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Catalog Number:
15245
CAS Number:
218608-99-2
Boc-2-fluoro-L-β-homophenylalanine
Purity:
≥ 98%
Synonym(s):
Boc-L-β-HomoPhe(2-F)-OH, Boc-(S-3-amino-4-(2-fluorophenyl)butyric acid
Documents
$65.40 /100MG
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Product Information

Boc-2-fluoro-L-b-homophenylalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued for its unique fluorinated phenyl group, which enhances the bioactivity and stability of peptides. Researchers in medicinal chemistry utilize Boc-2-fluoro-L-b-homophenylalanine to create novel peptide-based therapeutics, especially in the design of inhibitors and modulators for various biological pathways. Its ability to introduce specific steric and electronic properties makes it an essential building block for developing targeted therapies in oncology and neurology.

In addition to its applications in drug discovery, Boc-2-fluoro-L-b-homophenylalanine is also employed in the synthesis of complex natural products and in the study of protein interactions. The compound's protective Boc group allows for selective reactions, making it easier to manipulate during synthesis. This feature, combined with its fluorinated structure, provides researchers with a powerful tool for exploring new therapeutic avenues and optimizing existing compounds for enhanced efficacy.

Synonyms
Boc-L-β-HomoPhe(2-F)-OH, Boc-(S-3-amino-4-(2-fluorophenyl)butyric acid
CAS Number
218608-99-2
Purity
≥ 98%
Molecular Formula
C15H20FNO4
Molecular Weight
297.33
MDL Number
MFCD01076279
PubChem ID
21975848
Melting Point
108-114 °C
Appearance
White to off-white powder
Optical Rotation
[a]D21 = -19 ± 2º (C=1, in EtOH)
Conditions
Store at 0-8 °C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
Synonyms
Boc-L-β-HomoPhe(2-F)-OH, Boc-(S-3-amino-4-(2-fluorophenyl)butyric acid
CAS Number
218608-99-2
Purity
≥ 98%
Molecular Formula
C15H20FNO4
Molecular Weight
297.33
MDL Number
MFCD01076279
PubChem ID
21975848
Melting Point
108-114 °C
Appearance
White to off-white powder
Optical Rotation
[a]D21 = -19 ± 2º (C=1, in EtOH)
Conditions
Store at 0-8 °C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Boc-2-fluoro-L-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating modified peptides that can enhance biological activity.
  • Drug Development: Its unique fluorinated structure makes it a candidate for designing novel pharmaceuticals, especially in targeting specific receptors in the body.
  • Biotechnology: Used in the production of biologically active compounds, it helps in the development of therapeutic proteins and enzymes, contributing to advancements in biotechnology.
  • Research in Neuroscience: The compound's properties allow researchers to study interactions in neurological pathways, potentially leading to breakthroughs in treating neurological disorders.
  • Analytical Chemistry: It is employed in various analytical techniques to identify and quantify amino acids in complex mixtures, aiding in quality control and research applications.

Citations