2 Methoxypyridine 4 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

2-methoxypyridine-4-carboxylate

    Specifications

    HS Code

    453566

    Chemical Formula C7H7NO3
    Molar Mass 153.14 g/mol
    Appearance Solid (usually white or off - white)
    Melting Point N/A (specific value may vary, needs experimental determination)
    Boiling Point N/A (specific value may vary, needs experimental determination)
    Solubility In Water Low solubility, slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Pka Value N/A (specific value may vary, needs experimental determination)
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Odor Odorless or very faint odor

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    Frequently Asked Questions

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    What are the chemical properties of 2-methoxypyridine-4-carboxylate?
    2-Methoxypyridine-4-carboxylate, this is a group of organic compounds. It has many unique chemical properties and has attracted much attention in the field of organic synthesis.
    First of all, its structural characteristics are described. The pyridine ring is a nitrogen-containing six-membered heterocyclic ring with aromatic properties. The 2-position methoxy group is connected to the pyridine ring with an oxygen atom. The oxygen in the methoxy group has a solitary pair electron, which can be conjugated with the pyridine ring, affecting the electron cloud distribution of the ring, causing the electron cloud density of the pyridine ring to increase, which changes its electrophilic substitution activity. In the 4-position carboxylate group, the carboxyl negative ion exists stably, because in the carboxyl negative ion, the negative charge is delocalized by two oxygen atoms to reach a stable state.
    In addition to chemical activity, due to the change of electron cloud density of the pyridine ring, when the electrophilic substitution reaction occurs, the substituent tends to enter the position of higher electron cloud density of the pyridine ring. And because it contains carboxylate groups, it can complexe with metal ions to form metal complexes. Such complexes often have special uses in the field of catalysis or materials science. At the same time, carboxylate can react with acids to regenerate into carboxylic acids, or esterify with alcohols to form new ester compounds.
    In terms of solubility, the carboxylate group is ionic and has a certain solubility in water. However, the pyridine ring and the methoxy group are hydrophobic parts, so its solubility is also affected by factors such as solvent polarity and temperature. In organic synthesis, this solubility characteristic can be used for compound separation and purification.
    In terms of stability, under normal conditions, 2-methoxy pyridine-4-carboxylate is relatively stable. In case of strong acid, strong base or high temperature, strong oxidant and other extreme conditions, the structure may change. In case of strong acid, the carboxylate is converted to carboxylic acid; in case of strong oxidant, the pyridine ring or methoxy group may be oxidized.
    In summary, 2-methoxypyridine-4-carboxylate has broad application prospects in many fields such as organic synthesis, catalysis, and materials science due to its unique structure and various chemical properties.
    What are the common synthetic methods of 2-methoxypyridine-4-carboxylate?
    For the synthesis of 2-methoxypyridine-4-carboxylate, there are several common methods as follows.
    First, 2-methoxypyridine is used as the starting material and can be obtained by carboxylation. First, 2-methoxypyridine interacts with a suitable strong base, such as n-butyl lithium, to generate the corresponding lithium salt intermediate. This intermediate is very active, and then reacts with carbon dioxide gas at low temperature and without water and oxygen. After acidification, 2-methoxypyridine-4-carboxylic acid can be obtained. After that, it undergoes esterification reaction with alcohols under acid catalysis to generate 2-methoxypyridine-4-carboxylic acid. This approach needs to pay attention to the strict control of the reaction conditions. Because the lithium salt intermediate is extremely active, it is prone to side reactions in contact with water and oxygen.
    Second, it starts from pyridine-4-carboxylic acid. Pyridine-4-carboxylic acid is first reacted with methylating reagents such as dimethyl sulfate in an alkaline environment to achieve 2-position methoxylation, thereby obtaining 2-methoxypyridine-4-carboxylic acid, which is also converted into the corresponding carboxylic acid by esterification reaction. In this process, the amount of methylating reagent, reaction temperature and time have a great influence on the reaction yield and selectivity, and need to be carefully regulated.
    Third, a suitable halogenated pyridine is used as the raw material. For example, 2-halo-4-pyridyl carboxylate undergoes nucleophilic substitution reaction with methoxylating reagents such as sodium methoxide, and the halogen atom is replaced by methoxy group to form 2-methoxypyridine-4-carboxylate. The key to this method lies in the selection of halo-pyridine and the optimization of reaction conditions to ensure the efficient nucleophilic substitution reaction and reduce the occurrence of side reactions.
    All methods for synthesizing 2-methoxypyridine-4-carboxylate have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider factors such as raw material availability, cost, and difficulty of reaction conditions, and choose the appropriate synthesis path.
    In what areas is 2-methoxypyridine-4-carboxylate applied?
    2-Methoxypyridine-4-carboxylate, this is a chemical substance. It has applications in many fields, and let me explain it in detail.
    In the field of medicine, its significance is extraordinary. Due to its specific chemical structure and properties, it can act as a key intermediate for drug synthesis. In the development of many new drugs, 2-methoxypyridine-4-carboxylate is used as the starting material, and a series of delicate chemical reactions can be used to construct molecular structures with unique pharmacological activities. For example, when some innovative drugs are created for specific disease targets, it has made great contributions to the synthesis of drugs with precise curative effects and few side effects. < Br >
    In the field of materials science, it also has outstanding performance. Can participate in the preparation process of polymer materials. When introduced into the polymer polymerization reaction system, it can change the physical and chemical properties of the material. For example, it can improve the stability and solubility of the material. In the preparation of some functional coating materials or high-performance polymer materials, its addition can optimize the material properties and make it meet the needs of different scenarios, such as in the preparation of materials used in protective coatings for electronic devices or special environments.
    In the field of agricultural chemistry, 2-methoxy pyridine-4-carboxylate also plays a role. It can be used as an important component in the synthesis of new pesticides. With its unique chemical properties, the synthetic pesticides can exhibit high-efficiency insecticidal, bactericidal or weeding properties. Compared with traditional pesticides, pesticides based on this synthesis may have better environmental friendliness and targeting, ensuring the healthy growth of crops while reducing the adverse impact on the environment.
    What is the market outlook for 2-methoxypyridine-4-carboxylate?
    2-Methoxypyridine-4-carboxylate, a class of compounds in the field of organic chemistry. Its current market prospects, let me elaborate.
    The landscape of the chemical industry, the field of organic synthesis has a growing demand for new and efficient synthetic blocks. 2-methoxypyridine-4-carboxylate due to its unique structure, can be used as a key intermediate, and plays an important role in the synthesis of many complex organic compounds. In the field of medicinal chemistry, the construction of many drug molecules depends on these compounds. The ingenious combination of pyridine ring and methoxy group and carboxylate in its structure endows the molecule with specific physical and chemical properties and biological activity. It can be used in the process of drug development, or can be used as the core skeleton of lead compounds. It can be modified and modified to meet the needs of different disease treatment targets. Therefore, in the pharmaceutical market, its potential value is quite high and the prospect is also broad.
    Looking at the field of materials science, with the rapid development of functional materials, the demand for organic compounds with specific structures and properties is increasing. 2-methoxy pyridine-4-carboxylate can participate in the preparation of functional polymers, organic semiconductor materials, etc. With its unique electronic structure and reactivity, it may be able to impart novel electrical and optical properties to materials, and it may have outstanding performance in cutting-edge fields such as new display technologies, energy storage and conversion materials. The market potential is huge.
    However, its marketing activities also have challenges. The optimization of the synthesis process is crucial. To achieve large-scale production and cost control, it is necessary to continuously refine the synthesis route to improve the yield and purity. And market awareness still needs to be improved. The research and development of many potential application fields is still in its infancy. It is necessary for the industry, university and research community to work together and increase research efforts in order to fully tap its market value. Such compounds will bloom in the future chemical, pharmaceutical and materials markets and become an important force to promote industrial progress.
    How safe and toxic are 2-methoxypyridine-4-carboxylate?
    2-Methoxypyridine-4-carboxylate, the safety and toxicity of this substance are related to many aspects, let me explain in detail.
    First of all, its chemical properties, 2-methoxypyridine-4-carboxylate contains specific functional groups, methoxy groups are connected to pyridine rings, and the carboxylate part also has chemical activity. This structure gives it a certain reactivity, and it reacts with other substances in a specific chemical reaction environment. If it is not handled properly, it may cause accidental chemical reactions, which threatens safety.
    As for toxicity, although there is a lack of detailed and accurate research, it can be inferred from compounds with similar structures. Some of the pyridine compounds have certain toxicity, or irritate the skin, eyes and respiratory tract. The carboxylate part of 2-methoxypyridine-4-carboxylate, if it produces free acids or other metabolites during metabolism in the body, or affects the normal physiological function of organisms.
    In an industrial production environment, if workers are exposed to high concentrations of 2-methoxypyridine-4-carboxylate for a long time, or ingested by inhalation, skin contact, etc., or cause potential damage to health, such as respiratory inflammation, skin allergies, etc. In terms of the environment, if it enters the water body or soil, or has an unknown impact on the ecosystem due to chemical stability, or affects the structure and function of the microbial community, it will disturb the ecological balance.
    However, if you can correctly understand and follow the safety operating procedures, such as in production, storage and use, take appropriate protective measures, such as wearing protective equipment, ensuring good ventilation, and controlling the exposure dose and time, it can also effectively reduce risks and protect personnel safety and environmental health.