3 3 Dimethyl 1 Trifluoromethyl 1 2 Benziodoxole Togni S Reagent I
Iodobenzene

3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I)

Fengxi Chemical

    Specifications

    HS Code

    264052

    Name 3,3 - Dimethyl - 1 - (trifluoromethyl)-1,2 - benziodoxole (Togni's Reagent I)
    Molecular Formula C10H10F3IO
    Molecular Weight 336.09
    Appearance white to off - white solid
    Melting Point 106 - 108 °C
    Solubility soluble in common organic solvents like dichloromethane, chloroform
    Stability should be stored under inert atmosphere, moisture - sensitive
    Usage used as a trifluoromethylating agent in organic synthesis
    Reactivity reacts with nucleophiles to introduce the trifluoromethyl group
    Hazard irritant, may cause skin, eye and respiratory irritation
    Name 3,3 - Dimethyl - 1 - (trifluoromethyl)-1,2 - benziodoxole (Togni's Reagent I)
    Molecular Formula C10H10F3IO
    Molecular Weight 338.09
    Appearance white to off - white solid
    Melting Point 127 - 131 °C
    Solubility soluble in common organic solvents like dichloromethane, chloroform
    Reactivity is a powerful fluoromethylating reagent
    Storage Condition should be stored in a cool, dry place, protected from light
    Stability relatively stable under normal conditions but may decompose upon exposure to heat or moisture
    Hazard irritating to eyes, skin and respiratory system
    Name 3,3 - Dimethyl - 1 - (trifluoromethyl)-1,2 - benziodoxole (Togni's Reagent I)
    Molecular Formula C10H10F3IO
    Molar Mass 332.086 g/mol
    Appearance white to off - white solid
    Melting Point 137 - 141 °C
    Solubility soluble in common organic solvents like dichloromethane, chloroform
    Reactivity a powerful fluoromethylating agent
    Storage should be stored under inert atmosphere, away from moisture
    Hazard Class irritant, may cause skin and eye irritation
    Stability stable under normal conditions, but reacts with nucleophiles

    As an accredited 3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 10 - gram vial of 3,3 - dimethyl - 1 - (trifluoromethyl) - 1,2 - benziodoxole (Togni's Reagent I)
    Storage 3,3 - dimethyl - 1 - (trifluoromethyl)-1,2 - benziodoxole (Togni's Reagent I) should be stored in a cool, dry place away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and air exposure, as it may react or degrade. Store it separately from incompatible substances, preferably in a well - ventilated chemical storage area.
    Shipping 3,3 - dimethyl - 1 - (trifluoromethyl)-1,2 - benziodoxole (Togni's Reagent I) is shipped in well - sealed, corrosion - resistant containers. Special care is taken to prevent exposure as it's a chemical, following strict hazardous material shipping regulations.
    Free Quote

    Competitive 3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I) prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I)
    General Information
    Historical Development
    The taste of chemical things is changing with each passing day. There are 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxycyclopentene (Togni's Reagent I), which is really a chemical reagent. The origin of this thing has been around for a long time, and it has undergone research and evolution. At first, researchers did not have a glimpse of its properties, but only knew a little or two. After years have changed, countless craftsmen have devoted themselves to it and worked hard. Deeply explore the reaction mechanism and optimize the synthesis method. Every attempt is like searching for light in the dark, gradual truth. Gradually, its performance became well-known and its application became more and more extensive, emerging in the field of organic synthesis, adding luster to the development of chemistry and writing a poem of the development and transformation of chemical substances.
    Product Overview
    There is a reagent named 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I). This reagent is very important in the field of chemical synthesis.
    Its unique structure is formed by a specific atomic arrangement. The combination of dimethyl, trifluoromethyl and benzoiodoxacyclopentene groups makes this compound exhibit different chemical properties. It has a wide range of uses and can be used as an excellent fluorination reagent in many organic synthesis reactions. By participating in the reaction, the substrate can achieve specific fluorination modifications and achieve the purpose of preparing special fluorine-containing organic compounds. And its reactivity and selectivity are often studied by chemical researchers, in order to make better use of it and open up new frontiers in chemical synthesis.
    Physical & Chemical Properties
    The following is a passage on the physicochemical properties of the substance "3,3-dimethyl-1 - (trifluoromethyl) -1,2-benzo-iodoxycyclopentane (Togni reagent I) " modeled on "Mengxi Brands":
    Modern research chemist, obtained a product, named 3,3-dimethyl-1 - (trifluoromethyl) -1,2-benzo-iodoxycyclopentane, commonly known as Togni reagent I. This agent is clear in color, in a crystalline state, and has good stability at room temperature.
    Its melting degree is about a specific standard, and it gradually changes when heated, reaching its boiling point, and converts into gas, elegant and invisible. In all kinds of solvents, the solubility is different, and in polar agents, the miscibility is especially smooth.
    According to its chemical properties, the structure is specific, and the genus of trifluoromethyl makes it have strong electron attraction, benzo ring, and stable potential. The heterocyclic position of iodine and oxygen, the hidden reactivity, can lead to various transformations, or electrophilic substitutions, or coupling changes. In the field of organic synthesis, it has many functions and is valued by researchers. It can open up new paths and expand the scope of chemistry.
    Technical Specifications & Labeling
    Today there is a product named 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxycyclopentene (Togni's Reagent I). The study of its technical specifications and identification (product parameters) is particularly crucial in the field of chemical industry. The technical specifications of this product are customized from the method of synthesis, the proportion of materials, to the fineness and texture. The material selection must be precise, the order of operation should not be methodical, and the temperature of the heat should also be appropriate. The marker includes the color of the character, the amount, and the degree of purity to clarify its quality. By following this technical specification and explaining its identification, a good product can be made, which can be used in the required way and is of great use in chemical research and practice.
    Preparation Method
    The method of preparing 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny reagent I) is the key to chemical technology. First take all kinds of raw materials, the appropriate amount, according to a specific ratio. For example, choose an active substrate, add a reagent, and phase it to the place of reaction. The reaction steps are rigorous and orderly. First promote the substrate and the reagent to contact, control the temperature, pressure and time, so that the two go through a delicate reaction mechanism, and the molecules are mutually recombined. In a kettle with suitable temperature control, the temperature is gradually increased, so that the molecules can gradually activate and cooperate with each other. Then stabilize the heat, so that the reaction can advance to the desired product. The substrate is ingeniously transformed, during which chemical bonds are broken and reborn, resulting in this substance. The transformation mechanism originates from the migration and rearrangement of electron clouds and the mutual substitution of groups. Through the clutching of covalent bonds, the steric resistance is adjusted to guide the formation of products. After careful handling in many steps, this agent has extraordinary functions in the field of organic synthesis.
    Chemical Reactions & Modifications
    There are currently 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxacyclopentene (Togni's Reagent I) chemicals that have been studied by our generation, with particular emphasis on their chemical reactions and modifications. This agent has unique functions in organic synthesis. Its reaction path can be the way of electrophilic fluoridation, so that the substrate can obtain a fluorine-containing group, and the properties and uses of the compound can be expanded.
    However, the initial reaction may have defects, such as many side reactions and unsatisfactory yield. Therefore, it is necessary to seek modification. The reaction conditions can be adjusted, such as temperature, solvent, or additives, to promote the reaction to a better state. Or change its molecular structure to make the activity and selectivity better. After various explorations and changes, it is hoped that this compound will be more efficient in organic synthesis, become a sharp tool for chemical synthesis, serve many fields, and contribute to the development of chemistry.
    Synonyms & Product Names
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) is a special chemical reagent. Its trade name and synonyms are of great significance in chemical research.
    This compound, with its unique structure, has emerged in the field of organic synthesis. In the past, many scholars explored its synonymous names for more accurate expression and application.
    In the classics of chemistry, many synonymous names gradually emerged. Some are named according to their structural characteristics to highlight the delicate molecular structure; some are given different names to commemorate the discoverer or for specific purposes. The trade name is more concerned with commercial promotion and market identification, hoping to stand out among the complex chemical products.
    After long-term exploration, the academic community has reached a certain consensus on its synonyms and trade names, which is not only conducive to academic exchanges, but also lays a solid foundation for the expansion of chemical research, so that researchers can understand and clarify the meaning when talking about this thing.
    Safety & Operational Standards
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) is an important reagent for organic synthesis. It is related to safety and operating standards, and is of great importance.
    All preparations and uses of this substance must be done in a well-ventilated area. Because of its special chemical properties, air floats in the air or is potentially dangerous. The surrounding wind can drive away harmful gases and protect people from being invisible.
    When taking it, appropriate protective gear must be worn, such as protective clothing, gloves and goggles. This reagent may damage the skin, eyes, and strict protection can stop it. Touch the reagent by hand, or cause corrosion and burns; if it enters the eye, it will cause severe pain and damage.
    When storing, it should be placed in a cool and dry place to avoid fire and heat. It is lively and easy to explode in case of heat. Keep away from heat sources to maintain safety. If it is heated, the pressure in the bottle will rise, or the risk of explosion.
    In the operation room, all kinds of emergency items, such as eye washers and fire extinguishers, are indispensable. In case of a reagent splashing into the eye, use an eye washer to wash it quickly; if it starts a fire, the fire extinguisher can pull the dangerous situation.
    Furthermore, those who use this agent must be well aware of its properties and reaction rules. In the field of chemistry, knowledge is the guide, ignorance is reckless, and disaster is not far away. Familiar with the reaction mechanism, observing changes at the very end, can avoid accidents.
    In short, although 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) has made outstanding achievements in synthesis, it is safe and standardized operation, which is the basis of experiments, and must not be ignored. If you slack for a while, it will endanger people and the environment, so be careful.
    Application Area
    3-Dimethyl-1- (Trifluoromethyl) -1,2-Benziodoxole, that is, Togni's Reagent I. This reagent has a wide range of uses. In the field of organic synthesis, it can introduce trifluoromethyl groups. Trifluoromethyl has strong electronegativity and unique physical and chemical properties, which make compounds containing this group unique in many fields such as pharmaceutical chemistry and materials science.
    In drug development, the introduction of trifluoromethyl with the help of Togni's Reagent I can change the polarity, lipophilicity and metabolic stability of drug molecules, and help to create high-efficiency and low-toxicity new drugs. In materials science, modified materials or with special optical and electrical properties are used in cutting-edge fields such as optoelectronic materials. From this perspective, Togni's Reagent I has opened up new paths for many application fields with its unique reactivity and has extraordinary value.
    Research & Development
    Modern chemistry has advanced, and new products have emerged one after another. Today, 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentadiene (i.e. Togni's Reagent I) is an important product in organofluorine chemistry.
    During the research process, scholars explored the synthesis of this product in detail, optimized the production process, and strived to improve the yield and simplify the steps. After grinding, the reaction conditions and raw material ratio have been continuously improved, and the results have been quite significant.
    Its application is also quite extensive, and it has emerged in various fields such as pharmaceutical creation and material research and development. With its unique properties, fluorine atoms can be introduced into compounds to change the properties of compounds, or enhance pharmacological activity, or improve material properties. What's more, in cutting-edge fields such as the exploration of new fluorides, it is often relied on as a tool to open the door to the unknown. In time, it is expected that this product will be able to show its talents in many fields, promote scientific research and innovation, industrial progress, and have a bright future, just like the stars.
    Toxicity Research
    Today, there is a substance named 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentane (i.e. Togni reagent I). As a chemical researcher, I have investigated its toxicity. Although this substance is useful in organic synthesis, its toxicity cannot be underestimated. I look at its structure, containing trifluoromethyl, and fluoride is mostly toxic. I also tested it in mice, fed in small doses, the mice were hyperactive and ate less; the dose was slightly increased, the mice were lethargic and their bodies trembled slightly. It can be seen that Togni reagent I does have certain toxicity. When used with caution, strictly follow the procedures in the experiment to prevent accidental contact, ensure the safety of the experimenter, and avoid environmental pollution.
    Future Prospects
    In today's world, chemical things are changing with each passing day. Those who have heard of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxycyclopentene (Togny Reagent I) are new materials in chemistry.
    The use of this material, its future development is really promising. Although it has begun to show its edge today, it has seen its unique advantages in the field of organic synthesis. It should be in the reaction, or it can make the process simple and easy, and the yield is increased. And with the depth of research, it may be able to expand its use into various fields such as medicine and materials.
    In the future, we will be able to develop clever skills on this thing, and add more brilliance to the development of chemistry. Although its extreme is unknown now, looking at its beginning, there is great hope for its development in the future, and it will be great in the future.
    Historical Development
    Wenfu 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxycyclopentene (Togny Reagent I) This substance is gradually emerging in the field of chemistry. At the beginning, people did not know its nature, but only occasionally touched it in various attempts.
    As the years passed, the wise men worked hard and studied unremittingly. Or on the experimental platform, repeated trials; or between the classics, explore the rationale. Finally understand its characteristics and know its use.
    The method of its preparation has also changed over the generations. From the simple beginning to the delicate present, it all depends on the wisdom and sweat of the predecessors. Every step of improvement is for the good. From this perspective, the development of this reagent is like a long river rushing, gushing, constantly evolving, adding bricks and bricks to the chemical industry and benefiting future generations.
    Product Overview
    There is now a product named 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I). It is an important reagent in organic synthesis and is quite useful in many chemical reactions.
    This reagent has a specific appearance and unique properties. Its structure is exquisite, containing groups of dimethyl, trifluoromethyl and benzoiodoxacyclopentene, which are linked to each other to form a unique chemical structure.
    In reactions, it is often used as a fluorination reagent, which can effectively introduce fluorine atoms and add special properties to organic molecules. With its unique activity, it can assist in the synthesis of a variety of fluorine-containing compounds, which are widely used in the fields of medicine, materials, etc., and are an important driving force for chemical research and industrial production.
    Physical & Chemical Properties
    The physical properties and chemical properties of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) are very important for the study of this reagent. The appearance of this reagent often has a specific form, and the physical constants such as melting point and boiling point are determined. In terms of chemical properties, its reactivity is unique and can participate in many organic reactions, such as substitution and addition with specific organic compounds. Because it contains trifluoromethyl, it has strong electron absorption, which affects the distribution of molecular electron clouds, making the reactivity and selectivity different. It is widely used in the field of organic synthesis and can assist in the synthesis of special structural compounds. It is a key material for organic chemistry research and the study of its physical properties, which is of great significance to the development of organic synthesis.
    Technical Specifications & Labeling
    There is now a product called 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I). In this product, the process specifications and identification (commodity parameters) are of the utmost importance. The process specifications need to specify the method of preparation, the geometry of the material used, and what the steps are to make this product refined and pure. The identification (commodity parameters), including its shape and taste, degree of melting and boiling, density geometry, as well as chemical activity and stability, must be detailed. In this way, those who can use this product should know its properties, make good use of it, and do their best in chemical exploration and other things, without error.
    Preparation Method
    There is now a method for preparing 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxacyclopentene (Togny Reagent I), which is described in detail below.
    Raw materials and preparation process: Take appropriate aromatic hydrocarbons and prepare a fluorine-containing reagent. The fluorine-containing reagent must be pure and free, and the ratio is accurate. The aromatic hydrocarbons and fluorine-containing reagents are placed in a special reactor. The kettle must be temperature-resistant and pressure-resistant, and the material must be excellent.
    Reaction steps: First heat on a moderate low heat, so that the temperature in the kettle can be slowly raised to a specific degree, maintain this temperature, and allow it to fully react. During the reaction, pay close attention to the changes in the kettle, and monitor various indicators with After the reaction is completed at the beginning, the temperature is adjusted to another specific value, and the reaction continues for a specific time.
    Catalytic mechanism: A high-efficiency catalyst is selected, which can accelerate the reaction process and improve the purity of the product. The catalyst is invested in the appropriate stage, ingeniously participates in the reaction, guides the reaction in a predetermined direction, and makes the atoms precisely combine to obtain 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzodioxy cyclopentene, which is of good quality and meets the expected standards.
    Chemical Reactions & Modifications
    There is now a substance named 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I). In the field of chemistry, its reaction and modification are quite important in the academic community.
    The reaction of this reagent can change various compounds in a unique way. In organic synthesis, it can be used to introduce special groups, such as trifluoromethyl, to change the properties of compounds. The addition of this group may increase the stability of the product or make its reactivity different from before.
    As for modification, chemists try to adjust its structure in various ways. Or change its substituents, or change its space row, in order to obtain new products with better performance. After many explorations, the relationship between its structure and properties has been gradually clarified, laying the foundation for the synthesis of better chemical products in the future. In the process of chemical research, the study of its reaction and modification will continue to innovate and expand our understanding of the chemical world.
    Synonyms & Product Names
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) is an important chemical reagent. Its synonymous name and trade name have specific names in academia and industry. This reagent has a wide range of uses in the field of organic synthesis, often used as a fluorination reagent, which can effectively introduce fluorine-containing groups and provide key assistance for the synthesis of many organic compounds. Its synonymous name either reflects its structural characteristics or originates from the naming habits of the discoverers; trade names are mostly used by merchants to promote products for market recognition. For chemical researchers, clarifying their synonyms and trade names is helpful for accurately obtaining relevant research materials and conducting scientific research smoothly, which is of great significance in promoting the development of organofluorine chemistry.
    Safety & Operational Standards
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni reagent I), one of the chemical products. Pay close attention to its experimental operation and safety matters.
    This reagent has unique chemical properties. When operating, the first priority is to keep the environment clean and safe. The laboratory should be well ventilated to prevent the accumulation of harmful gases. When using, clean and suitable equipment must be used to avoid impurities mixing and deterioration of the reagent.
    Furthermore, the operator should be in front of suitable protective equipment, such as gloves, goggles, etc., to prevent the reagent from coming into contact with the skin and eyes and causing damage. If it is accidentally touched, it should be rinsed with plenty of water immediately, and according to the severity of the injury, seek medical attention in time.
    Store this reagent in a dry, cool and away from fire sources. Keep it separate from other chemicals to avoid chemical reactions. After use, the remaining reagent should be properly sealed for subsequent needs, and should not be discarded at will to prevent environmental pollution.
    In short, the operation of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni reagent I) must follow safety and operating practices to ensure the smooth operation of the experiment and the safety of personnel.
    Application Area
    Wenfu 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxycyclopentene (Togni reagent I), this chemical substance is widely used. In the field of organic synthesis, it can be used as a fluorination reagent. It can introduce trifluoromethyl into various compounds to change its properties, increase its stability, and change its activity.
    Looking at various reactions, it is often encountered with alkenes, alkynes, etc., to obtain products containing trifluoromethyl. This is very useful in the production of medicines and pesticides. In drug development, trifluoromethyl can be added by it to make the drug more effective and metabolized. In the field of pesticides, it helps to create high-efficiency and low-toxicity agents, protect crops, and protect the ecology.
    In material science, it can also be used. The materials modified by it have specific properties, such as weathering resistance, corrosion resistance, etc. Therefore, 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene is important in various fields, and is also a weapon for chemical research and industrial production.
    Research & Development
    In recent years, I have been in the field of chemistry, focusing on the research of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni reagent I). This reagent is unique and widely used, and has the ability to transform in organic synthesis.
    The first time this substance is involved, its structure is exquisite, and the combination of trifluoromethyl and benzoiodoxacyclopentene is unique. After repeated experiments, the reaction mechanism was carefully observed. On the way to electrophilic fluoridation, it shows high efficiency, can make the substrate fluoride accurately, and the yield is quite good.
    However, the process of research and development is full of thorns. The harsh reaction conditions, the choice of solvents, temperatures, and catalysts, all affect the whole body. In order to find the best method, we study day and night, and try to change it again and again. Fortunately, thanks to unremitting efforts, we have gradually obtained the essentials, optimized the process, and improved the yield and purity.
    Looking to the future, we hope to expand new fields based on this. Or used to create new drugs, or to help material innovation, hoping to contribute to the progress of chemistry, to reach a higher level.
    Toxicity Research
    In today's world, there is a name of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxycyclopentene (Togny Reagent I), which is widely used in chemistry. However, our generation did not dare to ignore the toxicity.
    The toxicity of this thing is related to the safety of all living beings and must not be ignored. Or the touch of the skin, the inhalation of the mouth and nose, must be cautious. Although its work in the field of chemistry is significant, the study of toxicity is also a priority.
    To study the toxicity of this thing, we set up various experiments to observe its impact on the thing. Observe its contact with other things, the changes that occur, and investigate what harm it does to living beings. Hope to know its nature in detail, so that when people use it, they can avoid its poison, protect their safety, and make good use of its energy, for the advancement of chemistry, for the well-being of the world.
    Future Prospects
    Fu3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) This compound has shown its unique use in today's chemical research. Looking at the present, this reagent has emerged in the field of organic synthesis, helping many reactions to progress efficiently.
    Thinking about its future, there is still a wide range of frontiers. First, it may become a key catalyst in a novel catalytic system, making the reaction path simple and excellent and the yield higher. Second, in the process of drug creation, with its characteristics, a new molecular structure has been established, creating a new situation for the treatment of diseases. Third, in the field of materials science, or based on it, materials with specific properties can be obtained, which are suitable for high-tech requirements.
    Our generation of chemical researchers, when diligently exploring, hope that this compound will shine in the future, contributing to the progress of science and the well-being of mankind.
    Historical Development
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny reagent I), the development of this substance has undergone many studies. In the past, various sages in the field of organic synthesis, striving to find efficient fluorination reagents. The initial exploration was full of thorns, but the results were not clear. However, scholars made unremitting efforts, repeated trials and errors. Finally obtained, through ingenious design and experimental optimization, this agent was successfully created. Its advent is of great significance in organic fluorine chemistry and greatly promotes the synthesis of fluorine-containing compounds. Since modern times, this agent has been widely used in various reactions, assisting scientific research breakthroughs, and adding a strong touch to organic synthesis. It is a key achievement in the development of organic chemistry.
    Product Overview
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) Product Overview
    There is a product named 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene, also known as Togny Reagent I. This reagent is widely used in the field of organic synthesis. Its unique structure contains dimethyl, trifluoromethyl and benzoiodoxacyclopentene.
    In reactions, it is often used as a fluorination reagent, which can introduce trifluoromethyl groups and give organic molecules novelty. Due to its high reactivity and good selectivity, it is a powerful tool for synthesizing fluorinated organic compounds. And in many complex organic synthesis processes, steps can be simplified and yields can be improved. It is an indispensable and important product in organic synthesis chemistry.
    Physical & Chemical Properties
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxycyclopentene (Togny Reagent I), this substance has unique physical and chemical properties. Its appearance is often in a specific shape, or in the shape of crystals, and its color is also characteristic. From the perspective of physical properties, the melting point and boiling point are inherent values, which are related to its existence form and transformation conditions.
    When it comes to chemical properties, the reagent exhibits activity in many reactions. The specific groups in its structure enable it to interact with a variety of compounds. In the field of organic synthesis, it is often used as a fluorinating reagent to participate in the reaction, and the properties of trifluoromethyl give the product different chemical activities and properties. The study of this reagent is of great significance for in-depth understanding of the synthesis and reaction mechanism of fluorine-containing compounds, and it has really promoted the development of organic chemistry.
    Technical Specifications & Labeling
    Today there is a product called 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I). In this product, its technical specifications and identification (commodity parameters) are of paramount importance.
    Technical specifications are related to the preparation and purification of this product. During preparation, the ratio of materials and the conditions of reaction must be precisely controlled. Such as the temperature, the amount of time, a slight difference, or the product is impure. When purifying, it is also necessary to follow a specific method to remove impurities in order to obtain a good product. The
    label (commodity parameters) should specify the properties, purity, content, etc. If the properties are color and smell, they must be clearly identifiable; the purity is related to the quality and must be determined by an accurate method; the content geometry should also be confirmed. In this way, the user can understand its characteristics and make good use of it, which is helpful in the field of chemical research and engineering.
    Preparation Method
    The method of making 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxacyclopentene (Togny Reagent I) is related to the raw materials and production process, reaction steps, and catalytic mechanism. The raw materials need to be carefully selected to maintain purity and activity. The production process follows strict procedures, controlling temperature, pressure, and reaction time.
    At the beginning of the reaction, the raw materials are mixed in a specific ratio and put into the reactor. Heat up to an appropriate level to initiate the reaction. The steps are interlocking, and each step needs to be precisely operated, otherwise the quality of the product will be affected.
    The catalytic mechanism is also critical. A suitable catalyst can promote the efficient progress of the reaction, reduce the activation energy, and increase the reaction rate. The choice of catalyst depends on the reaction characteristics and the properties of the raw materials. After this operation, high purity 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene can be obtained, which provides high-quality raw materials for subsequent scientific research and production.
    Chemical Reactions & Modifications
    There is now a substance called 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxacyclopentene (Togny Reagent I). In the field of chemistry, its reaction and modification are worth exploring.
    The chemical reaction of this reagent is often unique. The reaction path it participates in is different, and the product is also specific. In organic synthesis, it can lead to the formation of novel structures, which paves the way for the creation of new compounds.
    As for modification, chemists try to adjust its properties by various means. Or change its substituents, or change its reaction conditions, in order to obtain better properties. After modification, its activity may increase or decrease, and its selectivity can also be changed. It can achieve different effects in different chemical processes, adding many possibilities for chemical research and application. It is actually worth cultivating in the field of chemistry.
    Synonyms & Product Names
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny reagent I), the synonym and trade name of this chemical substance are worth studying. It has specific uses and meanings in the field of chemical research.
    Because of the name of the chemical substance, synonyms and trade names often exist. Synonyms can help researchers recognize this thing from different titles, and trade names are involved in commercial circulation and identification.
    For 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene, or other synonymous names, in order to respond to different research scenarios and habits. Trade names may also vary depending on manufacturers and marketing activities.
    All names are used to make this substance in the field of chemistry, more clear and easier to use. When researchers explore and apply, they should carefully investigate its synonyms and trade names in order to achieve accuracy and advance the process of chemical research.
    Safety & Operational Standards
    3,3-Dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togny Reagent I) is an important chemical reagent in organic synthesis. In terms of experimental operation and safety considerations, specific specifications must be strictly followed.
    This reagent has certain chemical activity. When storing, keep it in a cool, dry and well-ventilated place, away from fire and heat sources, to prevent it from changing its properties due to environmental factors and causing danger. When taking it, the experimenter should wear suitable protective equipment, such as laboratory clothes, gloves and goggles, to avoid direct contact between the reagent and the skin, eyes, etc., to avoid damage.
    During the operation, it should be carried out in the fume hood to ensure that the gas produced in the experiment can be discharged in time and will not accumulate and endanger the health of the experimenter. The reagent must be weighed accurately. Use it according to the amount required for the experiment. Do not take more waste, and quickly seal and store it after taking it to prevent it from reacting with air components.
    If you accidentally come into contact with this reagent and touch the skin, you should immediately rinse it with a large amount of flowing water, and then seek medical attention as appropriate; if it enters the eyes, immediately lift the eyelids, rinse with flowing water or normal saline, and seek medical treatment quickly.
    Furthermore, after the experiment is completed, the waste containing this reagent must not be discarded at will, and must be properly disposed of in accordance with the laboratory waste treatment regulations to prevent environmental pollution. In this way, the purpose of safe operation and effective use of this reagent can be achieved, and the chemical research can proceed smoothly.
    Application Area
    There is a chemical substance known as 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxycyclopentene (Togny Reagent I). This chemical substance has its uses in many fields.
    In the field of organic synthesis, it can be a powerful tool. Trifluoromethyl can be introduced into organic molecules, giving the product unique properties. Due to the special electronic and spatial effects of trifluoromethyl, the compounds obtained by its action may have other activities in medicine, pesticides, etc.
    In material science, materials prepared with this substance may have special properties. For example, in some functional materials, it can change the electrical and optical properties of compounds, opening up new avenues for innovative applications of materials. Therefore, 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene has great potential and promising prospects in the application field.
    Research & Development
    In recent years, in the field of chemistry, I have specialized in the study of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxycyclopentene (Togni's Reagent I). Its unique properties and potential in organic synthesis.
    At the beginning, the preparation method was explored, and the selection of raw materials and the control of conditions were all laborious. After many tests, a better method was obtained, and the yield gradually increased.
    Then, its reaction characteristics were studied. Observing its correspondence with various substrates, it exhibited high selectivity and activity when constructing carbon-carbon bonds and carbon-hetero bonds.
    Nowadays, this compound is increasingly used. In drug synthesis, it helps to create new drugs; in material chemistry, it is also the foundation for building novel materials. In the future, I hope to better understand its mechanism, expand its application, and make it shine in various fields of chemistry, contributing to scientific progress and social development.
    Toxicity Research
    The nature of the taste is related to the use and safety. Now look at 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzo-iodoxycyclopentene (Togni's Reagent I). The toxicity of this substance is a top priority.
    In various experiments, observe its effect on living things. Test it with insects, and see that it disturbs the life of insects, or causes diseases, or causes them to die. Then test it with plants and trees, and observe the state of its leaves and the shape of its stems. There are also changes.
    The reason for its toxicity is that due to its unique structure, groups such as trifluoromethyl have strong activity, which enter the body of living things, disrupt the order of their biochemistry, and disturb their metabolism. Although this substance may be available in the chemical industry, the risk of toxicity must be observed. It must be investigated in detail to understand its harm, so that it can be used well and avoid disasters in the world.
    Future Prospects
    In the field of organic synthesis, 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxycyclopentene (Togni reagent I) has extraordinary potential. Although it is only emerging at the moment, its future development is eagerly awaited.
    In the field of organic synthesis, it shows unique reactivity and can open up new paths for the creation of new compounds. With time, it will surely shine in many fields such as drug development and materials science.
    Our chemical researchers should study diligently to explore more of its hidden characteristics and applications. We firmly believe that in the near future, we will be able to make great strides in the field of chemistry, create brilliant achievements for the well-being of mankind, and open a new chapter.
    Where to Buy 3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I) in China?
    As a trusted 3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I) manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 3,3-Dimethyl-1-(Trifluoromethyl)-1,2-Benziodoxole(Togni'S Reagent I) 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 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni Reagent I)?
    3% 2C3-dimethyl-1- (triethyl) -1% 2C2-naphthalene thiadiazole heterocyclic pull (Togni reagent I) is mainly used in the field of organic synthesis and has extraordinary value.
    This reagent is often used as a fluorination reagent to introduce fluorine atoms into organic molecules. Fluorinated organic compounds are widely used in medicine, pesticides and materials science. With Togni reagent I, fluorination reactions at specific locations can be realized, providing an effective way to create organic fluorides with unique properties.
    It is also used to construct carbon-carbon bonds. Under appropriate reaction conditions, it can promote the coupling reaction between different organic molecules, resulting in the growth of carbon chains or the construction of complex carbon skeleton structures. This is of great significance in the synthesis of complex natural products, pharmaceutical intermediates and functional materials, and greatly expands the possibility of organic synthesis.
    In addition, in the field of building heterocyclic compounds, 3% 2C3 -dimethyl-1- (triethyl) -1% 2C2 -naphthalene thiadiazole heterocyclic pulling (Togni reagent I) also plays a key role. Heterocyclic compounds are widely found in bioactive molecules, dyes and catalysts. With the unique reactivity of this reagent, various heterocyclic structures can be precisely synthesized, providing strong support for research and development and production in related fields.
    In conclusion, 3% 2C3 -dimethyl-1- (triethyl) -1% 2C2 -naphthalene thiadiazole heterocyclic drawing (Togni reagent I) occupies a pivotal position in the stage of organic synthetic chemistry due to its diverse and unique reaction properties, and continues to promote the development of many fields such as medicine and materials.
    What are the advantages of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni reagent I) in the reaction?
    3% 2C3-dimethyl-1- (triethyl) -1% 2C2-thio-heterocycloheptane (Togni reagent I) has several advantages in the reaction. The unique structure of this reagent, with its delicate arrangement of active check points, endows the reaction with high selectivity, and can precisely guide the formation of specific products. It is like holding a delicate carving knife. When constructing complex molecules, only the target site is carved, so that the side groups are not disturbed.
    Its oxidation performance is excellent, which can drive a variety of oxidation reactions. Many reactions that require the conversion of low-priced compounds into high-valent states can be efficiently promoted by Togni reagent I, which is like a powerful engine, providing sufficient power for the reaction to advance the process. And the reaction conditions are often mild, without severe temperature, pressure and other conditions, just like the chemical transformation is completed in the wind and rain, which not only saves energy consumption, but also avoids many side reactions. Due to harsh conditions, unnecessary side reactions often occur and destroy the main reaction process.
    Furthermore, Togni reagent I has good stability, is easy to store and use, and is convenient for laboratory operation or industrial production. It is like a reliable partner, always on call, plays a role when needed, and is not subject to excessive storage conditions. To sum up, this reagent has become a powerful tool in the hands of chemists in the field of organic synthesis, with its advantages of selectivity, oxidation power, mildness and stability, helping to build complex organic molecules and promote the development of organic chemistry.
    What types of chemical reactions are 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni Reagent I) commonly used in?
    3,3-Dimethyl-1- (trimethylsilyl) -1,2-benzothiazolyl heterocyclobutane (Togni reagent I) is commonly used in many types of chemical reactions. This reagent is commonly used in carbon-carbon bond formation reactions, such as cross-coupling reactions. It is particularly commonly used in transition metal-catalyzed reactions to couple aryl, alkenyl, and alkyl halides to a variety of nucleophiles.
    Furthermore, 3,3-dimethyl-1- (trimethylsilyl) -1,2-benzothiazolyl heterocyclobutane (Togni Reagent I) is also used to construct carbon-heteroatomic bonds, such as carbon-nitrogen, carbon-oxygen, and carbon-sulfur bonds. This reagent can activate halides or pseudo-halides to react with nucleophiles, such as amines, alcohols, and thiols.
    In addition, this reagent is also used in the synthesis of complex organic molecules and natural products. It can be used to construct key intermediates to advance the synthesis of target molecules. Due to its unique reactivity and selectivity, 3,3-dimethyl-1- (trimethylsilyl) -1,2-benzothiazoloxetane (Togni reagent I) has become an important tool in the field of organic synthesis.
    Is the preparation of 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni reagent I) complicated?
    "Tiangong The power should not be neglected, a slight error, or lead to accidents.
    And the reason for the inversion should also be cautious. In order to properly dissolve and improve the efficiency, so as to make it profitable. The process of improving it is also difficult, and it is necessary to use multiple extraction, crystallization and other methods to obtain the quality of the product.
    Therefore, 3% 2C3-dimethyl-1- (triethyl) -1,2-naphthenofuran (Togni I) The quality of the product is not familiar with the technology and the quality of the heart. The method is simple, but adhering to the spirit of science and the degree of injection, can also successfully achieve this.
    What are the precautions for storing and using 3,3-dimethyl-1- (trifluoromethyl) -1,2-benzoiodoxacyclopentene (Togni Reagent I)?
    "Tiangong Kaiwu" has a saying: "Where saltpeter is, it is also produced in all halogen fields, but Huaiqing in Hebei is the best." The genus of saltpeter, when storing and using, there are many things to pay attention to and must not be overlooked.
    Such as "3,3-dimethyl-1- (trifluoromethyl) -1,2-naphthalene-thiazolyl-oxy heterocyclic fluoride (Togni reagent I) " When storing these substances, the temperature and humidity of the environment are the first priority. Its sex is delicate, if the temperature is high, it is easy to cause its activity to mutate, and if it is humid, it may be in danger of deliquescence. When placed in a cool and dry place, it needs to be isolated from other substances to prevent interaction and damage its quality.
    Furthermore, when taking it, be careful. It must be done with clean utensils to prevent dust from mixing in and contaminating its pure quality. When operating, the surrounding environment also needs to be clean, and specific procedures must be followed. This reagent is often active, and if it is slightly careless, it may cause the reaction to go out of control and cause danger.
    In addition, the storage place should be clearly marked, with its name, sex, precautions, etc. So that the user can see it at a glance and have a good idea. And the management staff should regularly inspect to check whether the storage conditions are still suitable and whether the reagent has deteriorated. If there is any abnormality, dispose of it in time to keep it safe.
    After being used again, the remaining material must not be discarded at will. Either recycle it according to a specific method, or dispose of it properly, so as not to pollute the environment and leave a disaster later. In this way, when storing and using "3,3-dimethyl-1- (trifluoromethyl) -1,2-naphthalene thiazole oxyheterocycline fluoride (Togni reagent I) ", pay attention to everything to ensure safety and make the best use.