Methyl 5 Bromopyridine 3 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

Methyl 5-bromopyridine-3-carboxylate

    Specifications

    HS Code

    322582

    Chemical Formula C7H6BrNO2
    Molar Mass 216.03 g/mol
    Appearance Solid (usually white or off - white)
    Melting Point Typically in the range of 80 - 85 °C (reported values may vary slightly)
    Solubility In Water Low solubility, as it is an organic ester with a bromine - containing aromatic ring
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
    Pka No acidic hydrogen in the molecule relevant for simple acid - base behavior in aqueous solution, no typical pKa value for this compound

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    Frequently Asked Questions

    As a leading Methyl 5-bromopyridine-3-carboxylate 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 Methyl 5-bromopyridine-3-carboxylate?
    Methyl-5-bromopyridine-3-carboxylate, this is an organic compound. Its physical properties are mostly solid under normal conditions, or liquid due to specific conditions. The characteristics of its melting point and boiling point are closely related to the intermolecular force and structure. Generally speaking, the melting point varies according to the regularity of the molecular structure and the strength of the force. The more regular the structure and the stronger the force, the higher the melting point; the same is true for the boiling point, which varies according to the size of the attractive force between molecules.
    In terms of chemical activity, the bromine atom in this compound is quite active. Bromine atoms have strong electron-absorbing properties, which reduce the density of their adjacent and para-position electron clouds, and are easily attacked by nucleophiles, triggering nucleophilic substitution reactions. For example, when encountering hydroxyl negative ions, bromine atoms may be replaced by hydroxyl groups to form corresponding alcohol derivatives.
    The ester group part also exhibits specific chemical properties. Under acidic or alkaline conditions, hydrolysis can occur. In acidic media, hydrolysis produces 5-bromopyridine-3-carboxylic acid and methanol; in alkaline environments, hydrolysis is more thorough, generating carboxylic acid and methanol. After acidification, 5-bromopyridine-3-carboxylic acid can be obtained.
    Due to the presence of pyridine rings, this compound is both basic. The solitary pair of electrons on the nitrogen atom of the pyridine ring can accept protons and react with acids to form salts. This basic property can be used in organic synthesis to adjust the reaction environment, or as a ligand to complex with metal ions, affecting the activity and selectivity of metal catalytic reactions.
    In addition, the compound can also participate in various organic reactions, such as reacting with Grignard reagents to construct more complex organic structures, in pharmaceutical chemistry, materials science and other fields, or as an important intermediate to synthesize compounds with specific biological activities or material properties.
    What are the synthetic methods of Methyl 5-bromopyridine-3-carboxylate?
    There are several common methods for preparing methyl 5-bromopyridine-3-carboxylic acid esters. One is to use 5-bromopyridine-3-carboxylic acid as the starting material to esterify it with methanol in the presence of acidic catalysts. Among them, the commonly used acidic catalysts are sulfuric acid, p-toluenesulfonic acid, etc. During the reaction, 5-bromopyridine-3-carboxylic acid and methanol are mixed in appropriate proportions, an appropriate amount of catalyst is added, and the reflux number is heated. After the reaction is completed, the target product can be obtained through neutralization, extraction, distillation and other steps.
    In the second method, 5-bromopyridine can be prepared by bromination reaction with pyridine as raw material, and then carboxyl groups can be introduced into the pyridine ring, and then esterified. In the bromination reaction, suitable brominating agents can be selected, such as liquid bromine, N-bromosuccinimide (NBS), etc. By introducing carboxyl groups, the corresponding Grignard reagent can be prepared by Grignard reagent reaction, then reacted with carbon dioxide, and then acidified to obtain 5-bromopyridine-3-carboxylic acid, and finally esterified to obtain methyl 5-bromopyridine-3-carboxylic acid ester. < Br >
    There are also other compounds containing pyridine structure as the starting material and converted through a series of reactions. However, no matter what method, it is necessary to choose carefully according to the availability of raw materials, the difficulty of reaction conditions, the purity and yield of the product and many other factors.
    Where is Methyl 5-bromopyridine-3-carboxylate used?
    Methyl-5-bromopyridine-3-carboxylic acid ester has a wide range of uses and has extraordinary applications in the field of pharmaceutical and chemical industry.
    First, the field of medicine. Because of its unique chemical structure, it can be used as a key intermediate for the creation of various drugs. For example, in the development of antimicrobial drugs, scientists can use its structural properties to build molecular structures that can inhibit or kill specific bacteria. Through carefully designed chemical reactions, linking it with other active groups to synthesize compounds with novel antimicrobial mechanisms, it is expected to provide new and effective drug options for the clinical treatment of bacterial infections. Furthermore, it can also be seen in the exploration of anti-tumor drugs. Researchers have gained insight into the growth and proliferation characteristics of tumor cells. Using methyl-5-bromopyridine-3-carboxylic acid ester as the starting material, through multiple steps and ingenious reactions, they construct drug molecules that specifically bind to tumor cell targets, thereby interfering with the metabolism and proliferation pathways of tumor cells, and contributing to the solution of cancer problems.
    In the chemical industry, it cannot be ignored. In the field of material synthesis, it can participate in the preparation of polymer materials with special functions. After polymerization, it is combined with other monomers to endow polymer materials with unique physical and chemical properties. If materials with high selective adsorption properties for specific gases are prepared, they can be applied to gas separation and purification processes. In the production of fine chemical products, it is used as an important raw material to synthesize high-quality dyes, fragrances, etc. Taking dye synthesis as an example, with its structural advantages, the color, stability and other properties of dye molecules can be adjusted to meet the diverse needs of different industries for dyes. For example, the dyes required by the textile printing and dyeing industry are sun-resistant, washable and colorful, and methyl-5-bromopyridine-3-carboxylate can play a key role in the synthesis process.
    What is the market price of Methyl 5-bromopyridine-3-carboxylate?
    Methyl-5-bromopyridine-3-carboxylic acid ester, the price of this product in the chemical market is quite variable for many reasons.
    The first to bear the brunt is the cost of raw materials. 5-bromopyridine-3-carboxylic acid and methanol are the key raw materials for synthesizing this product. If the supply of raw materials is in short supply or the market demand surges, its price will rise, which in turn will cause the production cost of methyl-5-bromopyridine-3-carboxylic acid ester to rise, and the price will also rise.
    Furthermore, the difficulty of the production process is closely related to the cost. If the synthesis process is complicated, special equipment, catalysts, or multi-step reactions or strict reaction conditions are required, all of which will increase production costs and eventually increase the price of the product. On the contrary, simple and efficient processes may reduce costs and make prices more affordable.
    The relationship between market supply and demand is also the main reason for the price. If at some time, this product is in strong demand in the fields of medicine, pesticides, etc., but the production supply is difficult to increase rapidly, and the supply is in short supply, the price will rise. On the contrary, if the market is saturated and the supply exceeds the demand, the manufacturer may reduce the price and promote it.
    In addition, different manufacturers have different cost control due to different technical levels, economies of scale, and management capabilities, and the price set is also different. Large factories may be able to reduce unit costs by virtue of their scale advantages, and their pricing may be more competitive.
    Overall, the market price of methyl-5-bromopyridine-3-carboxylate can range from hundreds of yuan per kilogram to more than 1,000 yuan. It is difficult to make a conclusion. It needs to be studied in detail according to the current market situation.
    What are the storage conditions for Methyl 5-bromopyridine-3-carboxylate?
    The existence of methyl-5-bromopyridine-3-carboxylic acid ester depends on its properties. This material is sensitive, and it should be avoided from water and fire, and it should be far away from things that can respond to it.
    This medicine should be stored in a cool and dry place, and the temperature should not be high to prevent it from changing. If the cover temperature is high, it may cause it to change, or cause it to change, which will damage its quality. And it should be placed in dark places. Light can also induce it to change, and keep its quality pure. Light is a taboo.
    And it must be solid when sealed, and it will prevent the invasion of air and water. The oxygen in the air and the wetness of the water can all respond to it, destroying its structure and changing its properties. Therefore, sealing is essential, and it is better to hide the utensils in glass bottles or plastic utensils.
    When storing this medicine, you should also pay attention to the things around it, and do not mix with alkalis, acids and strong oxidants. These numbers are easy to interact with methyl-5-bromopyridine-3-carboxylic acid esters, causing danger. Either burning or exploding, it is inevitable.
    In short, the hidden methyl-5-bromopyridine-3-carboxylic acid ester is cool, dark, sealed, and avoided. Only by preparing this number can it be kept stable and used without worry.