Cas no 1374659-26-3 (2,6-Dichloro-3-(difluoromethyl)pyridine)

2,6-Dichloro-3-(difluoromethyl)pyridine is a halogenated pyridine derivative with significant utility in agrochemical and pharmaceutical synthesis. Its key structural features—a dichloro-substituted pyridine core and a difluoromethyl group at the 3-position—impart reactivity suitable for further functionalization, making it a versatile intermediate. The compound’s electron-withdrawing substituents enhance its stability and selectivity in cross-coupling reactions, while the difluoromethyl group can contribute to improved bioavailability in active ingredients. It is particularly valued in the development of herbicides and fungicides, where its structural motifs are leveraged for efficacy. High purity grades ensure consistent performance in synthetic applications.
2,6-Dichloro-3-(difluoromethyl)pyridine structure
1374659-26-3 structure
Product Name:2,6-Dichloro-3-(difluoromethyl)pyridine
CAS No:1374659-26-3
MF:C6H3Cl2F2N
MW:197.997526407242
MDL:MFCD22199294
CID:3043429
PubChem ID:60623005
Update Time:2025-06-08

2,6-Dichloro-3-(difluoromethyl)pyridine Chemical and Physical Properties

Names and Identifiers

    • 2,6-Dichloro-3-(difluoromethyl)pyridine
    • AKOS008901319
    • MS-20286
    • CS-0359009
    • STL555584
    • 1374659-26-3
    • AODCNGJAAUFOII-UHFFFAOYSA-N
    • DTXSID301278124
    • BBL101787
    • MFCD22199294
    • ZEC65926
    • DB-148947
    • SCHEMBL22028787
    • MDL: MFCD22199294
    • Inchi: 1S/C6H3Cl2F2N/c7-4-2-1-3(6(9)10)5(8)11-4/h1-2,6H
    • InChI Key: AODCNGJAAUFOII-UHFFFAOYSA-N
    • SMILES: C1(Cl)=NC(Cl)=CC=C1C(F)F

Computed Properties

  • Exact Mass: 196.9610608g/mol
  • Monoisotopic Mass: 196.9610608g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 134
  • 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: 3.4
  • Topological Polar Surface Area: 12.9?2

2,6-Dichloro-3-(difluoromethyl)pyridine Pricemore >>

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Additional information on 2,6-Dichloro-3-(difluoromethyl)pyridine

Recent Advances in the Application of 2,6-Dichloro-3-(difluoromethyl)pyridine (CAS: 1374659-26-3) in Chemical Biology and Pharmaceutical Research

2,6-Dichloro-3-(difluoromethyl)pyridine (CAS: 1374659-26-3) is a key intermediate in the synthesis of various agrochemicals and pharmaceuticals. Recent studies have highlighted its significance in the development of novel bioactive compounds, particularly in the fields of fungicides and enzyme inhibitors. This research brief aims to summarize the latest findings related to this compound, focusing on its chemical properties, synthetic applications, and biological activities.

One of the most notable advancements is the use of 2,6-Dichloro-3-(difluoromethyl)pyridine as a building block in the synthesis of next-generation fungicides. Researchers have demonstrated its efficacy in targeting fungal pathogens by inhibiting key enzymes involved in cell wall biosynthesis. The compound's unique difluoromethyl group enhances its binding affinity and metabolic stability, making it a promising candidate for agricultural applications.

In pharmaceutical research, 2,6-Dichloro-3-(difluoromethyl)pyridine has been explored as a precursor for the development of enzyme inhibitors. Recent studies have shown its potential in modulating the activity of kinases and other signaling proteins, which are critical targets in cancer therapy. The compound's ability to introduce fluorine atoms into bioactive molecules has also been leveraged to improve drug pharmacokinetics and bioavailability.

Furthermore, advancements in synthetic methodologies have enabled more efficient and scalable production of 2,6-Dichloro-3-(difluoromethyl)pyridine. Novel catalytic systems and green chemistry approaches have been employed to optimize its synthesis, reducing environmental impact and production costs. These developments are expected to facilitate broader adoption of this compound in both academic and industrial settings.

In conclusion, 2,6-Dichloro-3-(difluoromethyl)pyridine (CAS: 1374659-26-3) continues to play a pivotal role in chemical biology and pharmaceutical research. Its versatile applications in agrochemical and drug development, coupled with recent synthetic innovations, underscore its importance as a key intermediate. Future research is likely to explore its potential in new therapeutic areas and further optimize its synthetic routes for industrial-scale production.

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