3 Fluoro 5 Trifluoromethyl Pyridine 2 Carbonitrile
pyridine pyrrole pyrazine piperidine piperazine

3-Fluoro-5-trifluoromethyl-pyridine-2-carbonitrile

    Specifications

    HS Code

    147367

    Chemical Formula C7H2F4N2
    Molecular Weight 190.098
    Appearance Solid (Typical)
    Solubility In Water Insoluble (Typical for this type of compound)

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    Frequently Asked Questions

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    What are the chemical properties of 3-fluoro-5-trifluoromethylpyridine-2-formonitrile?
    3-Hydroxy-5-trifluoromethylpyridine-2-formaldehyde, this is a class of organic compounds. Its parent, acetaldehyde, has multiple chemical properties.
    One of them is an addition reaction. The carbon and oxygen double bonds in the aldehyde group are electrophilic and can be added with many nucleophilic reagents. For example, with alcohols, under the catalysis of acids or bases, an addition reaction can occur to form hemiacetal, and then form acetal. Taking acetaldehyde and ethanol as an example, under acidic conditions, the carbonyl carbon atom of acetaldehyde is attacked by the nucleophilic attack of the oxygen atom in ethanol to form hemiacetal, which is then further reacted to form acetal. This reaction is often used as a carbonyl protection method in organic synthesis. It can also be added with hydrocyanic acid to form α-hydroxy nitrile. This product can be hydrolyzed to obtain α-hydroxy acid, which is an important intermediate in organic synthesis.
    The second is an oxidation reaction. Acetaldehyde is easily oxidized, and in the air, it can be slowly oxidized to acetic acid by oxygen; oxidized with a weak oxidant Torun reagent (silver ammonia solution), acetaldehyde is oxidized to ammonium acetate, and at the same time produces metallic silver, which adheres to the inner wall of the container to form a silver mirror. This reaction is called a silver mirror reaction, which is often used as an aldehyde group test method; reacted with Feilin reagent (an alkaline mixture of copper sulfate and potassium sodium tartrate), acetaldehyde is oxidized to acetic acid, and a brick-red cuprous oxide precipitate is formed at the same time, which is also used for aldehyde group test.
    < Using hydrogen as a reducing agent, in the presence of metal catalysts such as nickel and platinum, acetaldehyde carbonyl is reduced to hydroxyl to generate ethanol, which is a common method for preparing alcohols.
    The fourth is condensation reaction. In dilute alkali solution, acetaldehyde can undergo hydroxyl-aldehyde condensation reaction, and a molecule of acetaldehyde α-hydrogen atom is acted by base to form carbon negative ions, nucleophilic addition to another molecule of acetaldehyde carbonyl to generate β-hydroxyaldehyde. If heated, it can be further dehydrated to form α, β-unsaturated aldehyde. This reaction is an important way to increase carbon chain and synthesize complex organic compounds. As can be seen from the above, acetaldehyde is an important organic raw material with active chemical properties and is widely used in the field of organic synthesis.
    What are the main uses of 3-fluoro-5-trifluoromethylpyridine-2-formonitrile?
    3-Bromo-5-trifluoromethylpyridine-2-formaldehyde, namely 2-formyl-3-bromo-5-trifluoromethylpyridine, is an organic compound with important application value in the field of organic synthesis. Its main uses are as follows:
    First, in the field of pharmaceutical chemistry, it is often regarded as a key intermediate. Drug development aims to create compounds with specific biological activities and pharmacological properties. Taking the synthesis of some anti-cancer drugs as an example, 3-bromo-5-trifluoromethylpyridine-2-formaldehyde can be introduced into the target drug molecule through a series of chemical reactions by virtue of its unique chemical structure, thereby endowing the drug with high affinity and inhibitory activity against specific targets of cancer cells. Because the pyridine ring, bromine atom and trifluoromethyl in the structure can all participate in the interaction with biological macromolecules, it helps to improve the efficacy, selectivity and pharmacokinetic properties of drugs.
    Second, in the field of materials science, the compound can be used to synthesize functional materials. For example, when preparing organic optoelectronic materials, its structure can impart unique electrical and optical properties to the materials. The conjugated structure of the pyridine ring helps to transport electrons, and the energy level of the bromine atom and the trifluoromethyl can be adjusted. The interaction between the molecules makes the synthesized materials exhibit excellent properties in organic Light Emitting Diode (OLED), organic solar cells and other devices, such as improving luminous efficiency and enhancing stability.
    Third, it is also used in the field of pesticide chemistry. As an intermediate, it participates in the synthesis of new pesticides, and gives pesticides high insecticidal, bactericidal or herbicidal activities with its structural characteristics. Pyridine rings and halogenated groups have high affinity for specific targets of pests or pathogens, which can effectively inhibit their growth and reproduction, and help the development of environment-friendly and efficient pesticide products.
    What is the synthesis method of 3-fluoro-5-trifluoromethylpyridine-2-formonitrile?
    To prepare 3-alkyne-5-triethylpyridine-2-ethanol, the following ancient method can be used.
    First take an appropriate amount of acetylene, put it in a specific container, and apply suitable conditions to make it react with a halogenated hydrocarbon. The choice of this halogenated hydrocarbon needs to be carefully considered. Its structure should be in line with the alkynyl part of the target product, and the reaction mechanism of nucleophilic substitution should be used to generate an intermediate containing alkynyl groups.
    Then, this intermediate is combined with a specific pyridine derivative. The preparation of pyridine derivatives also needs to follow specific steps. After multiple reactions, the required substituents are introduced to make the structure similar to the structure of the pyridine part in the target product. When the two meet, under suitable catalyst and reaction environment, through clever reaction paths, the alkynyl group is connected to the pyridine part, and the basic structure of the target product is initially constructed.
    As for the introduction of the ethanol part, after the above structure is formed, a suitable alcohol derivative can be used as a raw material. This alcohol derivative needs to contain the basic fragment of ethanol, and through a series of transformation reactions, such as esterification, reduction, etc., it is connected to the formed molecular structure at an appropriate time. During the reaction process, it is necessary to pay close attention to the process and conditions of the reaction, such as temperature, pH, reaction time, etc., which have a profound impact on the formation and purity of the product. If the temperature is too high, it may cause frequent side reactions and the product is impure; if the temperature is too low, the reaction will be slow and take a long time. The regulation of pH is also related to the direction and rate of the reaction, which needs to be accurately grasped. After many debugging and operation, careful preparation can finally obtain 3-alkyne-5-triethylpyridine-2-ethanol.
    What are the precautions for the storage and transportation of 3-fluoro-5-trifluoromethylpyridine-2-formonitrile?
    Looking at your question today, it is related to the precautions for storage and transportation of dimethyl ether. Dimethyl ether has unique properties, so you should be cautious about these two things.
    The first word is storage. First, you must find a cool and well-ventilated place. Dimethyl ether is flammable and volatile. High temperature and unventilated places can easily cause it to evaporate and accumulate. In case of fire, it will cause an instant disaster and cause the danger of explosion. Second, storage containers need to be carefully selected. High-pressure and corrosion-resistant materials must be used, and the seal must be tight. Dimethyl ether may corrode ordinary materials, causing damage and leakage to the container, so choosing high-quality containers is the key. Third, in the storage area, fireworks and heat sources are strictly prohibited. Even small sparks can explode when exposed to dimethyl ether vapor, so there should be no open flames, electric heating appliances, etc. around. Fourth, leakage detection and alarm devices should be installed in the storage place. Once dimethyl ether leaks, it can be detected in time, so as to quickly take countermeasures and prevent problems before they occur.
    Second discussion on transportation. First, the transportation vehicle needs to be dedicated to its duties. It must be specially modified to have the ability of fire prevention, explosion prevention and anti-static. Vehicles need to be equipped with fire extinguishers, leakage emergency treatment equipment, etc., for emergencies. Second, during transportation, the speed of the vehicle should be stable and slow. Sudden brakes, sharp turns, etc. can easily cause the container to shake, collide, damage the container, and cause leakage. Third, transportation personnel should be professionally trained. Familiar with the characteristics, hazards and emergency response methods of dimethyl ether. Always pay attention during transportation, if there is any abnormality, report it quickly and handle it properly. Fourth, the transportation route planning needs to be careful. Avoid busy urban areas and densely populated places, choose open and smooth roads to reduce hazards during accidents.
    In the storage and transportation of dimethyl ether, strict regulations and precautions must be followed. If there is a slight mistake, it will cause a big disaster, so everything should not be ignored to ensure safety.
    What are the market prospects for 3-fluoro-5-trifluoromethylpyridine-2-formonitrile?
    Looking at the market prospects of 3-hydroxy- 5-trimethylpyridine-2-formaldehyde, it is worth exploring in depth.
    This compound has its uses in various fields. In the field of medicine, it may be the basis for the development of new agents. With its unique structure, it may be able to specifically combine with biomolecules in the body to help create new drugs with outstanding efficacy and minimal side effects. In materials science, it may participate in the synthesis of new functional materials, adding new substances to electronic and optical materials to meet the needs of rapid technological development.
    However, its market prospects are also influenced by a number of factors. First, the stability of raw material supply. If the raw materials are scarce or the supply channels are not smooth, the production must be stopped, which will make the output difficult to increase and affect the marketing activities. Second, the difficulty and cost of the synthesis process. If the process is complicated and the cost is high, even if the performance is superior, it is difficult to spread it widely in the market. Third, the guidance of regulations and policies. In the application of medicine and special materials, strict regulations are the only way for products to go on the market. Whether or not compliance is related to their market fate.
    At present, with the advance of science and technology, the research and application exploration of such compounds is in the ascendant. If we can break through the shackles of raw materials and processes and comply with regulations, 3-hydroxy- 5-trimethylpyridine-2-formaldehyde is expected to emerge in the market, causing ripples in related industries and creating a new situation.