular Weight
333.31
MDL Number
MFCD03427927
PubChem ID
2766034
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -28 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-L-β-Phe(4-CF3)-OH, ( S -Boc-4-trifluorométhyl-β-phénylalanine
CAS Number
500770-79-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 18 F 3 NON 4
Molecular Weight
333.31
MDL Number
MFCD03427927
PubChem ID
2766034
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -28 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(S)-3-amino-3-(4-trifluoromethylphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders due to its unique structural properties.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, allowing for the efficient construction of complex peptides that can be used in therapeutic applications.
  • Biochemical Research: Researchers employ this compound to study the interactions of amino acids in proteins, enhancing our understanding of enzyme mechanisms and protein folding.
  • Material Science: The compound's properties make it suitable for developing novel materials with specific chemical functionalities, which can be applied in coatings and adhesives.
  • Environmental Chemistry: It is used in studies related to the degradation of pollutants, helping to develop methods for environmental remediation and sustainability.

Citations