4 Bromomethyl 2 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

4-BROMOMETHYL-2-TRIFLUOROMETHYL-PYRIDINE

    Specifications

    HS Code

    825719

    Chemical Formula C7H5BrF3N
    Molecular Weight 240.02
    Appearance Typically a colorless to light - yellow liquid or solid
    Boiling Point Data may vary, around [X] °C (approximate value, exact depends on purity and conditions)
    Melting Point Data may vary, around [X] °C (approximate value, exact depends on purity and conditions)
    Density Data may vary, around [X] g/cm³ (approximate value, exact depends on conditions)
    Solubility Soluble in some organic solvents like dichloromethane, chloroform; less soluble in water
    Flash Point Data may vary, around [X] °C (approximate value, exact depends on conditions)
    Pka Data may vary, around [X] (approximate value for pyridine - related acidity)
    Vapor Pressure Data may vary, around [X] mmHg at [X] °C (approximate value, exact depends on conditions)
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 4-BROMOMETHYL-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 application fields of 4-bromomethyl-2-trifluoromethylpyridine
    4-Hydroxymethyl-2-trifluoromethylpyridine has a wide range of main application fields. In the field of medicine, this compound can be used as a key pharmaceutical intermediate. With its unique chemical structure, it can help synthesize many drugs with specific pharmacological activities. For example, when developing some targeted therapeutic drugs for specific diseases, it can be used as an important starting material for building drug molecular structures. With the modification and modification of its structure, the interaction between drugs and targets can be precisely regulated, thereby improving the efficacy and safety of drugs.
    In the field of pesticides, 4-hydroxymethyl-2-trifluoromethylpyridine also plays an important role. It can be used to prepare high-efficiency, low-toxicity and environmentally friendly new pesticides. Due to its chemical properties, it can enhance the specific effect of pesticides on pests or pathogens, while reducing the impact on non-target organisms, reducing pesticide residues, and meeting the needs of the current development of green agriculture. For example, some new pesticides and fungicides will be used in the synthesis of pesticides to improve the control effect of pesticides on pests and diseases.
    In the field of materials science, this compound also shows potential application value. It can participate in the synthesis of functional materials, giving materials unique physical and chemical properties. For example, in the preparation of some high-performance polymer materials, the introduction of 4-hydroxymethyl-2-trifluoromethylpyridine structural units can improve the material's heat resistance, chemical resistance, and optical properties, thus expanding the material's application range in high-end fields such as aerospace and electronics.
    What are the synthesis methods of 4-bromomethyl-2-trifluoromethylpyridine?
    There are various methods for the synthesis of 4-hydroxymethyl-2-trifluoromethyl pyridine. The first is to use pyridine as the starting material and go through a multi-step reaction. First, the pyridine is reacted with a specific reagent under suitable conditions to introduce hydroxymethyl groups. This process requires temperature control and time control, and an appropriate catalyst is selected to make the reaction proceed in the desired direction. Then, in a specific reaction system, trifluoromethyl is introduced. This step also requires fine regulation of the reaction conditions to improve the purity and yield of the product.
    Second, it can be started from other compounds containing pyridine structures. If a pyridine derivative with suitable substituents is found, through a series of functional group conversion reactions, one of the substituents is first modified to hydroxymethyl, and then trifluoromethyl is ingeniously introduced. This path requires careful design of the structure of the starting compound and familiarity with the reaction mechanism of each step in order to efficiently synthesize the target product.
    Third, there are also specific heterocyclic compounds as raw materials to construct pyridine rings through cyclization reactions, and hydroxymethyl and trifluoromethyl are introduced in an orderly manner during or after cyclization. This approach needs to accurately grasp the cyclization reaction conditions to ensure the accuracy of pyridine ring construction, and the subsequent steps of introducing substituents also need to be carefully operated to make the reaction of each step smooth, and finally obtain high-purity 4-hydroxymethyl-2-trifluoromethylpyridine.
    What is the market price of 4-bromomethyl-2-trifluoromethylpyridine?
    Today there is 4-hydroxymethyl-2-trifluoromethyl pyridine. What is the value of its market? This is a matter that is often inquired by the commercial market, which is related to the circulation of goods and wealth and the operation of the business. If you want to clarify its price, you must examine all things in detail.
    Looking at the source of its materials, if the materials it needs are easy to obtain and the quantity of production is wide, the price is flat. If the materials are rare and expensive, difficult to mine and difficult to make, their price is high. Such as the ancient treasures of mining, digging deep mountains, taking the labor, its value is even in the city; if the ordinary earth and stones are everywhere, the price is low. If the material of this compound is rare and complex, it is determined by the price, it is the most important. < Br >
    Furthermore, it depends on the craftsmanship. If the crafting method is simple, labor is saved, and energy consumption is minimal, the cost will drop, and the price will also drop. On the contrary, if the crafting technique is complex, it requires exquisite tools and people who specialize in it. It takes a long time and consumes a lot of money, and the price will be high. In the past, the art of swordsmithing was refined by the elite, and it took time and months, and the price of the sword was high; while the crude tools could be used in an instant, and the price was low.
    The supply and demand of the city is also the main reason. If there are many users, there are many who ask for it, and the supply is small, the price will rise. If there are few who need it, the goods will be piled up, although good and cheap. If you are hungry, you are thirsty for rice, and the price is several times higher; in a good year, the grain and wheat are in the warehouse, and the price is self-equalized. This compound is widely used in medicine, chemical industry, etc. Whether it is widely used or not, whether it is sought for prosperity or not, determines its price.
    There is also a situation of competition in the market. If there are many people who compete for this market, they compete with each other for their market, to attract customers to gain wealth, or reduce their price. If there is only one family, there is no other sub-name, and the right to operate the market, the price can be set by yourself. In ancient times, salt and iron were monopolized, and the officials were in charge of their profits, and the price was paid from the top; and later merchants competed, and the price moved with the market. < Br >
    Therefore, in order to know the market price of 4-hydroxymethyl-2-trifluoromethyl pyridine, it is necessary to look at the material source, technology, supply and demand, and competition, and weigh the reference to the school before obtaining its approximate price.
    What are the storage conditions for 4-bromomethyl-2-trifluoromethylpyridine?
    The storage conditions of 4-hydroxymethyl-2-trifluoromethyl pyridine should be handled with caution due to its special physical properties. It should be placed in a cool, dry and well ventilated place.
    Those who are cool should avoid high temperature. If it is in a warm place, it may cause chemical change due to heat, which will damage its quality. If the temperature is too high, it may promote its decomposition and deterioration, and lose its inherent properties. It is difficult to achieve the expected effect when used. Therefore, it is appropriate to not exceed 25 ° C. This temperature can slow down the rate of chemical change and keep its quality stable.
    Dry environment is also important. This substance is prone to reactions such as hydrolysis when exposed to water or moisture. Moisture can disrupt its molecular structure, causing its purity to decrease and activity to decrease. Therefore, the storage place must be moisture-proof, and it can be supplemented by desiccant to absorb surrounding water vapor and maintain its dry state.
    The best ventilation is to avoid the accumulation of harmful gases. If stored in an occluded place, this thing or volatile gas will accumulate and have a high concentration, which is dangerous to the human body, or will cause accidents due to the accumulation of gas, such as combustion, explosion, etc. And ventilation can disperse moisture in the environment and help keep it dry.
    In addition, when stored, it should be separated from oxidizing, reducing and other heterogeneous substances. With its chemical properties, if it encounters them or reacts violently, it will cause danger. It must be stored in a special container, which must be corrosion-resistant and well-sealed to prevent foreign objects from disturbing it, and to maintain its purity and stability. This is the key to the storage of 4-hydroxymethyl-2-trifluoromethyl pyridine.
    What are the physical and chemical properties of 4-bromomethyl-2-trifluoromethylpyridine?
    4-Hydroxymethyl-2-trifluoromethyl pyridine is a key intermediate in organic synthesis. Its physical and chemical properties are as follows:
    ** 1. Physical properties **
    1. ** Appearance **: Usually colorless to light yellow liquid, when pure, the color is lighter, if it contains impurities, the color may deepen. This appearance characteristic is in chemical production, and its purity status can be preliminarily determined by simple visual inspection.
    2. ** Boiling point **: The boiling point is within a specific range, and the exact value will vary according to the experimental conditions, roughly within a certain range. In the process of separation and purification, this boiling point characteristic can be separated by distillation according to the difference between its boiling point and other substances.
    3. ** Melting point **: It has an exact melting point, which is of great significance in the study of solid-state and liquid-state transformation and quality control. If the melting point of the product is in high agreement with the theoretical value, the side reflects its high purity.
    4. ** Solubility **: It shows good solubility in common organic solvents such as ethanol and ether, but its solubility in water is relatively limited. This difference in solubility allows for the selection of suitable solvents in organic synthesis reactions, which promotes the reaction to proceed more efficiently.
    ** Second, chemical properties **
    1. ** Nucleophilic Substitution Reaction Activity **: Hydroxymethyl groups and trifluoromethyl groups in the molecule change the electron cloud density distribution of the pyridine ring. Trifluoromethyl groups have strong electron-withdrawing effects, which reduce the electron cloud density of the pyridine ring, while the hydroxymethyl group is relatively weak. This makes the specific position on the pyridine ring attractive to nucleophiles, and nucleophilic substitution reactions can occur, which are widely used in reactions such as the construction of new carbon-heteroatomic bonds.
    2. ** Redox Properties **: Hydroxymethyl groups can be converted into aldehyde groups or carboxyl groups under appropriate oxidation conditions. If treated with mild oxidizing agents, hydroxymethyl groups can be selectively oxidized to aldehyde groups, providing a path for the synthesis of aldehyde-containing pyridine derivatives. At the same time, the pyridine ring itself can also participate in some redox reactions, achieving the reduction of the pyridine ring or the oxidation of pyridine nitrogen under different conditions.
    3. ** Acidic and basic **: From the perspective of acid and base, the pyridine nitrogen atom has a certain alkalinity and can react with acids to form salts. The hydrogen-oxygen bond on the hydroxymethyl group can also show a certain acidity under strong basic conditions, participating in acid-base related reactions. This property is quite important in some specific catalytic reaction systems.