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Catalog Number:
15573
CAS Number:
501015-17-4
Ácido Boc-( R -3-amino-3-(2-trifluorometilfenil)propiónico
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-D-β-Phe(2-CF3)-OH, ( R -Boc-2-trifluorometil-β-fenilalanina
Documents
$60.00 /250 mg
Tamaño
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Product Information

Boc-(R)-3-amino-3-(2-trifluoromethylphenyl)propionic acid is a versatile amino acid derivative that plays a crucial role in pharmaceutical research and development. This compound is particularly valued for its unique trifluoromethyl group, which enhances lipophilicity and biological activity, making it an excellent candidate for drug design and synthesis. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, facilitating the development of complex peptide structures and contributing to advancements in medicinal chemistry.

Researchers and industry professionals utilize Boc-(R)-3-amino-3-(2-trifluoromethylphenyl)propionic acid in the synthesis of bioactive compounds, particularly in the creation of peptide-based therapeutics. Its ability to improve the pharmacokinetic properties of peptides makes it a preferred choice for those looking to enhance drug efficacy. Additionally, its application in the development of inhibitors and modulators in various biological pathways underscores its importance in the field of drug discovery. With its unique properties and practical applications, this compound stands out as a valuable tool for advancing research and innovation in pharmaceuticals.

Synonyms
Boc-D-β-Phe(2-CF3)-OH, ( R -Boc-2-trifluorometil-β-fenilalanina
CAS Number
501015-17-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD03427963
PubChem ID
22309331
Melting Point
46-52 °C
Appearance
Sólido blanco
Optical Rotation
[a] D 25 = +14,0 ± 2º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-D-β-Phe(2-CF3)-OH, ( R -Boc-2-trifluorometil-β-fenilalanina
CAS Number
501015-17-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.31
MDL Number
MFCD03427963
PubChem ID
22309331
Melting Point
46-52 °C
Appearance
Sólido blanco
Optical Rotation
[a] D 25 = +14,0 ± 2º (C=1 en EtOH)
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-(R)-3-amino-3-(2-trifluoromethylphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in synthesizing 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 researchers to create complex peptides with high purity and yield, which is essential for therapeutic applications.
  • Biochemical Research: The compound is valuable in studying protein interactions and enzyme activities, helping scientists understand biological processes and develop new therapeutic strategies.
  • Fluorinated Compounds: Its trifluoromethyl group enhances the bioavailability and metabolic stability of compounds, making it a preferred choice in designing new drugs with improved efficacy.
  • Material Science: This chemical is also explored in the development of advanced materials, including polymers and coatings, due to its unique chemical properties that can enhance material performance.

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