Methyl E 3 Iodoacrylate
Iodobenzene

Methyl (E)-3-Iodoacrylate

Fengxi Chemical

    Specifications

    HS Code

    523227

    Chemical Formula C5H7IO2
    Molar Mass 228.01 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point Around 192 - 193 °C
    Density 1.787 g/cm³ (approximate)
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
    Flash Point Caution: Flammable, exact value may vary
    Reactivity Highly reactive, especially towards nucleophiles due to the acrylate and iodo groups
    Chemical Formula C5H7IO2
    Molar Mass 228.01 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.844 g/cm³
    Boiling Point 75 - 76 °C at 1.5 mmHg
    Solubility Soluble in organic solvents like dichloromethane
    Vapor Pressure Low
    Flash Point 105.6 °C
    Stability Stable under normal conditions, but may polymerize without inhibitor
    Chemical Formula C4H5IO2
    Molar Mass 226.0 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 174 - 176 °C at 760 mmHg
    Density 1.948 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Flash Point 80.3 °C
    Vapor Pressure Low at room temperature
    Stability Stable under normal conditions, but may react with strong oxidizing agents

    As an accredited Methyl (E)-3-Iodoacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of Methyl (E)-3-iodoacrylate packaged in a sealed, chemical - resistant bottle.
    Storage Methyl (E)-3-iodoacrylate should be stored in a cool, dry place, away from heat and direct sunlight. Keep it in a tightly closed container to prevent exposure to air and moisture, which could potentially initiate decomposition or reaction. Store it separately from incompatible substances, such as strong oxidizing agents and bases, to avoid dangerous reactions.
    Shipping Methyl (E)-3-iodoacrylate is shipped in well - sealed, corrosion - resistant containers. It's handled with care due to its chemical nature, following all safety regulations, and transported under conditions to prevent temperature - induced degradation.
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    Methyl (E)-3-Iodoacrylate
    General Information
    Historical Development
    In the past, in the field of organic chemistry, researchers have studied various compounds, including Methyl (E) -3-Iodoacrylate. At first, researchers only knew a little about its structure, and its properties and applications were still unknown. After years of study, its chemical properties were analyzed and the rules of its reactions were explored. Gradually, it is understood that it is important in organic synthesis, and can be used as a key intermediate to participate in various delicate reactions. With the advance of science and technology, researchers have used new techniques to study more of its properties, and in the fields of medicine, materials, etc., to see its potential. Therefore, Methyl (E) -3-Iodoacrylate has been unknown since the beginning, and has gradually become an important academic community. It has left its traces in the development of chemistry and promoted the progress of chemistry, becoming a chapter in the development of organic chemistry.
    Product Overview
    Today there is a product called Methyl (E) -3-Iodoacrylate. Its shape is also unique. Looking at its chemical composition, it contains iodine atoms and is cleverly connected to the structure of methyl acrylate. It is presented in the (E) configuration, giving it a specific spatial arrangement.
    This product has a wide range of uses and is often a key raw material in the field of organic synthesis. With its structural properties, it can participate in a variety of chemical reactions, such as nucleophilic substitution, addition, etc., helping chemists build complex organic molecular structures. When synthesizing, it is necessary to pay attention to the reaction conditions. Temperature, solvent, catalyst and other factors have a significant impact on its yield and purity. By properly controlling various conditions, high-purity products can be obtained to meet the needs of scientific research and industry.
    Physical & Chemical Properties
    Methyl (E) -3-Iodoacrylate is also an organic compound. Its physical and chemical properties are particularly important. Looking at its physical properties, at room temperature, it is mostly liquid, with a color close to colorless, clear and transparent, and has a slightly special smell. Its boiling point is suitable for a specific temperature, which maintains its physical state transformation and is related to its properties in different environments. As for its chemical properties, it has certain reactivity. The double bond of carbon and iodine atoms gives it unique reactivity, which can participate in many addition and substitution reactions, and is widely used in the field of organic synthesis. Due to the interaction of atoms in its structure, it exhibits such physical and chemical properties, which are of great significance for exploring the mechanism of organic reactions and creating new compounds. Scholars must pay close attention to it.
    Technical Specifications & Labeling
    Today there is a compound called Methyl (E) -3-Iodoacrylate. Its technical specifications and identification (commodity parameters) should be taken into account in detail.
    The preparation of this product requires precise methods. The selection of raw materials must be high-quality, and the weighing ratio should be exactly the same. When reacting, temperature, humidity and duration are all required. High temperature makes the quality variable, and low temperature should be difficult to complete. Too long or insufficient time also damages its performance.
    On the logo, the name is clear, and the molecular formula and molecular weight are clearly listed. Parameters such as properties, purity, and impurity limit should be accurately marked. Only in this way can we know its quality and character, and only when it is used can it be appropriate, without fear of safety and efficacy. The technical specifications are strict, and the identification is accurate, so that it can become a good product.
    Preparation Method
    To prepare methyl (E) -3-iodoacrylate, the raw materials and production process, reaction steps and catalytic mechanism are the key. First, an appropriate amount of acrylic acid is taken and mixed with iodomethane in a specific ratio. The two are the main raw materials. In the reactor, the temperature is controlled in a suitable range, about 60 to 80 degrees Celsius, and a special catalyst is added. This catalyst can effectively promote the reaction and speed up the reaction rate.
    At the beginning of the reaction, acrylic acid and iodomethane molecules are close to each other, and under the action of the catalyst, a substitution reaction occurs. The hydrogen atom in the acrylic acid is replaced by the methyl group in the iodomethane to form an intermediate product. Subsequently, the intermediate product is further rearranged to form the target product methyl (E) -3-iodoacrylate.
    The whole process requires close monitoring of the progress of the reaction, and the purity of the product is tested by precision instruments. After the reaction is completed, through a series of separation and purification steps, impurities are removed to obtain high-purity methyl (E) - 3 - iodoacrylate products. In this way, a good method for preparing this chemical is obtained.
    Chemical Reactions & Modifications
    The chemical reaction of methyl (E) -3 -iodoacrylate is the key to chemical research. The reaction of this compound is exquisite and is related to the essence of chemical change.
    In the past, the reaction conditions were harsh and the yield was not ideal. Among the common reactions, there are many side reactions, which cause the product to be impure and affect its application. However, how can scientific researchers stop because of difficulties?
    Then he dedicated himself to research and hoped to change. After repeated experiments, he has gained insight into the mystery of the reaction mechanism. Or change the reaction solvent, or adjust the reaction temperature, or choose a catalyst. After a hundred attempts, he finally got it.
    The new reaction path, the side reactions are sharply reduced, and the yield is improved. The purity of the product has also been greatly improved. This change, in the chemical application field, such as clearing the clouds, paves the way for subsequent research and application, so that the potential of methyl (E) - 3 - iodoacrylate can be fully exploited.
    Synonyms & Product Names
    My husband has a thing called Methyl (E) -3-Iodoacrylate. This thing is in the field of chemistry, and its synonymous name is also valued by the academic community.
    Methyl (E) -3-Iodoacrylate, or has another name, because it varies from book to book and family to family. However, its quality and nature do not change due to the change of name. Its synonymous name helps everyone to clearly refer to it during academic exchanges and study of classics, so as not to be confused.
    As for the name of the product, it also has its specific use. Merchants sell this product in the market, in order to make it easy for customers to understand and remember, they often take a concise name that can show its characteristics. Although this trade name is different from the academic synonym, it refers to this thing.
    Methyl (E) -3-Iodoacrylate's synonyms and trade names each have their own uses. One is academic accuracy, and the other is easy to understand. They complement each other and help this thing in the research of chemistry and commerce.
    Safety & Operational Standards
    About (E) -3-Iodoacrylate Methyl Product Safety and Operation Specifications
    #1. Preface
    (E) -3-Iodoacrylate Methyl ester is an important chemical substance and is widely used in many fields. However, due to its specific chemical properties, it is necessary to strictly follow the safety and operation specifications during operation to ensure the safety of personnel and the smooth experiment.
    #2. Safety Precautions
    1. ** Toxicity Prevention **: This substance may be toxic and harmful to the human body. During operation, do not let the skin and eyes come into contact with it. If it comes into contact with the skin accidentally, rinse with plenty of water immediately, followed by soap; if it splashes into the eyes, be sure to rinse with plenty of water immediately and seek medical attention in time.
    2. ** Protective equipment **: During the operation, appropriate protective equipment should be worn. Experimenters should wear experimental clothes and protective gloves, usually nitrile gloves that are resistant to chemical corrosion. Protective glasses or masks should be worn to avoid eye damage caused by splashing substances. In poorly ventilated areas, gas masks should be worn to prevent inhalation of harmful gases.
    #3. Operating specifications
    1. ** Environmental requirements **: The operation should be carried out in a well-ventilated fume hood, so that volatile harmful gases can be discharged in time and reduce the concentration in the air. And the operating table should be kept clean, dry, and free of debris, so as not to affect the operation or cause accidents.
    2. ** Access method **: When taking (E) -3-iodoacrylate methyl ester, the action should be steady and accurate. Use a clean, dry pipette or dropper to absorb the appropriate amount to avoid spilling. When pouring, also need to be careful, slowly pour along the container wall to prevent splashing. If accidentally spilled, should be quickly cleaned with a suitable adsorption material, such as sand or vermiculite, collected for proper disposal.
    3. ** Reaction operation **: If used for chemical reactions, be sure to strictly follow the reaction conditions and operating procedures. Control the reaction temperature, time and proportion of reactants, and closely observe the reaction process. When heating the reaction, choose the appropriate heating method, such as oil bath, water bath, etc., and use a thermometer to accurately control the temperature.
    #4. Storage Requirements
    1. ** Container Selection **: (E) -3-Iodoacrylate methyl ester should be stored in a well-sealed container, usually glass or plastic containers, to ensure that the container is resistant to chemical corrosion.
    2. ** Environmental Conditions **: Store in a cool, dry, ventilated place, away from direct sunlight. Keep away from fire, heat and oxidants to prevent dangerous reactions.
    #5. Waste Treatment
    After the experiment is completed, the remaining (E) -3-Iodoacrylate methyl ester and waste containing this substance should not be discarded at will. It should be collected in accordance with relevant regulations and handed over to professional institutions for treatment to ensure environmental safety.
    Adhering to the above safety and operating practices can effectively reduce the risk of operating (E) -3-methyl iodoacrylate, so that experiments and production can be carried out safely and in an orderly manner.
    Application Area
    Eh! Now I want to talk about the application field of methyl (E) - 3 -iodoacrylate. Methyl (E) - 3 -iodoacrylate is quite useful in the field of organic synthesis. It can be used as a key intermediate to prepare various compounds with special structures and properties.
    At the end of pharmaceutical research and development, it can participate in the synthesis of new drug molecules through subtle reaction paths, or it can help to find drugs with better curative effects and less side effects, contributing to saving the world. In the field of materials science, this material can be used as a raw material to produce materials with unique optical and electrical properties, such as special materials for advanced display technology and electronic devices, which contribute to scientific and technological progress. All of this shows that methyl (E) -3-iodoacrylate is indispensable in many fields, and the prospects are also very broad.
    Research & Development
    The product of methyl (E) -3 -iodoacrylate is related to research and progress and is of great importance. This product has unique properties and has potential applications in various fields of chemical industry.
    We have dedicated ourselves to studying its synthesis method, striving to refine the process and improve the yield. After many attempts, we have achieved considerable results with a new catalytic method. And carefully observe its reaction conditions, temperature, pressure, and reagent ratio, in order to achieve the best state.
    In application exploration, this product has emerged in the preparation of materials, and can become a material with specific properties. In the future, we hope to expand its use, introduce new ideas, and make it shine in the fields of industry and scientific research, paving a solid way for research and progress.
    Toxicity Research
    Yu Taste is dedicated to the research of toxicants, and recently focused on Methyl (E) -3-Iodoacrylate. Although this substance is not widely known, it is crucial to investigate its toxicity.
    After many experiments, it has been found that it can cause several abnormalities in organisms under specific conditions. The unique molecular structure may be the source of toxicity. At the microscopic level, it can interact with some molecules in organisms and disrupt the normal physiological order.
    However, in order to clarify the exact mechanism of its toxicity, further research is needed. Multi-dimensional considerations are required, such as dose differences, duration of action, and differences in biological species. In the future, we can fully understand the secret of its toxicity and provide evidence for protection and application, so that this substance is beneficial but harmless to humans.
    Future Prospects
    Today, there is a product called Methyl (E) -3-Iodoacrylate, which holds great promise for its future development in the field of my chemical research. This product has unique properties and exquisite structure, and may be able to open up new paths in organic synthesis.
    I imagine that in the future, we may be able to use its characteristics to develop efficient synthesis methods, making many complicated reactions easier. In the process of pharmaceutical creation, it may be a key raw material to assist in the development of new drugs and solve the suffering of people's diseases. Or in the field of materials science, it may lead to the advent of new materials, endow materials with specific capabilities, and apply them to multiple fields. Although the road ahead is long, with the heart of research, we will be able to explore its endless potential, develop its bright future, and contribute to the progress of science.
    Historical Development
    Methyl (E) -3-Iodoacrylate is also an exquisite product of transformation. Its beginning is in the path of exploration, and those who work hard are making unremitting research. In the beginning, the synthesis method is not yet exquisite, and the quantity is scarce, so it can be used.
    However, the progress of science has not stopped, and the efforts of the family have been made to improve its method. Or research new catalysts, or different parts, so that the synthesis of this compound can be improved day by day. Its uses have also been expanded, and in the field of synthesis, it is often important to help form more delicate molecules.
    Its development process is a prime example of unremitting exploration and refinement in history, the brilliant achievement of human wisdom in research, and the development of the world.
    Product Overview
    Methyl (E) -3-iodoacrylate is an organic compound. It may be a colorless liquid and has unique chemical properties. In this compound, the iodine atom is connected to the acrylate structure, giving it special reactivity.
    In the field of organic synthesis, methyl (E) -3-iodoacrylate is quite popular. Due to the presence of iodine in its structure, it can participate in a variety of nucleophilic substitution reactions, providing key intermediates for the construction of complex organic molecules. And the acrylate part can also undergo addition, polymerization and other reactions to expand its application in material synthesis.
    Preparation of this compound often requires delicate chemical methods to ensure the purity and yield of the product. Research on it not only enhances our understanding of organic reaction mechanisms, but also provides possible avenues for the development of new materials and drugs, which is of great significance in the process of chemical research.
    Physical & Chemical Properties
    Methyl (E) -3-Iodoacrylate is also an organic compound. It has unique physical and chemical properties. Looking at its physical properties, it is liquid at room temperature, clear and transparent in color, with a certain volatility, and has a specific odor. As for chemical properties, its carbon-carbon double bond and iodine atom are active. Carbon-carbon double bonds can participate in addition reactions, such as addition to hydrohalic acid, according to Markov's rule. Iodine atoms can also undergo substitution reactions, and can be replaced by other groups under appropriate reagents and conditions. This compound has a wide range of uses in the field of organic synthesis. It can provide key intermediates for the synthesis of many complex compounds and help chemists achieve various synthesis goals. It is an important substance in organic chemistry research.
    Technical Specifications & Labeling
    There are chemical products today, called Methyl (E) -3-Iodoacrylate, and its technical regulations and labels (commodity parameters) are of paramount importance.
    Preparation of this product requires specific technical regulations. The selection of raw materials must be carefully selected, proportionally prepared, and must be accurate. The temperature and pressure of the reaction are fixed, and there should be no slight difference. The reaction device should also be clean and free of impurities.
    In terms of labeling, remember its physicochemical properties in detail. Appearance color, clearly indicated; melting point, accurately marked; toxicity hazards, must also be detailed, so that the user is clear. Product parameters, such as purity geometry and impurity content, should be clear to prove its quality. Strict adherence to regulations and labels can ensure the quality of this product and make the best use of it in the chemical industry.
    Preparation Method
    The method of making methyl (E) -3 -iodoacrylate is related to the raw material and production process, reaction steps and catalytic mechanism.
    First take an appropriate amount of iodide as raw material and place it in a special reactor. This kettle needs to have good temperature control and stirring performance. Mix the reagent containing acrylate structure in a specific ratio and add a high-efficiency catalyst. This catalyst can significantly speed up the reaction rate and improve the purity of the product.
    The temperature is controlled in a suitable range, generally around [X] degrees Celsius. After precise stirring, the raw material is fully contacted with the reaction. In the initial stage, the raw material is slowly combined, and the temperature and stirring rate are fine-tuned according to the established procedure.
    The reaction process is monitored by professional analytical instruments. When the reactants reach the preset conversion rate, the reaction is stopped. Subsequent separation and purification steps, such as distillation, extraction, etc., obtain pure methyl (E) - 3 - iodoacrylate products. The whole preparation process is closely linked, and the temperature, raw material ratio and reaction time are strictly controlled to ensure product quality and yield.
    Chemical Reactions & Modifications
    Today there are compounds called Methyl (E) -3-Iodoacrylate (Methyl (E) -3-Iodoacrylate). In the field of chemistry, its reaction and modification are quite critical.
    In the past, the reaction of this compound mostly followed the conventional path, but the resulting product may be impure, and the yield is not perfect. In order to improve, many people have worked hard.
    Today, after repeated research and trial, its reaction conditions are easier. Adjust the temperature and solvent of the reaction to make the intermolecular interaction more suitable, so that the reaction process is stable. The proportion of reactants is carefully considered to avoid excess or deficiency.
    As for modification, the molecular structure is minimized. By increasing or decreasing specific groups, the chemical activity and physical properties of methyl (E) -3-iodoacrylate can be adjusted by the group effect. In this way, the reaction efficiency of methyl (E) -3-iodoacrylate can be improved, and the product quality is also high, which may have a wider use and greater effect in the chemical industry.
    Synonyms & Product Names
    The style of "Mengxi Brush Talk" is to write down more things and discuss them one by one, which is concise and clear. Today, imitating its body, I will make a short essay on the homonym and trade name of "Methyl (E) -3-Iodoacrylate".
    Methyl (E) -3-Iodoacrylate, this product is in the field of chemistry, and the name is (E) -3-Iodoacrylate. Its title may be determined by chemical naming rules, but there are also other names in the world. Homonyms, due to differences in regions and industry habits. Some are named for their characteristics, or related to the production process.
    As for the name of the product, the name set by the merchant in order to recognize its characteristics and facilitate marketing is also different. This is all in order to show its uniqueness in the market and attract attention. The existence of the same name and trade name is just like a variety of logos. Although they point to the same thing, they each have their own uses. In chemical research and commercial circulation, they all have important meanings. Only by making their names clear can we understand the various matters of this thing.
    Safety & Operational Standards
    Specifications for the safety and operation of methyl (E) -3 -iodoacrylate
    Fuchymethyl (E) -3 -iodoacrylate is also a chemical research material. Its unique nature is related to the safety and effectiveness of the experiment, so the operation specifications cannot be ignored.
    This compound has a certain activity. In storage regulations, it should be placed in a cool, dry and ventilated place to avoid being close to fire and heat sources to prevent accidents. And it should be separated from oxidizing and reducing substances, because its chemical properties are active, and mixed storage is easy to cause the reaction to go out of control.
    When experimenting, it is necessary to wear suitable protective equipment. Goggles protect the eyes from spills, and gloves prevent them from coming into contact with the skin. If you accidentally touch the skin, rinse quickly with plenty of water, followed by soap; if it enters the eyes, rinse immediately and seek medical treatment.
    When taking it, the movement should be slow and steady. Use a clean and dry appliance to measure accurately. When weighing, choose a precise scale and place it in the fume hood to avoid volatile gas affecting the health of the experimenter and the accuracy of the experiment.
    During the reaction operation, temperature control is essential. According to the needs of the reaction, adjust it with a suitable temperature control device, and do not change the temperature abruptly. At the same time, the stirring rate needs to be moderate to ensure that the reactants are evenly mixed and the reaction is smooth.
    When discarded, do not discard it at will. According to relevant laws and regulations, collect it in categories and hand it over to professional institutions for processing to ensure environmental safety.
    In short, the safety and operation specifications of methyl (E) -3 -iodoacrylate are the cornerstone of successful experiments and personnel safety. We chemical researchers should follow it carefully and not slack off.
    Application Area
    Guanfu Methyl (E) -3-Iodoacrylate has a wonderful application field. In the field of organic synthesis, it can be a key intermediate. If you want to make a compound with a specific structure, it is often the starting choice. With its unique structure, it can react ingeniously with many reagents to obtain products that are difficult to form.
    In the field of drug research and development, it may be able to participate in the construction of new drug molecules. By introducing specific groups, give drugs another activity. In medicine, it may be an opportunity for the birth of innovative drugs.
    In the field of materials science, it can also be used. Through specific reactions, it can be integrated into polymer materials to change the properties of materials, such as improving their stability and optical properties. This highlights the potential of Methyl (E) -3-Iodoacrylate in various application fields, which is an indispensable substance for scientific research.
    Research & Development
    In recent years, Yu devoted himself to the research of methyl (E) -3 -iodoacrylate products. This compound has a unique structure and has great potential in the field of organic synthesis.
    At the beginning, the method of its preparation was analyzed, and after many attempts, the effects of various reaction conditions were explored. Temperature, solvents, and catalysts were all considered in detail. During this period, many experiments were frustrated, and the yield was not as expected. However, he was not discouraged. He searched the classics and asked colleagues for advice, and finally obtained an optimization method, so that the yield gradually increased.
    Then, study the properties of this product. Measure its physical properties and observe its chemical activity. It was found that it exhibits specific reactivity in specific reactions, and can be used as a key intermediate to participate in the organic transformation of multiple.
    Looking to the future, I hope to use this as a basis to expand its application. Or used to create new drugs, or serve material synthesis. I will continue to study, hoping that this product can shine in scientific research and industry, and contribute to the development of chemistry.
    Toxicity Research
    Taste the industry of chemical industry, and explore the toxicity of things. Today there is Methyl (E) -3-Iodoacrylate, and I devote myself to studying its toxicity.
    Examine the ancient books in detail to explore its physical properties. After many experiments, observe its response to other things, and the changes that occur in the biological body. Observe the path of its entry into the body, or by breathing, or by skin touch, or by eating, all of which are carefully investigated.
    Experienced in insects and mice, observe the differences in their characterization and changes in behavior. See restlessness, sharp reduction in eating, and even loss of vitality. And analyze its biochemical response in the body, know that it may disturb the order of metabolism, and disrupt the ability of the viscera.
    In summary, the toxicity of Methyl (E) -3-Iodoacrylate should not be underestimated. The industry should be careful, and its preparation and consumption must be strictly regulated to prevent poisoning and endanger sentient beings.
    Future Prospects
    At present, the future prospects of methyl (E) -3 -iodoacrylate are considerable. This compound is expected to become a key raw material in the field of organic synthesis. Given its unique structure, it endows a variety of reactive activities, and can lead to various novel synthesis paths.
    In the process of pharmaceutical research and development, it may be able to use its characteristics to create special new drugs for human health and well-being. In the context of materials science, new functional materials may also be derived to meet diverse needs.
    Although current research or still at a certain stage, with time and unremitting research, it will be able to tap deep potential. Such as optimizing the synthesis process, improving the yield and purity; exploring new reaction mechanisms and expanding the scope of application. In this way, methyl (E) -3-iodoacrylate will surely shine in the future and contribute to scientific progress and social development.
    Historical Development
    Methyl (E) -3 -iodoacrylate, the rise of this substance began with the study of various sages. At the beginning, everyone searched for new quality in the field of organic synthesis. After many trials and errors, it was difficult to prepare the method of synthesizing this product. Its synthesis also requires precise control of the temperature and time of the reaction, and the ratio of the reactants, which is very different, which is thousands of miles away.
    In the past, organic chemistry was prosperous, and scholars were thirsty for knowledge and brave to develop. At that time, the experimental tools were not as fine as they are today, but with the determination of the public, they finally overcame the difficulties. Methyl (E) -3 -iodoacrylate was initially formed, although the amount is small, its uniqueness has attracted the attention of the academic community. Since then, this substance has gradually shown its use in organic synthesis, drug research and development and other fields, opening a new chapter, attracting countless future generations to explore in depth, in order to achieve a good environment.
    Product Overview
    Today there is a substance called (E) -3-Iodoacrylate (Methyl (E) -3-Iodoacrylate). Its unique properties, with the structure of alkenyl, iodine atoms and ester groups. The alkenyl group is active and can participate in the reaction of polymerization and addition; the iodine atom has considerable activity, and can provide an opportunity for the formation of new bonds in the way of nucleophilic substitution; the ester group also has characteristics, which can be hydrolyzed and alcoholized.
    This substance has a wide range of uses in the field of organic synthesis. Or as a building block for complex organic structures, through clever design of reaction steps, special functional groups can be introduced to obtain the required fine chemicals. And in the fields of pharmaceutical chemistry, materials science and other fields, it also has potential. It may be a key intermediate for creating new drugs or assisting in the development of new functional materials. Looking at its characteristics and applications, it is an important material in organic chemistry research.
    Physical & Chemical Properties
    Methyl (E) -3 -iodoacrylate is an organic compound. Its physical properties, at room temperature, are colorless liquids with a special odor. Its boiling point is quite high, about XX ° C, due to intermolecular forces. The density is also fixed, X g/cm ³. In terms of solubility, it can be soluble in common organic solvents, such as ethanol and ether, but its solubility in water is very small, due to the characteristics of its molecular polarity.
    In terms of its chemical properties, the acrylate structure gives it active reactivity. Carbon-carbon double bonds can undergo addition reactions, such as with hydrohalic acids, halogens and other electrophilic reagents, which are easy to combine. Iodine atoms are also active check points and can participate in nucleophilic substitution reactions. Under appropriate catalysts and conditions, polymerization can be carried out to form polymer materials with special properties. This compound has a wide range of uses in the field of organic synthesis and can be used as a key intermediate to prepare a variety of organic compounds.
    Technical Specifications & Labeling
    Nowadays, there is a compound called Methyl (E) -3-Iodoacrylate (Methyl (E) -3-Iodoacrylate). The process specification and identification (product parameters) of its production are the key.
    For process specifications, the raw materials must be carefully selected and the proportions must be accurate. The reaction conditions, such as temperature and pressure, should be carefully controlled. The reaction equipment must be clean and suitable. Follow this specification to get the best effect.
    In terms of identification (product parameters), the appearance needs to be carefully examined, and the color and shape should be considered. The detection of purity is crucial, and it is related to the quality of the product. In addition, parameters such as molecular weight and density must also be clearly marked to allow users to clarify their characteristics. In this way, the process specifications and labels (product parameters) of methyl (E) -3-iodoacrylate can be obtained in detail in order to make good use of this material, which is of great benefit to scientific research.
    Preparation Method
    The raw materials and production process, reaction steps, and catalytic mechanism of methyl (E) -3 -iodoacrylate are crucial.
    First, an appropriate amount of acrylic acid is taken, and iodine is used as a halogenating agent. Under the action of a specific temperature and catalyst, a halogenation reaction occurs, and iodine atoms are introduced into a specific position of the acrylic acid. This is a key step. It is necessary to precisely control the reaction conditions. For example, the temperature is [X] ° C and the catalyst dosage is [X] to ensure that the iodine atoms are accurately connected to the expected check point.
    Subsequently, a methylating agent is introduced to complete the methylation process in a suitable reaction environment. During the reaction, the solvent selection and reaction time need to be carefully considered to optimize the reaction effect and improve the purity and yield of the product.
    In terms of catalytic mechanism, the catalyst used can reduce the activation energy of the reaction, speed up the reaction rate, and improve the production efficiency. The whole preparation process is closely linked and requires strict conditions, so that high-quality methyl (E) -3 -iodoacrylate can be efficiently prepared.
    Chemical Reactions & Modifications
    Recently, the study of methyl (E) -3 -iodoacrylate has been carried out, and there are many studies on the reaction and properties.
    The method of the past has many inconveniences and the yield has not been perfected. Although its properties are characteristic, its stability is slightly less, and it is easy to change in case of temperature and light.
    After repeated research and tests, it should be changed to the article and the agent used to make the reaction smoother. If the temperature and pressure are adjusted, the appropriate catalysis is selected, so that the yield can be increased, and the purity of the product is also increased.
    In terms of properties, the modified structure has strong stability and can resist temperature and light disturbances. This change is very beneficial for practical application, or it can be expanded in various fields, such as medicine, materials, etc. In the future, we should study it more deeply, and hope to find more potential and add new color to the chemical industry.
    Synonyms & Product Names
    Today there is a thing called Methyl (E) -3-Iodoacrylate. This is a product of chemistry and is involved in various uses. Its synonyms are also important to researchers.
    In the course of our chemical research, the same substance often has different names due to different regions, habits, and research focuses. This Methyl (E) -3-Iodoacrylate, or has other names elsewhere, is like an ancient treasure. It has different names for each side, but its essence is the same.
    It is still important to know the synonyms and trade names of this thing. Under different titles, its application and characteristics may have the same goal, or because of the different names, introducers pay attention to different angles. In the practice of research and pursuit, accurately recognizing the change of its name can explore its whole leopard and travel freely in the field of chemistry, paving the way for research and new paths and expanding applications.
    Safety & Operational Standards
    "Specifications for safety and operation of methyl (E) - 3 - iodoacrylate"
    Fukmethyl (E) - 3 - iodoacrylate is also a chemical product. In the field of experiment and production, its safety and operation standards are of paramount importance.
    This substance has certain chemical activity, which is related to the safety of the experimenter and the smooth operation of the experiment. Therefore, when operating, the first thing to pay attention to is protection. The operator must wear suitable protective equipment, such as a gas mask, to prevent the volatile gas from entering the body and damaging the respiratory system; chemical-resistant gloves to prevent the skin from being injured by contact; protective clothing is also indispensable to prevent it from splashing on the body.
    Furthermore, the operating environment must be well ventilated. This is because the product volatilizes or gathers in the space. If the ventilation is not smooth, the concentration will gradually increase, which will endanger the health of the operator, and the safety of the operator. In case of open fire, or cause explosion. Therefore, the laboratory or production place should be equipped with an effective ventilation device to ensure the circulation of air.
    When storing, also pay attention to it. It should be placed in a cool, dry and ventilated place, away from fire and heat sources. Due to its chemical properties, or reaction with other substances, it should be stored separately from oxidants, acids, bases, etc., and should not be mixed. And the storage place should have corresponding leakage emergency treatment equipment and suitable containment materials.
    During the experimental operation, the amount should be accurate, according to the needs of the experiment, and do not be greedy for too much. The operation process should be rigorous, handle it with care, and avoid violent vibration and collision to prevent the container from being damaged and the product from leaking. If a leak unfortunately occurs, do not panic. In the case of a small amount of leakage, it can be absorbed by inert materials such as sand and vermiculite, and collected in a suitable container for proper disposal. If there is a large number of leaks, it is necessary to quickly evacuate the personnel from the leaked contaminated area to the safe area, and isolate them, and strictly restrict access. Emergency personnel should wear self-contained positive pressure breathing apparatus and anti-acid and alkali work clothes. Do not let leaks come into contact with combustible substances, rinse with plenty of water, dilute the washing water and put it into the wastewater system.
    In short, in the operation and use of methyl (E) -3-iodoacrylate, it is necessary to strictly observe safety and operating standards, so that the purpose of the experiment can be achieved, and the safety of personnel and the environment can be ensured.
    Application Area
    Nowadays, there is a chemical substance called Methyl (E) -3-Iodoacrylate, which is widely used. In the field of medicine, it can help pharmaceutical engineers develop innovative drugs to treat various diseases and save patients from pain. In the field of materials science, it can contribute to the research and development of new materials, making materials specific, whether strong or soft, or have strange electrical and thermal conductivity. In the process of organic synthesis, it is a key reagent, helping chemists build complex and delicate organic molecular structures and expanding the boundaries of organic chemistry. The application of this substance, such as the bright stars, emits light and heat in many fields, promotes the progress of science and technology, and seeks long-term benefits for human well-being.
    Research & Development
    I have always been interested in studying chemical substances. Recently, I have studied (E) -3-Iodoacrylate (Methyl (E) -3-Iodoacrylate). This substance has unique properties and has great potential in organic synthesis.
    At the beginning, I observed its structure, studied its bonding method carefully, and knew the wonder of its molecular combination. Then I explored its reaction properties, tried it with different reagents, and observed its changes. During the process, many difficulties arose, and the control of reaction conditions and the pursuit of product purity were all challenges.
    However, I did not give up, and after repeated attempts, I finally found the method. Under a specific temperature and pressure, with the help of a catalyst, the reaction effect gradually becomes apparent, and the quality and quantity of the product are considerable.
    At present, although the research on (E) -3 -Iodoacrylate methyl ester has been a small success, the road ahead is still far away. In the future, we should deepen our efforts and expand its application field, hoping to add a bright color to the field of chemistry, which will contribute to both academic and practical purposes.
    Toxicity Research
    Since modern times, chemical refinement has led to the emergence of various compounds. The toxicity of Methyl (E) -3-Iodoacrylate is of paramount importance.
    Detailed investigation of this compound, its unique structure, the combination of iodine atoms and methyl acrylate, or the toxicity is complex. In the experimental environment, all kinds of creatures were taken as samples to observe the signs after exposure to this compound. Small rodents were observed to be affected by it, with abnormal behavior and even physical discomfort.
    Examine the source of its toxicity, or because of the activity of iodine, it leads to a series of changes in organisms, disturbing the normal physiological order. Although the current research is not complete, the toxicity has begun to emerge. Subsequent efforts should be made to expand the research path, clarify the principle of poison and the degree of harm, so as to ensure the safety of all beings and the tranquility of the environment. When using this thing for the world, comprehensive strategies should be prepared to avoid disasters.
    Future Prospects
    In the field of chemical industry, methyl (E) -3 -iodoacrylate has extraordinary potential, and the future development is quite promising.
    This compound has a unique structure and specific reactivity, or it can open up a new path in organic synthesis. It can be used as a key intermediate to create new drugs, adding powerful wings to cure difficult diseases; it can also be used to develop high-end materials, making them have outstanding properties, and shine in the fields of aerospace and electronic technology.
    Although its cognition and research are still in progress, with time, in-depth exploration will surely be able to explore its potential. Our scientific researchers should be enthusiastic and diligent in their research, with a view to making methyl (E) -3-iodoacrylate contribute to the advancement of science and technology and the well-being of people's livelihood in the future, and draw a beautiful blueprint.
    Where to Buy Methyl (E)-3-Iodoacrylate in China?
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    Frequently Asked Questions

    As a leading Methyl (E)-3-Iodoacrylate 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 chemical properties of Methyl (e) -3-iodoacrylate?
    Methyl (E) -3-iodoacrylate, this is an organic chemical. It has the characteristics of an alkenyl ester and an iodine substitute. The alkenyl ester part has many reactivity due to its carbon-carbon double bond and ester group.
    Let's talk about the carbon-carbon double bond first, which can play an addition reaction. Just like olefin encounters bromine water, the double bond of methyl (E) -3-iodoacrylate can also be added to the bromine elemental substance, causing the bromine water to fade. This is a typical double bond reaction. Due to the high density of the double bond electron cloud, it is vulnerable to attack by electrophilic reagents.
    In terms of ester groups, it can be hydrolyzed. Under acidic conditions, the corresponding carboxylic acids and alcohols are gradually hydrolyzed; under alkaline conditions, the hydrolysis is more thorough and rapid, resulting in carboxylic salts and alcohols. This is the general nature of esters, because the carbonyl carbon in the ester group has a certain positive electricity, it is vulnerable to nucleophilic attack.
    Furthermore, iodine atoms, as halogen atoms, can undergo substitution reactions. Under the action of appropriate nucleophilic reagents, iodine atoms can be replaced, such as with sodium alcohols, iodine is replaced by alkoxy groups to form new organic compounds.
    In addition, due to the interaction of various parts in the structure, the overall chemical properties are complex and unique. This compound is often used as a key intermediate in the field of organic synthesis. With its diverse reactivity, it can build complex organic molecules and has important value in many fields such as medicinal chemistry and materials science.
    What are the preparation methods of Methyl (e) -3-iodoacrylate?
    The method of preparing methyl (E) -3 -iodoacrylate has been known for a long time. The method is multi-terminal, and the main one is selected.
    First, it can be prepared by the substitution reaction of acrylate and iodine reagent. Take an appropriate amount of acrylate and place it in a clean reaction vessel. The surrounding environment must be protected from strong light and moisture to prevent side reactions. Then, slowly add iodine reagent, such as iodine elemental substance combined with appropriate oxidizing agent, such as hydrogen peroxide combined with iodine. During the reaction, the temperature and reaction time need to be carefully adjusted. If the temperature is too high, the by-products will be plentiful, and if it is too low, the reaction will be slow. Usually, moderate low temperature is appropriate, such as in an ice water bath or near room temperature, depending on the specific reagent activity. During this period, stirring should be continued to fully contact the reactants and speed up the reaction process. After the reaction is completed, the product can be purified by extraction, distillation, etc., and methyl (E) -3 -iodoacrylate can be obtained.
    Second, react with an alkenyl-containing compound with an iodine source under the action of a specific catalyst. Select a compound with a suitable alkenyl structure and match it with a suitable catalyst, such as some transition metal catalysts. These two are placed in the reaction system together with the iodine source, and an appropriate amount of inert gas is introduced to create an anaerobic environment, because some catalysts are easily deactivated under aerobic conditions. Subsequently, the temperature is raised to a specific temperature, which needs to be explored through repeated experiments, depending on the activity of the catalyst and the characteristics of the reactants, or between tens of degrees Celsius and 100 degrees Celsius. During the catalytic reaction process, the progress of the reaction is closely monitored, which can be detected by means of thin-layer chromatography. After the reaction is completed, the impurities are removed through separation and purification steps, such as column chromatography, and the target product is finally obtained.
    Third, it is prepared by a multi-step reaction starting from an aldehyde or ketone. First, the aldehyde or ketone is reacted with a specific reagent to construct an intermediate containing an alkenyl structure. This process may involve a condensation reaction, etc. The intermediate is then reacted with an iodine reagent to complete the iodine substitution step. There are many steps in this way, and each step needs to strictly control the reaction conditions to ensure the purity and structure of the intermediate are correct, otherwise it will affect the yield and purity of the final product. Subsequent separation and purification operations are also required before methyl (E) - 3 - iodoacrylate can be prepared.
    Where is Methyl (e) -3-iodoacrylate used?
    Methyl (E) -3-iodoacrylate, which is used in various fields. In the field of pharmaceutical creation, it is a key material for the synthesis of delicate drug molecules. Gain iodine atoms have unique chemical activity, which can make drugs easier to combine with targets, thereby improving drug efficacy. And its acrylate structure can participate in a variety of chemical reactions, helping to build complex drug structures.
    In the place of material research and development, methyl (E) -3-iodoacrylate can also be used. It can be used for polymerization to obtain polymer materials with specific properties. For example, through specific polymerization methods, the resulting materials may have excellent optical properties, suitable for the preparation of optical materials such as optical lenses and optical fibers; or have good mechanical properties, which can be used to make high-end engineering plastics and improve the strength and toughness of materials.
    Furthermore, in the field of organic synthesis, it is an extremely important intermediate. Chemists can use it to carry out a series of reactions, such as nucleophilic substitution, addition, etc., to prepare a wide variety of organic compounds. This lays the foundation for the synthesis of new organic materials and fine chemicals, greatly enriching the variety of organic compounds and promoting the progress of organic synthesis chemistry. From this point of view, methyl (E) -3 -iodoacrylate plays an indispensable role in many fields such as medicine, materials, and organic synthesis, and has a profound impact on the development of related fields.
    What is the market outlook for Methyl (e) -3-iodoacrylate?
    Methyl (E) -3-iodoacrylate, which is a compound in the field of organic chemistry. Looking at its market prospects, it needs to be analyzed from multiple aspects.
    In the field of scientific research, there is a great demand for it in the field of organic synthesis. Because of its unique structure, it contains iodine atoms and acrylate groups, and iodine atoms are active, it can participate in a variety of chemical reactions, such as coupling reactions, and can form carbon-carbon and carbon-heteroatom bonds, providing an effective path for the synthesis of complex organic molecules. In the cutting-edge scientific research branches such as pharmaceutical chemistry and materials science, this raw material is often needed to synthesize novel structural compounds, so the market demand for scientific research is rising steadily.
    In the pharmaceutical industry, it also has potential. In drug research and development, specific structural compounds or key fragments of lead compounds. Methyl (E) -3-iodoacrylate can be chemically modified to integrate into drug molecules, giving drugs unique pharmacological activities, such as improving the ability of drugs to bind to targets and enhancing drug efficacy. Although there are not many drugs that use this as a direct component at present, it plays an important role as an intermediate in the research and development process. In the long run, with the deepening of pharmaceutical research and development, the market demand is expected to grow.
    In the field of materials, organic functional materials are developing rapidly. This compound can be polymerized and introduced into the main chain or side chain of polymer materials, giving the material special properties, such as changing the optical and electrical properties of the material. In the field of optoelectronic materials, it may be able to prepare materials with unique light response properties for use in sensors and optoelectronic devices. With the innovation of materials science and technology, the demand for them will gradually increase.
    However, its marketing activities also have challenges. The synthesis process may be more complex, and the cost restricts large-scale application. And the use of chemical substances needs to consider safety and environmental impact. With the advancement of science and technology, if the synthesis process can be optimized, the cost can be reduced, and the safety and environmental protection can be ensured, the market prospect of methyl (E) - 3 - iodoacrylate is broad, and it will play an important role in scientific research, medicine, materials and other fields, and the demand will continue to rise.
    What are the storage conditions for Methyl (e) -3-iodoacrylate?
    Methyl (E) -3-iodoacrylate is also a pure product. Its storage is essential, which is related to the preservation of quality and the safety of use, and cannot be ignored.
    This product should be stored in a cold and dry place to avoid sun exposure and heat contact. Exposure to the sun, close to hot objects, will cause the temperature to rise sharply, or the chemicity will change, damaging its pure quality. If it is wet, water vapor will easily enter, or it will cause hydrolysis to change, causing it to fail.
    And it must be far from fire, flame and heat sources. This product is flammable, and it will burn in case of fire, and even explode, which is very dangerous. And when it is stored separately from oxygen agents and strong acids and alkalis to prevent them from being triggered and dangerous.
    The receptacle must be strong and dense, and glass or plastic bottles and tanks should be selected. Seal it tightly to prevent the leakage of gas and liquid. Seal it immediately after use, and do not expose it to the gas for a long time.
    Every storage environment should be recorded in a book. The number of temperature and humidity should be recorded in detail when it is stored. Always check its equipment to see if there is any damage or leakage; observe its quality, and see that there is no change in color, taste, and state. If there is any abnormality, deal with it quickly to avoid serious trouble.
    In this way, methyl (E) -3-iodoacrylate can be stored for later use, to protect its quality and avoid its risks.