🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
04141
CAS Number:
114873-01-7
Boc-3-fluoro-L-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Phe(3-F)-OH, Boc- m -fluoro-L-Phe-OH, Boc-Phe(3-F)-OH
Documents
$29.34 /1G
Taille
Request Bulk Quote
Product Information

Boc-3-fluoro-L-phenylalanine is a valuable amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a unique fluorine substitution, which enhances its biological activity and stability, making it an essential building block for researchers in medicinal chemistry and biochemistry. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, facilitating the synthesis of complex peptides and proteins.

This compound is particularly useful in the development of pharmaceuticals targeting various diseases, including cancer and neurological disorders, where fluorinated amino acids can improve the efficacy and selectivity of therapeutic agents. Researchers appreciate its ability to modify peptide properties, leading to enhanced binding affinities and improved pharmacokinetic profiles. With its unique characteristics, Boc-3-fluoro-L-phenylalanine stands out as a versatile tool for scientists aiming to innovate in drug design and development.

Synonyms
Boc-L-Phe(3-F)-OH, Boc- m -fluoro-L-Phe-OH, Boc-Phe(3-F)-OH
CAS Number
114873-01-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 14 H 18 FNO 4
Molecular Weight
283.2
MDL Number
MFCD00672522
PubChem ID
3698526
Melting Point
75 - 77 °C
Appearance
Poudre blanche
Optical Rotation
[a] 25 D = 7 ± 2 ° (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-Phe(3-F)-OH, Boc- m -fluoro-L-Phe-OH, Boc-Phe(3-F)-OH
CAS Number
114873-01-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 14 H 18 FNO 4
Molecular Weight
283.2
MDL Number
MFCD00672522
PubChem ID
3698526
Melting Point
75 - 77 °C
Appearance
Poudre blanche
Optical Rotation
[a] 25 D = 7 ± 2 ° (C=1 dans MeOH)
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-3-fluoro-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of novel therapeutic agents.
  • Drug Development: Its unique fluorinated structure can enhance the bioactivity and stability of pharmaceutical compounds, making it a key player in drug formulation.
  • Biochemical Research: Researchers use it to study protein interactions and enzyme activities, providing insights into metabolic pathways and disease mechanisms.
  • Fluorine Chemistry: The incorporation of fluorine into organic molecules can improve their pharmacokinetic properties, leading to more effective drugs with fewer side effects.
  • Material Science: Its applications extend to the development of advanced materials, including polymers and coatings, due to its unique chemical properties.

Citations