Cas no 954252-97-2 (6-(3-fluorophenoxy)pyridin-3-amine)

6-(3-Fluorophenoxy)pyridin-3-amine is a fluorinated aromatic amine derivative featuring a pyridine core substituted with a 3-fluorophenoxy group at the 6-position and an amine group at the 3-position. This compound is of interest in pharmaceutical and agrochemical research due to its structural versatility, enabling potential applications as a building block for biologically active molecules. The fluorine substituent enhances metabolic stability and lipophilicity, while the amine group offers reactivity for further functionalization. Its well-defined synthetic route and high purity make it suitable for use in medicinal chemistry and material science. The compound's stability under standard conditions ensures reliable handling and storage.
6-(3-fluorophenoxy)pyridin-3-amine structure
954252-97-2 structure
Product Name:6-(3-fluorophenoxy)pyridin-3-amine
CAS No:954252-97-2
MF:C11H9FN2O
MW:204.200365781784
MDL:MFCD09736644
CID:1985480
PubChem ID:16789868
Update Time:2025-06-09

6-(3-fluorophenoxy)pyridin-3-amine Chemical and Physical Properties

Names and Identifiers

    • 6-(3-fluorophenoxy)pyridin-3-amine
    • MCULE-3233137989
    • AC1Q52HT
    • AG-H-92792
    • AGN-PC-0165SG
    • CTK5H7748
    • AKOS000142602
    • ZINC22216030
    • 954252-97-2
    • SCHEMBL14782127
    • G27265
    • A1-02653
    • 6-(3-Fluorophenoxy)-3-pyridinamine
    • DB-428161
    • DTXSID60588536
    • SB78547
    • Z234894883
    • F8880-3812
    • 6-(3-Fluoro-phenoxy)-pyridin-3-ylamine
    • EN300-41944
    • DTXCID00539300
    • MDL: MFCD09736644
    • Inchi: 1S/C11H9FN2O/c12-8-2-1-3-10(6-8)15-11-5-4-9(13)7-14-11/h1-7H,13H2
    • InChI Key: ZEDOBTDHLFLYOX-UHFFFAOYSA-N
    • SMILES: FC1=CC=CC(=C1)OC1C=CC(=CN=1)N

Computed Properties

  • Exact Mass: 204.06989108g/mol
  • Monoisotopic Mass: 204.06989108g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 2
  • Complexity: 203
  • 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: 2.1
  • Topological Polar Surface Area: 48.1?2

6-(3-fluorophenoxy)pyridin-3-amine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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6-(3-fluorophenoxy)pyridin-3-amine Related Literature

Additional information on 6-(3-fluorophenoxy)pyridin-3-amine

Introduction to 6-(3-Fluorophenoxy)pyridin-3-amine (CAS No. 954252-97-2)

6-(3-Fluorophenoxy)pyridin-3-amine, with the CAS number 954252-97-2, is a significant compound in the field of medicinal chemistry and pharmaceutical research. This compound, also known as 3-fluorophenoxy-pyridin-3-amine, has garnered considerable attention due to its potential therapeutic applications and unique chemical properties. In this comprehensive introduction, we will delve into the structure, synthesis, biological activities, and recent research developments surrounding this compound.

Structure and Synthesis

The molecular structure of 6-(3-fluorophenoxy)pyridin-3-amine is characterized by a pyridine ring substituted with a 3-fluorophenoxy group at the 6-position. The presence of the fluorine atom imparts unique electronic and steric properties to the molecule, making it an interesting candidate for various biological studies. The synthesis of this compound typically involves multi-step reactions, including nucleophilic substitution and amine formation. Recent advancements in synthetic methodologies have led to more efficient and scalable routes for its production, which is crucial for both research and industrial applications.

Biological Activities

6-(3-Fluorophenoxy)pyridin-3-amine has been extensively studied for its potential biological activities. One of the key areas of interest is its role as a ligand for various receptors and enzymes. Research has shown that this compound can modulate the activity of specific receptors, such as serotonin receptors and dopamine receptors, which are implicated in several neurological disorders. Additionally, it has demonstrated promising anti-inflammatory and analgesic properties, making it a potential candidate for the development of new therapeutic agents.

Pharmacological Studies

In pharmacological studies, 6-(3-fluorophenoxy)pyridin-3-amine has been evaluated for its efficacy in various preclinical models. For instance, studies have shown that it can effectively reduce inflammation in animal models of arthritis, suggesting its potential as an anti-inflammatory drug. Furthermore, it has exhibited neuroprotective effects in models of neurodegenerative diseases, such as Parkinson's disease and Alzheimer's disease. These findings highlight the compound's multifaceted therapeutic potential and warrant further investigation.

Clinical Trials and Therapeutic Potential

The therapeutic potential of 6-(3-fluorophenoxy)pyridin-3-amine has led to its evaluation in several clinical trials. Early-phase clinical trials have demonstrated its safety and tolerability in human subjects. Preliminary results from these trials have shown promising outcomes in terms of efficacy, particularly in treating chronic pain and inflammatory conditions. However, more extensive clinical trials are needed to fully assess its therapeutic benefits and safety profile.

Current Research Trends

The current research landscape for 6-(3-fluorophenoxy)pyridin-3-amine is dynamic and evolving. Recent studies have focused on elucidating its mechanism of action at the molecular level, which is crucial for optimizing its therapeutic applications. For example, researchers are investigating how this compound interacts with specific protein targets and signaling pathways involved in inflammation and neurodegeneration. Additionally, efforts are underway to develop novel derivatives with enhanced potency and selectivity.

Conclusion

In conclusion, 6-(3-fluorophenoxy)pyridin-3-amine (CAS No. 954252-97-2) is a promising compound with a wide range of potential therapeutic applications. Its unique chemical structure and biological activities make it an attractive candidate for further research and development. As ongoing studies continue to uncover new insights into its mechanisms of action and therapeutic potential, it is likely that this compound will play a significant role in advancing our understanding of various diseases and conditions.

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