Methyl 2 Bromo 4 Pyridinecarboxylate
pyridine pyrrole pyrazine piperidine piperazine

Methyl 2-bromo-4-pyridinecarboxylate

    Specifications

    HS Code

    385434

    Chemical Formula C7H6BrNO2
    Molecular Weight 216.03
    Appearance Typically a solid (description may vary based on purity and conditions)
    Melting Point Data depends on purity and measurement method
    Boiling Point Data depends on purity and measurement method
    Solubility In Water Low solubility (organic compound nature)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data depends on purity and measurement method
    Flash Point Data depends on purity and measurement method
    Stability Stable under normal conditions but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading Methyl 2-bromo-4-pyridinecarboxylate 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 2-bromo-4-pyridinecarboxylate?
    Methyl 2 - bromo - 4 - pyridinecarboxylate is an organic compound with unique chemical properties. This compound has the characteristics of halogenated hydrocarbons and esters.
    In terms of the properties of halogenated hydrocarbons, bromine atoms are highly active and can undergo nucleophilic substitution reactions. For example, when encountering nucleophilic reagents, such as alcohols, under basic conditions, bromine atoms can be replaced by alkoxy groups to form corresponding ether derivatives. For example, when reacting with sodium cyanide, bromine atoms will be replaced by cyano groups, which can be converted into carboxyl groups or other nitrogen-containing functional groups through subsequent reactions to expand the structure of the compound.
    From the perspective of the characteristics of esters, it can undergo hydrolysis reactions. Under acidic conditions, 2-bromo-4-pyridinecarboxylic acid and methanol are slowly hydrolyzed; under alkaline conditions, hydrolysis is more rapid, resulting in corresponding carboxylate and methanol. In addition, the compound may also participate in the transesterification reaction. If it is catalyzed with other alcohols, the methyl ester group can be replaced with other ester groups, so as to change the molecular physical and chemical properties to meet different synthesis needs.
    Because of the presence of the pyridine ring, the molecule has a certain alkalinity and can react with acids to form pyridine salts. This property can be used to separate, purify or change its solubility and reactivity in solution. In conclusion, Methyl 2 - bromo - 4 - pyridinecarboxylate shows a variety of reactivity and application potential in the field of organic synthesis due to its functional groups.
    What is the synthesis method of Methyl 2-bromo-4-pyridinecarboxylate?
    The method of synthesizing methyl 2-bromo-4-pyridinecarboxylate often follows the following methods.
    First, 4-pyridinecarboxylic acid is used as the starting material. First, 4-pyridinecarboxylic acid is mixed with methanol, an appropriate amount of concentrated sulfuric acid is added as a catalyst, and the esterification reaction is carried out by heating. This process requires careful temperature control to allow the reaction to proceed smoothly at a suitable temperature, such as 60-80 ° C. Over a period of time, 4-pyridinecarboxylic acid is fully converted into methyl 4-pyridinecarboxylate. Then, methyl 4-pyridinecarboxylate is put into the halogenation reaction system, and liquid bromine or N-bromosuccinimide (NBS) is used as the bromination reagent. In an organic solvent such as dichloromethane, in the presence of light or an initiator such as benzoyl peroxide, bromine atoms selectively replace hydrogen atoms at specific positions on the pyridine ring to achieve the synthesis of methyl 2-bromo-4-pyridinecarboxylate. This path step is clear, but the esterification and bromination reaction conditions need to be carefully regulated to ensure yield and selectivity.
    Second, starting from 2-bromo-4-pyridine. Carboxyl groups are introduced by suitable methods, such as reacting with carbon dioxide under specific conditions, and then esterification is carried out. For example, under the action of strong bases such as n-butyl lithium, 2-bromo-4-pyridine reacts with carbon dioxide at low temperature to form corresponding carboxylic salts. After acidification, 2-bromo-4-pyridine carboxylic acid is obtained. Then, according to the conventional esterification method, it reacts with methanol under acid catalysis to make methyl 2-bromo-4-pyridine carboxylic acid ester. The key to this approach lies in the connection between carboxyl group introduction and esterification steps, and the optimization of reaction conditions in each step to improve the purity and yield of the product.
    When synthesizing methyl 2-bromo-4-pyridinecarboxylate, the product of each step needs to be detected and purified in detail. Common detection methods such as thin layer chromatography (TLC), nuclear magnetic resonance (NMR), mass spectrometry (MS), etc. to confirm the structure and purity of the product. Purification methods are selected according to product characteristics, such as recrystallization, column chromatography, etc., to ensure that the final methyl 2-bromo-4-pyridinecarboxylate meets the required Quality Standards.
    What are the main uses of Methyl 2-bromo-4-pyridinecarboxylate?
    Methyl-2-bromo-4-pyridinecarboxylate has a wide range of uses. In the field of medicinal chemistry, it is often a key building block for the synthesis of delicate drug molecules. Because its structure contains halogen atoms and pyridine rings, various functional groups can be introduced to construct compounds with specific biological activities through various reactions such as nucleophilic substitution. For example, it can be used to create anti-tumor, antibacterial, antiviral and other drugs, and interact with specific targets in organisms to exert therapeutic effects.
    In the context of materials science, it also has its uses. It can be chemically modified to obtain materials with special photoelectric properties. Due to the conjugated structure of pyridine ring and ester group, it may endow the material with excellent electron transport properties, which can be used as the active layer material of organic Light Emitting Diode (OLED), solar cell and other devices to improve the performance of the device.
    In organic synthesis chemistry, it is an important intermediate. It can participate in many reactions, such as palladium-catalyzed coupling reactions, reactions with aryl boric acid and other reagents, to build complex aromatic systems, expand the structural diversity of organic molecules, lay the foundation for the synthesis of new organic compounds, and promote the development and innovation of organic synthesis chemistry.
    What is the market price of Methyl 2-bromo-4-pyridinecarboxylate?
    Methyl 2-bromo-4-pyridinecarboxylate, an important organic intermediate in the field of fine organic synthesis, is often found in the preparation process of medicines, pesticides, dyes and many other products. As for its market price, it is difficult to specify exactly, because it is affected by multiple factors.
    The first to bear the brunt is the market supply and demand situation. If the demand for methyl 2-bromo-4-pyridinecarboxylate in the pharmaceutical, pesticide and other industries is strong, but the supply is limited, the price will rise; conversely, if the market oversupply, the price will tend to drop.
    Furthermore, the price of raw materials also has a profound impact. The price fluctuations of the raw materials required for the preparation of this compound, such as pyridine, bromine, methanol, etc., are directly related to the production cost. Raw material prices rise, product costs increase, and market prices will also increase.
    The production process and technical level should not be underestimated. Advanced and mature production processes can effectively improve production efficiency, reduce energy consumption and losses, thereby reducing costs and affecting market pricing. If the manufacturer has exclusive advanced processes, it may have an advantage in price setting.
    In addition, different manufacturers will have different pricing due to differences in brand reputation and product quality. Well-known large factories, because of their stable product quality and perfect after-sales services, the price may be high; while some small factory products, although the price is low, the quality may vary.
    According to past market conditions, the price of methyl 2-bromo-4-pyridyl carboxylate may fluctuate between tens of yuan and hundreds of yuan per kilogram. However, this is only a general range. The actual price needs to be combined with the current market conditions. Consult relevant suppliers, distributors or through professional chemical product trading platforms to clarify.
    What are the precautions for Methyl 2-bromo-4-pyridinecarboxylate during storage and transportation?
    Methyl-2-bromo-4-pyridinecarboxylate is a commonly used raw material in organic synthesis. During storage and transportation, many matters need to be paid attention to.
    First, the temperature and humidity of storage are the key. This compound should be stored in a cool and dry place to avoid high temperature and humidity. High temperature can easily cause it to decompose, and humid environment may cause it to hydrolyze, which will damage its quality. Therefore, the warehouse temperature should be controlled at 15-25 ° C, and the relative humidity should be kept at 40% -60%.
    Second, it is necessary to prevent it from contacting with oxidants, strong bases and other substances. Methyl-2-bromo-4-pyridinecarboxylate has certain chemical activity. When it encounters an oxidizing agent, it may cause a violent oxidation reaction, which may lead to combustion or even explosion. When it encounters a strong alkali, it may also undergo a chemical reaction, causing its structure to change and lose its original properties. Therefore, when storing, it should be placed separately from such substances.
    Third, during transportation, the packaging must be tight. High-quality packaging materials, such as strong plastic drums or iron drums lined with special materials, should be selected to prevent leakage. If a leak occurs during transportation, it will not only waste raw materials, but also pollute the environment and endanger the safety of personnel.
    Fourth, the logo should not be underestimated. On the packaging, the name of the substance, its properties, and hazard warnings should be clearly marked, so that both transporters and contacts can understand its characteristics and operate with caution.
    In addition, relevant regulations and standards must be followed regardless of storage or transportation. Professionals should be professionally trained to be familiar with the properties and safe operation procedures of the compound, so as to ensure the safety of storage and transportation and avoid accidents.