5 6 Dibromopyridine 3 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

5,6-dibromopyridine-3-carboxylic acid

    Specifications

    HS Code

    872763

    Name 5,6 - dibromopyridine - 3 - carboxylic acid
    Molecular Formula C6H3Br2NO2
    Molecular Weight 279.90
    Appearance Solid (likely a powder or crystalline solid)
    Physical State Solid at room temperature
    Solubility Solubility characteristics would depend on solvent (e.g., may be sparingly soluble in water, more soluble in some organic solvents like DMSO)
    Chemical Stability Can be reactive due to the presence of bromine and carboxylic acid groups, may react with bases, reducing agents etc.

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    General Information
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    Frequently Asked Questions

    As a leading 5,6-dibromopyridine-3-carboxylic 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 main use of 5,6-dibromopyridine-3-carboxylic acid?
    5% 2C6-diethylamino-3-pyridinecarboxylic acid. The main uses of this compound are as follows:
    First, in the field of medicinal chemistry, it can be used as a key intermediate for drug synthesis. Because the pyridine ring coexists with active groups such as amine and carboxyl groups, it can build more complex drug molecules with the help of various chemical reactions. For example, by modifying the pyridine ring, changing its electron cloud density and spatial configuration, synthesizing compounds with specific pharmacological activities, or using the reactivity of amine and carboxyl groups to connect other functional fragments with biological activities to develop drugs for the treatment of specific diseases, such as the preparation of some drugs for the treatment of nervous system diseases or cardiovascular diseases, it may play an important intermediate role.
    Second, in the field of materials science, it can be used to prepare functional materials. In view of the characteristics of different groups in the molecular structure, it can be combined or reacted with other materials. For example, using its amine and carboxyl groups can cross-link with some polymers, thereby improving the properties of polymer materials, preparing materials with special adsorption, conductivity or optical properties, for the development of sensors, optical devices and other materials.
    Third, in organic synthetic chemistry, it is an extremely important synthetic building block. With the unique reactivity of amine groups, carboxyl groups, and pyridine rings, it can participate in many classic organic reactions, such as nucleophilic substitution reactions, condensation reactions, etc., to synthesize a series of organic compounds with different structures and functions, providing organic synthesis chemists with important starting materials for constructing complex organic molecular structures and assisting in the design and synthesis of new compounds.
    What are the synthesis methods of 5,6-dibromopyridine-3-carboxylic acid?
    The synthesis method of 5,6-dibromopyridine-3-carboxylic acid is an important research in the field of chemical synthesis. Its synthesis pathways are rich and diverse, and each has its own characteristics and application scenarios.
    First, pyridine is used as the starting material, and bromine atoms are introduced at specific positions of pyridine through halogenation reaction. Suitable halogenating reagents, such as bromine, N-bromosuccinimide (NBS), etc., can be selected. Under suitable reaction conditions, such as specific temperature, solvent and catalyst, the reaction is carried out to generate 5,6-dibromopyridine. Subsequently, carboxyl groups are introduced at the third position of the pyridine ring through carboxylation reaction. The commonly used carboxylation method is the Grignard reagent method, that is, the Grignard reagent of 5,6-dibromopyridine is first prepared, and then reacted with carbon dioxide. After subsequent treatment, the target product 5,6-dibromopyridine-3-carboxylic acid can be obtained.
    Second, the carboxyl-containing pyridine derivative can also be used as the starting material, and the carboxyl group can be properly protected to prevent it from being affected in the subsequent reaction. After that, the halogenation reaction is carried out, and the bromine atom is introduced at the 5th and 6th positions of the pyridine ring. After the reaction is completed, the protective group of the carboxyl group is removed to obtain 5,6-dibromopyridine-3-carboxylic acid. This path requires careful selection of protecting groups and deprotection conditions to ensure the smooth progress of the reaction and the purity of the product.
    Third, the coupling reaction strategy of transition metal catalysis is used. For example, the coupling reaction occurs under the action of transition metal catalysts such as palladium catalysts with suitable halogenated pyridine derivatives and carboxyl-containing nucleophiles. This method requires precise control of reaction conditions, such as the amount of catalyst, the selection of ligands, and the type and amount of bases, in order to achieve efficient and selective synthesis of 5,6-dibromopyridine-3-carboxylic acid.
    Different synthesis methods have their own advantages and disadvantages. The selection of starting materials, the difficulty of controlling the reaction conditions, and the yield and purity of the product are all key factors to consider. In actual synthesis, it is necessary to carefully choose the appropriate synthesis route according to specific needs and conditions to achieve the best synthesis effect.
    What is the market price of 5,6-dibromopyridine-3-carboxylic acid?
    At present, in the market, the price of 5% 2C6-dichloropyridine-3-carboxylic acid is related to all kinds of things. Its price often varies from time to time, and it also changes with the supply and demand of the market, the cost of production, and the regulation of government.
    If in terms of supply and demand, the demand is abundant and the supply is small, the price will be high. If the industry wants to increase 5% 2C6-dichloropyridine-3-carboxylic acid, but the production is not enough, the price will rise. On the contrary, if the supply exceeds the demand, the price will drop.
    The number of costs is also a major factor. The price of raw materials, the cost of labor, the loss of machinery, and the consumption of energy are all included in the cost. The price of raw materials is high due to the rarity of raw materials, or the increase in labor costs and energy consumption, the cost will rise, and the price will follow.
    The regulation of politics also has an impact. If strict laws are enacted to limit production and control pollution, the cost of producers will increase, and the price will also increase. On the contrary, the government promotes its business, and helps production reduce taxes, and the price may stabilize and drop.
    In the past, the price of this product has also changed. It is difficult to operate well at any time, and the raw materials are scarce, and the price is like a leap of the dragon; and the supply is slightly slower, but the price is gradually leveling without a big increase. < Br >
    Therefore, if you want to know the market price of 5% 2C6-dichloropyridine-3-carboxylic acid, you must look at the changes in supply and demand, the cost situation, and the measures of the government. The market is unstable, and the price is also unstable. Only when you are sensitive to all situations can you respond to it.
    What are the physicochemical properties of 5,6-dibromopyridine-3-carboxylic acid?
    5% 2C6-diyynylbenzene-3-carboxylic acid is an organic compound with unique physical and chemical properties. It is widely used in the fields of materials science and organic synthetic chemistry. The following are brief descriptions of its properties:
    1. ** Physical properties **:
    - ** Appearance **: Under normal conditions, 5% 2C6-diyynylbenzene-3-carboxylic acid is mostly solid, and its exact appearance varies according to the specific preparation method and purity, or it is white to light yellow crystalline powder. This appearance characteristic is easy to identify and handle.
    - ** Melting point **: The compound has a determined melting point, which is a key indicator for identifying purity and characteristics. Accurate melting point data need to be accurately determined experimentally. Due to differences in impurities or crystal forms, the melting point fluctuates slightly.
    - ** Solubility **: In common organic solvents, such as dichloromethane, N, N-dimethylformamide (DMF), 5% 2C6-diynylbenzene-3-carboxylic acid exhibits a certain solubility, and its solubility makes it act as a reactant or intermediate in solution chemical reactions. However, the solubility in water is poor, which is related to its molecular structure containing hydrophobic aromatic rings and alkynyl groups.
    2. ** Chemical properties **:
    - ** Acidic **: The molecule contains carboxyl groups, which are acidic and can neutralize with bases to form corresponding carboxylic salts. This property is used for the separation, purification and preparation of derivatives, such as the reaction with sodium hydroxide to form 5% 2C6-diynylbenzene-3-carboxylate sodium salt.
    - ** Alkynyl reactivity **: The alkynyl groups contained in 5% 2C6-diynylbenzene-3-carboxylic acids have high reactivity and can participate in a variety of chemical reactions. For example, under the action of a suitable catalyst, an alkynyl-alkynyl coupling reaction occurs to form a product containing a conjugated alkynyl chain structure, which has great potential for application in the field of organic semiconductor materials; it can also participate in the copper-catalyzed azide-alkynyl cycloaddition reaction (CuAAC) in click chemistry to construct heterocyclic compounds with diverse structures. < Br > - ** Aromatic ring reactivity **: As an important component of this compound, the benzene ring can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. Through such reactions, different functional groups can be introduced into the benzene ring to expand the chemical properties and application range of the compound.
    What are the precautions for storing and transporting 5,6-dibromopyridine-3-carboxylic acid?
    When storing and transporting 5% 2C6-diacetamide-3-pyridylic acid, there are several precautions that need to be paid attention to.
    First, when storing this compound, be sure to choose a cool, dry and well-ventilated place. Due to its nature, it may be affected by the ambient humidity and temperature, and the high temperature and humid place may cause it to deteriorate or decompose, which will damage the quality and efficiency. Therefore, in the warehouse, the temperature and humidity should be properly regulated, the temperature should be maintained within a specific range, and the humidity should not be too high to ensure its stability.
    Second, the storage place must be stored separately from oxidants, acids, bases and other substances. This is because 5% 2C6-diacetamide-3-pyridylic acid may react chemically with such substances, causing danger. Reactions such as oxidation reactions, acid-base neutralization, etc., may cause serious consequences such as heat generation, gas generation, and even explosion. Therefore, on the storage layout, the principle of classified storage should be strictly followed to prevent mixed storage.
    Third, when transporting, it is necessary to ensure that the packaging is intact. If the packaging is damaged, the compound may leak, not only polluting the environment, but also posing a threat to the safety of transporters. Packaging materials should have good sealing and corrosion resistance to effectively resist damage caused by external factors.
    Fourth, during transportation, it is also necessary to avoid violent vibrations and collisions. Violent vibrations or collisions may change the internal structure of the compound or cause damage to the packaging. The transportation vehicle should be smooth, and when the road conditions are not good, it is necessary to drive with caution to prevent accidents caused by excessive turbulence.
    In short, 5% 2C6-diacetamide-3-pyridylic acid needs to be carefully followed during storage and transportation, from the control of environmental conditions, to the specifications of material storage, to the operation of packaging and transportation, and strictly follow relevant procedures to ensure the safety of personnel and the quality of the compound.