Ethyl 2 Chloro 4 Pyridinecarboxylate
pyridine pyrrole pyrazine piperidine piperazine

Ethyl 2-chloro-4-pyridinecarboxylate

    Specifications

    HS Code

    788098

    Chemical Formula C8H8ClNO2
    Molecular Weight 185.607 g/mol
    Appearance Typically a colorless to light - yellow liquid
    Boiling Point Around 250 - 260 °C (decomposes)
    Density Approximately 1.25 - 1.30 g/cm³
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Flash Point Relatively high, potentially around 100 - 120 °C
    Odor May have a pungent or characteristic odor
    Stability Stable under normal conditions but may react with strong oxidizing agents

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    Frequently Asked Questions

    As a leading Ethyl 2-chloro-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 Ethyl 2-chloro-4-pyridinecarboxylate?
    Ethyl 2 - chloro - 4 - pyridinecarboxylate is an organic compound with specific chemical properties. Its molecules contain chlorine atoms, pyridine rings and ester groups, and these structures give it unique properties.
    In terms of physical properties, at room temperature, either liquid or solid, it has a certain melting point and boiling point. Due to the ester group, it has a certain solubility in organic solvents, such as common organic solvents such as ethanol and ether.
    In terms of chemical properties, ester groups can undergo hydrolysis. Under acidic conditions, hydrolysis produces 2 - chloro - 4 - pyridinecarboxylic acid and ethanol; under alkaline conditions, hydrolysis is more thorough and rapid, resulting in corresponding carboxylic salts and ethanol.
    Furthermore, chlorine atoms are active and can undergo substitution reactions. When nucleophiles attack, chlorine atoms can be replaced by other groups, and then various compounds can be derived. For example, when reacting with sodium alcohol, chlorine atoms can be replaced by alkoxy groups.
    Because the pyridine ring is aromatic, electrophilic substitution reactions can occur. However, the electron cloud density on the pyridine ring is relatively low compared to the benzene ring, and the electrophilic substitution reaction activity is slightly inferior to that of the benzene ring. Under appropriate conditions, other groups can be introduced at specific positions in the pyridine ring.
    Ethyl 2 - chloro - 4 - pyridinecarboxylate's chemical properties make it widely used in the field of organic synthesis and can be used as an intermediate for the preparation of a variety of bioactive or special functional compounds.
    What are the main uses of Ethyl 2-chloro-4-pyridinecarboxylate?
    Ethyl 2-chloro-4-pyridyl carboxylate, which is widely used. In the field of pharmaceutical synthesis, it is often a key intermediate. It can be skillfully converted into compounds with unique pharmacological activities through specific reaction steps, making outstanding contributions to the creation of new drugs to deal with diseases such as anti-infection and anti-tumor.
    In the field of pesticide research and development, it also plays an important role. With the help of chemical modification, highly efficient and low-toxic pesticide active ingredients can be constructed, showing strong inhibition or killing effect on pests, while reducing the adverse impact on the environment and protecting the growth of crops.
    In the field of materials science, ethyl 2-chloro-4-pyridyl carboxylate has also made a name for itself. It can participate in the synthesis of polymers or functional materials, endowing materials with unique physical or chemical properties, such as improving the stability and solubility of materials, so as to expand the application of materials in different scenarios.
    Furthermore, in the basic research of organic synthetic chemistry, it is a typical organic compound, providing an ideal model substrate for chemists to deeply explore the reaction mechanism and develop novel synthesis methods, and promoting the continuous development of the theory and technology of organic synthetic chemistry.
    What is the synthesis method of Ethyl 2-chloro-4-pyridinecarboxylate?
    There are various ways to synthesize ethyl 2-chloro-4-pyridine carboxylic acid esters. One common way is to use 4-pyridine carboxylic acid as the starting material.
    First, 4-pyridine carboxylic acid and ethanol are esterified under the condition of acid catalysis. In this process, the acid can be selected as sulfuric acid to provide protons for the reaction, which prompts the nucleophilic substitution of the carboxylic acid and the alcohol to form ethyl 4-pyridine carboxylic acid. The reaction mechanism is that the hydroxyl oxygen atom of the alcohol nucleophilically attacks the carbonyl carbon of the carboxylic acid, and the esterification is achieved through proton transfer and dehydration steps.
    Then, the 2-position of ethyl 4-pyridine carboxylate is chlorinated. In this chlorination step, chlorine gas or chlorine-containing reagents such as N-chlorosuccinimide (NCS) can be used. Taking NCS as an example, under the action of initiators such as benzoyl peroxide, NCS produces chlorine free radicals that attack the 2-position of the pyridine ring, and through radical substitution reaction, ethyl 2-chloro-4-pyridine carboxylate is obtained. During this process, the electron cloud distribution characteristics of the pyridine ring determine that the chlorine atom mainly attacks the 2-position.
    Another way is to chlorinate the pyridine ring first, and then esterify it. If 2-chloro-4-methylpyridine is used as the raw material, the methyl group is oxidized to the carboxyl group first, and a strong oxidant such as potassium permanganate can be selected. This oxidation reaction goes through multiple steps of intermediates, and finally 2-chloro-4-pyridine carboxylic acid is obtained. Then it is esterified with ethanol, and the conditions are similar to the above esterification, and ethyl 2-chloro-4-pyridine carboxylic acid ester can also be obtained.
    All synthesis methods have their own advantages and disadvantages. In actual operation, the choice should be based on the availability of raw materials, the difficulty of reaction conditions, the purity and yield of the product, and many other factors.
    Ethyl 2-chloro-4-pyridinecarboxylate What are the precautions in storage and transportation?
    Ethyl 2 - chloro - 4 - pyridinecarboxylate is an organic compound. When storing and transporting, many things need to be paid attention to.
    First, when storing, find a cool, dry and well-ventilated place. This is because the compound may be sensitive to heat and moisture. If it is exposed to high temperature and humid environment, it may deteriorate or undergo chemical reactions. For example, at high temperature, its molecular structure may change, which affects its chemical properties and application efficiency.
    Second, it must be kept away from fires and heat sources. Because of its flammability, it is easy to cause combustion in case of open flames and hot topics, causing the risk of fire. Once it catches fire, it will be difficult to fight or cause greater harm.
    Third, when storing this substance, it should be stored separately from oxidants, acids, alkalis, etc., and must not be mixed. Due to its active chemical properties, contact with the above substances may cause chemical reactions, or generate gas, heat, or even explosions.
    Fourth, during transportation, the packaging must be tight to ensure that the container is free of leakage. If there is a leak, it will not only waste raw materials, pollute the environment, but even more, leak or react with surrounding substances, endangering transportation safety.
    Fifth, transportation vehicles should also be selected and driven according to the specified route. To avoid densely populated areas and traffic arteries, prevent accidents from causing numerous casualties and major property losses.
    Sixth, those who handle and come into contact with this object should take protective measures, such as wearing protective gloves, goggles, etc. Because it may irritate the skin and eyes, if you accidentally come into contact, you should quickly rinse with plenty of water and seek medical treatment.
    What is the market price of Ethyl 2-chloro-4-pyridinecarboxylate?
    Fuethyl 2-chloro-4-pyridyl carboxylic acid ester, whose market value is determined by the number of. The quality of this substance is often affected by various factors. The supply of its raw materials is low, if the raw materials are rare or difficult to obtain, the price must be high; if the supply is abundant, it may be reduced. The method of manufacturing is also low, and the method of refining and multiplying, the cost will increase, and it will also be low; the method of easy, or it can be made slightly lower. In addition, the supply and demand of the market also depends on the lack of supply due to the demand. If the supply is low and the demand is low, or it will fall.
    However, the approximate direction of past transactions and the market, its value per gram may be 10 to 100. This is not a rough estimate. And different places, due to differences in performance and performance, also have different performance. And the suppliers are different, because of their cost control and strategic performance, the requirements are not uniform. Therefore, if you want to know its performance, you can only get the solution if you look at the market below and compare the quality of the suppliers.