2 Hydroxymethyl 3 Methyl 4 2 2 2 Trifluoroethoxy Pyridine
pyridine pyrrole pyrazine piperidine piperazine

2-hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine

    Specifications

    HS Code

    584713

    Chemical Formula C9H10F3NO2
    Molecular Weight 221.18
    Appearance Solid (usually)
    Melting Point Specific value would require experimental determination
    Boiling Point Specific value would require experimental determination
    Solubility In Water Limited solubility (predicted, actual value needs testing)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane (predicted)
    Density Specific value would require experimental determination
    Vapor Pressure Low (predicted, actual value needs testing)
    Flash Point Specific value would require experimental determination

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    Frequently Asked Questions

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    What is the main use of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine?
    2-Hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine is an organic compound. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry. Due to the unique structure of this compound, such as the presence of trifluoroethoxy and pyridine rings, it is endowed with specific chemical and physical properties. These properties can be chemically modified to achieve specific interactions with biological targets. Therefore, in the process of drug development, it may be used to construct molecular structures with specific biological activities, laying the foundation for the creation of new drugs.
    It also has its uses in the field of materials science. Due to its structure containing active functional groups, such as hydroxymethyl, it can participate in many chemical reactions or can be used to prepare functional polymer materials. By introducing this compound into the polymer skeleton, it may endow the material with special properties, such as improving the solubility, thermal stability or optical properties of the material, and then meet the special requirements of different application scenarios on material properties.
    In the field of pesticide chemistry, this compound may have certain biological activities due to its unique chemical structure. After reasonable modification and modification, it may be developed into a new type of pesticide, which shows good control effect on specific pests and diseases, and because of its fluorine-containing structure, it may have the advantages of high efficiency, low toxicity and environmental friendliness, which is in line with the current trend of pesticide development.
    In summary, 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine has potential application value in many fields such as medicine, materials and pesticides, providing an important material basis for scientific research and industrial development in related fields.
    What are the synthesis methods of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine
    2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine is an important organic compound, and its synthesis method has attracted much attention in the field of organic synthesis. Although the synthesis of this compound is not directly mentioned in Tiangong Kaiwu, the traditional process principles it contains have something in common with modern organic synthesis ideas, which can be used for reference.
    In modern organic synthesis, there are many methods for synthesizing 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine. One method is to introduce hydroxymethyl, methyl and trifluoroethoxy groups through a specific substitution reaction using a compound containing a pyridine ring as the starting material. For example, a pyridine derivative can be taken first, and a halogen atom can be introduced at a specific position in the pyridine ring by halogenation reaction, and then reacted with a nucleophile containing hydroxymethyl to generate a pyridine intermediate containing hydroxymethyl.
    Furthermore, the intermediate is treated with appropriate methylation reagents to achieve the introduction of methyl groups. In this process, the reaction conditions and reagents need to be carefully selected to ensure the selectivity and yield of the reaction. Finally, the resulting intermediate is reacted with 2,2,2-trifluoroethoxyl ethanol or its corresponding derivatives in the presence of a base or a catalyst to cause the trifluoroethoxy group to replace the halogen atom to form the target product 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine.
    In addition, there are other synthesis strategies, such as the gradual introduction of each substituent starting from the way of constructing the pyridine ring. First, the pyridine ring skeleton is constructed by organic reaction, and then hydroxymethyl, methyl and trifluoroethoxy are introduced in sequence. This strategy requires fine design of reaction steps and conditions to ensure the smooth progress of each step of the reaction, and precise control of the substituent position and configuration. In the synthesis process, a variety of organic synthesis techniques, such as separation and purification, structural identification, etc., are often used to ensure the purity and structural correctness of the product.
    In short, the synthesis of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine requires comprehensive consideration of raw material selection, reaction conditions optimization and reaction convergence of each step. Only by means of modern organic synthesis techniques and strategies can this compound be synthesized efficiently.
    What are the physical properties of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine
    2-Hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine, which is an organic compound. To understand its physical properties, it is necessary to observe its structural characteristics.
    From the structure, it can be seen that the molecule contains a pyridine ring, which is a six-membered nitrogen-containing heterocycle with certain stability and aromaticity. The nitrogen atom of the pyridine ring has lone pair electrons, which can participate in intermolecular interactions, such as the formation of hydrogen bonds, which affects the physical properties of the compound.
    Its 2-position hydroxymethyl (-CH -2 OH) and hydroxyl (-OH) have strong polarity and can form hydrogen bonds with water molecules, so it can improve the solubility of the compound in water. At the same time, due to the presence of hydroxyl groups, hydrogen bonds can be formed between molecules, which increases the intermolecular force and causes its melting point and boiling point to rise. Methyl (-CH) at the
    3 position is a non-polar group, which has a relatively small impact on the overall molecular polarity, but it will increase the molecular volume and have a slight impact on molecular accumulation and van der Waals forces.
    4-position 2,2,2-trifluoroethoxy (-OCH -2 CF), trifluoromethyl (-CF) has strong electron absorption, which will reduce the electron cloud density of the oxygen atoms connected to it, thereby affecting the molecular polarity and electron distribution. And trifluoromethyl increases the molecular volume and mass, coupled with its special electronic effects, it has a significant impact on the boiling point and density of compounds. Generally speaking, compounds containing trifluoromethyl have a relatively high boiling point and may also increase their density.
    Overall, 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine has complex physical properties because it contains a variety of different groups. It may be a solid or a high-boiling liquid, because the hydroxyl group can form a hydrogen bond with water and has a certain water solubility, and because of the existence of trifluoromethyl and pyridine rings, it also has a certain solubility in organic solvents. Its melting point and boiling point are affected by the combined action of intermolecular hydrogen bonds and van der Waals forces, or are in a relatively high range. Density may be higher due to the heavier trifluoromethyl. In addition, the compound may have certain volatility, but due to strong intermolecular forces, volatility or limited.
    What is the market outlook for 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine?
    2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine is an organic compound. Looking at its market prospects, it can be analyzed from various angles.
    From the field of medicine, fluoropyridine compounds often have unique biological activities and are very popular in drug development. This compound contains functional groups such as trifluoroethoxy and hydroxymethyl groups, or can be modified into lead compounds with specific pharmacological activities for the development of new drugs, such as antibacterial, antiviral or anti-tumor drugs. Therefore, if the exploration of compounds containing such structures in the field of pharmaceutical research and development continues, there may be considerable demand in the pharmaceutical raw material market.
    In the field of pesticides, fluorinated organic compounds are widely used in the creation of insecticides, fungicides and herbicides due to their excellent biological activity and good environmental compatibility. The structure of this compound may endow it with biological activities such as insecticides and bactericides. If further research and development are carried out, it is expected to become a new type of pesticide active ingredient and occupy a place in the pesticide market.
    From the perspective of chemical intermediates, as a key intermediate, it can be chemically converted to derive a variety of functional materials and fine chemicals. With the growth of demand for new functional materials in the chemical industry, if efficient synthesis routes can be developed to ensure stable supply, there will also be opportunities for development in the chemical intermediate market.
    However, its market expansion also faces challenges. The synthesis of this compound may require complex processes and specific reagents, and the production cost may be high, limiting its large-scale application. And the market competition is fierce, and continuous research and development and innovation are required to improve product quality and performance in order to stand out in the market.
    Despite the challenges, in view of the potential needs in the fields of medicine, pesticides and chemicals, if the technical and cost problems can be overcome, 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine should have broad market prospects.
    What are the storage conditions for 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine?
    2-Hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine is one of the organic chemicals. Its storage conditions are the most critical, related to the stability and quality of this substance.
    According to the concept of "Tiangong Kaiwu", everything needs to be suitable for its storage. This compound should be stored in a cool, dry and well-ventilated place. A cool place can avoid high temperature causing it to decompose or initiate chemical reactions. High temperature can promote molecular activity, cause structural changes, and damage its inherent properties. A dry place can prevent moisture erosion. Because moisture can cause reactions such as hydrolysis, the compound can deteriorate. Just like wood is perishable in case of moisture, this compound is also easily damaged in case of moisture.
    In addition, it must be kept away from fire, heat sources and oxidants. Fire and heat sources can cause combustion or explosion because of their flammability and certain chemical activity. Oxidants are prone to oxidation reactions with the like, changing the chemical structure and properties of compounds. And it should be stored separately, not mixed with other chemicals, to prevent interaction and unpredictable changes.
    Packaging should not be taken lightly. A well-sealed container must be used to keep it isolated from the outside world and prevent the intrusion of air, moisture, etc. If it is an ancient treasure, it must be firmly sealed to last for a long time. Therefore, according to the above storage conditions, 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine can be maintained in its proper properties and quality for subsequent scientific research and production.