2 Fluoro 5 Bromo 3 Methylpyridine
pyridine pyrrole pyrazine piperidine piperazine

2-fluoro-5-bromo-3-methylpyridine

    Specifications

    HS Code

    861779

    Chemical Formula C6H5BrFN
    Appearance Typically a solid (appearance can vary based on purity and conditions)
    Boiling Point Data may vary, approximate range might be in the region of organic heterocyclic compounds with similar structures
    Melting Point Specific melting point data would need to be sourced from literature, can be in a range based on purity
    Solubility In Water Limited solubility in water, being an organic heterocyclic compound with non - polar groups
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc., due to its organic nature
    Flash Point Flash point data would require experimental determination or reference to specific literature
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    General Information
    Where to Buy 2-fluoro-5-bromo-3-methylpyridine in China?
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    Frequently Asked Questions

    As a leading 2-fluoro-5-bromo-3-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 2-fluoro-5-bromo-3-methylpyridine?
    2-Fluoro-5-bromo-3-methylpyridine, this is an organic compound. Its main uses are quite extensive and play an important role in the field of medicinal chemistry.
    One is used in drug synthesis. In the development of many new drugs, this compound can be used as a key intermediate. Due to its specific chemical structure, it can participate in many complex reactions and help build molecular structures with specific pharmacological activities. For example, when developing some antibacterial drugs, 2-fluoro-5-bromo-3-methylpyridine can be introduced into drug molecules through a series of reactions to enhance the inhibition or killing ability of drugs against specific bacteria, adding help to human resistance to diseases.
    Second, it also has important applications in the creation of pesticides. With its unique chemical properties, it can be used to synthesize high-efficiency, low-toxicity and environmentally friendly pesticides. For example, for specific pests, pesticides synthesized from this raw material can precisely act on the physiological system of pests, interfering with their normal growth and reproduction, thus effectively protecting crops, ensuring food production safety, and laying the foundation for agricultural harvests.
    Third, in the field of materials science, 2-fluoro-5-bromo-3-methylpyridine has also emerged. In the preparation of some functional materials, it can be used as a structural modification unit to endow materials with special electrical and optical properties. For example, it is used to synthesize organic semiconductor materials with specific photoelectric conversion efficiency, which shows potential application value in solar cells and other fields, and contributes to the development of new energy.
    In short, although 2-fluoro-5-bromo-3-methyl pyridine is an organic compound, it plays an important role in many fields and has a profound impact on human life and technological development.
    What are 2-fluoro-5-bromo-3-methylpyridine synthesis methods?
    There are several common methods for synthesizing 2-fluoro-5-bromo-3-methylpyridine. First, it can be obtained from a series of reactions such as halogenation and methylation of compounds containing pyridine parent nuclei. Initially, appropriate pyridine derivatives are selected, and bromine atoms are introduced at specific positions in the pyridine ring through specific halogenating reagents, such as brominating agents, under suitable conditions. This process requires fine regulation of reaction conditions, such as temperature, solvent and reactant ratio, to ensure that bromine atoms fall precisely at the 5-position. Subsequently, fluorinated reagents are used to introduce fluorine atoms at the 2-position under similar conditions. In the methylation step, appropriate methylating reagents are selected to connect methyl groups to the 3-position. < Br >
    Second, it can also be based on the strategy of constructing pyridine rings. First, simple organic compounds containing fluorine, bromine and methyl are used as raw materials, and the pyridine ring structure is formed through multi-step cyclization reaction. The selection of starting materials for this route is crucial, and the activity and reaction check points of each raw material need to be reasonably designed. During the reaction process, each cyclization step needs to be carefully controlled to ensure the correct construction of the pyridine ring and the target position of each substituent.
    Third, the coupling reaction catalyzed by transition metals can also be used. Using halogenated aromatics containing fluorine, bromine and methyl or other suitable substrates, under the action of transition metal catalysts such as palladium catalysts, the coupling reaction is carried out with pyridine derivatives or intermediates capable of constructing pyridine rings. Such methods require precise control of the amount of catalyst, the selection of ligands and the reaction conditions in order to efficiently synthesize 2-fluoro-5-bromo-3-methyl pyridine. Each method has its own advantages and disadvantages. In practical application, it needs to be selected according to factors such as raw material availability, cost and reaction conditions.
    What are the physical properties of 2-fluoro-5-bromo-3-methylpyridine?
    2-Fluoro-5-bromo-3-methylpyridine is one of the organic compounds. Its physical properties are profound and are described in detail below.
    First appearance, usually a colorless to light yellow liquid, clear and with a special appearance, the observation can make the viewer observe its unique state. This liquid exhibits its specific physical form under normal temperature and pressure, which is a major characteristic of it.
    The boiling point is about a certain temperature range, and this temperature is the key node for its transition from liquid to gas. At this temperature, molecules are energized to escape from the liquid phase and enter the gas phase. The value of boiling point is related to their volatilization characteristics under different conditions, and is an important parameter in chemical operations, separation and purification.
    Furthermore, the melting point, although the relevant data may be difficult to obtain accurately, is also of great significance in the transition between solid and liquid states. Knowing the melting point can help to understand the physical state changes at low temperatures, which has a great impact on storage, transportation and other links.
    And density, which is different from water, this value reflects its mass characteristics per unit volume. From the density, its distribution in the mixed system can be inferred. When chemical production involves liquid-liquid mixing and other operations, density consideration is indispensable. < Br >
    In terms of solubility, it has a certain solubility in organic solvents such as ethanol and ether. This property makes it possible to dissolve it in organic synthesis reactions with suitable organic solvents to participate in the reaction and expand its application range. In water, the degree of solubility is relatively limited, which is related to the interaction between water molecules and the compound molecules, which affects its behavior in the aqueous phase system.
    In terms of volatility, it has moderate volatility due to a certain vapor pressure. In an open environment, it will gradually evaporate into the air. This property needs to be taken into account when storing, and appropriate sealing conditions should be selected to prevent its volatilization loss. The physical properties of 2-fluoro-5-bromo-3-methylpyridine are diverse, and it has an important impact on its application and treatment in many fields such as chemical industry and organic synthesis.
    What is the chemistry of 2-fluoro-5-bromo-3-methylpyridine?
    2-Fluoro-5-bromo-3-methylpyridine is one of the organic compounds. Its chemical properties are interesting and worthy of in-depth investigation.
    First of all, the structure of the pyridine ring gives this compound unique electronic properties. Fluorine atoms, bromine atoms and methyl atoms are respectively connected to specific positions in the pyridine ring, and the electronegativity of each atom interacts with spatial effects, which profoundly affects its chemical properties.
    In terms of reactivity, fluorine atoms have strong electronegativity, which can reduce the electron cloud density of the pyridine ring, making it difficult for electrophilic substitution reactions on the ring to occur. However, the electron cloud density of the adjacent and para-position is relatively higher, so under certain conditions, electrophilic reagents may react at these two positions. Although the electronegativity of
    bromine atom is not weak, its atomic radius is large, and the formation of C-Br bond is weak. In the nucleophilic substitution reaction, this bromine atom is easier to leave. In case of suitable nucleophilic reagents, such as alkoxides, amines, etc., nucleophilic substitution reactions can occur, and bromine atoms can be replaced by nucleophilic groups.
    methyl is attached to the pyridine ring, because it is a power supply group, it can increase the density of adjacent and para-position electron clouds, which affects the reaction selectivity to a certain extent. And methyl can undergo various reactions, such as being oxidized to carboxyl or aldehyde groups under the action of appropriate oxidants.
    In addition, under basic conditions, the nitrogen atom of 2-fluoro-5-bromo-3-methylpyridine can accept protons and form quaternary ammonium salts, thereby changing the solubility and reactivity of the compound. Under acidic conditions, the stability of the compound may be affected, depending on the type of acid and the reaction conditions.
    In conclusion, the chemical properties of 2-fluoro-5-bromo-3-methylpyridine are determined by its molecular structure, and the interaction of various substituents makes it exhibit diverse reactivity and application potential in the field of organic synthesis.
    What is the price range of 2-fluoro-5-bromo-3-methylpyridine in the market?
    I don't know what the market price range of 2-fluoro-5-bromo-3-methylpyridine is. The price of these compounds often varies due to many factors, and it is difficult to sum it up.
    First, the ease of preparation has a great impact. If the synthesis method is complicated, requiring many steps, expensive reagents and special conditions, the cost will be high, and the market price will also increase. On the contrary, if the synthesis is easier, the price may be relatively low.
    Second, the relationship between market supply and demand is also the key. If there are many buyers, the demand is strong, and the supply is limited, the merchant will raise the price. If the supply exceeds the demand, the price may be reduced in order to seek sales.
    Third, product purity is extremely important. High-purity 2-fluoro-5-bromo-3-methylpyridine is more expensive than low-purity products due to high purification costs. High-purity products commonly used in high-end scientific research, pharmaceutical synthesis and other fields are often expensive; while lower-purity products for industrial use may be slightly more affordable.
    Fourth, manufacturers and regions also have an impact. Different manufacturers have different pricing due to different technologies, scales, and cost control capabilities. And different regions have different prices due to different transportation costs and tax policies. Therefore, to know the exact price range of 2-fluoro-5-bromo-3-methylpyridine, it is necessary to check the chemical product trading platform, consult suppliers, and comprehensively consider the above factors to obtain a more accurate answer.