5 Bromo 3 Methylpyridine 2 Carbonitrile
pyridine pyrrole pyrazine piperidine piperazine

5-bromo-3-methylpyridine-2-carbonitrile

    Specifications

    HS Code

    515023

    Chemical Formula C7H5BrN2
    Molecular Weight 197.03
    Appearance Solid (likely white to off - white)
    Solubility In Water Low solubility, as it is a relatively non - polar organic compound
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
    Density Estimated based on similar compounds, around 1.5 - 1.7 g/cm³
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
    Reactivity Reactive at the bromo and nitrile functional groups, can participate in substitution and addition reactions

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    General Information
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    Frequently Asked Questions

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    What are the physical properties of 5-bromo-3-methylpyridine-2-formonitrile?
    5-Bromo-3-methylpyridine-2-formaldehyde is one of the organic compounds. Its physical properties are quite important, and I will describe them in detail for you.
    Looking at its appearance, 5-bromo-3-methylpyridine-2-formaldehyde is mostly white to light yellow crystalline powder at room temperature. This form is easy to observe and handle, and in many experiments and industrial processes, this appearance characteristic makes it easy to identify and use.
    As for the melting point, the melting point of this compound is about a certain range. The melting point is the critical temperature at which a substance changes from a solid state to a liquid state, which is of great significance for its purity and characteristics. Accurate determination of the melting point can help researchers determine whether the substance is pure. If impurities are mixed, the melting point will often change, or increase, or decrease, or the melting range will become wider.
    Solubility is also a key physical property. 5-Bromo-3-methylpyridine-2-formaldehyde exhibits a certain solubility in organic solvents, such as common ethanol and dichloromethane. Ethanol is a commonly used organic solvent, and there is a specific interaction between it and 5-bromo-3-methylpyridine-2-formaldehyde, which makes the compound soluble in ethanol. In water, its solubility is relatively poor. This difference in solubility has far-reaching implications in the separation, purification and reaction of compounds. For example, when separating a mixture, a suitable solvent can be selected for extraction operation according to its solubility in different solvents, so as to achieve effective separation.
    Furthermore, the compound has a certain stability. At room temperature and pressure without special chemical environment influence, it can maintain its own structure and properties relatively stable. However, in case of special conditions such as high temperature, strong oxidizing agent or reducing agent, its chemical structure may change, triggering a chemical reaction. Understanding its stability can help to take appropriate measures during storage and use to avoid deterioration of the compound due to environmental factors.
    In summary, the physical properties of 5-bromo-3-methylpyridine-2-formaldehyde, such as appearance, melting point, solubility, and stability, play a crucial role in its application in chemical research, industrial production, and other fields. Researchers should understand it in detail in order to make good use of it.
    What are the chemical properties of 5-bromo-3-methylpyridine-2-formonitrile?
    5-Hydroxy-3-methylpyridine-2-formamide has unique chemical properties. This substance has certain stability, and can maintain a relatively stable state under normal temperature, and is not prone to spontaneous violent chemical changes.
    Its solubility is quite critical, slightly soluble in water, but slightly better in some organic solvents, such as ethanol and acetone. This solubility makes it possible to choose a suitable solvent for separation, purification or reaction according to actual needs in many chemical experiments and industrial production processes.
    In terms of acidity and alkalinity, 5-hydroxy- 3-methylpyridine-2-formamide is weakly basic. This is because the nitrogen atom of the pyridine ring has an unshared electron pair and can accept protons. This weakly basic property enables it to react with acids to form corresponding salts. This reaction is of great significance in the field of organic synthesis. It can achieve precise control of the reaction process and products by adjusting the pH of the reaction system.
    Furthermore, it has a certain reactivity. Hydroxyl, methyl and formamide groups in the molecular structure are all active check points. Hydroxyl groups can participate in esterification reactions and form ester compounds with acids under suitable conditions. Although methyl groups are relatively stable, they can also be oxidized under the action of specific strong oxidants. Formamyl groups can participate in hydrolysis reactions, and in acidic or alkaline environments, hydrolysis generates corresponding acids and amines.
    In addition, 5-hydroxy- 3-methylpyridine-2-formamide can also participate in a variety of nucleophilic and electrophilic substitution reactions. Due to the distribution of electron clouds in the pyridine ring, it is vulnerable to attack by nucleophiles or electrophilic reagents at specific locations, and then generate various derivatives, providing rich possibilities for organic synthesis.
    What is the main synthesis method of 5-bromo-3-methylpyridine-2-formonitrile?
    5-Hydroxy-3-methylglutaric acid-2-methyl ester, the method of synthesis of this substance has been recorded in ancient books, and has been studied in later generations. The method can be divided into various categories, which are described in this article.
    First, ethyl acetoacetate is used as the starting material and obtained through several steps of reaction. First, ethyl acetoacetate is mixed with sodium methoxide, and the reaction is carried out at an appropriate temperature to exchange the ester group of ethyl acetoacetate with sodium methoxide. This step is intended to activate the molecular structure and lay the foundation for the subsequent reaction. Then halogenated hydrocarbons are introduced, and the halogen atoms of halogenated hydrocarbons are active. They can be substituted with specific positions of ethyl acetoacetate derivatives, and groups such as methyl are cleverly integrated into the molecule. Subsequently, through hydrolysis, decarboxylation and other steps, the molecular structure is finely regulated to finally obtain 5-hydroxy- 3-methylglutaric acid-2-methyl ester. This process is like a craftsman's carving utensil. Each step requires precise control of temperature, time, material ratio and other factors to obtain the ideal product.
    Second, citric acid is used as the starting material. Citric acid has a special structure and has multiple activity check points. First, citric acid is properly modified, such as esterification reaction, which converts some of its carboxyl groups into ester groups to change the molecular polarity and reactivity. Then, through reduction reaction, the oxidation state of some functional groups in the molecule is precisely adjusted, so that the molecule gradually approaches the target product structure. After a series of complex reactions such as condensation and rearrangement, the carbon skeleton and functional group layout of 5-hydroxy- 3-methylglutaric acid-2-methyl ester are ingeniously constructed. This path requires familiarity with various chemical reaction mechanisms in order to strategize in complicated steps to ensure the smooth progress of the synthesis.
    Third, specific olefins are used as raw materials to synthesize by addition and oxidation. Olefins have unsaturated double bonds and are chemically active. First, the olefin is added to a suitable reagent, and the required functional groups, such as hydroxyl groups, carboxyl groups and other precursors, are introduced. After that, the functional groups are further transformed by oxidation reaction, and the molecular structure is carefully shaped. Through the coordination of multi-step reactions, the complete structure of the target product is gradually constructed. This method requires strict reaction conditions and requires the help of specific catalysts, solvents, etc., to guide the reaction in the expected direction, just like piloting a ship to a given harbor between waves.
    In which fields is 5-bromo-3-methylpyridine-2-formonitrile used?
    For 5-3-methylpyridine-2-formamide, its use is involved in a wide range of domains.

    , this compound is often an important raw material. Because of its specific chemical properties, it can be reversed by a series of reversals to obtain high-efficiency products such as oil and bacteria. For example, other compounds can be combined, replaced, etc., and molecules with specific crop disease control activities can be constructed to help produce crops, improve crop yields, and ensure good quality.
    Some derivatives can be used as anti-tumor compounds in the field, through the generation of stem cells, inhibit tumor angiogenesis, etc., for the purpose of inhibiting tumor growth. Or, it can be used to treat myeloid diseases.
    Furthermore, in the field of materials science, 5-3-methylpyridine-2-formamide can be used for the synthesis of functional materials. For example, it can be used for the synthesis of gold molecular coordination, gold molecular framework materials (MOFs). This material has the characteristics of high specific surface area, high pore size, and excellent performance in adsorption and catalytic reaction. It can efficiently adsorb specific molecules and mix them with each other. In catalytic reaction, it can provide specific active sites, accelerate the reaction process, and improve the reaction performance.
    Therefore, 5-3-methylpyridine-2-formamide plays an important role in many fields such as reaction, reaction, and materials, promoting the development of each phase.
    What is the market price range for 5-bromo-3-methylpyridine-2-formonitrile?
    There is now a market price range for pentachlorotrimethylheptadiene. I should examine all the things in detail to understand the implications of its price.
    Looking at the supply and demand of the city, if there are many people seeking this product, but there are few suppliers, the price will increase; on the contrary, if the supply exceeds the demand, the price will be reduced. And if the place where this product is produced is widely abundant and convenient for transportation, its price will be flat; if the place of origin is remote and difficult for transshipment, its price will also increase.
    Also observe the simplicity of the craftsmanship. If the technique of making this product is simple and the labor cost is low, the price is also low; if the art is complicated and requires multiple materials and multiple workmanship, the cost is high and the price is expensive.
    Let's consider the competition in the city again. If there are many businesses in the city, competing for profits and competing, the price will decline; if there are few businesses, and it is almost a single market, the price will be set by them, or higher.
    And the economic trend of the world is also related to its price. The economy is prosperous, the people are rich and need a wide range, and the price may rise; the economy is depressed, it needs to decrease and the market is cold, and the price will fall.
    To sum up, the market price of pentacan trimethylheptadiene is related to supply and demand, origin, craftsmanship, competition, and economic trends. The range of its price is as little as [lower price] and as much as [upper price]. This is just a rough estimate, market conditions change, and the actual price should be subject to real-time conditions.