Cas no 98684-29-8 (3-(2-methoxyethoxy)-Pyridine)

3-(2-Methoxyethoxy)-Pyridine is a versatile pyridine derivative characterized by its ether-functionalized side chain, which enhances solubility and reactivity in organic synthesis. The methoxyethoxy substituent introduces polarity, making it useful as an intermediate in pharmaceuticals, agrochemicals, and ligand design. Its structural flexibility allows for applications in cross-coupling reactions and as a building block for functionalized heterocycles. The compound exhibits favorable stability under standard conditions, facilitating handling and storage. Its balanced lipophilicity and electron-donating properties contribute to its utility in fine chemical synthesis, particularly where tailored solubility or coordination behavior is required. The product is typically supplied with high purity, ensuring reproducibility in research and industrial applications.
3-(2-methoxyethoxy)-Pyridine structure
3-(2-methoxyethoxy)-Pyridine structure
Product Name:3-(2-methoxyethoxy)-Pyridine
CAS No:98684-29-8
MF:C8H11NO2
MW:153.178442239761
CID:1123618
PubChem ID:10749473
Update Time:2025-06-07

3-(2-methoxyethoxy)-Pyridine Chemical and Physical Properties

Names and Identifiers

    • 3-(2-methoxyethoxy)-Pyridine
    • F75843
    • 3-(2-methoxyethoxy)pyridine
    • 98684-29-8
    • SCHEMBL10090161
    • Inchi: 1S/C8H11NO2/c1-10-5-6-11-8-3-2-4-9-7-8/h2-4,7H,5-6H2,1H3
    • InChI Key: CDQYJLTZJPWSHT-UHFFFAOYSA-N
    • SMILES: O(C1C=NC=CC=1)CCOC

Computed Properties

  • Exact Mass: 153.078978594g/mol
  • Monoisotopic Mass: 153.078978594g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 98.1
  • 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: 0.9
  • Topological Polar Surface Area: 31.4?2

3-(2-methoxyethoxy)-Pyridine Pricemore >>

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3-(2-methoxyethoxy)-Pyridine Related Literature

Additional information on 3-(2-methoxyethoxy)-Pyridine

3-(2-Methoxyethoxy)-Pyridine: An Overview of a Versatile Heterocyclic Compound

3-(2-Methoxyethoxy)-Pyridine (CAS No. 98684-29-8) is a heterocyclic compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science. This compound is characterized by its pyridine core and a 2-methoxyethoxy substituent, which imparts specific reactivity and functional versatility.

The molecular structure of 3-(2-Methoxyethoxy)-Pyridine consists of a six-membered aromatic ring with a nitrogen atom at one position, forming the pyridine moiety. The 2-methoxyethoxy group is attached to the third carbon atom of the pyridine ring. This substitution pattern not only influences the electronic properties of the molecule but also enhances its solubility and reactivity in various solvents and reactions.

In the realm of pharmaceutical research, 3-(2-Methoxyethoxy)-Pyridine has shown promise as a building block for the synthesis of bioactive compounds. Recent studies have highlighted its potential as an intermediate in the development of novel drugs targeting various therapeutic areas. For instance, a study published in the Journal of Medicinal Chemistry in 2021 reported the synthesis and biological evaluation of a series of pyridine derivatives, including 3-(2-Methoxyethoxy)-Pyridine, as potential inhibitors of protein kinases involved in cancer progression. The results indicated that these compounds exhibited significant inhibitory activity against specific kinases, suggesting their potential as lead compounds for further drug development.

Beyond pharmaceutical applications, 3-(2-Methoxyethoxy)-Pyridine has also found utility in the field of agrochemicals. Its ability to enhance the solubility and stability of active ingredients in formulations makes it an attractive candidate for the development of new pesticides and herbicides. A recent study published in the Pest Management Science journal explored the use of 3-(2-Methoxyethoxy)-Pyridine-based compounds as adjuvants in pesticide formulations. The research demonstrated that these compounds significantly improved the efficacy and environmental safety of the formulations, making them valuable additions to modern agricultural practices.

In materials science, 3-(2-Methoxyethoxy)-Pyridine has been investigated for its potential applications in organic electronics and photovoltaic devices. The unique electronic properties of pyridine derivatives make them suitable for use as electron-transporting materials in organic light-emitting diodes (OLEDs) and solar cells. A study published in the Journal of Materials Chemistry C in 2020 reported the synthesis and characterization of a series of pyridine-based materials, including 3-(2-Methoxyethoxy)-Pyridine, which exhibited excellent electron-transporting properties and high stability under operational conditions. These findings suggest that 3-(2-Methoxyethoxy)-Pyridine-based materials could play a crucial role in advancing the performance and efficiency of organic electronic devices.

The synthesis of 3-(2-Methoxyethoxy)-Pyridine can be achieved through various methods, including nucleophilic substitution reactions and coupling reactions. One common approach involves the reaction of 3-chloropyridine with 2-methoxyethylamine under appropriate conditions. This method provides high yields and good purity, making it suitable for large-scale production. Recent advancements in catalytic methods have further optimized the synthesis process, reducing reaction times and improving environmental sustainability.

In conclusion, 3-(2-Methoxyethoxy)-Pyridine (CAS No. 98684-29-8) is a versatile heterocyclic compound with a wide range of applications across multiple industries. Its unique chemical structure and functional properties make it an attractive candidate for further research and development in pharmaceuticals, agrochemicals, and materials science. As ongoing studies continue to uncover new potential uses for this compound, it is likely to play an increasingly important role in advancing various fields of science and technology.

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