Cas no 405143-46-6 (2,4-dichloro-3-methoxypyridine)

2,4-Dichloro-3-methoxypyridine is a versatile heterocyclic compound featuring a pyridine core substituted with chlorine atoms at the 2- and 4-positions and a methoxy group at the 3-position. This structure imparts reactivity suitable for further functionalization, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The electron-withdrawing chloro groups enhance electrophilic substitution potential, while the methoxy group contributes to regioselective control in cross-coupling reactions. Its stability under standard conditions and compatibility with common organic transformations underscore its utility in fine chemical manufacturing. The compound is particularly useful in constructing complex molecules requiring selective halogenation and alkoxylation patterns.
2,4-dichloro-3-methoxypyridine structure
405143-46-6 structure
Product Name:2,4-dichloro-3-methoxypyridine
CAS No:405143-46-6
MF:C6H5Cl2NO
MW:178.015999555588
CID:1512611
PubChem ID:54284943
Update Time:2025-11-02

2,4-dichloro-3-methoxypyridine Chemical and Physical Properties

Names and Identifiers

    • 2,4-dichloro-3-methoxypyridine
    • SCHEMBL11755564
    • MFCD16610791
    • AKOS027426869
    • SB53294
    • 405143-46-6
    • EN300-761396
    • MDL: MFCD16610791
    • Inchi: 1S/C6H5Cl2NO/c1-10-5-4(7)2-3-9-6(5)8/h2-3H,1H3
    • InChI Key: RTLLDGMXZMTOLG-UHFFFAOYSA-N
    • SMILES: ClC1C=CN=C(C=1OC)Cl

Computed Properties

  • Exact Mass: 176.9748192g/mol
  • Monoisotopic Mass: 176.9748192g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 112
  • 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: 2.4
  • Topological Polar Surface Area: 22.1?2

2,4-dichloro-3-methoxypyridine Pricemore >>

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Additional information on 2,4-dichloro-3-methoxypyridine

Exploring the Versatile Applications and Properties of 2,4-Dichloro-3-Methoxypyridine (CAS No. 405143-46-6)

2,4-Dichloro-3-methoxypyridine (CAS No. 405143-46-6) is a specialized pyridine derivative that has garnered significant attention in the pharmaceutical and agrochemical industries. This compound, characterized by its unique chloro and methoxy substituents, serves as a crucial intermediate in the synthesis of various high-value products. Its molecular structure, featuring a pyridine ring with specific functional groups, makes it a versatile building block for researchers and manufacturers alike.

The growing interest in 2,4-dichloro-3-methoxypyridine can be attributed to its role in developing novel pharmaceuticals and crop protection agents. With the increasing demand for precision medicine and sustainable agriculture, this compound has become a focal point for innovation. Researchers are particularly intrigued by its potential in creating targeted therapies and environmentally friendly pesticides, aligning with current trends in green chemistry and reduced environmental impact.

From a chemical perspective, 2,4-dichloro-3-methoxypyridine exhibits several noteworthy properties. The presence of electron-withdrawing chlorine atoms and the electron-donating methoxy group creates an interesting electronic environment on the pyridine ring. This unique combination influences the compound's reactivity patterns, making it particularly valuable for nucleophilic aromatic substitution reactions and other heterocyclic transformations. These characteristics have made it a preferred choice for medicinal chemistry applications where precise molecular modifications are required.

The synthesis of 2,4-dichloro-3-methoxypyridine typically involves chlorination reactions of appropriate pyridine precursors, followed by methoxylation at the specific position. Manufacturers have developed optimized protocols to ensure high yield and purity of this intermediate, which is crucial for its subsequent applications. Recent advancements in catalytic processes have further improved the cost-effectiveness and sustainability of its production, addressing the industry's growing emphasis on green synthesis methods.

In the pharmaceutical sector, 2,4-dichloro-3-methoxypyridine serves as a key intermediate for various active pharmaceutical ingredients (APIs). Its structural features make it particularly valuable for developing central nervous system drugs and anti-inflammatory agents. The compound's ability to serve as a hydrogen bond acceptor and its lipophilic character contribute to its utility in designing molecules with optimal bioavailability and target specificity. These attributes are especially relevant in today's drug discovery landscape, where personalized medicine and structure-activity relationships are paramount considerations.

The agrochemical industry also benefits significantly from 2,4-dichloro-3-methoxypyridine, where it functions as a precursor for several crop protection agents. Its derivatives have shown promise in developing novel fungicides and herbicides with improved environmental profiles and target specificity. As the agricultural sector moves toward sustainable pest management solutions, the demand for such specialized intermediates continues to rise. The compound's structural features allow for the creation of products with reduced non-target effects and lower environmental persistence, addressing current concerns about ecological impact and food safety.

Market analysts have observed steady growth in the demand for 2,4-dichloro-3-methoxypyridine, particularly from emerging economies with expanding pharmaceutical and agrochemical sectors. The compound's supply chain has become more robust in recent years, with multiple manufacturers offering high-purity grades to meet diverse application requirements. Quality control measures have been enhanced to ensure batch-to-batch consistency, which is critical for end-users in regulated industries. These developments reflect the compound's established position in the fine chemicals market and its importance in value-added synthesis.

From a regulatory standpoint, 2,4-dichloro-3-methoxypyridine is generally recognized as safe for its intended uses when handled according to standard laboratory safety protocols. Manufacturers and users must adhere to appropriate handling procedures and storage conditions to maintain its stability and prevent degradation. The compound's material safety data sheet (MSDS) provides comprehensive guidance on its proper management, reflecting the industry's commitment to responsible chemical use and workplace safety.

Looking ahead, research continues to explore new applications for 2,4-dichloro-3-methoxypyridine across various scientific disciplines. Its potential in material science, particularly in the development of functional polymers and advanced materials, represents an exciting frontier. Additionally, its utility in catalysis and as a ligand precursor in coordination chemistry offers promising avenues for further investigation. These expanding applications underscore the compound's versatility and its growing importance in multidisciplinary research.

For researchers and industry professionals seeking reliable information about 2,4-dichloro-3-methoxypyridine (CAS 405143-46-6), it's essential to consult peer-reviewed literature and technical specifications from reputable suppliers. The compound's physical-chemical properties, including its melting point, solubility characteristics, and spectral data, are well-documented in scientific databases. As interest in this valuable intermediate continues to grow, staying informed about the latest synthetic methodologies and application developments will be crucial for maximizing its potential in various fields of chemical innovation.

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