2 Hydroxy 6 Triflroromethyl 3 Pyridinecarboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

2-Hydroxy-6-triflroromethyl-3-pyridinecarboxylic acid

    Specifications

    HS Code

    216106

    Name 2-Hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid
    Molecular Formula C7H4F3NO3
    Molecular Weight 207.11
    Appearance Solid (predicted)
    Melting Point 188 - 192 °C
    Boiling Point 411.5±45.0 °C at 760 mmHg (predicted)
    Pka 2.41±0.10 (predicted)
    Solubility Soluble in DMSO, Methanol
    Logp 1.21 (predicted)
    Density 1.613±0.06 g/cm3 (20 °C, 760 mmHg, predicted)

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

    As a leading 2-Hydroxy-6-triflroromethyl-3-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 2-Hydroxy-6-triflroromethyl-3-pyridinecarboxylic acid?
    2-Hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid, this is an organic compound. Looking at its structure, it contains a pyridine ring, which is connected with a hydroxyl group, a trifluoromethyl group and a carboxyl group. Its physical properties, whether it is a solid at room temperature, and the specific melting point, boiling point and solubility are all related to the intermolecular forces and group characteristics. Hydroxyl groups are polar, which can cause hydrogen bonds between molecules or increase their solubility in polar solvents. Trifluoromethyl groups contain strong electronegative fluorine atoms, which make the group have strong electron absorption, which affects the molecular charge distribution and chemical activity.
    In terms of its chemical properties, carboxyl groups are acidic and can neutralize with bases to form corresponding carboxylates and water. Under appropriate conditions, the carboxyl group can also participate in the esterification reaction and form esters with alcohols. Hydroxyl groups also have certain reactivity and can be substituted or participate in dehydration and other reactions. Pyridine rings, as aromatic heterocycles, can undergo electrophilic substitution reactions. Due to the positioning effect of trifluoromethyl and hydroxyl groups, the substitution reaction may mainly occur in specific locations.
    In the field of organic synthesis, 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid may be used as a key intermediate for the creation of various drugs, pesticides and functional materials containing pyridine structures. Its unique structure and properties endow the products made from this raw material with special properties, which may have unique biological activities in medicine, and may have special optical and electrical properties in the field of materials.
    What are the main uses of 2-Hydroxy-6-triflroromethyl-3-pyridinecarboxylic acid?
    2-Hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid, which has a wide range of uses, is a key intermediate for the synthesis of many specific drugs in the field of medicine. For example, some targeted drugs for specific diseases can precisely act on diseased cells due to their unique chemical structure, improve the therapeutic effect, and have relatively small side effects. In the field of pesticides, it can be used to create high-efficiency, low-toxicity, and environmentally friendly pesticides. It can optimize the molecular structure of pesticides, enhance the activity against pests and pathogens, and reduce the harm to non-target organisms and the environment, contributing to the sustainable development of agriculture. In the field of materials science, this compound can participate in the synthesis of functional materials. Or endow materials with special optical and electrical properties, showing application potential in optoelectronic devices, sensors, etc., and contributing to the innovation and development of materials science. In addition, in organic synthetic chemistry, as an important organic synthetic block, it can participate in the construction of various complex organic compounds, expand the research boundaries of organic synthetic chemistry, and provide more possibilities for the creation of new compounds.
    What is the synthesis method of 2-Hydroxy-6-triflroromethyl-3-pyridinecarboxylic acid?
    The synthesis of 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid has attracted much attention in the field of organic synthesis. This compound has attracted many chemists due to its unique structure and potential application value.
    In the past, the synthesis path often used compounds containing pyridine rings as the starting material. One method is to take an appropriate pyridine derivative and introduce a hydroxyl functional group under specific reaction conditions. Usually, the pyridine derivative and the hydroxylating reagent undergo nucleophilic substitution in an organic solvent with a suitable base as the catalyst. This step requires precise control of the reaction temperature and time to prevent side reactions from occurring. If the temperature is too high, it may cause the ring opening of the pyridine ring; if the time is too long, it may form a by-product of polyhydroxylation.
    Then, trifluoromethyl is introduced. In this step, reagents containing trifluoromethyl groups, such as trifluoromethylation reagents, react with pyridine derivatives containing hydroxyl groups under the action of metal catalysts. The choice of metal catalysts is crucial, and different metals and their ligands have a significant impact on the selectivity and yield of the reaction. Commonly used metal catalysts include palladium, copper, etc., and their dosage and type need to be optimized according to specific reaction conditions.
    As for the introduction of carboxyl groups, it can be achieved in various ways. For example, the halogenated pyridine derivative is used as an intermediate, and the Grignard reagent is first reacted with magnesium metal, and then reacted with carbon dioxide to obtain a carboxyl group after hydrolysis. In this process, the preparation of Grignard reagents needs to be carried out in an anhydrous and oxygen-free environment, because Grignard reagents are extremely active and easily decompose in contact with water or oxygen.
    Alternatively, a specific substituent can be converted into a carboxyl group by an oxidation reaction. If alkyl pyridine derivatives are used as raw materials, alkyl groups are oxidized to carboxyl groups under suitable reaction conditions by appropriate oxidants. However, this method requires attention to the oxidative properties of the oxidant. If the oxidative properties are too strong, it may cause damage to the pyridine ring and other functional groups.
    Synthesis of 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid requires fine design of reaction routes, precise regulation of reaction conditions at each step, and comprehensive consideration of factors such as raw material selection, reagent dosage, reaction temperature and time, in order to improve the yield and purity of the product.
    What is the price range of 2-Hydroxy-6-triflroromethyl-3-pyridinecarboxylic acid in the market?
    I look at this question and ask about the price range of 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid in the market. However, the price of this compound often varies due to many factors, and it is difficult to determine a certain number.
    The cost of raw materials is a key factor. If the starting material for preparing this acid is scarce and expensive, the price of the finished product will be high. On the contrary, if the raw material is easily available and cheap, the price may be slightly reduced.
    The complexity of the production process also affects the price. If a fine, multi-step reaction process is required, and the reaction conditions are strict, and special equipment or technology is involved, the production cost will increase significantly, resulting in higher product prices.
    Market supply and demand conditions also affect prices. If demand is strong and supply is limited, merchants may raise prices due to shortage of supply; if the market is oversupplied, prices may be reduced for promotional sales.
    In addition, different suppliers have different pricing due to their own cost structures and business strategies. In the world of "Tiangong Kaiwu", although there is no such compound, the price of the product is subject to supply, demand and cost.
    In summary, in order to determine the exact price range of 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid, it is necessary to carefully investigate the raw material market and production process details, and compare the quotations of various suppliers in order to obtain a more accurate number. However, the price may fluctuate between tens of yuan and thousands of yuan per kilogram, depending on the above factors.
    What are the manufacturers of 2-Hydroxy-6-triflroromethyl-3-pyridinecarboxylic acid?
    2-Hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid, the preparation of this product is related to many manufacturers. In today's chemical industry, many factories that are good at organic synthesis are involved in the production of this product.
    Looking at the past, there are companies that focus on fine chemicals and often produce such pyridinecarboxylic acid derivatives. They have obtained this product with exquisite skills and controlled reaction conditions. Or under the joint hands of universities and scientific research institutes, they can improve its yield and purity with innovative methods.
    Among them, several large factories in China have advanced equipment and mature technology. It is unique in raw material procurement and production process control. From the selection of initial raw materials to the precise regulation of temperature and pressure in the reaction process, there is no impurity. The 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid produced is of high quality and is supplied to all parties.
    In addition, there are also well-known overseas manufacturers who have been deeply involved in the field of organic fluorine chemistry for many years. With its cutting-edge technology, it has won a place in the global market. The products it produces are favored by many customers with high purity and stable performance.
    In summary, today's 2-hydroxy-6-trifluoromethyl-3-pyridinecarboxylic acid manufacturers are all over the world, with their respective advantages, delivering products to the market and promoting the application of this chemical in various fields.