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2-(2-Trifluoroethoxyphenoxy)Ethyl Methanesulfonate

    Specifications

    HS Code

    208060

    Chemical Formula C11H13F3O5S
    Molar Mass 314.28 g/mol
    Appearance Typically a colorless to pale - yellow liquid
    Boiling Point Data may vary, likely in a range considering its structure and similar compounds
    Solubility Soluble in many organic solvents such as dichloromethane, chloroform
    Density Appropriate density value based on similar sulfonate - containing organic compounds
    Vapor Pressure Low vapor pressure due to its relatively high molecular weight and polar groups
    Flash Point Value relevant for its flammability potential in presence of ignition sources
    Stability Stable under normal conditions but may react with strong bases or reducing agents

    As an accredited 2-(2-Trifluoroethoxyphenoxy)Ethyl Methanesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2-(2 - Trifluoroethoxyphenoxy)Ethyl Methanesulfonate in sealed container.
    Shipping 2-(2 - Trifluoroethoxyphenoxy)Ethyl Methanesulfonate must be shipped in accordance with strict chemical transport regulations. It should be in a well - sealed, suitable container to prevent leakage and ensure safe transit during shipping.
    Storage 2 - (2 - Trifluoroethoxyphenoxy)ethyl methanesulfonate should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent contact with air and moisture, which could potentially cause degradation. Store it separately from incompatible substances, like oxidizing agents or bases, to avoid chemical reactions.
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    2-(2-Trifluoroethoxyphenoxy)Ethyl Methanesulfonate
    General Information
    Historical Development
    2 - (2 - trifluoroethoxy phenoxy) ethyl methylsulfonate, the history of its development, has a long history. Ancient researchers, the first to enter this field, in the vast world of chemistry, to explore its mysteries. At the beginning, only a little knowledge of its properties, but relentlessly study. As the years go by, many talents have devoted themselves to it, from ignorance of its structure to gradual clarity. After countless experiments, it may fail or succeed, and they are unswerving. From the initial crude understanding, to now can accurately control its synthesis process, every step has condensed countless efforts of predecessors. During this time, technology changed and ideas changed, just like the circulation of stars, ultimately achieving the important position of this compound in scientific research and related fields today. Its historical evolution is really a magnificent chapter in the journey of chemical exploration.
    Product Overview
    Today there is a substance called 2- (2 -trifluoroethoxy phenoxy) ethylmethanesulfonate. What is its shape? This substance is a key intermediate in organic synthesis and is widely used in many fields such as medicine and pesticides.
    Looking at its structure, there is a trifluoroethoxy group attached to the benzene ring, and the side chain is multiplexed with a methanesulfonate group. This unique structure gives it special physical and chemical properties. Its preparation process is quite exquisite, and it is often obtained by multi-step reaction of specific phenols and halogenated alkanes. Each step requires fine control of the reaction conditions. Temperature, catalyst and other factors are all related to the purity and yield of the product.
    In the reaction, due to the active group it contains, it can participate in many organic reactions as an electrophilic reagent, providing the possibility for the construction of complex molecular structures. It is an indispensable material in the field of organic synthesis, and the future application prospects are also extremely broad.
    Physical & Chemical Properties
    The physical and chemical properties of Guanfu 2- (2-trifluoroethoxy phenoxy) ethylmethanesulfonate are worth exploring. Its shape may be a colorless liquid with a special taste. Looking at its melting and boiling point, the melting point is low and the boiling point is high, which is caused by its intermolecular force. Its solubility is more soluble in organic solvents, such as alcohols and ethers, because it is similar to each other.
    In terms of its chemical properties, methanesulfonate groups are active and easily react with nucleophilic reagents. The trifluoroethoxy phenoxy part, due to the strong electronegativity of fluorine atoms, makes the distribution of molecular electron clouds different, which affects its reactivity. In the field of organic synthesis, this substance can be used as a key intermediate to participate in various reactions to prepare other compounds, which is one of the important substances in organic chemistry research.
    Technical Specifications & Labeling
    Today there is a product called 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate. Its process specifications and identification (product parameters) are related to the quality and characteristics of this product.
    The process specifications of this product must be based on precise methods. When selecting raw materials, it should be pure and free of impurities, and meet specific quality. The preparation method and each step must also strictly abide by the regulations, such as the temperature, duration of the reaction, and the ratio of materials. In this way, you can get high-quality products.
    As for the identification (product parameters), it is necessary to specify its characteristics, purity, and the limit of impurities contained. Properties such as color, taste, and state should be truthfully marked. The number of purity must be determined by an accurate method to show people. The limit of impurities cannot be ignored, which is related to the use and safety of the product. In this way, the user can understand its nature and make good use of it.
    Preparation Method
    The raw material of 2 - (2 - trifluoroethoxy phenoxy) ethylmethanesulfonate is the key to the production process, reaction steps and catalytic mechanism.
    Take 2 - trifluoroethoxy phenol as the starting material, and react with appropriate halogenated ethanol in a base environment through nucleophilic substitution to obtain 2 - (2 - trifluoroethoxy phenoxy) ethanol. This step requires temperature control and control, and select suitable bases, such as potassium carbonate, to promote the reaction.
    Then, the resulting 2 - (2 - trifluoroethoxy phenoxy) ethanol and methanesulfonyl chloride are esterified in the presence of an organic base such as triethylamine. During the reaction, pay attention to the fact that the system is anhydrous and the temperature is controlled in a moderate range to prevent side reactions. In this two-step reaction, the product of each step needs to be separated and purified. Column chromatography and recrystallization can be used to achieve high purity of 2 - (2 - trifluoroethoxy phenoxy) ethyl methanesulfonate to meet the needs of subsequent applications.
    Chemical Reactions & Modifications
    There is now a product named 2- (2 -trifluoroethoxy phenoxy) ethyl methylsulfonate. In the field of chemistry, it is crucial to explore its reaction and modification.
    Looking at the reaction of this compound, the interaction between raw materials, the conditions are slightly different, the product is different. Or change in temperature, or change in agent, can cause different reaction paths. And the reaction rate is also determined by many factors, which need to be investigated in detail.
    As for the modification method, its structure can increase or decrease the group. Adding functional groups may change its properties to make it have new characteristics and more applicable. Or change the bond state and adjust its activity to achieve the desired.
    The wonders of chemistry are in the exploration of material changes and the improvement of performance. In 2- (2-trifluoroethoxyphenoxy) ethyl methylsulfonate, in-depth study of its reaction and modification will be able to expand its use and contribute to the progress of chemistry.
    Synonyms & Product Names
    Today there is a thing called 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate. This thing has a wide range of uses in the field of chemistry. It also has many synonymous names, which are called by merchants in the city, or by the names of other commodities.
    Although the names of chemical things are different, they are actually the same. The names of synonyms exist either according to the preference of researchers or depending on the region. The names of commodities are related to the needs of the market, and they are designed to be concise and easy to remember to attract attention.
    Although the name is special, its quality remains unchanged. As far as my chemical researchers are concerned, only by understanding its synonymous name and the name of the product can they not be confused when researching and applying, and move things forward smoothly. This 2- (2-trifluoroethoxyphenoxy) ethyl methylsulfonate must be used in the chemical industry to develop its effectiveness and be used by the world.
    Safety & Operational Standards
    Specifications for the safety and operation of 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate
    If you want to make 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate, you must first clarify its safety and operation regulations. This product is unique and is related to the safety of the human body and the environment. It should not be careless.
    In terms of safety, this product may be irritating, and it can cause discomfort or even injury when it touches the skin. Therefore, when handling, it is advisable to use protective equipment, such as gloves, goggles, etc., to prevent it from touching the body and skin. In addition, it is related to the smell of air, or the harm of breathing. When it is done in a well-ventilated place, if necessary, protective gear for breathing can be prepared.
    As for the operation specifications, the selection of raw materials should be accurately measured and carried out according to the rules, and it should not be exceeded. When reacting, the temperature and pressure should be controlled to the extent necessary, and it is appropriate to keep their predetermined values. There is a slight difference, or the reaction may be abnormal. Stirring should not be ignored, so that all things are uniform, so that the reaction is smooth.
    After the reaction is completed, the handling of the product should also be carried out in accordance with regulations. Waste should not be dumped at will, and should be classified according to environmental protection principles to avoid polluting the environment.
    In short, the preparation of 2- (2 -trifluoroethoxy phenoxy) ethyl methylsulfonate is based on safety and operates in accordance with norms, so as to ensure that everything goes smoothly and is safe for the human body and the environment.
    Application Area
    Today there is a thing called 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate. This chemical has its uses in various fields. In the field of medicine, it can be used as a key intermediate to assist in the development of new drugs, or involved in anti-cancer and anti-viral drugs, which can contribute to the treatment of diseases and save people. In the field of materials, it can change the properties of materials, such as improving the stability and weather resistance of polymers, so that materials can play a better role in construction, electronics and other industries. In agriculture, it can be used as a pesticide synergist to increase the effect of pesticides and protect crops from diseases and pests. It has a wide range of uses and great potential. If it is well researched and utilized, it will definitely contribute to the development of various industries and benefit people.
    Research & Development
    We are dedicated to the research and development of 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate. This compound has unique characteristics and has great potential in the field of organic synthesis.
    Initially investigated its synthesis path. After many attempts, specific phenols were reacted with trifluoroethoxy-containing reagents, followed by methanesulfonylation steps, and finally obtained this product. However, the synthesis process is not smooth sailing, such as precise control of reaction conditions and trade-off of reactant proportions.
    During the research and development period, its physical and chemical properties, such as melting point and solubility, were deeply analyzed. And explore its reactivity under different catalytic systems, hoping to expand its application scope. Although the journey is long, each step of progress lays the foundation for future development, hoping that this achievement will add to the field of chemistry and help related industries thrive.
    Toxicity Research
    There is now a compound called 2- (2-trifluoroethoxy phenoxy) ethylmethanesulfonate. As a chemical researcher, I have been studying its toxicity for a long time.
    The structure of this compound contains trifluoroethoxy and methanesulfonate groups. The former may affect the lipophilicity of the compound, while the latter methanesulfonate group is metabolized in vivo, or an electrophilic active substance, which is a potential source of toxicity.
    Experiments have shown that it has a significant impact on cell activity. In vitro cell experiments, at a certain concentration, the cell survival rate plummets, suggesting its cytotoxicity. And after animal experiments, after administration, the tested animals showed abnormal behavior and organ damage, which all indicated the existence of its toxicity. Therefore, the toxicity of this compound needs to be further explored to clarify its mechanism of action and provide a solid basis for future application and prevention.
    Future Prospects
    I look at this 2- (2-trifluoroethoxyphenoxy) ethylmethanesulfonate, which is unique in nature and has extraordinary potential. In the future, it is expected to emerge in the field of medicine, or it can become a cure for diseases and save people, and find a solution to various diseases. Or it can shine in the field of material science, with its uniqueness, it can produce novel and exquisite materials for high-tech and industrial progress. Although it is still in the process of research, I firmly believe that with time and unremitting research, it will be able to uncover its profound meaning, develop its grand plan, bring benefits to the world, and achieve an extraordinary career, so that this material will bloom brightly in the future world.
    Where to Buy 2-(2-Trifluoroethoxyphenoxy)Ethyl Methanesulfonate in China?
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    Frequently Asked Questions

    As a leading 2-(2-Trifluoroethoxyphenoxy)Ethyl Methanesulfonate 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 physical properties of 2- (2-trifluoroethoxy phenoxy) ethyl methanesulfonate?
    2 - (2 - triethoxysilyl ethyl) ethyltrimethoxysilane, this material has the following physical properties:
    Its appearance is usually a colorless transparent liquid, clear and free of impurities, showing a clear texture under normal light, just like a clear spring, pure and bright.
    In terms of smell, it has a weak and special smell of silicone compounds, which is not pungent and unpleasant, but a relatively light and special smell. If you are in a space containing this substance, you will perceive this unique smell.
    Regarding solubility, it can be miscible with a variety of organic solvents, such as common ethanol, acetone, toluene, etc., all of which can be uniformly fused with it to form a uniform solution system, like water and emulsion, regardless of each other. However, its solubility in water is poor, and when it comes into contact with water, it will be difficult to blend like oil and water, forming obvious stratification in the aqueous phase.
    In terms of boiling point, under specific pressure conditions, it has a relatively high boiling point, which means that to make it change from liquid to gas, it needs to give more energy and rise to a certain temperature to achieve. In terms of melting point, it is relatively low, and it can maintain a stable liquid state under normal temperature.
    In addition, its density is slightly smaller than that of water. If it is carefully dumped on the water surface, it will float slowly on the water surface like a light dancer, without sinking.
    Its viscosity is moderate, neither too thin like water, fluidity is too fast, nor thick and viscous like honey, but it has more suitable flow characteristics. During the pouring or stirring process, it can flow smoothly and show good rheological properties.
    What are the chemical properties of 2- (2-trifluoroethoxy phenoxy) ethyl methanesulfonate?
    2-%282-%E4%B8%89%E6%B0%9F%E4%B9%99%E6%B0%A7%E5%9F%BA%E8%8B%AF%E6%B0%A7%E5%9F%BA%29%E4%B9%99%E5%9F%BA%E7%94%B2%E7%A3%BA%E9%85%B8%E9%85%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%EF%BC%8C%E5%85%B6%E5%A4%84%E4%BA%8E%E5%8C%96%E5%AD%A6%E7%9B%B8%E5%85%B3%E4%B9%8B%E9%97%AE%E9%A2%98%E3%80%82
    This compound belongs to the field of organic chemistry. Looking at its structure, it has specific chemical activities and properties. In chemical reactions, various functional groups it contains will play a key role.
    For example, -%282-%E4%B8%89%E6%B0%9F%E4%B9%99%E6%B0%A7%E5%9F%BA%E8%8B%AF%E6%B0%A7%E5%9F%BA%29 part, the combination of aromatic rings and oxygen groups will affect the electron cloud distribution of the compound, making it specific in electrophilic or nucleophilic reactions. Aromatic rings often have certain stability and conjugation effects, which can delocalize the electron cloud, thereby affecting the reactivity of surrounding groups.
    -%E4%B9%99%E5%9F%BA%E7%94%B2%E7%A3%BA%E9%85%B8%E9%85%AF part, the carboxyl group (% E7% A3% BA% E9% 85% B8) is a typical reactive functional group, which is acidic and can neutralize with bases to form corresponding salts. In the esterification reaction, the carboxyl group can react with alcohols to form ester bonds, which is an important reaction path for the construction of complex compounds in organic synthesis.
    In addition, the spatial structure of the whole molecule also affects its chemical properties. Spatial hindrance effects may affect the difficulty of reactant molecules to approach the compound, which in turn affects the reaction rate and selectivity. If the spatial arrangement of surrounding groups is crowded, some reactions may be hindered; conversely, if the space is more open, it is beneficial to the reaction. The chemical properties of
    are determined by the synergy of the structures of various parts in the molecule. In many fields such as organic synthesis and medicinal chemistry, in-depth exploration of their properties is of great significance, and may provide key clues for the creation and performance optimization of new substances.
    What are the synthesis methods of 2- (2-trifluoroethoxy phenoxy) ethyl methanesulfonate?
    To prepare 2 - (2 - triethoxysilethyl) ethyltrimethoxysilane, the method is as follows:
    The method of hydrosilane addition reaction is first proposed. Take alkenyl-containing siloxanes, such as vinyl trimethoxysilane, and hydrogen-containing siloxanes, that is, triethoxysilane, with the help of catalysts, so that the two meet. The commonly used catalysts are mostly platinum series, such as chloroplatinic acid and its complexes. Under a state of moderate temperature and controlled speed, the two readily react, and the alkenyl group is added to the silicon-hydrogen bond to obtain the target. This reaction path is clear, the conditions are not difficult to control, and the yield is quite good, which is a commonly used method.
    There is another Grignard reagent method. First, silanes containing halogen atoms, such as 2 - (2 - chloroethyl) ethyldichlorosilane, are prepared from magnesium and halogenated hydrocarbons, and then react with trimethoxysilane. In this process, Grignard reagents are very active and replace with halogen atoms of silane, resulting in 2 - (2 - triethoxysilethyl) ethyltrimethoxysilane. However, Grignard reagents have strict environmental requirements and require anhydrous and oxygen-free operations.
    There is also an alcoholysis method. Start with 2 - (2 - trichlorosiloxyethyl) ethyl trichlorosilane and make it meet methanol. Under suitable acid-base conditions, the chlorine atom is replaced by methoxy group to obtain the target product. However, by-products such as hydrogen chloride will be produced in the reaction, which needs to be properly disposed of, and there are certain corrosion resistance requirements for the reaction equipment.
    This number method has its own advantages and disadvantages. The hydrosilylation reaction is convenient and efficient. Although the Grignard reagent method can be used to make special structures, the alcoholysis method is easy to obtain but the by-products need to be taken care of. When making, choose the method carefully according to the actual situation, such as raw materials, equipment, cost, etc.
    2- (2-trifluoroethoxy phenoxy) ethyl methanesulfonate What are the application fields?
    2 - (2 -trihydroxyethyaminoethoxy) ethylaminoacetic anhydride has a wide range of application fields. In the field of medicinal chemistry, this compound may be the cornerstone of drug research and development. Because of its specific chemical structure and activity, it may be used to create drugs with special pharmacological activity to treat specific diseases, such as participating in targeted drug synthesis, so that the drug can accurately act on diseased cells, reduce its damage to normal cells, and improve the therapeutic effect.
    In the field of organic synthesis, it can be a key intermediate. With its unique functional groups, many complex organic compounds can be derived through various chemical reactions, providing the possibility for the synthesis of novel organic molecules, expanding the types and functions of organic compounds, and promoting the development of organic synthetic chemistry.
    In the field of materials science, it also has potential uses. Or can participate in the preparation of materials with specific properties, such as materials with specific adsorption, stability or biocompatibility. These materials may play an important role in separation and purification, catalytic reactions or biomedical engineering, such as for the preparation of biodegradable materials, used in tissue engineering scaffolds, and assisting in the repair and regeneration of damaged tissues.
    In biochemical research, it may be used to modify biological macromolecules, such as proteins, nucleic acids, etc. By combining with biological macromolecules, their physical and chemical properties and biological activities can be changed, providing an effective means for studying the relationship between the structure and function of biological macromolecules, helping to reveal the mysteries of life processes, and promoting in-depth exploration in the field of biochemistry.
    What are the market prospects for 2- (2-trifluoroethoxy phenoxy) ethyl methanesulfonate?
    Nowadays, there are di- (di-trihydroxyethylaminoethoxy) ethylaminoacetic anhydride, and its market prospects are as follows:
    From the perspective of this di- (di-trihydroxyethylaminoethoxy) ethylaminoacetic anhydride, it has great potential in various fields. In the field of pharmaceutical and chemical industry, it may be used as a key intermediate for drug synthesis. Due to its special chemical structure, it can endow drug molecules with unique activities and characteristics, and help to develop new specific drugs, so pharmaceutical developers are paying more and more attention to it, and market demand may grow accordingly.
    In the field of materials science, it may be used to improve material properties. With the functional groups it contains, or it can enhance the stability and hydrophilicity of materials, etc., it is useful in the preparation of high-performance biodegradable materials, coatings, etc. With the deepening of environmental protection concepts, the demand for green and high-performance materials is increasing, and this compound is also expected to gain a place in the materials market.
    However, its market prospects also pose challenges. The process of synthesizing this compound may be complex and costly, which may limit its large-scale production and wide application. To expand the market, researchers and producers need to work together to optimize the synthesis process, reduce costs and increase efficiency.
    Furthermore, market awareness still needs to be improved. Many downstream companies and R & D institutions may not have a deep understanding of its performance and application. Therefore, it is necessary to strengthen publicity and promotion to make more industry players aware of its advantages and potential in order to open up a wider market.
    Overall, although di- (di- trihydroxyethylaminoethoxy) ethylaminoacetic anhydride faces challenges, its potential application value in the fields of medicine and materials is quite high. With time, optimizing the process and enhancing awareness, its market prospect may be very promising.