4 Pyridinecarboxylic Acid 2 Bromo 6 Methyl Methyl Ester
pyridine pyrrole pyrazine piperidine piperazine

4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester

    Specifications

    HS Code

    545217

    Chemical Formula C8H8BrNO2
    Molar Mass 230.06 g/mol
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Low (organic ester)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data needed
    Flash Point Data needed
    Vapor Pressure Low (due to solid nature at room temp)
    Stability Stable under normal conditions, may react with strong oxidizing agents

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    Frequently Asked Questions

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    What are the physical properties of 4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester
    This is methyl 2-bromo-6-methyl-4-pyridinecarboxylate, and its physical properties are as follows. Looking at its properties, it is often colorless to pale yellow liquid, or a crystalline solid. The appearance of this form depends on the conditions such as ambient temperature and pressure. It has a certain melting point. If it is a solid, the melting point or within a specific range is essential for the identification and purification of this substance. However, the exact melting point needs to be determined by precise experiments.
    When it comes to solubility, it has good solubility in organic solvents such as ethanol, ether, chloroform, etc. This is because the molecular structure of the substance can form a suitable interaction force with the organic solvent molecules, so it can be well miscible. However, in water, its solubility is relatively limited. Due to the fact that the polarity of water does not match the polarity of the molecules of the substance perfectly, the degree of solubility in water is not high.
    Then talk about density, which is one of the important physical properties of the substance, reflecting its mass per unit volume. Compared with similar compounds, its density value may be unique and can be accurately obtained by density measurement experiments. This value is of great significance in the separation, storage and related process design of substances.
    In addition, the substance may have a certain degree of volatility. Under specific temperatures and environments, it can evaporate from the liquid or solid surface to the gas phase. The strength of volatility is also closely related to factors such as intermolecular forces and temperatures. Understanding its volatility is crucial for environmental control and safety during production and use.
    Its refractive index is also an important physical property. When light passes through the substance, it will refract. The refractive index reflects the degree of change in the speed and direction of light propagation in it. This property can be used in the fields of material purity identification and composition analysis.
    What are the chemical properties of 4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester
    Methyl 2-bromo-6-methyl-4-pyridinecarboxylate, this is an organic compound. Its chemical properties are unique and have the following numbers.
    Looking at its structure, it contains a pyridine ring, which is a nitrogen-containing hexa-membered heterocycle, which endows the compound with aromaticity. The nitrogen atom of the pyridine ring has a solitary pair of electrons, making it alkaline and can form salts with acids. Moreover, the electron cloud distribution of the pyridine ring is uneven, and electrophilic substitution can occur at specific positions, while the substitution of 2-bromo and 6-methyl affects the electron cloud density and reactivity on the ring. < Br >
    2-bromine atoms have high activity and can participate in nucleophilic substitution reactions. When encountering nucleophilic reagents, bromine ions are easy to leave, and nucleophilic reagents are replaced by nucleophilic reagents, such as reacting with sodium alcohol, corresponding ether compounds can be formed; when reacting with amines, nitrogen-containing derivatives can be obtained.
    6-methyl as the power supply group, through induction effect and superconjugation effect, the electron cloud density of the pyridine ring increases, especially the ortho and para-sites. This change not only affects the activity and selectivity of the pyridine ring electrophilic substitution reaction, but also in some oxidation reactions, methyl groups can also be oxidized to form carboxyl groups and other functional groups. The methyl formate group at the
    4-position has the general properties of ester compounds. Under acidic conditions, hydrolysis can occur to form 2-bromo-6-methyl-4-pyridinecarboxylic acid and methanol; under alkaline conditions, hydrolysis is more thorough to obtain carboxylate and methanol. At the same time, the ester group can participate in the transesterification reaction, and under the action of different alcohols in catalysts, new ester compounds are formed.
    In addition, the compound contains multiple functional groups, and the interaction between the functional groups makes it complex and rich in chemical properties. It can be used as a key intermediate in the field of organic synthesis to construct organic compounds with diverse structures through a series of reactions.
    What is the main use of 4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester
    4-Pyridine carboxylic acid, 2-bromo-6-methyl-, methyl ester are widely used in the field of chemical and pharmaceutical.
    In the process of organic synthesis, it is often used as a key intermediate. Its structure is unique, containing pyridine rings, bromine atoms, methyl and methyl ester groups, which endow it with active chemical activity. Bromine atoms can introduce various functional groups through nucleophilic substitution reactions, thereby expanding the complexity of molecular structures. Pyridine rings are also active checking points for various reactions, and can participate in many heterocyclic construction reactions, helping to synthesize compounds with specific biological activities or physical properties.
    In the pharmaceutical field, this is used as a starting material. After a series of reactions, many molecules with potential medicinal value can be created. Due to its structural characteristics, it may interact with specific targets in organisms, such as certain enzymes or receptors, thus exhibiting biological activities such as antibacterial, anti-inflammatory, and anti-tumor. Chemists modify its structure to fine-tune the physicochemical properties and biological activities of compounds in order to find drug lead compounds with high efficiency and low toxicity.
    Furthermore, in the field of materials science, through specific chemical reactions, it can be introduced into the structure of polymer materials to endow materials with special properties, such as improving the stability, solubility, or optical properties of materials. Therefore, 4-pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester has important uses in chemical, pharmaceutical and materials science fields, and is the cornerstone of many chemical synthesis and application studies.
    What are the synthesis methods of 4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester
    There are several ways to synthesize methyl 2-bromo-6-methyl-4-pyridinecarboxylate.
    First, 2-methyl-4-pyridinecarboxylic acid can be used. First, a suitable bromination reagent, such as liquid bromine, is carried out in the presence of a suitable catalyst, such as iron powder or iron tribromide. During this process, bromine atoms selectively replace hydrogen atoms at the 2-position on the pyridine ring to form 2-bromo-6-methyl-4-pyridinecarboxylic acid. Then, the obtained product is heated with methanol under the action of esterification catalyst such as concentrated sulfuric acid to carry out esterification reaction, so as to obtain methyl 2-bromo-6-methyl-4-picolinecarboxylate.
    Second, 2-bromo-6-methyl pyridine can also be used as raw material. First, the methyl on the pyridine ring is oxidized to carboxyl groups by using a suitable oxidant, such as potassium permanganate, to obtain 2-bromo-6-methyl-4-picolinecarboxylic acid. Subsequently, the target product 2-bromo-6-methyl-4-pyridinecarboxylate was obtained by esterification reaction with methanol catalyzed by an acidic catalyst.
    Another idea is to start from a suitable pyridine derivative and construct the desired substituent through a multi-step reaction. For example, methyl and bromine atoms are introduced first, then carboxyl groups are introduced at the 4-position of the pyridine ring through a specific reaction, and finally esterified with methanol. However, this pathway is relatively complicated, and the conditions of each step need to be carefully controlled to ensure high yield and selectivity. In conclusion, there are various methods for synthesizing this compound, each with its own advantages and disadvantages. It is necessary to choose the appropriate synthesis path according to the actual situation, such as the availability of raw materials, cost and reaction conditions.
    4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester What are the precautions in storage and transportation
    4-Pyridinecarboxylic acid, 2-bromo-6-methyl-, methyl ester This substance needs to be paid attention to in storage and transportation.
    First, when storing, it must find a cool and dry place. This substance is prone to change when heated, and the temperature is too high or its chemical properties are unstable, and even deteriorate. Therefore, in the warehouse, it should be stored in a low temperature area, protected from direct sunlight, and the warehouse should be well ventilated to prevent heat accumulation.
    Second, moisture prevention is also crucial. Because of its chemical structure, it is easy to absorb moisture. If it is damp, or causes reactions such as hydrolysis, it will damage its quality. Therefore, the humidity of the storage environment should be controlled within a certain range. Desiccant can be placed at the storage place, and the packaging must be tight to prevent moisture from invading.
    Third, when transporting, appropriate packaging materials should be used. Because the substance has a certain chemical activity, improper packaging or leakage. Use sturdy and chemically resistant containers to ensure that there is no risk of leakage during transportation. Loading and unloading should be handled with care to prevent packaging damage.
    Fourth, this substance may have certain toxicity and irritation. Storage and transportation personnel should be professionally trained to be familiar with its characteristics and safety protection measures. When operating, protective clothing, protective gloves and goggles are required. If you come into contact accidentally, rinse with plenty of water and seek medical treatment.
    Furthermore, the storage and transportation process should follow relevant regulations and standards. Operate strictly in accordance with the regulations on the management of hazardous chemicals, and keep records of entry and exit warehouses and transportation for traceability and supervision. In this way, the safety of 4-pyridinecarboxylic acid, 2-bromo-6-methyl -, and methyl ester during storage and transportation can be guaranteed to avoid accidents.