5 Bromo 2 Fluoro 6 Methylpyridine
pyridine pyrrole pyrazine piperidine piperazine

5-bromo-2-fluoro-6-methylpyridine

    Specifications

    HS Code

    414354

    Chemical Formula C6H5BrFN
    Appearance Solid (Typical for this class of compounds, but exact appearance can vary)
    Solubility In Water Low (Expected due to non - polar nature of the aromatic ring)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Hazard Class Irritant (Typical for halogenated aromatic compounds, but exact classification may vary)

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    General Information
    Where to Buy 5-bromo-2-fluoro-6-methylpyridine in China?
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    Frequently Asked Questions

    As a leading 5-bromo-2-fluoro-6-methylpyridine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 5-bromo-2-fluoro-6-methylpyridine?
    5-Bromo-2-chloro-6-methylpyridine has a wide range of main uses. In the field of pharmaceutical synthesis, this compound plays a crucial role. For example, in the development of some antibacterial drugs, 5-bromo-2-chloro-6-methylpyridine can be used as a key intermediate. Due to its unique chemical structure, it can be cleverly combined with other compounds through a series of chemical reactions to construct drug molecular structures with specific antibacterial activities, helping to develop better and more targeted antibacterial drugs, providing powerful weapons for human beings to fight bacterial infectious diseases.
    In the field of pesticides, 5-bromo-2-chloro-6-methylpyridine also has an indispensable position. It can be used to synthesize a variety of efficient pesticides and fungicides. In agricultural production, pests and diseases have always been a major problem affecting crop yield and quality. Pesticides synthesized based on 5-bromo-2-chloro-6-methylpyridine can precisely act on specific physiological links of pests and pathogens, or damage their nervous system, or interfere with their metabolic processes, thus effectively killing pests, inhibiting the growth of pathogens, ensuring the healthy growth of crops, and enhancing the efficiency of agricultural production.
    In addition, in the field of materials science, 5-bromo-2-chloro-6-methylpyridine also shows certain application potential. Researchers can use it to synthesize polymer materials with special properties. By carefully designing the reaction path, the compound is involved in the polymerization of polymers, endowing the material with unique properties such as better stability, electrical conductivity, or optical properties, meeting the needs of different fields for special materials, and promoting the continuous progress and innovation of materials science.
    What are the synthesis methods of 5-bromo-2-fluoro-6-methylpyridine?
    There are many synthetic methods of 5-bromo-2-chloro-6-methylpyridine, which are described in detail below.
    First, pyridine is used as the starting material. First, an appropriate halogenation reagent, such as a brominating agent and a chlorinating agent, is used to halogenate the pyridine ring under specific reaction conditions, introducing bromine atoms and chlorine atoms, and then methyl groups are introduced at the designated position through methylation reaction, so that the target product can be obtained. The raw material of this method is pyridine, which is relatively common, and the reaction steps are relatively clear. However, the regioselectivity of the halogenation reaction may need to be finely regulated to introduce bromine and chlorine atoms into the target position.
    Second, a methyl-containing pyridine derivative is used as the starting material. If methyl groups already exist on the starting pyridine ring, they can be halogenated first. Through rational selection of halogenation reagents and reaction conditions, bromine atoms and chlorine atoms are introduced at specific positions to synthesize 5-bromo-2-chloro-6-methyl pyridine. This path may simplify some reaction steps because the starting materials already contain methyl groups, but suitable methyl-containing pyridine derivative raw materials may need to be specially prepared or purchased, and the cost may vary.
    Third, the coupling reaction catalyzed by palladium. First, intermediates such as pyridine halide or borate containing different substituents are prepared, and then under the action of palladium catalyst, the parts are connected through coupling reaction to construct the structure of the target product. This method has the advantages of high efficiency and good selectivity, and can accurately realize the formation of carbon-carbon and carbon-heteroatomic bonds. However, palladium catalysts are more expensive, the reaction conditions may be more severe, and the requirements for reaction equipment and operation are also high.
    Fourth, the reaction involving organometallic reagents is used. For example, organolithium reagent or Grignard reagent can be prepared first, and its reaction with halogenated pyridine derivatives can be used to introduce substituents and construct structures, and then 5-bromo-2-chloro-6-methylpyridine can be synthesized. This method has high reactivity, but organometallic reagents are sensitive to water and air, and strict anhydrous and anaerobic conditions are required during operation, which increases the difficulty and cost of experiments.
    What is the market price of 5-bromo-2-fluoro-6-methylpyridine?
    The market price of 5-hydroxy- 2-thio-6-methylpyridine is often due to multiple reasons.
    First, the balance between supply and demand is the main reason. If there are many applicants and few suppliers, the price will tend to rise. If the industry is prosperous, the demand for 5-hydroxy- 2-thio-6-methylpyridine will increase, but the producers will not increase rapidly to respond, and the market price will rise. On the contrary, if the supply exceeds the demand, the stock is difficult to sell, and the price will trend down. < Br >
    Second rule, the price of raw materials is also related. The preparation of 5-hydroxy- 2-thio-6-methylpyridine requires various raw materials. The price of raw materials rises and falls, and the price of the finished product also changes accordingly. Suppose the production of raw materials is due to the time of day, place or other reasons, causing its price to rise, then the production of 5-hydroxy- 2-thio-6-methylpyridine increases, and the market price has to be higher.
    Repeat, the clumsiness of the process also affects the price. If a new law is created that saves labor costs and increases efficiency, the price may be reduced. On the contrary, if the craftsmanship is old-fashioned, the cost is too much and the efficiency is too low, and the price is difficult to reduce.
    Also, the regulations of the decree and the rate of taxation can affect the price. If the decree is strict, the producer may increase the fee, and the price will be higher because of it; if the tax is heavy, it will also increase the cost, and the market price will be expensive.
    And the competition in the market is also the key. There are many people in the same industry, competing to sell, or to reduce the price to attract customers. However, if there are no competitors, or if they are only in their own interests, the price will be exclusive. < Br >
    The market price of 5-hydroxyl-2-thio-6-methylpyridine is not determined at one end, but depends on the interaction of supply and demand, raw materials, processes, decrees, and competition. It is based on its constant price change, and it cannot be said in a word.
    What are the precautions for storing and transporting 5-bromo-2-fluoro-6-methylpyridine?
    In the storage and transportation of 5-bromo-2-chloro-6-methylpyridine, the following things must be paid attention to:
    First, because of its chemical activity, the packaging material requirements are strict. Packaging that can withstand its chemical action, such as specific plastic materials or specially treated metal containers, should be selected to prevent material leakage caused by corrosion of the packaging. And the packaging should be well sealed to avoid contact with outside air, moisture, etc.
    Second, temperature and humidity have a great impact on its stability. It should be stored in a cool, dry place, away from heat and water sources. High temperature can easily promote chemical reactions, and high humidity may cause deliquescence and other conditions, resulting in damage to its quality.
    Third, 5-bromo-2-chloro-6-methylpyridine may be toxic and irritating. When transporting and storing, be sure to take protective measures. Operators need to wear professional protective equipment, such as protective clothing, gloves, protective masks, etc., to prevent the human body from coming into contact with it or inhaling its volatile gases.
    Fourth, this substance should be stored and transported separately from oxidants, reducing agents, acids, bases, etc. Because it is prone to chemical reactions with these substances, it may even cause violent reactions, endangering safety.
    Fifth, storage areas and transportation vehicles should be kept clean and free of other impurities. And there should be obvious warning signs to remind personnel of its danger. During transportation, it is necessary to ensure stability and avoid vibration and collision to prevent packaging damage.
    What are the physical and chemical properties of 5-bromo-2-fluoro-6-methylpyridine?
    5-1-2-pentyne-6-methylpyridine is a unique chemical compound, and its physicalization is of great significance.
    As far as physical properties are concerned, the fusion of this compound is affected by the effects of alkynyl groups, alkyl groups, and pyridine groups in its molecules. The incompatibility of alkynyl groups makes the molecular force present a special orientation, and the alkyl groups can form alkyl groups. The aromaticity of pyridine groups also affects the molecular interaction. Usually, the presence of alkyl groups increases the boiling force of the compound, which increases the molecular attractiveness force. The melting properties also vary due to the integrity of the molecule. The properties of alkynyl pyridine and the properties of pyridine groups may make the molecular arrangement more orderly.
    In terms of solubility, due to the weak solubility of the water-based group and the weak solubility of the pyridine group, it may have a certain solubility in the soluble group such as alcohol and water (if the proportion of alkyl groups such as alkyl groups is appropriate); and the alkyl group in the molecule makes it soluble to a certain extent in non-soluble groups such as alkyl groups. However, due to the shadow of alkynyl groups, pyridine groups, and alkyl groups, the solubility non-solubility law can be summarized.
    In terms of the solubility, the alkyl group has anti-activity, can be esterified and reversed, and the carboxylic acid forms an ester under the action of catalysis. This is a common reaction in the synthesis. Alkynyl groups can perform addition and inverse reactions, such as the addition of alkyls, acids, etc., to generate phase additives, and can also provide a way for some gold catalysis. The nitrogen atom of pyridine has solitary molecules, so that it can be used as an acid reaction, or a gold coordination to form complexes, which may be useful in the field of catalysis and materialization. In addition, the co-chemical system of the compound molecule is composed of alkynyl pyridine, which may give it special photophysical properties. It may have research value in optical materials and the like.