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Catalog Number:
15574
CAS Number:
500770-77-4
Acide boc-( S -3-amino-3-(2-trifluorométhylphényl)propionique)
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-β-Phe(2-CF3)-OH, ( S -Boc-2-trifluorométhyl-β-phénylalanine
Documents
$55.00 /250 mg
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Product Information

Boc-(S)-3-amino-3-(2-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 trifluoromethylphenyl group contributes to its lipophilicity, facilitating interactions with biological membranes and enhancing bioavailability in medicinal applications. Researchers often leverage this compound in the design of novel therapeutics, particularly in the development of inhibitors and modulators targeting specific biological pathways.

In addition to its applications in drug discovery, Boc-(S)-3-amino-3-(2-trifluoromethylphenyl)propionic acid serves as a valuable building block in the synthesis of complex organic molecules. Its ability to undergo various chemical transformations allows for the creation of diverse derivatives, expanding its utility in medicinal chemistry. This compound is particularly relevant for professionals engaged in the synthesis of fluorinated compounds, which are known for their enhanced metabolic stability and improved pharmacokinetic properties. With its unique structural features and practical applications, this compound stands out as a key resource for researchers and industry professionals alike.

Synonyms
Boc-L-β-Phe(2-CF3)-OH, ( S -Boc-2-trifluorométhyl-β-phénylalanine
CAS Number
500770-77-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 18 F 3 NON 4
Molecular Weight
333.31
MDL Number
MFCD03427925
PubChem ID
22309331
Appearance
Poudre blanche
Optical Rotation
[a]D25 = -12 to -14 °(C=1 in Ethanol)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-L-β-Phe(2-CF3)-OH, ( S -Boc-2-trifluorométhyl-β-phénylalanine
CAS Number
500770-77-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 18 F 3 NON 4
Molecular Weight
333.31
MDL Number
MFCD03427925
PubChem ID
22309331
Appearance
Poudre blanche
Optical Rotation
[a]D25 = -12 to -14 °(C=1 in Ethanol)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(S)-3-amino-3-(2-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 creation of complex peptides that can be used in therapeutic applications, enhancing the efficiency of drug design.
  • Biochemical Research: Researchers leverage this compound to study protein interactions and enzyme activities, providing insights into biological processes and potential therapeutic targets.
  • Material Science: Its unique chemical structure makes it suitable for developing advanced materials, including polymers that exhibit specific mechanical and thermal properties, beneficial in various industrial applications.
  • Fluorinated Compounds Research: The trifluoromethyl group enhances the compound's bioactivity and stability, making it a valuable subject in studies aimed at developing new fluorinated pharmaceuticals with improved efficacy.

Citations