3 Bromo 6 Chloro 2 Pyridinecarboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

3-Bromo-6-chloro-2-pyridinecarboxylic acid

    Specifications

    HS Code

    383284

    Chemical Formula C6H3BrClNO2
    Molar Mass 236.45 g/mol
    Appearance Solid (usually)
    Color May vary, often off - white to light - colored solid
    Melting Point Data may vary, needs experimental determination
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF
    Acidity Pka Relevant to the carboxylic acid group, data may vary
    Purity Can be specified by manufacturers, e.g., 95%, 98% etc.

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    General Information
    Where to Buy 3-Bromo-6-chloro-2-pyridinecarboxylic acid in China?
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    Frequently Asked Questions

    As a leading 3-Bromo-6-chloro-2-pyridinecarboxylic acid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemistry of 3-Bromo-6-chloro-2-pyridinecarboxylic acid?
    3-Bromo-6-chloro-2-pyridinecarboxylic acid, this is an organic compound with specific chemical properties. Its physical properties are mostly solid, and its appearance may be white to off-white crystalline powder. It has good stability at room temperature and pressure.
    When it comes to solubility, the substance has different solubility in organic solvents. Common organic solvents such as methanol, ethanol, dichloromethane, etc., may have a certain solubility in them. This is due to the interaction between the polarity of the organic solvent and the molecular structure and the compound. However, the solubility in water may be limited, although its molecular structure contains carboxyl groups that can form hydrogen bonds with water, the presence of bromine, chlorine atoms and pyridine rings makes its overall polarity not high, and the interaction with water is difficult to dissolve.
    Chemical activity, the presence of carboxyl groups makes the compound acidic, and can neutralize with bases to form corresponding salts. Under suitable conditions, carboxyl groups can participate in many organic reactions, such as esterification reactions, and form esters with alcohols under the action of catalysts. Bromine and chlorine atoms, as halogen atoms, are highly active and can participate in nucleophilic substitution reactions. For example, in the presence of appropriate nucleophiles, bromine and chlorine atoms can be replaced by nucleophiles to generate new organic compounds. This property provides a path for the synthesis of more complex pyridine derivatives. The pyridine ring also gives the compound a certain chemical activity and can participate in the substitution reaction on the ring. Due to the distribution of electron clouds in the pyridine ring, the electrophilic substitution reaction mostly occurs in specific locations.
    The chemical properties of this compound are of great significance in the field of organic synthesis. It provides key intermediates for the preparation of new medicines, pesticides and materials. Chemists can use its properties to design and synthesize organic compounds with specific functions.
    What are the common synthesis methods of 3-Bromo-6-chloro-2-pyridinecarboxylic acid?
    The common synthesis methods of 3-bromo-6-chloro-2-pyridinecarboxylic acid generally include the following.
    One is to use pyridine as the starting material. First, pyridine is interacted with halogenating reagents under specific conditions, such as using suitable brominating agents and chlorinating agents, carefully adjusting the reaction temperature, time and reagent dosage, introducing bromine atoms and chlorine atoms at specific positions in the pyridine ring, and then introducing carboxyl groups at the second position of the pyridine ring through carboxylation reaction. This carboxylation reaction can be achieved by using suitable carboxylating reagents, such as a combination of carbon dioxide and metal reagents, under corresponding reaction conditions. < Br >
    Second, it can start from the pyridine derivative containing specific substituents. For example, the pyridine compound with some substituents selectively introduces bromine and chlorine atoms at the desired position through the halogenation reaction, and then converts other substituents, and finally builds a carboxyl group through a multi-step reaction. In this process, the halogenation reaction needs to select the appropriate halogenation reagent and reaction conditions according to the activity and selectivity of the substrate to ensure the accurate introduction of bromine and chlorine atoms into the target check point. When converting other substituents, the appropriate reaction path should be selected according to their characteristics to accurately achieve the transformation to carboxyl groups.
    Third, the coupling reaction catalyzed by transition metals. Pyridine derivatives containing bromine and chlorine atoms were selected as substrates and coupled with carboxyl-containing reagents under the action of transition metal catalysts. This method requires careful selection of catalysts, ligands, reaction solvents and bases to improve the efficiency and selectivity of the reaction. For transition metal catalysts such as palladium and nickel, the electronic effect and steric resistance of ligands have a great impact on the reaction, and careful consideration is required to achieve efficient synthesis of 3-bromo-6-chloro-2-pyridinecarboxylic acid.
    Where is 3-Bromo-6-chloro-2-pyridinecarboxylic acid used?
    3-Bromo-6-chloro-2-pyridinecarboxylic acid, which is used in many fields. In the field of medicine, it is a key intermediate for the synthesis of specific drugs. Taking the creation of antibacterial drugs as an example, its unique chemical structure can undergo a series of reactions to ingeniously introduce drug molecules, giving the drug a targeted effect on specific bacteria, helping the drug to more accurately attack bacteria and improve antibacterial efficacy.
    In the field of pesticides, it also plays an important role. After rational design and reaction, it can be converted into highly efficient pesticide ingredients. For example, for some common crop pests, the pesticides can interfere with the physiological activities of pests, or destroy their nervous system, or hinder their normal metabolism, effectively prevent and control pests, and ensure crop yield and quality. < Br >
    In the field of materials science, it has also made its mark. It can be used as a starting material for the construction of special functional materials. By polymerizing or modifying with other compounds, materials with unique optical and electrical properties are prepared. For example, in organic optoelectronic materials, it can adjust the electron transport and luminescence properties of materials, providing the possibility for the development of new display technologies and optoelectronic devices.
    In addition, in chemical research, it is often used as an important reagent for researchers to explore new chemical reaction paths and study reaction mechanisms. Because its structure contains a variety of active check points, it can trigger a variety of chemical reactions, contributing to the development of organic synthetic chemistry.
    What is the market price of 3-Bromo-6-chloro-2-pyridinecarboxylic acid?
    3-Bromo-6-chloro-2-pyridinecarboxylic acid, the market price of this substance is difficult to determine. The price of the cover often changes due to a variety of reasons, such as the trend of supply and demand, the method of preparation, the price of the material, the difference in market conditions and the difference in regions.
    First of all, the trend of supply and demand, if there are many people in the market, and there are few people who produce, the price will rise; on the contrary, if the supply exceeds the demand, the price will drop.
    The method of preparation is also the key. The new method may reduce its cost and make the price lower; the old method, the cost may be high, and the price will also be high.
    The price of the material also affects its market value. If the price of raw materials rises, in order to ensure profitability, the price of the finished product will also increase; if the price of raw materials falls, the price of the product may also decrease.
    The difference in market conditions is also huge. During the period of economic prosperity, all industries are booming, and the demand may be prosperous, and the price may rise; when the economy is depressed, the demand may decrease, and the price may also decrease.
    The difference in regions also makes the price different. Where transportation is convenient and industries are concentrated, the cost may be low, and the price may be cheap; where transportation is inconvenient and industries are sparse, the cost may be high, and the price may be expensive.
    To know the exact price, you can consult chemical raw material suppliers or explore chemical product trading platforms to obtain a timely and accurate price. However, this price is not static and requires constant attention to know its dynamics.
    What are the storage conditions for 3-Bromo-6-chloro-2-pyridinecarboxylic acid?
    3-Bromo-6-chloro-2-pyridinecarboxylic acid, this is an organic compound. Its storage conditions are quite important, which is related to the stability and quality of the compound.
    According to the concept of "Tiangong Kaiwu", each product has its own suitable storage place in order to maintain its characteristics. When this compound is stored, the first environment is dry. Because of the humid gas, it is easy to cause reactions such as hydrolysis and deterioration. Therefore, when placed in a dry place, such as supplemented by desiccant, it can keep the environment less humid.
    Furthermore, temperature is also the key. It should be stored in a cool place to avoid high temperature. High temperature is easy to promote its chemical reaction and cause structural changes. Generally speaking, the temperature is preferably 2-8 ° C, which can effectively reduce the rate of decomposition or other adverse reactions.
    Storage containers should also be considered. Corrosion-resistant containers should be used, because the compound has a certain chemical activity, ordinary containers or react with it. Glass containers or some specific plastic containers can be well selected if they can be ensured not to chemically react with them.
    And it needs to be separated from other chemicals such as oxidizing agents and reducing agents. Due to its chemical properties, it coexists with other chemicals, or reacts violently, causing safety hazards.
    In conclusion, to properly store 3-bromo-6-chloro-2-pyridinecarboxylic acid, it is necessary to place it in a dry, cool environment, choose a suitable container, and reasonably separate it from other chemicals, so as to ensure its quality and stability.