4 Bromo 2 6 Dimethylpyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Bromo-2,6-dimethylpyridine

    Specifications

    HS Code

    949612

    Name 4-Bromo-2,6-dimethylpyridine
    Molecular Formula C7H8BrN
    Molecular Weight 186.05
    Appearance Colorless to light yellow liquid or solid
    Boiling Point 204 - 206 °C
    Melting Point 23 - 25 °C
    Density 1.396 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents like ethanol, ether
    Flash Point 85 °C
    Pka ~ 4.1 (estimated for pyridine - like nitrogen)
    Cas Number 53673-32-4

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    General Information
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    Frequently Asked Questions

    As a leading 4-Bromo-2,6-dimethylpyridine 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 chemical properties of 4-Bromo-2,6-dimethylpyridine?
    4-Bromo-2,6-dimethylpyridine is one of the organic compounds. Its chemical properties are unique and valuable to explore.
    In this compound, the bromine atom is connected to the pyridine ring and methyl group, and the structure gives it special reactivity. In the nucleophilic substitution reaction, the bromine atom is active and easy to be replaced by nucleophilic reagents. Geyne bromine has a certain electronegativity, which makes the electron cloud of the C-Br bond biased towards bromine, making the carbon atom positively charged, and the nucleophilic reagent is easy to attack. For example, when reacted with sodium alcohol, corresponding ether compounds can be formed; when reacted with amine, nitrogen-containing derivatives can be obtained.
    Furthermore, the presence of the pyridine ring makes it alkaline to a certain extent. The nitrogen atom of the pyridine ring has lone pairs of electrons and can accept protons. However, due to the power supply effect of the methyl group on the ring, the alkalinity is slightly different from that of the pyridine. The methyl supply increases the electron cloud density around the nitrogen atom, and the alkalinity is slightly stronger than that of the pyridine.
    In addition, the substitution of 2,6-dimethyl group has an impact on the spatial structure of the molecule and the distribution of the electron cloud. In space, the methyl group occupies a certain position, which affects the proximity of the reagent and the reaction selectivity during the reaction. In terms of electrons, the methyl ion increases the electron cloud density of the pyridine ring, and the localization effect is also reflected in the electrophilic substitution reaction. The reaction check point is mostly in the higher electron cloud density of the pyridine ring.
    In short, 4-bromo-2,6-dimethylpyridine can be used as an important intermediate in the field of organic synthesis due to its own structural characteristics. It can participate in a variety of chemical reactions and build various organic compounds with its special chemical properties.
    What are the main applications of 4-Bromo-2,6-dimethylpyridine?
    4 - Bromo - 2,6 - dimethylpyridine is a key compound in organic synthesis. It has a wide range of uses and has important applications in many fields.
    First in the field of medicinal chemistry. This compound is often used as a key intermediate in the creation of new drugs. Due to its pyridine ring structure and the specific substitution mode of bromine atoms and methyl groups, it endows the molecule with unique chemical and physical properties, which can participate in a variety of chemical reactions and help to construct complex drug molecular structures. For example, in the development of specific targeted anti-cancer drugs, 4-Bromo-2,6-dimethylpyridine can be linked to other active groups through a series of reactions to form molecules with specific biological activities to precisely act on cancer cell targets and inhibit their growth and diffusion.
    Furthermore, it is also indispensable in the field of materials science. It can be used to prepare functional materials, such as organic optoelectronic materials. By participating in polymerization reactions or modification reactions, the photoelectric properties of materials can be improved. For example, in the preparation of organic Light Emitting Diode (OLED) materials, the introduction of this compound structure can adjust the luminous efficiency and color purity of the material, and improve the display quality and performance of OLED displays.
    In addition, it also plays an important role in the field of pesticide chemistry. It can be used as a starting material for the synthesis of new pesticides. Its structural characteristics enable it to derive compounds that are highly effective in killing or repelling pests, and have relatively little impact on the environment. For example, the synthesis of pesticides with selective insecticidal activity only targets specific pests, reducing damage to beneficial insects and the environment, and realizing the needs of precision agriculture.
    In summary, 4-Bromo-2,6-dimethylpyridine plays a crucial role in the fields of medicine, materials and pesticides, providing an important chemical basis and material support for the development of various fields.
    What are the synthesis methods of 4-Bromo-2,6-dimethylpyridine?
    The synthesis of 4-bromo-2,6-dimethylpyridine has been known for a long time. There are many methods, and the ones mentioned above are almost common.
    First, 2,6-dimethylpyridine is prepared by bromination reaction with 2,6-dimethylpyridine as the starting material. This reaction often requires the assistance of brominating agents, such as bromine ($Br_2 $). Under suitable reaction conditions, such as specific temperatures, solvents and catalysts, bromine can selectively replace the 4-position hydrogen atom on the pyridine ring to obtain the target product. In this process, temperature control is crucial. If the temperature is too high, side reactions may occur, resulting in impure products; if the temperature is too low, the reaction rate will be slow and take a long time.
    Second, 2-methyl-6-acetylpyridine can also be used as a raw material. It is first brominated to obtain 4-bromo-2-methyl-6-acetylpyridine, and then through a suitable method, such as reduction reaction, the acetyl group is converted to methyl, and finally 4-bromo-2,6-dimethylpyridine is obtained. This route step is slightly complicated, but the reaction conditions at each step are relatively mild, and the product is easy to separate and purify.
    Furthermore, the desired structure can be constructed by multi-step reaction from suitable pyridine derivatives. For example, a pyridine derivative with appropriate substituents is selected, and bromine atoms and methyl groups are gradually introduced through a series of reactions such as substitution and deprotection, so as to achieve the purpose of synthesis. Although this method is complex, the reaction can be flexibly regulated, which is quite beneficial for the synthesis of specific needs.
    All synthesis methods have their own advantages and disadvantages. It is necessary to choose carefully according to the actual situation, such as the availability of raw materials, cost considerations, product purity requirements, etc., in order to achieve the purpose of efficient synthesis of 4-bromo-2,6-dimethylpyridine.
    What is the market price of 4-Bromo-2,6-dimethylpyridine?
    4-Bromo-2,6-dimethylpyridine, the value of this substance in the market, it is difficult to judge. Its price is not constant, but varies with many factors.
    The first one to bear the brunt is the state of supply and demand in the market. If there are many people who want it, it will be used in various chemical synthesis, pharmaceutical research and development and other industries, and if the supply is small, the price will rise. On the contrary, if there are few people who want it, the supply will exceed the demand, and the price will drop.
    Furthermore, the difficulty of preparation and the cost will also affect the price. Its preparation requires complicated steps, the materials used are rare, the process is precise and strict, and the cost will be high, and the price will follow. If the preparation method is simple and the materials used are widely available, the cost can be reduced and the price will also decrease.
    The difference in origin is also related to the price. In different places, due to differences in resources, manpower, and taxes, the cost of the product produced is different, and the price is also different.
    In addition, the state of market competition has a great impact on the price. If there are many players competing for profit, in order to occupy the market seat, there may be a move to reduce the price. On the contrary, if there are few competitors in the market, the price may be high.
    In summary, in order to know the exact market price of 4-bromo-2,6-dimethylpyridine, it is necessary to check the market information of chemical raw materials in real time, consult the industry merchants, brokers, or refer to the quotations of relevant trading platforms, in order to obtain a more accurate number.
    What are the precautions for 4-Bromo-2,6-dimethylpyridine during storage and transportation?
    4-Bromo-2,6-dimethylpyridine is a commonly used raw material for organic synthesis. During storage and transportation, many matters must be paid attention to to to ensure its quality and safety.
    First storage. This compound should be placed in a cool, dry and well-ventilated place. Because it is quite sensitive to heat and easy to decompose or deteriorate at high temperature, it is essential to keep away from heat sources and open flames. And direct sunlight should be avoided, because it contains bromine atoms, which can cause light or photochemical reactions and damage the material structure. Furthermore, the storage must be separated from oxidants, acids, bases, etc., to prevent dangerous chemical reactions. Because 4-bromo-2,6-dimethylpyridine has a certain chemical activity, it encounters oxidants or acids and bases, or reacts violently, and even causes explosions.
    As for transportation. Packaging must be tight and reliable for the purpose of leak-proof and shock-proof. During transportation, it is necessary to ensure that the temperature is stable and avoid bumps and collisions. Because it is under vibration or impact, or the structure is damaged, or the package is damaged, causing leakage. In the event of leakage, surrounding personnel need to be evacuated to a safe area quickly, and emergency personnel should wear professional protective equipment and clean up to prevent harm to human body and the environment.
    In summary, when storing and transporting 4-bromo-2,6-dimethylpyridine, strict treatment of environmental conditions, isolated storage, packaging protection, etc. is required to ensure its safety and lay a good foundation for subsequent use.