3 Amino 2 Fluoro 4 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3-Amino-2-fluoro-4-(trifluoromethyl)pyridine

    Specifications

    HS Code

    764039

    Chemical Formula C6H4F4N2
    Molecular Weight 180.10
    Appearance Solid (Typical)

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    General Information
    Where to Buy 3-Amino-2-fluoro-4-(trifluoromethyl)pyridine in China?
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    Frequently Asked Questions

    As a leading 3-Amino-2-fluoro-4-(trifluoromethyl)pyridine 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 main application fields of 3-Amino-2-fluoro-4- (trifluoromethyl) pyridine
    3-Amino-2-fluoro-4- (trifluoromethyl) pyridine is widely used in the fields of medicine, pesticides, and materials.
    In the field of medicine, this compound is often a key intermediate for the creation of new drugs due to its special fluorine atom and pyridine structure. The introduction of fluorine atoms can significantly change the physical, chemical and biological activities of compounds. With its structural properties, highly specific and highly active drugs can be developed, such as inhibitors targeting specific disease-related targets. Or for the development of anti-cancer drugs, by binding to specific proteins of cancer cells to block their abnormal proliferation signaling pathways, to achieve therapeutic effect; or drugs related to nervous system diseases, because the structure is similar to neurotransmitters, can regulate neurotransmission, such as depression, anxiety and other diseases.
    In the field of pesticides, 3-amino-2-fluoro-4 - (trifluoromethyl) pyridine is also an important raw material. Its structure endows the compound with good stability and biological activity, and the prepared pesticide has the characteristics of high efficiency, low toxicity and wide range. It can be used to produce insecticides, which can bind to specific receptors in the insect's nervous system, interfere with their nerve conduction, and cause insect paralysis and death; or as fungicides, inhibit the activity of key enzymes for the growth and reproduction of pathogens, protect crops from disease infestation, and maintain agricultural harvests.
    In the field of materials, due to its unique structure and properties, it can be used to prepare special functional materials. For example, for photoelectric materials, its electronic structure and conjugated system make the material have excellent photoelectric conversion properties, which can be applied to organic Light Emitting Diode (OLED), solar cells and other devices to improve its efficiency and stability; or to prepare high-performance polymer materials, the introduction of this structure can modify the thermal stability, chemical stability and mechanical properties of the polymer, and expand the application range of
    In summary, 3-amino-2-fluoro-4- (trifluoromethyl) pyridine plays an extraordinary role in the fields of medicine, pesticides, materials, etc. With the development of science and technology, its application prospects will be broader.
    What are the physical properties of 3-Amino-2-fluoro-4- (trifluoromethyl) pyridine
    3-Amino-2-fluoro-4- (trifluoromethyl) pyridine is a kind of organic compound. Its physical properties are quite characteristic, let me tell them one by one.
    When it comes to appearance, this compound is often in the form of a white to light yellow crystalline powder, which is delicate in appearance and resembles the essence of precipitation over time. Its properties are relatively stable at room temperature and pressure, but it needs to be properly stored to prevent changes due to environmental factors.
    The melting point is within a certain range, which is crucial for the identification and purification of this substance. By accurately measuring the melting point, its purity geometry can be determined. If the melting point is accurate and the melting range is narrow, it indicates that the purity of the substance is quite high; conversely, if the melting range is wide, it may contain impurities and needs to be further purified.
    Solubility is also one of its important physical properties. In organic solvents, such as common ethanol and dichloromethane, it has a certain solubility. This property facilitates its use as a reactant or intermediate in organic synthesis reactions. In suitable solvents, it can better contact and react with other reactants, promoting the smooth progress of chemical reactions. However, in water, its solubility is relatively poor. This difference is due to the characteristics of its molecular structure. The structure of fluorine atoms and pyridine rings in the molecule affects its interaction with water molecules.
    Furthermore, its density also has a specific value. Although in general operation, this parameter may not be as important as melting point and solubility, in some research scenarios involving accurate measurement and phase equilibrium, accurate knowledge of density is indispensable. It determines the quality of a certain volume of the substance, and provides key data support for material ratio and process design in actual production and scientific research.
    In summary, the physical properties of 3-amino-2-fluoro-4- (trifluoromethyl) pyridine, from appearance, melting point, solubility to density, are all interrelated and have a profound impact on its application in the chemical field. In many fields such as organic synthesis and drug development, it is necessary to fully understand and rationally utilize these physical properties in order to better play the role of this compound and promote the progress of related science and technology.
    What are the synthesis methods of 3-Amino-2-fluoro-4- (trifluoromethyl) pyridine
    The synthesis method of 3-amino-2-fluoro-4- (trifluoromethyl) pyridine has been known for a long time. There are many methods, which are described by you today.
    One is to start with fluorine-containing pyridine derivatives and borrow the method of nucleophilic substitution. First take a suitable fluorine-containing pyridine substrate, place it in a specific reaction vessel, add an appropriate amount of nucleophilic reagents, such as ammonia. Adjust the reaction temperature, pressure and time, so that the nucleophilic reagent attacks the specific check point on the pyridine ring and replaces the corresponding group, then 3-amino-2-fluoro-4 - (trifluoromethyl) pyridine is obtained. This process requires fine control of the reaction conditions. If the temperature is too high or too low, the reaction yield and selectivity can change.
    Second, through the construction strategy of pyridine rings. First, the appropriate small organic molecules are used as raw materials to build a pyridine ring structure through multi-step reactions. For example, the organic fragments containing fluorine and trifluoromethyl are selected, and the compounds containing amino groups are reacted with condensation and cyclization to build a pyridine ring. This process has many steps, but each step is crucial. When condensation, suitable catalysts and reaction solvents need to be selected to promote the efficient progress of the reaction; when cyclization, attention should also be paid to the reaction conditions so that the pyridine ring structure is correctly generated and the desired substituent position is reached.
    Third, the path of photocatalytic synthesis. In the presence of a photocatalyst, a suitable fluorine-containing, amino-containing and trifluoromethyl-containing starting material is irradiated with light of a specific wavelength. The photocatalyst absorbs light energy and produces an excited state, which prompts the electron transfer and chemical reaction of the starting molecule to gradually generate the target product. This method is relatively novel and the reaction conditions are relatively mild, but the selection of photocatalysts and the photoreaction device are quite demanding. The activity and stability of the photocatalyst directly affect the efficiency and success of the reaction; the design of the photoreaction device should also ensure that the light energy acts evenly and efficiently on the reaction system.
    What is the price range of 3-Amino-2-fluoro-4- (trifluoromethyl) pyridine in the market?
    The exact price of 3 - Amino - 2 - fluoro - 4 - (trifluoromethyl) pyridine in Wuwei City. However, if you want to know its price, you can ask it on the chemical raw material trading platform and reagent supplier. Vendors have different pricing depending on supply, purity and quantity.
    Common chemical raw material trading platforms, such as Gade Chemical Network, gather many chemical product suppliers and often list the prices of various products. Or you can find the price of this compound at professional reagent suppliers such as Sinopharm Group Chemical Reagent Co., Ltd., search banner reagent network, etc.
    If the purchase quantity is small, it is used for laboratory trials. Due to the cost of packaging, transportation, etc., the price per gram may be higher, or tens or even hundreds of yuan. If it is industrial mass production and large-scale procurement, the price per kilogram may be reduced due to economies of scale, or reduced to hundreds of yuan per kilogram. But these are all speculative prices, and the actual price must be subject to the quotations of suppliers in the market.
    What are the storage conditions for 3-Amino-2-fluoro-4- (trifluoromethyl) pyridine?
    3-Amino-2-fluoro-4- (trifluoromethyl) pyridine is a very important chemical substance, and its storage conditions require special attention. This substance should be stored in a cool, dry and well-ventilated place.
    A cool environment can prevent it from causing many unstable conditions due to excessive temperature. Excessive temperature may cause changes in its chemical reactivity, which in turn affects its quality and performance. A dry environment is also crucial, because moisture may react with the substance or cause adverse changes such as hydrolysis. Humid environments can easily deteriorate the substance and reduce its purity.
    Furthermore, good ventilation is also indispensable. In this way, even if the substance evaporates a little gas, it can be discharged in time to avoid accumulation in a limited space to prevent danger, such as explosion or damage to human health.
    In addition, when storing such chemicals, make sure that the container is well sealed. Sealed containers can effectively prevent the mixing of external air, moisture and other impurities, and maintain the purity and stability of the substance. At the same time, storage areas should be kept away from fire sources, heat sources and strong oxidants, etc., due to 3-amino-2-fluoro-4- (trifluoromethyl) pyridine or violent reactions with these substances, resulting in safety accidents. For storage facilities, regular inspections should also be carried out to check whether the container is damaged or leaking, so as to detect and deal with problems in a timely manner and ensure the safe storage of the substance.