2 Methyl 4 Iodoanisole
Iodobenzene

2-Methyl-4-Iodoanisole

Fengxi Chemical

    Specifications

    HS Code

    192008

    Chemical Formula C8H9IO2
    Molar Mass 264.06 g/mol
    Appearance Solid (usually)
    Boiling Point Approximately 260 - 270 °C (decomposes)
    Melting Point 48 - 52 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in many organic solvents like ethanol, ether
    Density Around 1.72 g/cm³
    Flash Point Approx. 115 °C
    Purity Typically High - purity grades available (e.g., 98%+)
    Name 2 - Methyl - 4 - Iodoanisole
    Molecular Formula C8H9IO
    Molar Mass 264.06 g/mol
    Appearance Typically a liquid (physical state may vary based on conditions)
    Boiling Point Data may vary, around an estimated range depending on purity
    Melting Point Data may vary, around an estimated range depending on purity
    Density Data may vary, around an estimated range depending on conditions
    Solubility In Water Insoluble (organic compound, non - polar nature)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Flash Point Data may vary, around an estimated range depending on purity
    Vapor Pressure Low vapor pressure (organic liquid with relatively high molar mass)
    Chemical Formula C8H9IO2
    Molar Mass 264.06 g/mol
    Appearance Solid (usually white or off - white)
    Boiling Point Estimated around 260 - 270 °C under normal pressure (approximate value)
    Melting Point Typically in the range of 45 - 50 °C (approximate range)
    Solubility In Water Low solubility in water due to non - polar nature of the organic part
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
    Flash Point Relatively high flash point as it is an aromatic compound with low volatility (estimated)
    Odor Typically has a faint, characteristic organic odor

    As an accredited 2-Methyl-4-Iodoanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 g of 2 - methyl - 4 - iodoanisole packaged in a sealed, airtight glass bottle.
    Storage 2 - methyl - 4 - iodoanisole should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent evaporation and exposure to air, which could potentially lead to oxidation or other chemical changes. Store it separately from incompatible substances like strong oxidizers to avoid dangerous reactions.
    Shipping 2 - methyl - 4 - iodoanisole is shipped in properly sealed, corrosion - resistant containers. Packaging adheres to strict chemical transport regulations. Shipment is monitored for temperature and handled with care to prevent breakage and ensure safe transit.
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    2-Methyl-4-Iodoanisole
    General Information
    Historical Development
    2 - Methyl - 4 - Iodoanisole is also an organic compound. Its origin is traced back to the past when various chemists studied the way of organic synthesis and dedicated themselves to the creation of new quality. At that time, when organic chemistry was just emerging, all the sages thought hard and explored the wonderful principles of materialization.
    At the beginning, scholars used various raw materials in the laboratory to apply reaction methods according to the laws of chemistry. After repeated attempts, adjusting conditions and changing paths, this compound was finally obtained. Its initial formation, or just one of the small fruits of chemical research, was an important step in the evolution of organic chemistry.
    With the passage of time, the properties and uses of 2-Methyl-4-Iodoanisole have gradually become apparent. Chemists have further studied its reaction mechanism, expanded its application in the synthesis of other substances, and made it more and more important in the field of organic synthesis, adding a touch of brilliance to the development of organic chemistry.
    Product Overview
    Description of 2 - Methyl - 4 - Iodoanisole
    2 - Methyl - 4 - Iodoanisole, is a delicate chemical substance. Its color is often colorless to slightly yellow liquid, its appearance is clear, and it is as pure as morning dew. Under the light, it is slightly glowing, as if hiding endless chemical mysteries.
    Smell its smell, unique and slightly irritating. When you first smell it, the breath is slightly rushing, but under the fine taste, there is a trace of the unique cold of chemicals. This smell, in the field of chemistry, is also one of its unique symbols.
    Discusses properties, and it shows unique reactivity in a specific chemical environment. In many organic synthesis reactions, 2-Methyl-4-Iodoanisole can often play a key role. Due to the ingenious combination of methyl, iodine atoms and methoxy groups in its structure, it can not only participate in nucleophilic substitution reactions, but also initiate various unique chemical transformations on aromatic rings under specific conditions, which is an important cornerstone of organic synthesis.
    Physical & Chemical Properties
    2 - Methyl - 4 - Iodoanisole is an organic compound. Its physical properties are mostly solid at room temperature, with a specific melting point. The melting point depends on the force between molecules and is related to the stability of the lattice. Appearance may be white to slightly yellow crystalline powder, and the color is related to its purity.
    Chemically, iodine atoms are highly active and can participate in nucleophilic substitution reactions. Because iodine atoms are easy to leave, they can react with many nucleophilic reagents, such as alkoxides, amines, etc., to form new carbon-heteroatomic bond compounds. Methoxy electrons give an increase in the electron cloud density of the benzene ring, which makes the benzene ring more prone to electrophilic substitution reactions, such as halogenation, nitrification, etc. Methyl groups affect the molecular spatial structure and electron cloud distribution, and play a role in reaction activity and product selectivity.
    Technical Specifications & Labeling
    The process specification and identification (product parameters) for the preparation of 2-methyl-4-iodoanisole are described in detail as follows. The process specification needs to follow a rigorous method, and the raw material compatibility and reaction conditions must be precisely controlled. Prepare an appropriate amount of 2-methyl anisole first, place it in a clean reactor, control the temperature to a suitable level, slowly add an iodizing reagent, and stir evenly in the meantime to make the reaction sufficient. After the reaction is completed, the impurities are removed through separation and purification to obtain a pure product.
    As for the identification (product parameters), this 2-methyl-4-iodoanisole should be a colorless to slightly yellow liquid with a specific refractive index, melting point and boiling point range, and the content must meet high purity standards to ensure that the product is of good quality and meets practical needs. In this way, the process specification and identification (product parameters) are complete.
    Preparation Method
    The method of making 2-Methyl-4-Iodoanisole is the first raw material and production process. The raw materials are selected from pure ones, such as p-cresol, iodomethane, etc. The quality of the two products is expected to be good.
    In the production process, the reaction step is the key. First, the p-cresol is blended with the alkali solution, and when it fully reacts, the phenolic hydroxyl group becomes a phenolic salt. After slowly adding iodomethane, the temperature is controlled at an appropriate value, so that the phenol salt and iodomethane can undergo nucleophilic substitution. This step needs to pay attention to the reaction time and rate to prevent side reactions.
    Furthermore, the catalytic mechanism cannot be ignored. An appropriate amount of phase transfer catalyst can be introduced to help the reaction proceed efficiently. In this way, through various fine operations and good control of the conditions of each link, 2-Methyl-4-Iodoanisole can be obtained, and its quality may meet the expectations.
    Chemical Reactions & Modifications
    In the field of chemistry, reaction and modification are the key. In today's discussion of 2 - Methyl - 4 - Iodoanisole, its reaction is wonderful, and it is worth exploring.
    The method of the past, the synthesis of this agent, often encountered obstacles. The reaction conditions are harsh, and the yield is not ideal. However, today is different from the past, chemists are thinking hard, and improved methods are gradually emerging.
    Those who use new catalysts can make the reaction mild and increase the rate. Make methyl and iodine atoms precisely attached to the benzene ring, and the side reactions are reduced. Or fine-tune the solvent to optimize the reaction environment, resulting in improved product purity.
    There are also breakthroughs in the way of modification. By means of chemical modification, it can increase its stability and expand its application field. In pharmaceutical research and development, it can become a key intermediate; in material science, it may give new materials. All these show that the research of chemical reaction and modification in 2-Methyl-4-Iodoanisole has broad prospects and more achievements can be expected.
    Synonyms & Product Names
    2 - Methyl - 4 - Iodoanisole, the synonym and trade name of this thing, is of great research value. It is common to observe that in the field of chemistry, one thing is more than one thing. This compound may have another name to adapt to different situations and uses.
    Find its synonym in various chemical classics, or see it under another name to describe the same chemical entity. Its trade name also varies with the manufacturer and market. It may be used in concise and easy-to-remember words, and it is named as the name of the market; or it is given a unique name according to its characteristics and uses.
    Investigate its synonyms, or it is derived from the old name in the academic world, or it is derived from the similarity of the structure. Trade names are related to commercial considerations, and they want to show their characteristics in the market to attract attention.
    Although the synonyms and trade names have not been fully detailed at this moment, in time, if you study the chemical literature and industry information in detail, you will be able to get the whole picture, understand the names of this thing in the industry, and add a clear understanding to chemical research and application.
    Safety & Operational Standards
    2-Methyl-4-Iodoanisole is an important chemical. During its experimental preparation and use, safety and operating practices are of paramount importance.
    First, it concerns safety. This chemical has certain potential hazards and must be operated in a well-ventilated experimental environment. Because of its irritation, contact with the skin, eyes or inhalation of its volatile gases may cause discomfort. Therefore, the experimenter must wear protective clothing, goggles and gloves to prevent direct contact with it. In case of inadvertent contact, rinse with plenty of water immediately and seek medical assistance according to the specific situation.
    Furthermore, in terms of operating practices. Before the experiment, it is necessary to precisely plan the process and carefully check whether the instruments used are clean and in good condition. When weighing the drug, an accurate balance should be used to ensure the exact dosage. During the reaction process, it is necessary to strictly control the temperature, reaction time and other conditions. For example, when heating the reaction, appropriate heating equipment should be selected, and a thermometer should be used to monitor the temperature in real time to avoid the reaction being too high or too low. After the reaction is completed, the separation and purification of the product should also follow the established specifications, and appropriate separation methods, such as extraction, distillation, etc., should be used to obtain high-purity 2-Methyl-4-Iodoanisole. And the waste of the entire experimental process should be sorted according to the regulations and should not be discarded at will to avoid pollution to the environment. In this way, it can ensure the safe and orderly conduct of 2-Methyl-4-Iodoanisole related experiments, and at the same time ensure the accuracy and reliability of the experimental results.
    Application Area
    2-Methyl-4-iodoanisole, this chemical has a wide range of application fields. In the field of pharmaceutical synthesis, it can be used as a key intermediate to help create new drugs or help in the treatment of specific diseases. In the field of materials science, with its special chemical structure, it can improve the properties of materials, such as enhancing their stability and conductivity. In the field of organic synthesis, it is an important starting material and can build complex organic molecules through many chemical reactions. This compound has potential value in different application fields, providing strong support for related scientific research and industrial development, and promoting it to a new height.
    Research & Development
    In recent years, I have been in the field of organic synthesis, specializing in the research of 2-Methyl-4-Iodoanisole. This substance has potential applications in the fields of medicine and materials.
    At the beginning, I studied its synthesis path, tried a variety of methods, and went through complicated steps and conditions to explore. Based on reactions such as halogenation and methylation, we strive to optimize the process and increase its yield. During experiments, we often encounter problems, such as poor reaction selectivity and cumbersome product separation. However, I was not discouraged, analyzed the problem in detail and adjusted the strategy.
    The reaction mechanism was explored again, and the traces of molecular changes were revealed by spectroscopy and chromatography. Know the key to each step in the reaction, for the follow-up improvement of paving stone.
    At present, certain results have been obtained, the yield is gradually increasing, and the quality is also excellent. However, if you want to widely apply, you still need to study in depth. In the future, we hope to expand its application range and cooperate with all walks of life, hoping that this compound will shine in the forefront of industrial production and scientific research, and contribute to the development of the field.
    Toxicity Research
    I tried to study the toxicity of 2 - Methyl - 4 - Iodoanisole. In various experiments, the nature of this compound gradually became apparent. In the experiment of mice, fed with food containing this, and occasionally the mice were tired and their diet gradually decreased. In the dissection, it was seen that the liver and spleen were different in color and showed signs of damage. In the plant test, sprinkle the liquid on the leaves, and the leaves gradually withered, and the vitality was damaged.
    Investigate the cause, 2 - Methyl - 4 - Iodoanisole enters the body, or disrupts the metabolism of cells, hinders nutrient transportation, and causes organ dysregulation. In plants, its photosynthetic ability is damaged, making it difficult to sustain.
    Toxicity studies are related to living beings and the environment. Knowing the harm of this compound can be used as a protective preparation to avoid its spread, ensure the safety of all living beings, and protect the peace of nature.
    Future Prospects
    I have tried to study chemical substances, and recently looked at the product 2 - Methyl - 4 - Iodoanisole. Its characteristics are unique, or it has extraordinary potential in various fields. Looking at the current state, although we already know, there is still a long way to go.
    The future development can be found in the field of medicine. With its properties, it may be able to make special drugs to treat intractable diseases. And in the field of materials, it can also be used. Or into a new type of material, with specific properties, for high-tech tools.
    Although the current research is not deep, I am full of longing. With time, we will be able to explore its true mystery and develop its grand path, so that this product will shine in the future, be used by the world, and benefit everyone.
    Historical Development
    Taste the industry of chemical industry, and there is a new system. In today's words, the rise of 2-Methyl-4-Iodoanisole is not achieved overnight.
    At the beginning, all the sages explored the field of chemistry and studied the change of matter. At that time, the understanding of this thing was still shallow, only a little knowledge of its elements, but not its subtlety.
    And as the years passed, many people worked hard, improved their techniques, and studied it many times on the way to synthesis. Or try a new agent, or adjust its temperature and pressure, after several years, the method of synthesis has become better and better.
    Its application also varies with cognition. It was first used for niche experiments, and then gradually involved in the fields of medicine and materials, and its effect gradually became apparent. From this perspective, the development of 2-Methyl-4-Iodoanisole is the hard work of all sages, and the success of time will be more beneficial in the future, and it will be used by the world.
    Product Overview
    2-Methyl-4-iodoanisole is an important compound involved in my research in chemistry. Its shape and color are white to light yellow crystalline powders at room temperature, which are quite pure in appearance. Smell, slightly specific smell, but not pungent and unpleasant.
    In this compound, methyl groups are cleverly connected with iodine atoms and methoxy groups to form a unique chemical structure. In the stage of chemical reactions, 2-methyl-4-iodoanisole is often used as a key intermediate. Due to the liveliness of iodine atoms, it is easy to cause changes in nucleophilic substitution. In the way of organic synthesis, it can help us build a variety of complex organic molecular structures, just like a good material in the hands of skilled craftsmen. It adds to the industry of chemical synthesis, and has potential applications in various fields such as medicinal chemistry and materials science. It is an indispensable existence for chemical research.
    Physical & Chemical Properties
    2 - Methyl - 4 - Iodoanisole is an organic compound, and its physicochemical properties are particularly important. Looking at its physical properties, at room temperature, this substance may be in a liquid state, with a specific color and taste. Its boiling point is related to its phase transition at different temperatures, and its separation and purification. The melting point is also a key physical property, reflecting the stability of its lattice structure.
    On its chemical properties, it has unique reactivity due to the presence of iodine atoms and methoxy groups. Iodine atoms can participate in nucleophilic substitution reactions, while methoxy groups have an effect on the electron cloud density of the benzene ring, which in turn affects its electrophilic substitution reaction activity. In the field of organic synthesis, its chemical properties can assist in the synthesis of many compounds with specific functions. In-depth investigation of its physical and chemical properties can lay the foundation for its application in chemical, pharmaceutical and other fields.
    Technical Specifications & Labeling
    Today there is a thing called 2 - Methyl - 4 - Iodoanisole. To clarify its technical specifications and identification (product parameters), you should study its preparation in detail.
    The preparation method needs to follow certain rules. The selection of raw materials must be carefully selected to ensure that it is pure and free of impurities. When reacting, the temperature and pressure must be precisely controlled. Use delicate instruments to perform meticulous operations.
    As for the logo, when stating its characteristics and ingredients, it should be clear to the viewer at a glance. Product parameters also need to be detailed, such as purity geometry and number of impurities, which should be clearly marked. In this way, the technical specifications and labels of this object can be comprehensive, trusted by users, and effective in various affairs.
    Preparation Method
    To prepare 2 - Methyl - 4 - Iodoanisole, the raw materials and production process, reaction steps and catalytic mechanism are very important. First take an appropriate amount of p-methoxytoluene as the initial raw material and place it in a clean reaction vessel. Introduce iodine elemental substance and catalyze with an appropriate amount of catalyst. This catalyst may be a specific metal salt, which can effectively promote the reaction.
    Control the temperature in a suitable range, about [X] degrees Celsius, so that the two slowly react. During this period, pay close attention to the process of the reaction, and fine-tune the ratio of temperature and reactants according to the reaction phenomenon. The reaction takes several times until the reaction is sufficient.
    After separation and purification, impurities are removed by delicate distillation or extraction to obtain pure 2-Methyl-4-Iodoanisole. This preparation process requires fine control of each link to ensure the purity and yield of the product.
    Chemical Reactions & Modifications
    The wonders of chemical industry are related to the change of substances, especially the reaction and modification. Now take 2-Methyl-4-Iodoanisole as the theory.
    The reaction of its synthesis, chemists are exhausted. Or take an aromatic hydrocarbon, through halogenation, introduce iodine atoms, and then follow the methylation step to obtain this product. However, in the reaction, obstacles are often encountered. The temperature and the proportion of reagents are all key. A little carelessness, the product is not pure, and the yield is also low.
    As for modification, it is designed to optimize its performance. Or make it more stable to adapt to different environments; or enhance its activity for special reactions. Chemists study the mechanism and adjust its molecular structure with exquisite methods. Looking at the reaction and modification of this substance is like writing a book, one stroke at a time, all of which need to be precise in order to obtain the best work of chemical industry, paving the way for various applications.
    Synonyms & Product Names
    Today there is a thing named 2 - Methyl - 4 - Iodoanisole. This thing has attracted much attention in my chemical research. It also has many synonymous names, or according to its chemical structure characteristics, or according to its use properties.
    As far as its synonymous names are concerned, it is due to the variety of chemical naming rules and different research perspectives. If viewed from a certain aspect of the structure, there can be different names, but they all refer to the same substance. As for the trade name, merchants either choose another name to sell it in order to highlight its characteristics or to make it easy to remember and promote.
    Although the names are different, their essence is one. For our researchers, it is necessary to understand that many terms refer to this specific chemical in order to avoid confusion during research exchanges and literature studies, and to accurately grasp its properties and uses in order to facilitate the advancement of scientific research.
    Safety & Operational Standards
    Safety and Handling Specifications for 2-Methyl-4-Iodoanisole
    Fu 2-methyl-4-iodoanisole is an important substance in chemical research. During its experimental operation and use, many safety and operating specifications must be followed in detail.
    Safety, the first protection. Experimenters must wear appropriate protective clothing, including laboratory gowns, gloves, etc. This substance may be sensitive or irritating to the skin and eyes, so protective gloves are selected with good chemical resistance to prevent it from coming into contact with the skin. Eye protection, goggles are essential to prevent accidental splashing of the eyes.
    Furthermore, ventilation is critical. 2-Methyl-4-iodoanisole may be volatile. In places with poor ventilation, its steam may accumulate, which not only endangers health, but also increases the risk of fire. Therefore, the experimental operation should be carried out in the fume hood to ensure that the harmful steam is discharged in time.
    The operating specifications should not be underestimated. When weighing, precise measuring tools are indispensable to ensure accurate dosage, and the operation should be rapid to avoid long-term exposure to air. Mixing or reaction steps, temperature, time and other conditions need to be strictly controlled. When heating, appropriate heating devices, such as oil baths and water baths, should be used to prevent local overheating from causing uncontrolled reactions.
    For storage, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. Due to its certain chemical activity, it is advisable to store it separately because it is mixed with other substances or causes dangerous reactions.
    Waste disposal is also in accordance with regulations. Waste containing 2-methyl-4-iodoanisole should not be discarded at will. It should be collected and properly disposed of according to the chemical waste treatment process to avoid environmental pollution and human hazards.
    In conclusion, in the research and use of 2-methyl-4-iodoanisole, safety and operation standards are essential to ensure smooth experiments, personnel safety, and environmental friendliness, and must not be neglected.
    Application Area
    2 - Methyl - 4 - Iodoanisole is also a chemical material. Its use, in the field of, can be synthesized as a raw material. With the characteristics of this product, it can be reversed in many ways, helping to form the active group of the product. For example, in some painful processes, in its synthesis process, 2 - Methyl - 4 - Iodoanisole or to angle, can be generally transformed, can be used for specific effects.
    In the field of materials, it is also useful. Or can be polymerized and reversed to obtain special polymers. Such polymers may have low resistance, light resistance, etc. According to the molecular arrangement of the controllable polymer, the specific properties of the material can be given, which is used in the field of optical devices.
    Furthermore, in the research of synthesis, 2-Methyl-4-Iodoanisole is often important. The chemist, by virtue of its general performance, can be used to synthesize the new molecule.
    Research & Development
    In recent times, it has been restored, chemistry has been refined, and material research has been pursued, which is new and new. Today there is a thing called 2-Methyl-4-Iodoanisole, and I devote myself to it.
    Begin to study its properties in detail, observe its shape and quality, and measure its physical and chemical characteristics. After repeated experiments, explore its reaction rules. Under various conditions, observe its changes, observe its transformation, and clarify its characteristics.
    Then seek a method for its preparation. Try all kinds of paths, either complex or simple, or successful or failed. However, I am determined to persevere, and repeatedly investigate, and finally find one or two usable methods.
    As for its use, it is also widely explored. It can be used for the preparation of medicinal stones, or it can help the research of materials. Although the road ahead is long, I believe that this substance will be used in the process of research, shine brightly, and be beneficial to the progress of science. In the future, I should continue to study it to promote its development, and do my best for the prosperity of chemistry.
    Toxicity Research
    The industry of chemical industry is related to the people's livelihood, but the investigation of poisons in it cannot be ignored. Now take 2-Methyl-4-Iodoanisole as the theory, and examine its toxicity in detail.
    Husband 2-Methyl-4-Iodoanisole, among chemical products, although not widely known, the study of toxicity should not be taken lightly. We must follow the scientific method to investigate its nature. After various experiments, observe its response to living things, and observe its response to the environment. Or changes in cells, or in ecological methods, all need to be investigated carefully.
    The study of toxicity is not a one-day effort. It must be accumulated over the months and years, and many people will participate in the school. It is hoped to obtain the true fruit, so as to clarify the advantages and disadvantages of this thing in life and nature, and lead the right path for the chemical industry, avoid disasters, protect the well-being of the people, and protect the peace of heaven and earth.
    Future Prospects
    Today, there is a thing called 2-Methyl-4-Iodoanisole, and our generation of chemical researchers has carefully studied it. It has shown its uniqueness in the present, but our eyes are more focused on its future development.
    Looking at this substance, the structure is exquisite and the characteristics are also potential. In time, in the field of medicine, it may emerge. It can help create new drugs and open up new ways for the treatment of diseases.
    On top of the industry, it may become a key raw material, making the production technology more exquisite, and the quality of the product has to soar.
    And the scientific exploration of the husband has no end. 2-Methyl-4-Iodoanisole hidden mysteries, waiting for us to dig deeper. In the future, we will be able to expand our understanding and build a scientific grand building based on it, so as to make immeasurable contributions to the well-being of mankind. We should have great ambitions and study it unremittingly, looking forward to seeing this material shine and develop infinite possibilities in the future.
    Historical Development
    In the past, our generation studied a thing in the field of chemistry, called "2-Methyl-4-Iodoanisole". It has not been noticed by the academic community at the beginning, but we have investigated the reality with sensitivity and determination.
    At the beginning, we explored the method of preparation, but encountered many thorns. All kinds of attempts, or the raw materials were difficult to find, or the reaction was bad. However, we have not been discouraged, and we have failed again and again. After months of research, we gradually obtained the wonderful method of preparation.
    After that, we have also struggled to explore the nature. Its physical properties, color, shape, and melting point have all been investigated in detail; its chemical properties, and the reactions of various things, are recorded one by one. As the years go by, its mysteries are gradually revealed.
    Today, "2-Methyl-4-Iodoanisole" is gradually becoming more and more important in the chemical industry. Or it is the basis for the synthesis of new substances, or it is available in the research and development of medicine. Looking back on the past, from its invisibility to today, it is important for people. This hardship is the proof of my generation's research, and I hope that future generations will follow our aspirations and go further and further in the road of chemistry.
    Product Overview
    2 - Methyl - 4 - Iodoanisole Description
    2 - Methyl - 4 - Iodoanisole is a chemical substance that we have been working hard on. It has unique properties and has important applications in the field of organic synthesis.
    Looking at its structure, methoxy and methyl are connected to the benzene ring, and the iodine atom is also at a specific position, so the structure gives it a different chemical activity. During the preparation process, after many fine steps, the reaction conditions are strictly controlled, such as temperature, reagent ratio, and slight difference, which will affect the yield and purity.
    This substance can be used as a key intermediate in many reaction systems. Either nucleophilic substitution or coupling reactions can play a key role in the generation of compounds with complex structures and special functions.
    In the scene of industrial production and academic research, 2-Methyl-4-Iodoanisole has attracted attention. Our researchers continue to explore more potential properties and application paths, hoping to contribute to the development of the chemical field.
    Physical & Chemical Properties
    2 - Methyl - 4 - Iodoanisole is an organic compound. Its physical properties are mostly solid at room temperature, with a specific melting point, which can be accurately determined by a melting point meter. Looking at its appearance, it may be a white to light yellow crystalline powder with a certain luster. This substance has considerable solubility in organic solvents, such as ethanol, ether, etc., but poor solubility in water.
    When it comes to chemical properties, its iodine atom has high activity and is easy to participate in nucleophilic substitution reactions. Methoxy and methyl groups also affect its chemical activity. Methoxy groups have a donator effect, which increases the density of electron clouds in the benzene ring and makes it more prone to electrophilic substitution reactions. Methyl groups change the molecular spatial structure and electron cloud distribution. This compound is widely used in the field of organic synthesis and can be used as a key intermediate to prepare complex organic molecules through a series of reactions.
    Technical Specifications & Labeling
    Today there is a product called 2-Methyl-4-Iodoanisole. Its process specifications and identification (commodity parameters) are the key. If you want to make this product, you should first clarify the precision and proportion of the materials used, and the operation should follow the law. There should be no mistakes. In the reaction environment, the temperature and duration need to be carefully checked to ensure that everything goes well.
    After it is made, check its logo. Examine the parameters of the product carefully, and observe its color, purity geometry, and taste. The size specifications are also in line with the previous regulations. In this way, you can get a good product, and the process specifications and identification are correct and can be used.
    Preparation Method
    The method of preparing 2-methyl-4-iodoanisole is related to raw materials, production process, reaction steps and catalytic mechanism. Taking anisole as the base, with an appropriate halogenating agent, such as iodine elemental compound and a suitable oxidizing agent, after halogenation reaction, iodine atoms can be introduced into the anisole phenyl ring. The reaction system needs to be temperature-controlled and controlled, and a mild temperature, such as 30 to 50 degrees Celsius, is selected to ensure an orderly reaction. The choice of catalysis can be found with high activity and selectivity, such as specific metal salts or organic ligands, to help the reaction be efficient. The reaction step is to prepare anisole and halogenating agent in the reactor, adjust the temperature and then add catalysis, stir to promote mixing and reaction. After the reaction is completed, the pure 2-methyl-4-iodoanisole is obtained by extraction and distillation. This process focuses on the precise ratio of raw materials and strict control of conditions to achieve the purpose of high yield and excellent yield.
    Chemical Reactions & Modifications
    The chemical and anti-chemical modification of 2-methyl-4-iodoanisole is the most important research. In the past, the reverse route of this compound was often followed by the usual method, and the method of iodine substitution and methylation was carried out. However, such methods have their drawbacks.
    The reverse method is often produced by the side reaction, resulting in high quality of the product. And the reverse parts are harsh, requiring high cost, high cost or special catalysis, which is expensive and costly.
    Now if you want to modify it, you need to do something else. New catalytic systems can be developed, or integrated and introduced, in the hope of promoting high efficiency and high efficiency. If you explore new types of gold catalysts, it is hoped that under the new method and the new method, the iodine atom will be replaced and the side reaction will be suppressed. In this way, the efficiency of 2-methyl-4-iodoanisole may be greatly improved, making it more suitable for work and production, and promoting the development of the chemical field.
    Synonyms & Product Names
    2 - Methyl - 4 - Iodoanisole This product, its identity is an important part of the study of the product name. I can explore the general characteristics of the product in the field of chemistry, and the same product name cannot be ignored.
    2 - Methyl - 4 - Iodoanisole, or there are different uses for it. The same product, such as exploring the seclusion, seeks accuracy.
    As for the product name, sell it in different languages, or take a special name. However, whether it is the same or the product name, it depends on the origin of the product, and cannot be managed.
    For those of us who are researching and researching 2-Methyl-4-Iodoanisole, we can only use this product in all parties to facilitate research, communication and application, and make the wisdom of chemistry more complete.
    Safety & Operational Standards
    2-Methyl-4-iodoanisole is an important chemical product that is essential for its safety and operating practices.
    In the operating area, it is necessary to maintain good ventilation to prevent the accumulation of harmful gases. Operators should wear appropriate protective clothing, protective gloves and goggles to avoid contact with skin and eyes. In case of inadvertent contact, rinse immediately with plenty of water and seek medical attention according to the specific situation.
    In terms of storage, 2-methyl-4-iodoanisole should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. At the same time, it should be stored separately from oxidants, acids, etc., and should not be mixed to prevent dangerous chemical reactions. The storage area should be equipped with suitable materials to contain leaks.
    If a leak occurs, the personnel in the leaked contaminated area should be quickly evacuated to a safe area and quarantined to strictly restrict access. Emergency personnel should wear self-contained positive pressure breathing apparatus and anti-toxic clothing. Cut off the source of leakage as much as possible to prevent it from flowing into restricted spaces such as sewers and drainage ditches. In the event of a small leak, it can be absorbed by sand, vermiculite or other inert materials. In the event of a large number of leaks, embankments or pits should be built to contain them, covered with foam to reduce vapor disasters, and then transferred to a tanker or a special collector with an explosion-proof pump, recycled or transported to a waste treatment site for disposal.
    In short, the safety and operating standards for 2-methyl-4-iodoanisole should be followed carefully, so as to ensure the safety of personnel, avoid environmental pollution, and ensure the smooth progress of chemical experiments or production.
    Application Area
    2-Methyl-4-iodoanisole, this compound is useful in many fields. In the field of medicinal chemistry, it can be used as a key intermediate to help synthesize drugs with specific pharmacological activities, or involve antibacterial and anti-inflammatory effects. In the field of materials science, it may be able to participate in the synthesis of materials with special photoelectric properties, such as application in new display materials. In organic synthetic chemistry, with its structural properties, it can provide an effective path for the construction of complex organic molecules, introduce different functional groups through various chemical reactions, and expand the diversity of organic compounds. Its potential in various application fields is like jade waiting to be carved, opening the door to exploration and innovation for chemical researchers to tap more practical value.
    Research & Development
    I am dedicated to the research of 2 - Methyl - 4 - Iodoanisole. At the beginning, I explored the method of its synthesis, and after several attempts, I found a delicate way. With a certain method, the yield was not as expected, so I repeatedly considered and adjusted various conditions, such as temperature and reagent dosage.
    And its properties were observed, and its solubility and stability differed in different solvents. This property is crucial in practical applications. Then consider its application domain, which can be used in the preparation of certain types of drugs, or in materials science.
    Now looking at this product, although it has been obtained, there is still room for expansion. In the future, we should explore more deeply, optimize the synthesis process, improve the yield and purity, and expand its application range, hoping to make it shine in more fields and contribute to the development of science and the progress of society.
    Toxicity Research
    Study on the toxicity of 2-Methyl-4-Iodoanisole
    Taste the nature of things, there are good and evil, especially in chemical products. 2-Methyl-4-Iodoanisole is also a product of chemical products. In fact, today, explore the mystery of its toxicity.
    Looking at its shape, or something that is pure in color and taste, it should not be judged by its appearance. The poison of this thing is related to the safety of the living being. In the genus of microinsects, if you apply it in moderation, you can see that its behavior is abnormal, or impatient or slow, and the signs of life are gradually weakening.
    The reason is to cover its molecular structure, which can disturb the physiological order of living things. Entering the body, or disturbing the metabolism of cells, or blocking the conduction of nerves. Although it is not fully known, the appearance of toxicity cannot be ignored.
    Those who study, should be careful, observe its changes, remember its feelings, for the prevention of the world. When its nature is known, when it is used, avoid its harm and promote its benefits, and protect the safety of all things.
    Future Prospects
    I tried to study 2 - Methyl - 4 - Iodoanisole and thought about its future prospects.
    In today's world, science and technology are changing day by day. This compound may open up new avenues in the field of medicine. Its unique structure may help doctors make special drugs and save patients from suffering. In materials science, it is also possible. With its characteristics, it may be able to develop exotic materials for use in high-tech, such as electronic devices, to improve performance.
    Although the current research is not perfect, it has a good future. With time, everyone will be able to explore its endless potential, use it for the world, make extraordinary achievements, create infinite benefits, and shine brightly in the future, leading the trend of science and technology, and blessing all people.
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    Frequently Asked Questions

    As a leading 2-Methyl-4-Iodoanisole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 2 - methyl - 4 - iodoanisole?
    The chemical structure of 2 + -methyl-4-iodoanisole is described as follows: The core of this compound is a benzene ring, which is a typical structure of aromatic hydrocarbons. Above the benzene ring, there is a methyl group (-CH 🥰) at position 2, which is composed of one carbon atom and three hydrogen atoms, and is connected to the benzene ring in a tetrahedral shape. At position 4, there is an iodine atom (-I), which is relatively large and has a great influence on molecular properties. At the same time, the first position of the benzene ring is connected to a methoxy group (-OCH 🥰). The methoxy group is composed of an oxygen atom and a methyl group. The oxygen atom is covalently connected to the benzene ring, and the methyl group at the other In this way, the atoms and groups are connected by covalent bonds in a specific order and spatial position to construct the chemical structure of 2-methyl-4-iodoanisole, which endows the compound with specific physical and chemical properties. It is of great significance in many reactions and application fields of organic chemistry.
    What are the main physical properties of 2 - methyl - 4 - iodoanisole?
    The main physical properties of 2 + -methyl-4-iodoanisole are as follows:
    This substance is mostly liquid at room temperature, with a clear and transparent appearance or a slight yellowish sheen. The color state is due to factors such as electronic transitions and conjugated systems in the molecular structure. It has a special odor. This odor is derived from the molecular composition and structure of the organic substance. The smell is emitted, which can be sensed by the sense of smell or has a certain irritation. However, due to individual differences in the sense of smell, the perception is also different.
    When it comes to the melting point, its melting point is about -13 ° C, and the boiling point is about 247 ° C. The value of the melting point reflects the strength of the force between molecules. Below -13 ° C, the thermal motion of the molecules weakens, and the arrangement of each other gradually becomes orderly, so they become solid states; the value of the boiling point indicates that when the temperature reaches 247 ° C, the molecules gain enough energy to break free from the attractive forces between molecules, and change from liquid to gaseous state.
    In terms of density, it is about 1.65 g/cm ³, which is heavier than water. If mixed with water, it will sink underwater. This density characteristic is determined by the relative mass of the molecules and the degree of accumulation between molecules. The molecules contain iodine atoms, and the atomic weight is large, resulting in an increase in the overall relative mass and then a higher density. In terms of solubility, it is slightly soluble in water, but easily soluble in organic solvents such as ethanol, ether, and chloroform. This is because water is a polar solvent, and although 2-methyl-4-iodoanisole contains methoxy groups with a certain polarity, the polarity is weaker overall due to factors such as benzene rings and iodine atoms. According to the principle of "similar miscibility", it is more soluble in non-polar or weakly polar organic solvents.
    What are the common applications of 2 - methyl - 4 - iodoanisole in organic synthesis?
    2 + -Methyl-4-iodoanisole, which is widely used in organic synthesis.
    First, it can be used as a key intermediate for the synthesis of other organic compounds. Due to its structure containing both methyl, iodine atoms and methoxy groups, these functional groups have unique reactivity and can be converted into other functional groups through many organic reactions, such as nucleophilic substitution, coupling reactions, etc., to construct more complex organic molecules. For example, in the Suzuki coupling reaction, the iodine atom in 2-methyl-4-iodoanisole can react with boron-containing reagents to form new carbon-carbon bonds, providing an effective way for the synthesis of polyaryl compounds, which is of great significance in the fields of medicinal chemistry and materials science.
    Second, in the field of drug synthesis, it is often regarded as a starting material. Its structure can be modified and modified to meet the needs of specific drug targets. Pharmaceutical chemists can develop new drugs with specific pharmacological effects by derivatizing its functional groups and adjusting the physicochemical properties and biological activities of molecules.
    Third, in the field of materials science, it is also useful. Introducing it into the structure of a polymer material through a suitable reaction can endow the material with unique properties, such as changing the optical and electrical properties of the material. For example, by connecting it to the polymer backbone through a specific reaction, it is expected to prepare organic polymer materials with special photoelectric properties, which may have applications in fields such as organic Light Emitting Diodes (OLEDs) and solar cells.
    What are the synthesis methods of 2 - methyl - 4 - iodoanisole?
    The synthesis of 2 + -methyl-4-iodoanisole is an important topic in organic synthetic chemistry. There are two common methods for preparing this substance.
    First, 2-methyl-4-hydroxyanisole is used as the starting material and can be obtained by halogenation reaction. In this reaction, it is crucial to select a suitable halogenating reagent. Commonly used ones are the combination of potassium iodide and hydrogen peroxide. In an acidic environment, potassium iodide can be oxidized by hydrogen peroxide to an active iodine elemental substance, and then the phenolic hydroxyl group of 2-methyl-4-hydroxyanisole undergoes electrophilic substitution reaction to form 2-methyl-4-iodoanisole. During the reaction, it is necessary to pay attention to the regulation of the reaction temperature and time. If the temperature is too high or the time is too long, it may cause side reactions, such as the formation of polyhalogenated products.
    Second, it can be synthesized from 2-methylanisole through multiple steps such as nitration, reduction, diazotization and iodine substitution. First, 2-methylanisole and mixed acid (a mixture of sulfuric acid and nitric acid) undergo nitration reaction, and nitro is introduced into the phenyl ring. This step requires strict control of the temperature and the ratio of mixed acid to prevent excessive nitrification. The resulting nitro compound can be converted into the corresponding amino compound after reduction, such as iron powder and hydrochloric acid as reducing agents. Then, the amino compound reacts with sodium nitrite and hydrochloric acid to undergo diazotization to form a diazonium salt. Finally, the diazonium salt reacts with potassium iodide, and the diazonium group is replaced by the iodine atom to obtain the target product 2-methyl-4-iodoanisole. Although this route has many steps, the reaction selectivity of each step is better and the product purity is easy to control.
    The above two methods have advantages and disadvantages. The former step is relatively simple, but the selectivity of the halogenation reaction is sometimes poor; the latter step is complicated, but it can better control the structure and purity of the product. In actual synthesis, the optimal method should be selected according to specific needs and conditions.
    What is the approximate market price for 2 - methyl - 4 - iodoanisole?
    I don't know what the market price of 2 - + - methyl - + - 4 -iodoanisole is. The market price of these substances often changes due to various reasons, such as the trend of supply and demand, the distance of origin, the difficulty of preparation, the quality and quality, and the price demanded by the vendors in the market may also be different.
    If you want to know the exact price, you should consult the chemical material merchants, chemical mall platforms, or in the chemical industry forums and communities, and ask those who know this. They may be able to give a more accurate price according to the current market situation. However, the price is difficult to say in a word, and it must be checked in real time before it can be accurate.