🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15580
CAS Number:
500770-78-5
Ácido Boc-( S )-3-amino-3-(3-trifluorometilfenil)propiónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-β-Phe(3-CF3)-OH, ( S )-Boc-3-trifluorometil-β-fenilalanina
Documents
$65.00 /250 mg
Tamaño
Request Bulk Quote
Product Information

Boc-(S)-3-amino-3-(3-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 medicinal chemistry applications. Its unique trifluoromethylphenyl group contributes to its lipophilicity, allowing for improved interactions in biological systems, which is particularly beneficial in drug design and development.

Researchers and industry professionals can leverage Boc-(S)-3-amino-3-(3-trifluoromethylphenyl)propionic acid in the synthesis of bioactive peptides and as a building block in the creation of novel therapeutic agents. Its ability to facilitate the formation of complex structures while maintaining high purity levels makes it a valuable asset in the pharmaceutical industry. Additionally, its distinctive properties may lead to enhanced efficacy and selectivity in drug formulations, paving the way for innovative treatments in various therapeutic areas.

Synonyms
Boc-L-β-Phe(3-CF3)-OH, ( S )-Boc-3-trifluorometil-β-fenilalanina
CAS Number
500770-78-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD03427926
PubChem ID
22309332
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -14 ± 2 º (C=1 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-β-Phe(3-CF3)-OH, ( S )-Boc-3-trifluorometil-β-fenilalanina
CAS Number
500770-78-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD03427926
PubChem ID
22309332
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -14 ± 2 º (C=1 en CHCl 3 )
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-(S)-3-amino-3-(3-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 ability to modulate neurotransmitter activity.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, where its protective Boc group allows for selective reactions, making it easier to construct complex peptide chains.
  • Biochemical Research: Researchers utilize this compound to study protein interactions and enzyme activities, providing insights into metabolic pathways and potential therapeutic targets.
  • Material Science: The compound's unique trifluoromethyl group enhances its properties in developing advanced materials, including coatings and polymers with improved thermal and chemical resistance.
  • Agricultural Chemistry: It has applications in the formulation of agrochemicals, where its structural characteristics can improve the efficacy and stability of pesticides and herbicides.

Citas