2 6 Difluoro 4 Pyridinecarboxylicacid
pyridine pyrrole pyrazine piperidine piperazine

2,6-Difluoro-4-pyridinecarboxylicacid

    Specifications

    HS Code

    217189

    Chemical Formula C6H3F2NO2
    Molar Mass 159.09 g/mol
    Appearance Solid (usually a powder or crystalline solid)
    Physical State At Room Temp Solid
    Melting Point Specific value would need experimental determination
    Boiling Point Specific value would need experimental determination
    Solubility In Water Limited solubility expected, as it is a heterocyclic carboxylic acid with fluorine substituents
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, DMSO, etc. to some extent
    Pka Value Characteristic value related to its acidic strength (experimental determination required)
    Density Specific density value would need experimental determination
    Odor May have a faint, characteristic odor

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    Frequently Asked Questions

    As a leading 2,6-Difluoro-4-pyridinecarboxylicacid 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 2,6-difluoro-4-pyridinecarboxylic acid?
    2% 2C6-diene-4-pentanoic acid is an organic compound with multiple unique chemical properties.
    It has an unsaturated bond, that is, a carbon-carbon double bond and a carbon-carbon triple bond, so it exhibits the characteristics of an addition reaction. Take the reaction with halogen elements (such as bromine water) as an example, the bromine molecule will be added to the carbon-carbon double bond or triple bond, causing the bromine water to fade. This is a common method for identifying such unsaturated compounds. Due to the high density of double-bond and triple-bond electron clouds, it is susceptible to attack by electrophilic reagents. For example, when adding hydrogen halide, follow the Markov rule. Hydrogen atoms are added to unsaturated carbon atoms with more hydrogen, and halogen atoms are added to those with less hydrogen.
    2% 2C6-diene-4-valerynic acid is also acidic. Because of its carboxyl group (-COOH), in aqueous solution, the carboxyl group can ionize hydrogen ions and is acidic. It can neutralize with bases to form corresponding carboxylic salts and water. And its acidity is affected by other groups in the molecule. The presence of unsaturated bonds will change the distribution of electron clouds, which in turn affects the acidity of carboxyl groups.
    The compound may also undergo polymerization. Due to the existence of multiple unsaturated bonds in the molecule, under suitable catalysts and reaction conditions, double or triple bonds can be opened and connected to each other to form polymeric polymers. This polymerization reaction may have important applications in the field of materials science, and can prepare polymer materials with special properties.
    In addition, due to the different functional groups, 2% 2C6-diene-4-valerynic acid can participate in a variety of organic synthesis reactions. It is an important intermediate in organic synthesis and can be converted into other organic compounds with specific structures and functions through a series of reactions.
    What are the main uses of 2,6-difluoro-4-pyridinecarboxylic acid?
    2% 2C6-diene-4-valerynic acid, which may make great progress in the fields of pharmaceutical research and development, organic synthesis and materials science.
    In the field of pharmaceutical research and development, its unique chemical structure can be used as a key intermediate to create compounds with specific biological activities. Or by modifying and modifying this structure, new drugs for specific diseases can be developed, such as anti-cancer drugs. Cancer cell growth and spread depend on specific biomolecules and signaling pathways. Designed compounds containing this structure may be able to precisely target these key targets, block the proliferation and metastasis pathways of cancer cells, and provide new opportunities to conquer cancer.
    In the field of organic synthesis, it can be used as a cornerstone for the construction of complex organic molecules. Because it contains alkylene and alkyne functional groups, it can participate in a variety of chemical reactions, such as cyclization reactions, addition reactions, etc. By ingeniously designing reaction steps and taking advantage of these reaction characteristics, complex and novel organic molecules can be synthesized, which opens up new directions for organic synthetic chemistry, enriches the variety of organic compounds, and promotes the development of organic synthesis technology.
    In the field of materials science, it is introduced into polymer materials or endows materials with unique properties. Ethylene and alkyne functional groups can participate in polymerization reactions to form polymers with special structures and properties. Or make materials have excellent optical properties, such as fluorescence properties, for the manufacture of luminescent materials; or improve the mechanical properties of materials, enhance their strength and toughness, and be used in aerospace, automobile manufacturing and other fields that require strict material properties.
    To sum up, 2% 2C6-diene-4-valerynic acid has shown broad application prospects in the fields of medicine, organic synthesis and materials science due to its unique structure. With the deepening of research, it is expected to bring more innovative achievements and breakthroughs.
    What are the preparation methods of 2,6-difluoro-4-pyridinecarboxylic acid?
    2% 2C6-diene-4-valerynic acid is an organic compound, and there are many ways to prepare it. In ancient Chinese,
    First, it can be prepared by the reaction of the corresponding halogenated hydrocarbon and the alkynide through nucleophilic substitution. When the halogenated hydrocarbon encounters the alkynide, the two are combined in phase, and the halogen atom is replaced by the alkynyl group, so the precursor of this acid is formed, and then the appropriate functional group is converted, such as oxidation, to obtain 2% 2C6-diene-4-valerynic acid. This is a common method, but the reaction conditions need to be finely regulated. The activity of halogenated hydrocarbons and alkynides, the solvent of the reaction, the temperature, and the type and amount of bases are all related to the success or failure of the reaction and the yield.
    Second, conjugated dienes and alkynes can also be formed into its key intermediates through the Diels-Alder reaction. Conjugated dienes and alkynes interact under suitable conditions to form a cyclic structure. Then, a series of reactions are applied to the cyclic product, either ring opening or carboxyl groups are introduced, and various transformations are carried out to obtain 2% 2C6-diene-4-valerynic acid. This reaction requires attention to the configuration and electronic effects of the reactants to promote the smooth occurrence of the reaction, and the subsequent conversion steps also need to be carefully designed.
    Third, dehydration of alkynyl alcohol and further functional group modification can also be used as a preparation method. Under the action of appropriate dehydrating agents, alkynyl alcohol dehydrates a molecule of water to form an unsaturated alkyne structure, and then reacts such as halogenation and carboxylation to gradually build the structure of the target product. In this process, the selectivity of the dehydration reaction and the localization selectivity of the subsequent reaction are all key considerations.
    All kinds of preparation methods have their own advantages and disadvantages, and they need to be selected according to actual needs, such as the availability of raw materials, the difficulty of reaction, and the purity of the product, in order to achieve the purpose of preparation.
    What is the market price of 2,6-difluoro-4-pyridinecarboxylic acid?
    I don't know what the current market value of 2,6-diene-4-pentynyl butyric acid is. The market size often varies due to factors such as location, supply and demand. It may be used in chemical research, chemical synthesis, etc. However, factors such as the required amount, ease of improvement, and cost of production will all cause its price.
    If it is used in the chemical industry, its price may vary according to the price and package price. High-quality products have high cost due to high cost of extraction, and the price is not cheap; low-quality products may be relatively low. And if it is purchased in batches, suppliers may give discounts due to large quantities, and the price will also vary.
    And in different regions, due to the difference in cost and cost, the price also varies. In places with convenient transportation and chemical industry, due to the convenience and low production cost, the price may be relatively flat; in places with partial cost, the cost is high, and the price may be higher.
    For this, in order to know the market value, it is necessary to identify the suppliers, chemical trading platforms, or recent market transactions.
    What are the precautions for storing and transporting 2,6-difluoro-4-pyridinecarboxylic acid?
    When storing and transporting 2% 2C6-diene-4-valerynic acid, there are many key points to be paid attention to.
    First, this substance has special properties, and the storage environment must be dry and cool. Because it may be extremely sensitive to temperature and humidity, high temperature and humidity can easily cause deterioration or other chemical reactions, so it needs to be stored in a well-ventilated place, away from heat and fire sources, so as to avoid danger such as thermal decomposition or fire.
    Second, when transporting, the packaging must be solid and tight. Suitable packaging materials need to be selected to ensure that the packaging will not be damaged due to bumps and collisions during transportation, resulting in material leakage. Because of its certain chemical activity, once it leaks or causes pollution to the environment, it may also endanger the safety of transportation personnel.
    Third, whether it is storage or transportation, it must be strictly separated from oxidants, acids, alkalis and other substances. This substance is chemically active and in contact with the above substances, it is prone to violent chemical reactions, which may cause serious consequences such as explosions.
    Fourth, the storage area and transportation vehicles should be equipped with corresponding emergency treatment equipment and appropriate protective equipment. In the event of an unexpected situation, such as leakage, effective measures can be taken quickly to deal with it, and at the same time, relevant personnel can be protected in time to avoid harm.
    Fifth, detailed records of the storage and transportation process should be kept. It includes information such as the quantity of the substance, the time of entry and exit, the transportation route, and the handling personnel, so that the cause can be quickly traced and identified in the event of a problem.