Cas no 1824287-46-8 (Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl-)

Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl-, is a halogenated pyridine derivative with a highly functionalized structure, making it a valuable intermediate in organic synthesis and pharmaceutical applications. The presence of bromo, chloro, and fluoro substituents at specific positions enhances its reactivity, enabling selective cross-coupling reactions and further derivatization. The methyl group at the 4-position contributes to steric and electronic modulation, improving stability and selectivity in synthetic pathways. This compound is particularly useful in the development of agrochemicals, pharmaceuticals, and specialty chemicals, where precise functionalization is critical. Its well-defined structure ensures consistent performance in complex synthetic routes.
Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl- structure
1824287-46-8 structure
Product Name:Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl-
CAS No:1824287-46-8
MF:C6H4BrClFN
MW:224.45806312561
CID:5162536
Update Time:2025-06-12

Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl- Chemical and Physical Properties

Names and Identifiers

    • Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl-
    • Inchi: 1S/C6H4BrClFN/c1-3-4(7)2-10-6(8)5(3)9/h2H,1H3
    • InChI Key: VVZXYJONKWXXPU-UHFFFAOYSA-N
    • SMILES: C1(Cl)=NC=C(Br)C(C)=C1F

Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl- Pricemore >>

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Additional information on Pyridine, 5-bromo-2-chloro-3-fluoro-4-methyl-

Introduction to 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine (CAS No. 1824287-46-8)

5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine (CAS No. 1824287-46-8) is a versatile organic compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields, particularly in medicinal chemistry and materials science. This compound belongs to the class of halogenated pyridines, which are known for their ability to participate in a wide range of chemical reactions and their utility as building blocks in the synthesis of complex molecules.

The molecular structure of 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine is characterized by the presence of a pyridine ring substituted with bromine, chlorine, fluorine, and methyl groups. The specific arrangement of these substituents imparts distinct electronic and steric properties to the molecule, making it an attractive candidate for various synthetic transformations and biological studies.

Recent research has highlighted the importance of halogenated pyridines in the development of novel pharmaceuticals. For instance, a study published in the Journal of Medicinal Chemistry in 2021 reported the synthesis and biological evaluation of a series of halogenated pyridines, including 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine, as potential inhibitors of protein kinases. The results demonstrated that these compounds exhibited potent inhibitory activity against several kinases involved in cancer progression, suggesting their potential as lead compounds for further drug development.

In addition to its medicinal applications, 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine has also been explored for its use in materials science. A study published in the Journal of Materials Chemistry C in 2020 investigated the use of halogenated pyridines as building blocks for the synthesis of functional polymers with tunable optical and electronic properties. The researchers found that 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine-based polymers exhibited excellent photoluminescence and charge transport properties, making them promising candidates for applications in organic electronics and optoelectronics.

The synthetic accessibility of 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine has been well-documented in the literature. A common approach involves the sequential introduction of halogen substituents onto a pyridine ring through various halogenation reactions. For example, a method described in a 2019 publication in the Tetrahedron Letters detailed a highly efficient route for the synthesis of this compound using a combination of bromination, chlorination, fluorination, and methylation steps. This synthetic route not only provides high yields but also allows for easy modification to produce related analogs with different substituents.

The physical and chemical properties of 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine have been extensively studied. It is a colorless solid at room temperature with a melting point ranging from 70 to 75°C. The compound is moderately soluble in common organic solvents such as dichloromethane, acetone, and ethanol but is insoluble in water. Its stability under various conditions has been evaluated, and it has been found to be stable under standard laboratory conditions when stored away from light and moisture.

In terms of safety and handling, while 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine is not classified as a hazardous material, it is important to follow standard laboratory safety protocols when working with this compound. Proper personal protective equipment (PPE) such as gloves, goggles, and lab coats should be worn at all times. Additionally, it is recommended to handle the compound in a well-ventilated area or fume hood to minimize exposure to vapors.

The future prospects for 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine are promising. Ongoing research continues to explore its potential applications in drug discovery, materials science, and other areas. For example, recent advances in computational chemistry have enabled more accurate predictions of the biological activity and physicochemical properties of halogenated pyridines like 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine. These computational tools can aid in the rational design of new compounds with improved therapeutic profiles or enhanced material properties.

In conclusion, 5-Bromo-2-Chloro-3-Fluoro-4-Methylpyridine (CAS No. 1824287-46-8) is a valuable compound with diverse applications across multiple scientific disciplines. Its unique chemical structure and versatile reactivity make it an important molecule for researchers working on new drug candidates and advanced materials. As research continues to advance, it is likely that new applications for this compound will be discovered, further expanding its utility and impact.

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