3 Amino 2 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3-Amino-2-(trifluoromethyl)-Pyridine

    Specifications

    HS Code

    117995

    Name 3 - Amino - 2 - (trifluoromethyl)Pyridine
    Molecular Formula C6H5F3N2
    Molecular Weight 162.11
    Appearance Typically a solid or liquid, appearance may vary
    Melting Point Data may vary depending on purity, usually needs experimental determination
    Boiling Point Data may vary depending on purity and conditions, usually needs experimental determination
    Solubility Solubility characteristics can vary, may have some solubility in organic solvents
    Density Value depends on experimental conditions, usually needs experimental determination
    Pka Relevant to its acidic - basic properties, specific value needs experimental determination
    Flash Point Data may vary depending on purity, usually needs experimental determination

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    Frequently Asked Questions

    As a leading 3-Amino-2-(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 uses of 3-Amino-2- (trifluoromethyl) Pyridine?
    3-Amino-2- (trifluoromethyl) pyridine is widely used in the field of organic synthesis. First, it can be used as an intermediary for pharmaceutical synthesis. Its unique structure can introduce special functional groups to help create new drugs. For example, in the preparation of some antidepressant drugs, this compound can be connected with other organic molecules through specific reactions to construct structural units with specific biological activities, thereby affecting the interaction between drugs and biological targets, adjusting the efficacy and selectivity of drugs.
    Second, it also has important functions in the field of pesticides. Due to its fluoride-containing properties, it can enhance the stability and biological activity of pesticides. It can be used as a key raw material for the synthesis of high-efficiency and low-toxicity pesticides. After a series of chemical reactions, pesticide products that target specific pests or diseases can be prepared. For example, the synthesis of insecticides with special effects on the nervous system of insects can achieve the purpose of efficient insecticide by interfering with the nerve conduction of pests, and has a small impact on the environment.
    Furthermore, in the field of materials science, 3-amino-2- (trifluoromethyl) pyridine can participate in the synthesis of functional materials. It can be polymerized with other monomers to prepare polymer materials with special properties. For example, the synthesis of polymer materials with excellent optical and electrical properties can be applied to optoelectronic devices, sensors and other fields. The amino group and trifluoromethyl group contained in this compound can change the electron cloud distribution of the material, endow the material with unique physical and chemical properties, and expand the application scope of the material.
    What are the physical properties of 3-Amino-2- (trifluoromethyl) Pyridine
    3-Amino-2- (trifluoromethyl) pyridine is one of the organic compounds. It has unique physical properties and is related to the application of chemical and pharmaceutical fields.
    When it comes to appearance, this compound is often in the form of a white to light yellow crystalline powder, with a fine texture and a good luster when viewed in natural light. This form is conducive to its storage and transportation, and it is easy to mix with other substances in many reactions to improve the efficiency of the reaction.
    Its melting point is quite critical, between about 108-110 degrees Celsius. The characteristics of the melting point can help to identify the purity of this compound, and also provide key parameters for its heat treatment process. When the temperature rises near the melting point, the substance gradually melts from the solid state to the liquid state. This transition process needs to be precisely controlled, which is related to the effectiveness of the subsequent process.
    Solubility is also an important physical property. 3-Amino-2 - (trifluoromethyl) pyridine is slightly soluble in water, but it can be better dissolved in organic solvents such as ethanol and dichloromethane. This difference in solubility is of great significance in the selection of separation, purification and reaction solvents. In organic synthesis, the selection of suitable organic solvents can make the reaction easier and improve the yield of the product.
    Furthermore, its density also has a specific value, about 1.429g/cm ³. The characteristics of density are indispensable in the measurement and mixing ratio of substances. In industrial production, the precise measurement of this substance requires consideration of its density to ensure the accuracy of the reaction system.
    In addition, the vapor pressure of this compound cannot be ignored. Although the vapor pressure is low at room temperature, it gradually increases with the increase of temperature. This property is related to its volatility in a confined space and is extremely important for safe production and storage.
    The many physical properties of 3-amino-2- (trifluoromethyl) pyridine play a key role in the application of chemical industry, medicine and other fields, providing a solid foundation for the design and implementation of related processes.
    What are the chemical properties of 3-Amino-2- (trifluoromethyl) Pyridine
    3-Amino-2- (trifluoromethyl) pyridine is an important member of organic chemicals. Its chemical properties are unique and contain many wonders. Let me tell you one by one.
    Let me first talk about the properties of its amino groups. Amino groups are basic groups. Because nitrogen atoms have lone pairs of electrons, they can react with acids to form corresponding salts. Just like when encountering strong acids, amino groups will readily accept protons and become positively charged ions.
    Furthermore, the influence of trifluoromethyl groups cannot be ignored. Trifluoromethyl groups are rich in highly electronegative fluorine atoms, which greatly change the electron cloud distribution of pyridine rings by virtue of their powerful electron-absorbing effects. In this way, the electron cloud density of the pyridine ring decreases, and the activity of the electrophilic substitution reaction also decreases. However, from another perspective, it enhances the attractiveness of the pyridine ring to nucleophiles, making nucleophilic substitution reactions easier to occur.
    In addition, the compound also exhibits certain stability. The existence of trifluoromethyl groups, due to the high bond energy of C-F bonds, imparts additional stability to the molecule, making it difficult to decompose under some common chemical reaction conditions.
    In the field of organic synthesis, 3-amino-2 - (trifluoromethyl) pyridine is often used as a key intermediate due to its unique chemical properties. Its amino groups and trifluoromethyl groups can be used as reaction check points. Through ingeniously designed chemical reactions, combined with other organic compounds, organic molecules with more complex structures and functions can be constructed. In this way, it has made great contributions to the development of organic synthetic chemistry and has shown broad application prospects in many fields such as medicinal chemistry and materials science.
    What are the synthesis methods of 3-Amino-2- (trifluoromethyl) Pyridine
    The synthesis methods of 3-amino-2 - (trifluoromethyl) pyridine have been used in ancient times, and there are many methods, each with its own wonders.
    First, the compound containing the pyridine structure is used as the starting material, and the method of substitution reaction is borrowed. First, under specific conditions, the parent pyridine meets the reagent containing the trifluoromethyl group, so that the trifluoromethyl group cleverly replaces the atom at a specific position on the pyridine ring, and then introduces the trifluoromethyl group. Then, the introduction step of the amino group is carefully designed. The aminolysis reaction can be carried out, and the target position can be formed at the appropriate temperature, pressure and catalyst with the assistance of a suitable amination reagent, so that the 3-amino-2 - (trifluoromethyl) pyridine can be obtained. This path requires fine control of the reaction conditions, and the reaction conditions of each step are slightly different, which may affect the yield and purity.
    Second, start with the strategy of building a pyridine ring. Organic small molecules containing trifluoromethyl groups are selected to directly build a pyridine ring through cyclization reaction with compounds containing amino groups or potential sources of amino groups. For example, by means of condensation reaction, the relevant small molecules are connected to each other, and when the ring is formed, trifluoromethyl groups and amino groups are precisely arranged at the target position at the same time. Although the starting materials of this route are relatively common and easy to find, the reaction mechanism is complex and involves multi-step series reactions. The reaction process needs to be carefully regulated in order to make the reaction proceed smoothly and achieve the desired product.
    Third, the use of transition metal catalysis means. Transition metal complexes are used as catalysts to make the reaction substrate containing trifluoromethyl and amino groups efficiently couple to form the target product under mild reaction conditions. Transition metal catalysts can precisely activate substrate molecules, guide the directional occurrence of reactions, and improve the selectivity and efficiency of the reaction. However, this method is very careful about the choice and dosage of catalysts, and the cost of catalysts may be a factor restricting large-scale production.
    The above synthesis methods have their own advantages and disadvantages, and it is necessary to choose carefully according to the specific experimental conditions, the availability of raw materials and the use of the target product.
    What is the price range of 3-Amino-2- (trifluoromethyl) Pyridine in the market?
    The price of 3-amino-2 - (trifluoromethyl) pyridine in the market is difficult to determine. Its price is often caused by many changes, and it cannot be limited to a certain number.
    Looking at the past, the price of chemical products was often tied to the balance between supply and demand. If there are many people who want this product, but the supply is small, the price will rise; on the contrary, if the supply exceeds demand, the price may decline. And the cost of its production is also the main reason. The price of raw materials, the process of preparation, and the cost of energy consumption will all be involved in the cost, which will then affect the price in the market.
    In addition, the competition in the market cannot be ignored. If multiple merchants compete to sell this product, in order to compete for profits, or reduce its price; if there are few merchants and control the market, the price may be high.
    In addition, changes in luck and government regulations will also affect its price. In case of natural and man-made disasters, production is blocked, or government orders are tightened, limiting production, the price can fluctuate.
    Therefore, if you want to know the exact price of 3-amino-2- (trifluoromethyl) pyridine, you need to observe the current market situation and consult all merchants to obtain its near-real number, and it is difficult to hide its price range.