Cas no 1807257-52-8 (5-Chloro-2,4-difluoropyridine)

5-Chloro-2,4-difluoropyridine is a fluorinated pyridine derivative widely used as a key intermediate in pharmaceutical and agrochemical synthesis. Its structure, featuring chlorine and fluorine substituents, enhances reactivity and selectivity in nucleophilic substitution and cross-coupling reactions. The electron-withdrawing properties of the fluorine atoms improve stability while facilitating further functionalization. This compound is particularly valuable in the development of active ingredients due to its ability to modulate biological activity and metabolic stability. High purity grades are available to meet stringent industry requirements. Proper handling under inert conditions is recommended due to its sensitivity to moisture and potential reactivity.
5-Chloro-2,4-difluoropyridine structure
5-Chloro-2,4-difluoropyridine structure
Product Name:5-Chloro-2,4-difluoropyridine
CAS No:1807257-52-8
MF:C5H2ClF2N
MW:149.525887012482
CID:4902349
PubChem ID:130054786
Update Time:2025-11-01

5-Chloro-2,4-difluoropyridine Chemical and Physical Properties

Names and Identifiers

    • 5-Chloro-2,4-difluoropyridine
    • F74873
    • BS-52365
    • 1807257-52-8
    • EN300-7175428
    • Inchi: 1S/C5H2ClF2N/c6-3-2-9-5(8)1-4(3)7/h1-2H
    • InChI Key: BKEHDGPFLXDGDC-UHFFFAOYSA-N
    • SMILES: ClC1C=NC(=CC=1F)F

Computed Properties

  • Exact Mass: 148.9843831g/mol
  • Monoisotopic Mass: 148.9843831g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 101
  • 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
  • Topological Polar Surface Area: 12.9

5-Chloro-2,4-difluoropyridine Pricemore >>

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Additional information on 5-Chloro-2,4-difluoropyridine

5-Chloro-2,4-difluoropyridine: A Comprehensive Overview

5-Chloro-2,4-difluoropyridine, also known by its CAS number 1807257-52-8, is a heterocyclic aromatic compound with significant applications in various fields. This compound belongs to the pyridine family, characterized by a six-membered ring containing one nitrogen atom. The presence of chlorine and fluorine substituents at specific positions imparts unique chemical and physical properties to this molecule, making it a valuable compound in both academic and industrial research.

The synthesis of 5-Chloro-2,4-difluoropyridine involves multi-step processes that typically include nucleophilic substitution and electrophilic aromatic substitution reactions. Recent advancements in synthetic chemistry have enabled the development of more efficient and environmentally friendly methods for its production. For instance, researchers have explored the use of microwave-assisted synthesis to accelerate reaction rates while minimizing the formation of by-products. These innovations not only enhance the scalability of the synthesis but also align with the growing demand for sustainable chemical processes.

5-Chloro-2,4-difluoropyridine exhibits a wide range of applications due to its structural versatility. In the field of materials science, this compound has been utilized as a precursor for the synthesis of advanced materials such as conductive polymers and metal-organic frameworks (MOFs). Its ability to coordinate with metal ions makes it particularly useful in constructing MOFs with high surface area and porosity, which are highly sought after for gas storage and catalytic applications.

In the pharmaceutical industry, 5-Chloro-2,4-difluoropyridine serves as an intermediate in the synthesis of bioactive compounds. Recent studies have highlighted its potential as a building block for developing drugs targeting various diseases, including cancer and infectious diseases. For example, researchers have reported the use of this compound in designing inhibitors for kinases, which are key enzymes involved in cell signaling pathways. The fluorinated substituents on the pyridine ring contribute to the molecule's lipophilicity and bioavailability, making it an attractive candidate for drug development.

The electronic properties of 5-Chloro-2,4-difluoropyridine also make it a promising candidate for applications in optoelectronics. Its conjugated π-system enables efficient charge transport, which is essential for devices such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Recent research has focused on modifying the molecule's structure to optimize its electronic characteristics further. For instance, introducing electron-withdrawing groups like chlorine and fluorine has been shown to enhance its stability and efficiency in electronic devices.

In terms of environmental impact, 5-Chloro-2,4-difluoropyridine has been studied for its potential role in pollution control. Its ability to act as a catalyst in degradation reactions has been explored for breaking down organic pollutants in water. Fluorinated pyridines like this compound have demonstrated high catalytic activity due to their strong electron-withdrawing effects, which facilitate redox reactions. This application holds significant promise for addressing environmental challenges associated with industrial waste and water contamination.

The toxicity profile of 5-Chloro-2,4-difluoropyridine has also been a subject of recent research interest. While it exhibits moderate toxicity towards certain organisms, studies suggest that its environmental risk is relatively low compared to other chemicals in similar classes. Regulatory agencies have established guidelines for safe handling and disposal of this compound to minimize its impact on ecosystems.

In conclusion, 5-Chloro-2,4-difluoropyridine, with its CAS number 1807257-52-8, is a versatile compound with diverse applications across multiple disciplines. Its unique chemical properties make it an invaluable tool in both academic research and industrial development. As advancements in synthetic methods and material science continue to unfold, the potential uses of this compound are expected to expand further, contributing significantly to technological progress and environmental sustainability.

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