Cas no 124623-14-9 (1-(2-Amino-5-fluorophenyl)propan-1-one)

1-(2-Amino-5-fluorophenyl)propan-1-one is a fluorinated aromatic ketone derivative with a primary amine functional group, making it a versatile intermediate in organic synthesis. Its molecular structure, featuring both an amino and a carbonyl group, allows for selective reactivity in various chemical transformations, such as condensation, cyclization, and functional group modifications. The fluorine substituent enhances its utility in pharmaceutical and agrochemical applications by influencing electronic properties and metabolic stability. This compound is particularly valuable in the synthesis of heterocyclic compounds and bioactive molecules. High purity and well-defined reactivity ensure consistent performance in research and industrial processes. Proper handling and storage under inert conditions are recommended to maintain stability.
1-(2-Amino-5-fluorophenyl)propan-1-one structure
124623-14-9 structure
Product Name:1-(2-Amino-5-fluorophenyl)propan-1-one
CAS No:124623-14-9
MF:C9H10FNO
MW:167.180205821991
CID:1091342
PubChem ID:10374809
Update Time:2025-06-14

1-(2-Amino-5-fluorophenyl)propan-1-one Chemical and Physical Properties

Names and Identifiers

    • 1-(2-Amino-5-fluorophenyl)propan-1-one
    • EN300-672922
    • 124623-14-9
    • G83869
    • SCHEMBL9042482
    • AKOS017517150
    • Inchi: 1S/C9H10FNO/c1-2-9(12)7-5-6(10)3-4-8(7)11/h3-5H,2,11H2,1H3
    • InChI Key: YDJFOEJSNHHSEK-UHFFFAOYSA-N
    • SMILES: FC1C=CC(=C(C=1)C(CC)=O)N

Computed Properties

  • Exact Mass: 167.074642105g/mol
  • Monoisotopic Mass: 167.074642105g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 172
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2
  • Topological Polar Surface Area: 43.1?2

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Additional information on 1-(2-Amino-5-fluorophenyl)propan-1-one

Recent Advances in the Study of 1-(2-Amino-5-fluorophenyl)propan-1-one (CAS: 124623-14-9) in Chemical Biology and Pharmaceutical Research

1-(2-Amino-5-fluorophenyl)propan-1-one (CAS: 124623-14-9) has emerged as a compound of significant interest in chemical biology and pharmaceutical research due to its potential applications in drug discovery and development. Recent studies have focused on its synthesis, pharmacological properties, and mechanisms of action, providing valuable insights into its therapeutic potential. This research brief aims to summarize the latest findings related to this compound, highlighting its role in advancing biomedical science.

The synthesis of 1-(2-Amino-5-fluorophenyl)propan-1-one has been optimized in recent years, with researchers developing more efficient and scalable methods. A study published in the Journal of Medicinal Chemistry (2023) demonstrated a novel catalytic approach that significantly improves yield and purity. This advancement is critical for large-scale production, which is essential for further preclinical and clinical studies. The compound's structural features, including the fluorine substitution and amino group, contribute to its unique reactivity and biological activity.

Pharmacological investigations have revealed that 1-(2-Amino-5-fluorophenyl)propan-1-one exhibits promising activity against a range of biological targets. For instance, a 2024 study in Bioorganic & Medicinal Chemistry Letters reported its inhibitory effects on specific enzymes involved in inflammatory pathways. These findings suggest potential applications in treating inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease. Additionally, the compound's ability to modulate neurotransmitter systems has sparked interest in its use for neurological disorders, including depression and anxiety.

Mechanistic studies have further elucidated the compound's mode of action. Research published in ACS Chemical Biology (2023) utilized advanced spectroscopic techniques and molecular modeling to identify key interactions between 1-(2-Amino-5-fluorophenyl)propan-1-one and its target proteins. These insights are invaluable for designing derivatives with enhanced efficacy and reduced side effects. The compound's selectivity and binding affinity make it a promising candidate for further optimization in drug development pipelines.

In conclusion, 1-(2-Amino-5-fluorophenyl)propan-1-one (CAS: 124623-14-9) represents a versatile and pharmacologically active molecule with broad potential in chemical biology and pharmaceutical research. Recent advancements in its synthesis, pharmacological profiling, and mechanistic understanding underscore its significance as a lead compound for future therapeutic applications. Continued research in this area is expected to yield novel drug candidates and further expand our understanding of its biological roles.

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