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Catalog Number:
15443
CAS Number:
479064-88-5
Boc-(S-3-amino-3-(4-fluorophenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-β-Phe(4-F)-OH, (S-Boc-4-fluoro-β-phenylalanine
Documents
$65.40 /250MG
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Product Information

Boc-(S)-3-amino-3-(4-fluorophenyl)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative is particularly valuable in the synthesis of peptide-based drugs, where its unique structure enhances the stability and bioactivity of the resulting compounds. The presence of the Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, making it an ideal choice for chemists looking to streamline their synthetic pathways.

In addition to its applications in drug development, Boc-(S)-3-amino-3-(4-fluorophenyl)propionic acid serves as a crucial building block in the creation of novel therapeutic agents targeting various diseases. Its fluorinated phenyl group can improve the pharmacokinetic properties of the final products, offering researchers a significant advantage in developing more effective treatments. With its robust profile and practical applications, this compound is essential for professionals aiming to innovate in the field of medicinal chemistry.

Synonyms
Boc-L-β-Phe(4-F)-OH, (S-Boc-4-fluoro-β-phenylalanine
CAS Number
479064-88-5
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18FNO4
Molecular Weight
283.3
MDL Number
MFCD03427919
PubChem ID
2734583
Appearance
White to off-white solid
Optical Rotation
[a]D25 = -36 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(4-F)-OH, (S-Boc-4-fluoro-β-phenylalanine
CAS Number
479064-88-5
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18FNO4
Molecular Weight
283.3
MDL Number
MFCD03427919
PubChem ID
2734583
Appearance
White to off-white solid
Optical Rotation
[a]D25 = -36 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-3-amino-3-(4-fluorophenyl)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.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, allowing researchers to create complex peptides with specific functionalities, enhancing drug delivery systems.
  • Biochemical Research: The compound is valuable in studying protein interactions and enzyme activities, providing insights into metabolic pathways and disease mechanisms.
  • Drug Design: Its unique structure aids in the design of selective inhibitors, particularly in cancer research, where targeting specific pathways can lead to more effective therapies.
  • Material Science: The compound can be incorporated into polymeric materials, improving their properties for use in drug delivery systems and biomedical applications.

Citations