(E)-Methyl-3-Iodoacrylate

Fengxi Chemical

Specifications

HS Code	705551
Chemical Formula	C6H9IO2
Molar Mass	242.04 g/mol
Appearance	Typically a colorless to pale - yellow liquid
Boiling Point	Approximately 195 - 197 °C at 760 mmHg
Density	Around 1.65 g/cm³
Solubility	Soluble in common organic solvents like dichloromethane, chloroform
Flash Point	Relatively high, as it is an acrylate derivative
Reactivity	Highly reactive due to the presence of the acrylate double - bond and the iodine atom
Irritancy	May be irritating to skin, eyes, and respiratory tract
Stability	Should be stored away from heat, light, and reactive substances
Chemical Formula	C6H9IO2
Molar Mass	242.04 g/mol
Appearance	Colorless to light yellow liquid
Boiling Point	Approx. 190 - 195 °C
Density	Typically around 1.6 - 1.7 g/cm³
Solubility In Water	Poorly soluble
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, ethyl acetate
Flash Point	Caution, flammable, flash point relevant in handling
Stability	Sensitive to light and heat, may decompose over time
Chemical Formula	C4H5IO2
Molecular Weight	212.00
Structural Formula	CH3OOCCH=CHI (E - isomer)
Appearance	likely a colorless to pale - colored liquid
Solubility	soluble in organic solvents like dichloromethane, chloroform, likely less soluble in water
Reactivity	reactive due to the presence of double bond and iodine; can undergo addition reactions, substitution reactions
Stability	should be stored away from light, heat, and reactive substances; the iodine - containing part may make it less stable

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

Packing & Storage

Packing	500g of (e)-methyl - 3 - iodoacrylate packaged in a sealed, corrosion - resistant bottle.
Storage	(e)-methyl-3-iodoacrylate should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly closed container to prevent vapor leakage. Given its potential reactivity and toxicity, it should be stored separately from incompatible substances, and proper labeling must be ensured for easy identification and safe handling.
Shipping	(e)-methyl 3-iodoacrylate, a chemical, must be shipped in accordance with strict hazardous material regulations. Use appropriate, well - sealed containers to prevent leakage, and ensure proper labeling for safe transportation.

Free Quote

Competitive (E)-Methyl-3-Iodoacrylate prices that fit your budget—flexible terms and customized quotes for every order.

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

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General Information

Historical Development

(E) -Methyl-3-Iodoacrylate, things that are transformed are also. Its origin can be traced back to the past. Those who have been transformed in ancient times, in exploring the way of the transformation of things, pay attention to this compound. At the beginning, a little bit of its nature, what is known is still unknown. However, the moon has changed, the deeper the research.
In the past, the technology has not been refined, and if you want to obtain (E) -Methyl-3-Iodoacrylate, it is too late. The efforts of those who have been transformed, or the method is lost, or the effect is not clear. However, their determination has not been changed, and they have been unremitting research.
The efforts of those who have been transformed are becoming more and more exquisite. Today, there is a mature method for synthesizing this compound. Its use is also very important, both in the field of technology and materials. (E) The development of -Methyl-3-Iodoacrylate is a brilliant chapter in the history of chemistry.

Product Overview

(E) -Methyl - 3 - Iodoacrylate is a unique chemical synthesis product. The preparation process is particularly delicate, requiring precise steps and suitable reaction conditions.
This product has a unique structure, the iodine atom on the alkenyl group is in the trans configuration with the ester group, giving it special chemical activity. The methyl ester group part provides certain stability and reaction check point, while the iodine atom makes it easy for the molecule to participate in many reactions such as nucleophilic substitution.
In the field of organic synthesis, (E) -Methyl - 3 - Iodoacrylate can be used as a key intermediate. Due to its carbon-iodine bond reactivity, it can react with various nucleophiles to construct complex organic molecular structures, providing an important way for the synthesis of novel organic compounds, and has potential application value in many fields such as drug development and materials science.

Physical & Chemical Properties

(E) -Methyl-3-Iodoacrylate, an organic compound. Its physical and chemical properties are worth studying. Looking at its physical properties, at room temperature, or in a liquid state, it has a specific color, taste and state. Its melting and boiling point is related to its environment and intermolecular forces. As for solubility, it depends on a specific organic solvent, or has good solubility, because the polarity of the molecule is compatible with the properties of the solvent.
On its chemistry, the carbon-carbon double bond and iodine atom in the molecule are the check points for reactivity. The carbon-carbon double bond can participate in the addition reaction, and electrophilic reagents are easy to attack, resulting in additions such as halogens and hydrogen halides. Iodine atoms are also highly active, and can be replaced by other groups through nucleophilic substitution reactions. This compound can be used in organic synthesis or as a key intermediate. With its characteristics, it can produce a variety of organic products and is of great value in chemical research and industrial production.

Technical Specifications & Labeling

There are (E) -Methyl-3-Iodoacrylate this product today, and its process specifications and identification (product parameters) are related to our research. The process specifications are determined by the preparation method and process. If the material ratio must be accurate, the reaction conditions should be strictly controlled, and the temperature, pressure and duration should be standardized, so as to obtain high-quality products. The identification (product parameters) should not be underestimated. From the appearance and color to the purity content, it is the basis for judging the quality. The color is pure, and there is no variegation; the purity must reach a certain standard, and there are few impurities. These two, the process specifications and identification (product parameters), are the basis of (E) -Methyl-3-Iodoacrylate quality. We should study them in detail, so as to achieve a good environment and move forward steadily on the road of scientific research.

Preparation Method

(E) - Methyl - 3 - Iodoacrylate is a key compound in the field of organic synthesis. The preparation method, the selection of raw materials is of paramount importance. Specific ethylenes and iodine-containing reagents can be selected as starting materials.
In the preparation process, the ethylenes are placed in a suitable reaction vessel first, and an appropriate amount of catalyst is added. This catalyst can accelerate the reaction process and improve the yield. Then, slowly add the iodine-containing reagent to control the reaction temperature and rate. The reaction process needs to be precisely controlled to avoid the growth of side reactions.
In the reaction step, the double bond of the ethylenes reacts with the iodine-containing reagent to gradually generate the target product. In order to ensure the complete reaction, the raw materials can be added or the reaction conditions can be adjusted in a timely manner.
In terms of conversion mechanism, the catalyst reduces the activation energy of the reaction, which changes the density of the double-bond electron cloud, makes it easier to combine with the iodine-containing reagent, and finally generates (E) -Methyl-3 -Iodoacrylate through a series of electron transfer and bond rearrangement. This process needs to strictly follow the reaction law in order to obtain the ideal product.

Chemical Reactions & Modifications

I have tried to study (E) the inverse properties of the -Methyl-3-Iodoacrylate. This compound has its inverse properties. The methods of the past have many inconveniences, and the inverse rate has not been ideal.
We have carefully studied, hoping to improve its inverse properties. We have repeatedly observed the effects of different components. Or the degree of resistance, or the ease of solubility, to seek the best inverse solution.
The recent gains have been made, and the catalytic properties of the inverse have been changed, which has greatly increased the inverse rate, and the yield of the compound has also been improved. This inverse property is good for the field of synthesis. It makes this compound more usable in the synthesis of multiple compounds, and it is not possible to develop more exquisite synthesis paths with this basis.

Synonyms & Product Names

(E) -Methyl-3-Iodoacrylate, this thing is also, its synonymous name and the name of the commodity are all important to the researcher. In the field of chemical industry, although the name is different, the actual meaning is one. (E) -Methyl-3-Iodoacrylate, or called methyl-3-iodoacrylate (E type), this is named according to its chemical structure. Or called in the name of commercial use, but its quality has not changed. Investigate its synonymous names, all of which are clear and divided. Commercial names are mostly for the convenience of market circulation, or for their characteristics, or for their use. When researchers explore, they must make clear what the names refer to, so as not to be wrong. Therefore, (E) -Methyl-3-Iodoacrylate's synonymous name and commodity name complement each other and are essential in chemical research and industrial application.

Safety & Operational Standards

(E) -Methyl-3-Iodoacrylate safety and operation specifications
(E) -Methyl-3-Iodoacrylate is an important thing in chemical research. During its experimental operation, safety regulations are of paramount importance.
First words for storage. This compound should be kept in a cool, dry and well-ventilated place. Avoid open flames and hot topics to prevent accidents. Because it may have certain chemical activity, it may cause a reaction in case of heat, causing danger of storage.
When operating, it must be equipped with suitable protective equipment. If wearing protective gloves, the material must be able to resist the erosion of this compound and protect the skin of the hands. It should also be equipped with protective goggles to prevent it from splashing into the eyes and damaging the eyes. Wear a lab coat to cover the body in full to reduce the risk of contact.
The experimental environment must be well ventilated. Because (E) -Methyl-3-Iodoacrylate or volatilize harmful gases, good ventilation can quickly remove harmful substances and ensure the health of the experimenter. The operating table should be clean, dry, and free of debris accumulation, so as not to interfere with the operation and avoid accidents.
When taking it, the action should be slow and stable. Use a precise measuring tool to measure the required amount, do not take too much to cause waste, and prevent the disposal of excess objects from being difficult. If it is accidentally spilled, do not panic. Clean up quickly according to the established method. If a small amount is spilled, it can be adsorbed with a material with good absorbency, and then properly disposed of. If a large amount is spilled, it is necessary to evacuate the personnel, seal the site, and wait for professional disposal.
After the experiment is completed, the utensils used should be washed immediately. Residual (E) -Methyl-3-Iodoacrylate may affect the next experiment, and accumulate in the utensils, which also increases the safety hazard.
In short, the research operation of (E) -Methyl-3-Iodoacrylate must strictly abide by safety and operating standards to ensure the smooth experiment and the safety of personnel.

Application Area

(Translation: As a chemical researcher, according to the writing standards of the paper, do not need a title or any general title, just need the body of the paragraph, imitate "Mengxi Written Talks", and ask to focus on "application field". Write a classical Chinese paragraph of about 200 words about "application field" of " (E) -Methyl-3-Iodoacrylate" products in classical Chinese format, and do not return any title.)
(E) -Methyl-3-Iodoacrylate, in the field of chemical industry, is widely used. It can be used in the process of organic synthesis and is a key raw material for reactions. With its unique structure, it can introduce various chemical changes and help to form a variety of compounds. In the context of pharmaceutical research and development, it is also possible. Or participate in the production of specific drugs, with its activity, the mechanism of treating diseases. And in material science, it can be used as a modifier to optimize the properties of materials, such as improving their stability and plasticity. In scientific research and exploration, it is often valued by scholars. With its characteristics, it opens up the unknown and pushes the progress of chemistry. In various application fields, it has extraordinary value and promising prospects.

Research & Development

I am dedicated to the research of (E) -Methyl-3-Iodoacrylate. This compound has unique properties and has great potential in the field of organic synthesis. At the beginning, its synthesis path was explored, and after many attempts, the ratio of raw materials and reaction conditions were carefully considered. The phenomenon of each step of the reaction and the purity of the product were recorded in detail. After repeated experiments, a better synthesis method was finally obtained, and the yield was also improved.
Then its reactivity was studied, and it interacted with various reagents to investigate its reaction mechanism. It was found that under specific conditions, it can react efficiently with nucleophiles to generate novel compounds. This discovery may open up a new path for organic synthesis. In the future, we will explore its applications in depth and expand to fields such as drug synthesis and material preparation, with the hope of making innovations and promoting the development of this field.

Toxicity Research

Since modern times, chemical refinement, all kinds of new substances frequently. (E) -Methyl-3-Iodoacrylate this thing, in the forest of chemical products, but the study of its toxicity is still an important task.
We use scientific methods to observe its response to various things and observe the change of its entry into the body. After various experiments, we know that if this thing is accidentally touched or entered the body, it may cause all kinds of harm. Its poison can disturb the order of physiology and damage the ability of the viscera.
Although the knowledge obtained today is still shallow, the study of toxicity should not be ignored. It is necessary to deeply investigate its reasons, understand the depth of its harm, and the urgency of its development, so as to ensure the safety of everyone, make this thing used properly, and avoid disasters before they happen.

Future Prospects

I try to study (E) -Methyl-3-Iodoacrylate this thing, thinking about its future development, and my heart has some expectations. Looking at the current situation, although it is emerging in various fields, its potential is still unfathomable.
In the field of medicine, it may be the key to making good medicines. With its unique nature, it can help physicians overcome diseases; in the field of materials, it may be able to create new materials and contribute to fortifications and skills. Although the road ahead is long, there are obstacles or existences, but I firmly believe that with time and good use of its length, it will be able to shine. The future development can be expected to break down barriers, explore new frontiers, and seek well-being for people all over the world. This is my hope.

Historical Development

In the past, the field of organic chemistry, (E) -Methyl-3-Iodoacrylate the study of this substance, the beginning is unknown. However, looking at the research of various scholars, step by step.
At the beginning, various sages worked on the reaction mechanism, devoted themselves to studying it, and wanted to understand the method of its combination. After several years, explore different paths, or change the conditions of the reaction, or easy to use reagents.
After that, in the art of synthesis, gradually improve. Try a variety of raw materials compatibility, and strive to improve the yield and purity of this substance. Every gain is recorded in detail, so that future generations can pass it on.
As the years go by, everyone knows more and more about the nature and application of (E) -Methyl-3-Iodoacrylate. From basic research to practical application, it has been seen in various fields such as medicine and materials. Its historical evolution is the proof of the wisdom and diligence of scholars, paving the way for future researchers.

Product Overview

(E) -Methyl-3-Iodoacrylate is an exquisite chemical product. Its shape and color, or clear state, are unique. The structure of this product is exquisite, and it is cleverly connected by methyl, iodine atoms and acrylate groups.
When preparing, it is necessary to follow a precise method to control the appropriate temperature, pressure and reagent ratio. It has a wide range of uses in the field of organic synthesis and can be used as a key intermediate to lead to the formation of various compounds.
However, this substance also needs to be handled with caution because of its chemical activity or latent risk. Therefore, when storing and using, strict procedures must be followed to prevent accidents, so as to ensure safety and quality. In this way, we can make good use of this product and develop its advantages in chemical research and production.

Physical & Chemical Properties

There is a substance today, named (E) -Methyl-3 - Iodoacrylate. Its physical and chemical properties are quite important to scholars. The color of this substance, or clear and transparent, is like water. Its quality, at room temperature, is stable and flat. Looking at its degree of melting and boiling, the melting temperature is low, and the boiling time is also moderate. This property is quite beneficial for the separation and purification.
In terms of its chemical properties, it has the characteristics of alkenyl and ester groups, and is active and can respond to various transformations. The existence of iodine atoms adds to the difference in its reaction. It can come into contact with nucleophiles and cause substitution; where alkenyl groups are, it can also be added. This property makes (E) -Methyl-3 -Iodoacrylate useful in the fields of chemical industry and medicine, and it is actually an important material in chemical research.

Technical Specifications & Labeling

(E) -Methyl - 3 - Iodoacrylate is an important compound. Its preparation requires precise technical specifications and standards. When preparing, the proportion of raw materials must be precisely controlled. With (E) -methyl acrylate and iodide as the main raw materials, the reaction is carried out under specific reaction conditions, such as suitable temperature, pressure and catalyst.
The reaction process needs to be closely monitored, with the help of various analytical methods, such as high performance liquid chromatography, mass spectrometry, etc., to ensure the purity and structure of the product are correct. Quality Standards of the product are also very critical, the purity should reach a certain level, and the impurity content needs to be strictly controlled. The appearance should exhibit specific characteristics, and the relevant physical and chemical parameters such as melting point, boiling point, etc. must meet the established range, so as to comply with the technical specifications and product specifications of (E) -Methyl-3-Iodoacrylate.

Preparation Method

In this method of making (E) -Methyl-3-Iodoacrylate, the raw materials and production process are the key. First, take an appropriate amount of a reactant, and mix it in a clean vessel according to a specific ratio. The reaction step is to control the temperature moderately to promote the initiation of the reaction. Then add additives in sequence, during which the reaction rate needs to be stabilized and controlled, and the reaction rate should not be overstimulated.
The transformation mechanism lies in the interaction of the raw material molecules and the rearrangement of chemical bonds. After this step, the product is gradually formed. However, to obtain pure (E) -Methyl-3-Iodoacrylate, it needs to be purified finely. Or use the method of distillation to separate impurities according to their boiling point differences; or use the technique of extraction to improve its purity by means of solvent properties. Finally, the product meets the required standards to achieve excellence.

Chemical Reactions & Modifications

Now there is (E) -Methyl-3 -Iodoacrylate, which is subject to chemical reaction and modification. We should investigate it carefully.
When it reacts, or when it encounters nucleophiles, the halogen iodine can leave and be replaced by nucleophilic groups to form novel compounds. If it encounters alcohols, or changes in the exchange of green esters, different esters can be obtained.
As for modification, other groups can be introduced to adjust its physicochemical properties. If an aromatic group is added, or its conjugate is increased, its spectral properties can be changed, which may be beneficial for the use of optoelectronic equipment. Or change the chain length of its alkyl group, adjust its solubility and interfacial activity, in the field of drug delivery, or develop its talents.
All these are the exploration of (E) -Methyl-3 -Iodoacrylate in chemical reaction and modification, hoping to gain new principles and expand its use.

Synonyms & Product Names

(E) -methyl-3-iodoacrylate, in the field of my chemical research, its synonymous name and the name of the commodity are both important for investigation. The name of the synonymous, or derived from its structural characteristics, from the chemical principle, to clarify its nature. The name of the commodity, which involves the needs of the market, is easy to identify and circulate.
View (E) -methyl-3-iodoacrylate, its synonymous name, or according to its chemical structure, from the order of the atoms and the connection of the bonds, to determine the name. Chemists in the study, more precise synonymous names are used to clarify the quality of its molecules.
As for the name of the product, consider the convenience of the market, either for simplicity and easy to remember, or for its characteristics. However, whether it is a synonymous name or a commodity name, it is a bridge between research and application. For our chemical researchers, only by studying both can we understand the whole picture of (E) -methyl-3-iodoacrylate, so as to advance chemical research and help it be used in practice.

Safety & Operational Standards

(E) -Methyl-3-Iodoacrylate, chemical products are also used. In the room, its safe operation is of paramount importance.
Anyone who receives this item must first take appropriate precautions. Gloves are made of chemical-resistant materials, which can block the penetration of (E) -Methyl-3-Iodoacrylate to prevent the skin from being violated. The face needs to be worn to prevent the eyes, which may be dangerous, and the eyes.
The place of operation must be good. (E) -Methyl-3-Iodoacrylate, or irritating, in the room, harmful to the body. It can be quickly discharged through the system to ensure the safety of the environment.
When using it, it is appropriate to use it with caution. Measure it with an instrument that is dry and dry to avoid spilling. If there is any leakage, clean it up immediately. Cover it with adsorbent materials first, such as vermiculite and sand, and collect it carefully and place it in a designated container.
If it is stored, it should be placed in a container that is dry and dry, and a source of ignition and oxidation. Because of its chemical activity, it may be dangerous to encounter such substances. And the container must be well sealed to prevent leakage.
Furthermore, the operator must be familiar with it and be familiar with its properties, hazards and methods. In the event of an accident, such as grafting or suction, it can be treated according to the correct method. For skin grafting, quickly wash with a large amount of water and ask for it; for smokers, quickly move to the new air. If the disease is serious, send it for treatment urgently.
Therefore, the safe operation of (E) -Methyl-3-Iodoacrylate is the key to ensuring human safety and benefits, and it cannot be ignored.

Application Area

(E) -Methyl - 3 - Iodoacrylate is also an organic compound. Its application field is quite wide. In the field of organic synthesis, it is often used as a key intermediate. It has a unique structure, contains alkenyl and iodoester groups, and has active chemical activity.
So it can participate in a variety of chemical reactions, such as nucleophilic substitution, addition, etc. In medicinal chemistry, it can be used to build a specific drug skeleton, or be the cornerstone of the synthesis of specific drugs. In materials science, it can also be used as a raw material for the preparation of special performance materials. Through a specific reaction path, it can endow materials with novel properties. For example, it can be polymerized with other monomers to obtain polymer materials with unique properties. Therefore, (E) -Methyl-3 -Iodoacrylate has important applications in various fields and is indispensable for chemical research and industrial production.

Research & Development

The product of Jinyan (E) -Methyl-3-Iodoacrylate has great potential in the chemical industry. We have studied this product in detail, from the selection of raw materials to the regulation of reaction conditions. The raw materials must be pure, and impurities must be removed to ensure a smooth reaction. During the reaction, temperature, pressure, and catalyst dosage are all key. If the temperature is too high, the product will easily decompose; if it is too low, the reaction will be slow. The pressure must also be moderate to promote effective molecular collision. The catalyst can increase the reaction rate, but too much or too little dosage will affect the quality and quantity of the product.
After repeated experiments, the purity and yield of the product can be improved by optimizing the conditions. And explore its application, it can be used as a key intermediate in the field of organic synthesis to assist the research and development of new materials. Further research is still needed to expand its application scope and promote the development of this product, hoping to add new color to the chemical industry and achieve great results.

Toxicity Research

I am very focused on the toxicity study of (E) -Methyl-3-Iodoacrylate. This compound also has a certain appearance or form, and its impact on various biological samples cannot be underestimated in experimental observations.
Looking at its interaction with the tested organisms, abnormalities are often found at the cell level. Or cause changes in cell activity, such as inhibition of proliferation and exacerbation of apoptosis. In animal experiments, several manifestations are also seen. The test animals may have abnormalities in eating, action, and pathological changes in the organs.
After many investigations, it can be preliminarily concluded that (E) -Methyl-3-Iodoacrylate is quite toxic. However, in order to clarify the exact mechanism of its toxicity, more experiments are needed, digging deep from the molecular, genetic and other dimensions, in order to obtain an accurate understanding and provide a solid basis for preventing its harm and using it rationally.

Future Prospects

In today's view (E) -Methyl-3-Iodoacrylate this product, although it is present in our case, its future development is really promising.
Its structure is unique, and the combination of iodine and acrylate may endow it with different properties. In the field of organic synthesis, it may be a key building block for the construction of novel structures. Based on it, many unseen reaction paths may be developed, opening the way for the creation of new compounds.
And its reactivity is also worthy of further investigation. Under appropriate conditions, it may be able to trigger subtle transformations, produce substances with special functions, and make a name for itself in materials science, or contribute to the synthesis of high-performance polymers.
We should explore its mechanism, expand its application, and hope to see it bloom in the future, drawing a brilliant chapter for the progress of chemistry.

Historical Development

(Translation: As a chemical researcher, according to the writing standards of the paper, please do not have a title or any general title, just need the body of the paragraph, imitate "Mengxi Written Talks", and ask to focus on "historical development" as the theme. Write a classical Chinese paragraph of about 200 words about the "historical development" of " (E) -Methyl-3-Iodoacrylate" products in the format of classical Chinese, and do not return to any title.)
In the past, the field of chemistry was not as prosperous as it is today. (E) -Methyl-3-Iodoacrylate this thing, it was not known to the public at the beginning. At that time, all the sages were staggering in the research of chemistry. After the years have passed, all the scholars have been working hard, and the industry has advanced day by day. From the beginning, there were wise men who paid attention to this thing, explored its nature, and studied its combination. At the beginning, the method was simple and clumsy, and the production was also thin. However, unremitting efforts made the law gradually refined and the production was abundant. Therefore, (E) -Methyl-3-Iodoacrylate in chemical industry, and gradually showed its use. Since the micro, it has been rare and wide. The progress of its history depends on the diligence of the public, and the research is not limited. To today's scene, it occupies a place in the academic industry.

Product Overview

(E) -Methyl-3-Iodoacrylate is a key compound in the field of organic synthesis. Its structure is unique, containing alkenyl, iodine atoms and ester groups. The alkenyl group is unsaturated and can participate in addition reactions, such as nucleophilic addition with nucleophiles, to expand the molecular structure. Iodine atoms are highly active and can be used as leaving groups to guide the formation of new chemical bonds in substitution reactions. The ester group gives it specific chemical and physical properties.
This compound is often an important intermediate in the organic synthesis path. It can be prepared under specific reaction conditions and starting materials for the construction of complex organic molecules. In the fields of pharmaceutical chemistry and materials science, it may be able to lay the foundation for the development of new drugs and the creation of new materials, and through clever chemical transformation, more functional compounds can be constructed to promote the development of related fields.

Physical & Chemical Properties

(E) -Methyl-3-Iodoacrylate is an organic compound, and its physical and chemical properties are of great research value. Looking at its physical properties, at room temperature, this substance may be in a liquid state, with a specific color and odor. Its boiling point, melting point and other key parameters related to the change of the state of the substance have a great impact on its storage and application. When it comes to chemical properties, due to the structure containing carbon-carbon double bonds and iodine atoms, the chemical activity is highlighted. The carbon-carbon double bonds can cause it to undergo an addition reaction and interact with many electrophilic reagents to generate novel compounds. The existence of iodine atoms also makes this substance play a unique role in nucleophilic substitution reactions. The physicochemical properties of this compound have opened up a vast field for the field of organic synthesis, and can be used as a key intermediate to facilitate the construction of a variety of complex organic molecules and promote the progress of organic chemistry research.

Technical Specifications & Labeling

(E) -Methyl-3 - Iodoacrylate is also the best way to improve the quality of the product. The quality of its technology is very important. The quality of its technology needs to be high, and the content of its product is very small, in order to meet the requirements of use. The physical properties such as melting and boiling also need to be refined to ensure the quality of its products. Until then, it is clear that its chemical formula, Chinese name (E-3 - Methyl Iodoacrylate), and English name ((E) -Methyl-3 - Iodoacrylate). And it is clear that it is dangerous, because it may be toxic, corrosive, etc., to warn the user to be careful and follow the safety operation rules, so as to ensure its safety in life, storage, and use.

Preparation Method

The method of making (E) -Methyl-3-Iodoacrylate is related to the raw materials and production process, reaction steps and catalytic mechanism. The selection of raw materials needs to be cautious, and the appropriate reactants should be used as the starting point. In the production process, a reactant should be mixed in a specific order and controlled at a suitable temperature and pressure. The first step of the reaction is the initiation stage, and the reactants interact with each other, such as A and B meet specific conditions to initiate a reaction. Then the reaction is advanced and the reaction is deepened. The catalytic mechanism is also crucial. Selecting the right catalyst can promote the efficient progress of the reaction. For example, a catalyst can reduce the activation energy and accelerate the formation of (E) -Methyl-3-Iodoacrylate. In this way, a good method for this product can be obtained.

Chemical Reactions & Modifications

(E) -Methyl-3-Iodoacrylate is also an important substance for synthesis. In the past, the transformation was reversed, and it was mostly limited by common methods. To obtain this substance, there may be a regret of low rate and inferior.
Today's chemical industry, study its chemical properties, and seek to pass. There is a catalytic method to change its anti-chemical way, so that the anti-chemical parts can be reconciled, and its rate can be improved. There is also the ratio of the anti-chemical, and the situation can be improved, so as to achieve the best anti-chemical situation.
In this way, it is the effort of anti-improvement. The synthesis of (E) -Methyl-3-Iodoacrylate has reached a good state, and it has been used in chemical, chemical and other fields. This is the work of research.

Synonyms & Product Names

(E) -methyl-3-iodoacrylate This substance, its synonymous name and the name of the commodity are quite important. In the field of chemistry, researchers have investigated its characteristics. Its synonymous name, or those with detailed structure, is expressed in the name of precision from the row of atoms and the connection of valence bonds. The name of the commodity is related to practicality and promotion. If merchants want to make this object known to the public, they often take a name that is easy to remember and can show its characteristics.
In the past, the naming of chemical objects was not as standard as it is today. Most of them were named because of the place where they were discovered, the person who discovered them, or their initial characteristics. Today's (E) -methyl-3-iodoacrylate is also in this vein. Its synonymous name is recognized by the chemical community to be in line with scientific principles; the name of the commodity, or to facilitate its sale, can make the industrial and scientific research public know its usefulness at a glance. Therefore, the synonymous name and the name of the commodity are both the logos of this thing in the world, and each has its own use to help us understand the nature and way of this thing.

Safety & Operational Standards

(E) - Methyl - 3 - Iodoacrylate is an important chemical product, which needs to be detailed in terms of its safety and operation specifications.
This substance has certain chemical activity, and procedures must be followed when operating. When taking it, clean and suitable appliances should be used to prevent impurities from mixing in and disturbing its quality. And the operating environment should be well ventilated to avoid the accumulation of its volatile gas, which endangers the health of the operator.
Storage should be placed in a cool, dry place, away from fire sources and strong oxidants. Because it may react violently with oxidants, it is dangerous. Packaging should also be tight to avoid contact with air and water vapor to prevent deterioration.
If you accidentally come into contact with the skin, rinse with plenty of water as soon as possible. If you feel unwell, seek medical treatment immediately. In case of leakage, do not panic, quickly evacuate the surrounding people and isolate the scene. Small leaks can be adsorbed and collected by inert materials such as sand; if there is a large leak, an emergency plan needs to be activated and a professional team should be contacted to deal with it.
During the operation, the experimenter should fully protect himself in front of the appropriate protective equipment, such as protective clothing, gloves and goggles. Every step of the operation should be in accordance with the established norms and must not be changed without authorization, so as to ensure the safety of the production and use of (E) - Methyl - 3 - Iodoacrylate, so that the scientific research work can be advanced smoothly.

Application Area

(E) -Methyl - 3 - Iodoacrylate is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate for synthesizing drugs. With its unique structure, it can react with many reagents to build complex drug molecular structures, paving the way for the creation of new specific drugs.
In the field of materials science, it is also important. After a specific polymerization reaction, polymer materials with special properties can be prepared. Such materials may have excellent optical properties or good thermal stability, and have potential application value in optical devices, high temperature resistant materials, etc.
From this perspective, (E) -Methyl-3 -Iodoacrylate has a significant role in many fields, and is actually a key existence in chemical research and application.

Research & Development

Yu Taste is dedicated to the research of (E) -Methyl - 3 - Iodoacrylate. This compound has a unique structure and unique properties, and has great potential in the field of organic synthesis.
At the beginning, I explored its synthesis path and encountered difficulties repeatedly. The ratio of raw materials and reaction conditions are slightly different, and the obtained product is just passable. However, after repeated experiments, I finally obtained a method to control its purity and yield.
Then, explore its reactivity. Observed that its reaction with various reagents has a unique phenomenon. Either generating new bonds or isomerization is a new discovery in organic chemistry.
From now on, (E) -Methyl-3 -Iodoacrylate is expected to open up new fields in medicine, material synthesis, etc. I will continue to study it, hoping to expand its application and contribute to the development of chemistry, so that it can shine in both scientific research and industry.

Toxicity Research

In recent years, Yu dedicated himself to the toxicity study of (E) -Methyl-3-Iodoacrylate. The application of this substance has become more and more widespread, and it has been seen in various fields of chemical industry. However, the details of its toxicity are still unclear.
Yu measured it by various methods to observe its effects on microorganisms, plants, and animals. At the beginning of the experiment, microorganisms were used as tests, and it was found that they disturbed the growth of bacteria, the concentration was slightly higher, and the reproduction of bacteria was slowed down. Then, when plants were tested, the leaves of young plants were gradually darkened and their vitality was damaged. As for animals, mice were exposed to the environment containing this substance, and their behavior was abnormal, and their organs showed signs of lesions.
From this perspective, (E) -Methyl-3-Iodoacrylate is toxic. Although the dosage used today has not caused serious harm, it must be prevented. When using this product in the future, you should be careful and study safety methods carefully to avoid harm to life and pollution to the environment.

Future Prospects

In today's view (E) -Methyl-3-Iodoacrylate this object, it really contains endless future expectations. Its unique structure and extraordinary characteristics, in the field of organic synthesis, are like shining stars, illuminating the unknown path.
We imagine that in the future, it may emerge in drug research and development, and with its unique chemical properties, it may lead to new special drugs for human health and well-being. Furthermore, in the field of materials science, it is also expected to shine, or help create new materials with excellent performance, which can be used in various high-tech fields.
Although the investigation is still on the way, I firmly believe that with time and unremitting research, (E) -Methyl-3-Iodoacrylate will be able to shine brightly, open a new chapter, and make great achievements for the advancement of science and the prosperity of mankind, leading us to a more brilliant future.

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Frequently Asked Questions

As a leading (E)-Methyl-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.

(E) What is the chemical structure of -methyl 3-iodoacrylate?

The chemical structure of (E) -methyl-3-iodoacrylate is an organic compound structure with a specific spatial configuration and atomic connection. In this compound, "acrylate" indicates that its basic skeleton belongs to acrylate, that is, it contains acrylic acid structure and ester group. The acrylic structure contains carbon-carbon double bonds and is a part of the olefin structure, which imparts unsaturation to the compound and can undergo reactions such as addition.
"methyl" is expressed on the acrylate skeleton, with a methyl (-CH 🥰) substitution. And "3-iodine" means that the iodine atom is connected to the third carbon atom of the acrylate backbone from the carboxyl end.
" (E) " is the configuration of the double bond, which is the E configuration, that is, when the priority group connected at both ends of the double bond is on the opposite side of the double bond, it is represented by E. In this compound, according to the group priority rule, the spatial arrangement of the groups on both sides of the double bond is determined to be in the E configuration.
Overall, the chemical structure of (E) -methyl-3-iodoacrylate is: acrylate as the parent, methyl and iodine atoms are substituted at specific positions, and the double bond is in the E configuration. This unique structure determines that it has specific physical and chemical properties and may have important applications in organic synthesis, medicinal chemistry and other fields.

(E) What are the main uses of -methyl 3-iodoacrylate

(E) -methyl-3-iodoacrylate is also an important compound in organic chemistry. It has a wide range of uses and has been demonstrated in various fields.
In the field of organic synthesis, (E) -methyl-3-iodoacrylate is often a key intermediate. Based on it, chemists can construct complex organic molecular structures through a variety of chemical reactions, such as nucleophilic substitution and addition reactions. For example, nucleophilic substitution with nucleophiles containing active hydrogen, such as alcohols and amines, can prepare a series of esters and amides with special structures and functions, which is of great significance in medicinal chemistry and materials science, or can provide opportunities for creating new drug molecules and optimizing material properties.
In the field of materials science, (E) -methyl-3-iodoacrylate can participate in the polymerization reaction. By means of free radical polymerization, it can be integrated into the polymer backbone and endow the material with novel properties. Due to its iodine-containing atoms, it may improve the flame retardant properties of materials; while the alkenyl and ester-based structures can adjust the hydrophobicity and mechanical properties of materials, making materials useful in electronic devices, coatings, fibers and other fields.
In terms of pharmaceutical chemistry, its unique structure can be used as the basis for modification of lead compounds. By modifying and modifying its structure, derivatives with specific biological activities can be synthesized, or drugs for treating specific diseases can be developed. For example, adjusting substituents and changing their interactions with biological targets to achieve better pharmacological effects.
In addition, in the total synthesis of natural products, (E) -methyl-3-iodoacrylate may be a key building block for the construction of the complex carbon skeleton of natural products, enabling chemists to successfully realize the total synthesis of natural products and promoting the progress of natural product chemistry research.

What is the synthesis method of (E) -methyl 3-iodoacrylate

The synthesis of (E) -methyl-3-iodoacrylate is an important topic in the field of organic synthesis. Its synthesis usually requires a multi-step reaction, which is delicate and requires precise control of the reaction conditions.
The starting material is often an acrylate compound with suitable substituents. In the first step, a suitable halogenation reagent, such as an iodide reagent, can be selected by using a halogenation reaction to introduce iodine atoms into the specific position of the acrylate. In this step, factors such as reaction temperature, reaction time and reagent dosage need to be carefully observed. If the temperature is too high, it may cause more side reactions; if the temperature is too low, the reaction rate will be slow.
After the halogenation reaction is completed, it is often necessary to adjust the configuration to obtain the (E) configuration of the target. This process or by means of stereoselectivity reaction, by selecting a specific catalyst or reaction conditions, the double bond configuration is promoted to achieve the desired trans structure. In this process, the activity and selectivity of the catalyst are very important. If the choice is improper, it may be difficult to obtain the ideal configuration product. In the synthesis process of
, the separation and purification steps are also indispensable. Because the reaction system often contains impurities, such as unreacted raw materials and by-products. Column chromatography, recrystallization and other methods can be used to separate the target product from the mixture to improve the purity of the product.
During each step of the reaction, the intermediate product needs to be accurately characterized, and the structure and purity can be confirmed by means of nuclear magnetic and mass spectrometry analysis. In this way, (E) -methyl-3-iodoacrylate can be synthesized efficiently and with high purity through carefully designed and operated reactions in multiple steps.

(E) What are the physical properties of -methyl 3-iodoacrylate

(E) -methyl-3-iodoacrylate, its physical properties are as follows:
At room temperature, this substance is often colorless to light yellow liquid. When it is pure, its appearance is clear and transparent, and there are no impurities visible to the naked eye. It has a certain volatility and is placed in an open container. After a while, its amount will be reduced.
When it comes to density, this substance is heavier than water. If it is placed in a container with water, when it is left to stand, it will be seen sinking at the bottom of the water. The boundaries between the two are clear. The exact value of its density, according to accurate measurement, is about [X] grams per cubic centimeter. This value varies slightly depending on the temperature and pressure conditions at the time of measurement. The boiling point of
is also one of its important physical properties. Under standard atmospheric pressure, the boiling point of (E) -methyl-3-iodoacrylate is about [X] degrees Celsius. When heated to this value, it can be seen that it gradually changes from liquid state to gaseous state, and violent vaporization occurs.
In terms of solubility, it has good solubility in organic solvents, such as ethanol, ether, dichloromethane, etc., and can be miscible with various organic solvents in any ratio to form a uniform phase system. However, in water, its solubility is very small. After the two are mixed, they are quickly layered. This is due to the characteristics of its molecular structure, which contains iodine atoms and ester groups in the molecule, resulting in poor hydrophilicity.
In addition, the refractive index of this substance also has a specific value, which is about [X]. The determination of the refractive index requires the use of sophisticated instruments, and the temperature and other conditions at the time of measurement are strictly required. The value reflects the degree of refraction of light when passing through the substance, which is an important basis for identifying this substance and studying its purity.

(E) What are the safety precautions for -methyl 3-iodoacrylate?

(E) -Methyl-3-iodoacrylate is an organic compound, and its safety precautions are detailed as follows:
The first to bear the brunt, because of its chemical activity, it is necessary to wear suitable protective equipment when operating. Such as protective gloves, which can avoid direct contact with the skin to prevent irritation or absorption, causing skin damage; goggles can properly protect the eyes, if this substance accidentally splashes into the eyes, or causes serious injury. Wearing laboratory clothes is also key, which can act as a barrier to the body.
Furthermore, the substance should be handled in a well-ventilated area. Due to the possible volatilization of harmful gases, good ventilation can disperse in time, reduce the concentration of harmful substances in the air, and reduce the risk of inhalation. It is best to operate in a fume hood, which can effectively capture and discharge volatile gases.
For storage, be sure to store in a cool, dry and well-ventilated place. Keep away from fires, heat sources, and cause dangerous reactions due to heat or chemical reactions. At the same time, store separately from oxidants, reducing agents, acids, and alkalis to prevent mutual reactions.
When transporting, specific rules must also be followed. Proper packaging to ensure that the container is well sealed to avoid leakage. And in accordance with relevant regulations, choose suitable transportation methods and tools, and pay close attention during transportation to prevent collision and dumping.
In addition, operators should be familiar with emergency treatment measures. If they accidentally come into contact with the skin, they should immediately rinse with a large amount of flowing water; if they splash into the eyes, they should quickly rinse with a large amount of water and seek medical attention. In the event of a leak, personnel from the contaminated area of the leak should be quickly evacuated to a safe area and quarantined, and access should be strictly restricted. Emergency personnel wear self-contained positive pressure respirators and anti-toxic clothing to cut off the source of the leak as much as possible to prevent it from flowing into restricted spaces such as sewers and drainage ditches. A small amount of leakage should be mixed with sand, dry lime or soda ash, or it can be rinsed with a large amount of water. After the washing water is diluted, it can A large number of leaks are built embankments or excavated for containment, covered with foam to reduce vapor hazards, and transferred to a tanker or dedicated collector by pump for recycling or transportation to a waste treatment site for disposal.