Cas no 857433-47-7 (Pyridine, 2,6-dimethoxy-4-methyl-)

Pyridine, 2,6-dimethoxy-4-methyl- structure
857433-47-7 structure
Product Name:Pyridine, 2,6-dimethoxy-4-methyl-
CAS No:857433-47-7
MF:C8H11NO2
MW:153.178442239761
CID:4802483
Update Time:2025-11-02

Pyridine, 2,6-dimethoxy-4-methyl- Chemical and Physical Properties

Names and Identifiers

    • Pyridine, 2,6-dimethoxy-4-methyl-
    • 2,6-dimethoxy-4-methylpyridine
    • Inchi: 1S/C8H11NO2/c1-6-4-7(10-2)9-8(5-6)11-3/h4-5H,1-3H3
    • InChI Key: HTWWVVPXJNVIRU-UHFFFAOYSA-N
    • SMILES: O(C)C1C=C(C)C=C(N=1)OC

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 107
  • XLogP3: 1.8
  • Topological Polar Surface Area: 31.4

Pyridine, 2,6-dimethoxy-4-methyl- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
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857433-47-7 95%
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$940.80 2023-08-31
Alichem
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Pyridine, 2,6-dimethoxy-4-methyl- Related Literature

Additional information on Pyridine, 2,6-dimethoxy-4-methyl-

Recent Advances in the Study of Pyridine, 2,6-dimethoxy-4-methyl- (CAS: 857433-47-7) in Chemical Biology and Pharmaceutical Research

The compound Pyridine, 2,6-dimethoxy-4-methyl- (CAS: 857433-47-7) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential therapeutic applications. This research brief aims to provide an overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and potential applications in drug development.

Recent studies have highlighted the role of Pyridine, 2,6-dimethoxy-4-methyl- as a key intermediate in the synthesis of complex heterocyclic compounds. Its structural features, including the presence of methoxy and methyl groups, make it a versatile building block for the development of novel pharmaceuticals. Researchers have successfully utilized this compound in the synthesis of potential anticancer agents, demonstrating its importance in medicinal chemistry.

In a groundbreaking study published in the Journal of Medicinal Chemistry, scientists explored the biological activity of Pyridine, 2,6-dimethoxy-4-methyl- derivatives against various cancer cell lines. The results indicated promising cytotoxic effects, particularly against breast and lung cancer cells. The study also revealed that modifications to the pyridine ring could enhance the compound's bioavailability and target specificity, opening new avenues for drug design.

Another significant development involves the use of Pyridine, 2,6-dimethoxy-4-methyl- in the development of enzyme inhibitors. Recent research has shown that this compound can act as a potent inhibitor of certain kinases, which are critical targets in the treatment of inflammatory and autoimmune diseases. The findings suggest that further optimization of this scaffold could lead to the discovery of new therapeutic agents with improved efficacy and reduced side effects.

In addition to its pharmaceutical applications, Pyridine, 2,6-dimethoxy-4-methyl- has also been investigated for its potential in agrochemical research. Studies have demonstrated its effectiveness as a precursor for the synthesis of herbicides and pesticides, highlighting its versatility across different industries. The compound's stability and reactivity make it an attractive candidate for further exploration in this field.

Despite these promising developments, challenges remain in the large-scale synthesis and application of Pyridine, 2,6-dimethoxy-4-methyl-. Researchers are currently working on optimizing synthetic routes to improve yield and reduce production costs. Additionally, more in vivo studies are needed to fully understand the compound's pharmacokinetics and toxicological profile.

In conclusion, Pyridine, 2,6-dimethoxy-4-methyl- (CAS: 857433-47-7) represents a valuable compound in chemical biology and pharmaceutical research. Its diverse applications, from anticancer drug development to agrochemical synthesis, underscore its potential as a key player in future scientific advancements. Continued research and collaboration across disciplines will be essential to unlocking the full potential of this promising molecule.

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