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Catalog Number:
15539
CAS Number:
500789-03-7
Boc-(R-3-amino-3-(2-fluorophenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-β-Phe(2-F)-OH, (R-Boc-2-fluoro-β-phenylalanine
Documents
$65.40 /250MG
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Product Information

Boc-(R)-3-amino-3-(2-fluorophenyl)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative, characterized by its unique fluorophenyl group, plays a crucial role in the synthesis of peptide-based therapeutics and drug candidates. Its Boc (tert-butyloxycarbonyl) protecting group enhances stability and facilitates ease of handling during chemical reactions, making it an ideal choice for researchers focused on complex organic synthesis.

The compound's specific structure allows for the exploration of novel drug formulations, particularly in the development of inhibitors and modulators targeting various biological pathways. Its application extends to the creation of advanced materials and bioconjugates, showcasing its potential in both medicinal chemistry and materials science. Researchers appreciate its ability to enhance bioactivity and selectivity in drug design, paving the way for innovative therapeutic solutions.

Synonyms
Boc-D-β-Phe(2-F)-OH, (R-Boc-2-fluoro-β-phenylalanine
CAS Number
500789-03-7
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18FNO4
Molecular Weight
283.3
MDL Number
MFCD03427955
PubChem ID
2756795
Appearance
White to off white powder
Optical Rotation
[a]D25 = +34 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-β-Phe(2-F)-OH, (R-Boc-2-fluoro-β-phenylalanine
CAS Number
500789-03-7
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18FNO4
Molecular Weight
283.3
MDL Number
MFCD03427955
PubChem ID
2756795
Appearance
White to off white powder
Optical Rotation
[a]D25 = +34 ± 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-(R)-3-amino-3-(2-fluorophenyl)propionic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceuticals, particularly in developing drugs targeting neurological disorders due to its structural similarity to amino acids.
  • Peptide Synthesis: It is frequently used in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield, which are essential for therapeutic applications.
  • Bioconjugation: The compound can be employed in bioconjugation processes, facilitating the attachment of drugs to antibodies or other biomolecules, enhancing targeted delivery in cancer therapies.
  • Research in Neuroscience: Its unique fluorophenyl group makes it valuable in studies investigating receptor interactions and signaling pathways in the nervous system, helping to advance our understanding of neuropharmacology.
  • Analytical Chemistry: The compound is useful in developing analytical methods for quantifying amino acids in biological samples, aiding in nutritional studies and metabolic research.

Citations