Ethyl 2-Iodobenzoate

Fengxi Chemical

Specifications

HS Code	203139
Chemical Formula	C9H9IO2
Molecular Weight	262.07
Appearance	Typically a liquid
Boiling Point	Approximately 283 - 285 °C
Melting Point	N/A (usually liquid at room temperature)
Density	Around 1.68 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Flash Point	Approximately 125 °C
Odor	Characteristic odor
Hazard Class	Irritant, harmful if swallowed, inhaled or in contact with skin
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Colorless to light yellow liquid
Boiling Point	Around 260 - 262 °C
Density	Typically around 1.69 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Odor	Characteristic, somewhat pungent
Stability	Stable under normal conditions, but light - sensitive
Chemical Formula	C9H9IO2
Molecular Weight	262.07
Appearance	Liquid (usually)
Boiling Point	Around 260 - 265 °C
Density	Typically around 1.7 - 1.8 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Flash Point	Caution - flammable, flash point data varies but in flammable range
Odor	Characteristic, likely pungent

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

Packing & Storage

Packing	100g of Ethyl 2 - iodobenzoate packaged in a sealed, chemical - resistant glass bottle.
Storage	Ethyl 2 - iodobenzoate should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. It should be kept in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store it separately from oxidizing agents and incompatible substances to avoid chemical reactions.
Shipping	Ethyl 2 - iodobenzoate is shipped in well - sealed, corrosion - resistant containers. Shipment adheres to strict chemical transport regulations, ensuring proper handling to prevent leakage and maintain product integrity during transit.

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General Information

Historical Development

Ethyl 2-Iodobenzoate is an organic compound. At the beginning of its birth, chemists studied and searched hard, and in the laboratory, after many attempts, they made it appear with exquisite methods. At that time, the technology was not as developed as it is today, and the preparation was difficult, and very little was obtained.
With the passage of time, science and technology have advanced, and the preparation methods have become more and more sophisticated. Researchers continue to explore and improve their skills, so that the output of Ethyl 2-Iodobenzoate has increased and the quality is also excellent. In the past, the preparation required cumbersome steps and took a long time, but now the process is simplified and the efficiency is improved.
This compound is increasingly important in the field of organic synthesis. Or as an intermediate, it participates in various reactions and assists in the synthesis of other substances. Its historical evolution has witnessed the development of chemistry, from its initial difficult exploration to its increasing application today, which is indeed the achievement of scientific and technological progress.

Product Overview

Ethyl 2 - Iodobenzoate is an important compound in organic synthesis. It is a colorless to light yellow liquid with a special odor. In the molecular structure, the benzene ring ortho-position of ethyl benzoate is replaced by iodine atoms.
Its preparation is often made of ethyl benzoate, and iodine atoms are introduced through halogenation reaction. The reaction conditions need to be strictly controlled, and the temperature and the proportion of reagents affect the yield.
This compound has a wide range of uses in the field of medicinal chemistry and can be used as an intermediate to participate in the synthesis of various drugs. In materials science, it may also be a key component in the preparation of special functional materials. Its unique chemical properties are derived from the synergistic action of benzene ring, ester group and iodine atom, which makes it have specific reactivity and physical properties, and has potential application value in many fields.

Physical & Chemical Properties

Ethyl 2-Iodobenzoate is an organic compound with unique physical and chemical properties. Its appearance is colorless to light yellow liquid, which is one of its physical properties.
When it comes to chemical properties, the iodine atom in this compound is quite active. Due to the difference in electronegativity of iodine atoms, it is easy to participate in nucleophilic substitution reactions. In case of nucleophilic reagents, iodine atoms are easily replaced to form new derivatives. Under alkaline conditions, hydrolysis can occur, and ester groups are broken to form 2-iodobenzoic acid and ethanol.
In terms of physical properties, Ethyl 2-Iodobenzoate has a density greater than that of water and is insoluble in water, but soluble in common organic solvents such as ethanol and ether. Its boiling point and melting point are also specific values. The boiling point causes the compound to change from liquid to gaseous state at the corresponding temperature, and the melting point determines the transition temperature between solid and liquid states, which are all important physical properties.

Technical Specifications & Labeling

"Technical Specification and Labeling of Ethyl 2-Iodobenzoate (Commodity Parameters) "
Ethyl 2-Iodobenzoate is a chemical product I have studied. Its technical specification is the key. The synthesis method requires precise steps to fuse all raw materials according to a specific ratio. The temperature and time of the reaction should be carefully controlled. If the temperature is controlled within a certain range, the reaction can be guaranteed to be smooth and a pure product can be obtained.
In terms of labeling, the product parameters must be clear. On the packaging, the chemical name Ethyl 2-Iodobenzoate should be written in detail, and the molecular formula and molecular weight should be marked. The number of purity cannot be ignored, which is essential for measuring quality. In addition, there are storage methods, dangerous signs, etc., which should be detailed in accordance with regulations, so that users can see at a glance and operate correctly to ensure safety and quality.

Preparation Method

To prepare Ethyl 2-Iodobenzoate, the raw materials, production process, reaction steps and catalytic mechanism are as follows. First, ethyl benzoate is taken as the raw material, supplemented by an appropriate amount of iodizing reagent, which is the foundation of the reaction. The first temperature of the reaction step is controlled, and moderate temperature is appropriate. It should not be overheated or overcooled. If it is overheated, the side reaction will be raw, and if it is too cold, the reaction will be slow. In the meantime, a specific catalyst is added, which can effectively reduce the activation energy of the reaction and speed up the reaction rate. The catalytic mechanism lies in the formation of an intermediate transition state with the reactants, which promotes the smooth breaking and recombination of chemical bonds. After this step, ethyl benzoate fully reacts with the iodizing reagent, and after a series of transformations, Ethyl 2-Iodobenzoate is finally obtained, and the yield is considerable and

Chemical Reactions & Modifications

Ethyl 2-Iodobenzoate is an organic compound. In chemical research, its reaction and modification are of great importance to us.
The method of the past, the preparation of Ethyl 2-Iodobenzoate, has many cumbersome steps, and the yield is not ideal. The reaction conditions are harsh, often requiring high temperature and high pressure, and the reagents used may be toxic and corrosive, which is unfavorable to the environment and human body.
Today, with advanced scientific research and in-depth study of its reaction mechanism, there are improved methods. The new way is guided by green chemistry, selects mild reagents, optimizes the reaction conditions, and allows the reaction to occur in a milder state. In this way, not only the yield is increased, but also the harm to the environment is reduced. For example, the use of new catalysts can accelerate the reaction process, reduce side reactions, and improve product purity. With this modification, the preparation of Ethyl 2-Iodobenzoate is more efficient and environmentally friendly, and its application in the chemical industry is also more promising.

Synonyms & Product Names

Ethyl 2 - Iodobenzoate, also known as ethyl iodobenzoate. It is sold in the market under this name.
This product is used in the field of chemistry. It is often used in the process of synthesis and is an important raw material. Its properties are not determined, but when encountering specific chemical problems, it can also generate new compounds.
We study this product, study its properties and uses, and hope to be able to improve the process of transformation. We hope to use a better method to reduce the cost and increase the quantity, so as to meet the needs of labor and scientific research. In this way, it is beneficial to the development of chemistry.

Safety & Operational Standards

Ethyl 2 - Iodobenzoate
Ethyl 2 - Iodobenzoate is an important organic compound that is widely used in chemical research and related industries. However, in order to ensure the smooth operation of the experiment and the safety of personnel, it is essential to strictly abide by the safety and operation standards.
In terms of safety, Ethyl 2 - Iodobenzoate has certain potential hazards. It may be irritating to the skin, eyes and respiratory tract. Therefore, when operating, appropriate protective equipment, such as laboratory clothes, gloves and goggles, must be worn to protect the skin from direct contact with the eyes. And the operation should be carried out in a well-ventilated environment or in a fume hood to prevent inhalation of its volatile aerosols and damage to the respiratory tract.
Furthermore, Ethyl 2 - Iodobenzoate is at risk of burning in case of open flame, hot topic or. Therefore, the operation site must be kept away from fire and heat sources, smoking is strictly prohibited, properly stored, placed in a cool, dry and ventilated place, avoid mixing with prohibited compounds such as oxidants, to prevent violent chemical reactions and endanger safety.
As for the operating specifications, read the relevant chemical safety technical instructions carefully before use, and be familiar with its physical and chemical properties and emergency treatment methods. When weighing and measuring Ethyl 2 - Iodobenzoate, use precise instruments and operate carefully according to the amount required for the experiment to avoid waste and excessive use. During the experiment, stirring, heating and other operations should also be carried out according to the established procedures and parameters, and the reaction situation should be closely monitored to prevent accidents.
If you accidentally come into contact with Ethyl 2-Iodobenzoate and splash on the skin, you should immediately rinse with a large amount of flowing water; when entering the eyes, immediately lift the eyelids, rinse with flowing water or normal saline, and seek medical attention immediately. In case of fire, choose a suitable fire extinguishing agent according to its nature.
In short, when operating Ethyl 2-Iodobenzoate, adhere to a rigorous attitude and strictly abide by safety and operating standards, in order to effectively avoid risks and ensure the safety and success of the experiment.

Application Area

Ethyl 2-Iodobenzoate is also a chemical material. Its use is important in the field of research and development, and it can be used as an important raw material. With this material, there are many synthetic reactions, helping to create special effects.
In the field of materials, it also has its place. It can be used for specific processes, chemical properties and special materials, or with good performance, or excellent quality, for different needs.
Furthermore, in the research of chemistry, Ethyl 2-Iodobenzoate is often used. Its special transformation can lead to various subtle reactions, in order to explore new transformation paths and promote the synthesis of the next step. Therefore, it plays an indispensable role in the field of multiple applications.

Research & Development

In recent years, Yu has dedicated himself to the research of the organic compound Ethyl 2-Iodobenzoate. This compound has unique properties and has great potential in the field of organic synthesis.
Initially, explore its synthesis method. After repeated experiments, try different reaction conditions and raw material proportions. Or change the temperature, or change the solvent, to find the best synthesis path. In the exploration of the reaction mechanism, no effort has been spared to observe the changes of each step in detail, showing the wonders of the interaction between molecules.
Then, study its application and expand. Try it on the preparation of new materials and observe its impact on material properties. Observe whether it can improve material stability, conductivity, etc. Also explore its role in drug synthesis, hoping to find a breakthrough for the development of new drugs.
Although the research process has encountered many obstacles, such as difficult to increase productivity and difficult to remove impurities. However, I worked tirelessly with the team to study, and failed repeatedly. Now it has achieved a little success, the synthesis efficiency has gradually increased, and the application prospect has become clear. In the future, with continuous improvement, Ethyl 2-Iodobenzoate can shine in scientific research and industry, contributing to the development of related fields.

Toxicity Research

Since modern times, Yu has focused on the toxicity study of chemical substances. In today's discussion of Ethyl 2-Iodobenzoate, its toxicity is quite important.
At first, the chemical structure of Ethyl 2-Iodobenzoate was carefully observed, including the groups of iodine and ethyl benzoate. The structure is often related to the toxicity characteristics. After various experiments, small animals were used as samples to observe their state after ingesting Ethyl 2-Iodobenzoate. It may appear to be slow to move and poor diet, and there are subtle changes in internal organs.
However, the study of toxicity is not just based on the appearance. The metabolic pathway of Ethyl 2-Iodobenzoate in organisms is re-explored, and it is known that it may affect the activity of specific enzymes and cause disorders in physiological processes. And under different doses, toxic reactions vary. At low doses, the body can still compensate; if the dose is slightly increased, the reaction will be exacerbated.
In summary, the toxicity of Ethyl 2-Iodobenzoate cannot be ignored. Follow-up studies should be more in-depth to clarify its harm and provide evidence for protection and application.

Future Prospects

Ethyl 2-Iodobenzoate is a chemical product that I have been working on recently. Although the current preparation process still has limitations, I am full of hope for its future development.
In the synthesis method, I am exploring more subtle and efficient ways to improve yield and reduce costs. It is hoped that in the future, this process will be mature, realize large-scale production, and be widely used in medicine, materials and many other fields.
In the performance exploration, I hope to gain in-depth insight into its characteristics and explore potential uses. With time, or with its unique properties, it may provide an opportunity to solve some of the current difficult scientific problems and emerge in cutting-edge research.
I firmly believe that through unremitting efforts, Ethyl 2-Iodobenzoate will be able to shine in the future and contribute to the progress of science and the development of society.

Historical Development

Ethyl 2-Iodobenzoate is also an organic compound. Its traces can be found in the path of chemical evolution. In the past, chemists explored the properties of substances, the method of synthesis and separation, and worked tirelessly in the field of organic synthesis.
At that time, the exploration of halogenated benzoate esters was gradually emerging, and chemists worked hard to find a good method for preparation. The synthesis of Ethyl 2-Iodobenzoate has developed gradually with the improvement of chemical theory and the advancement of technology. From initial ignorance and probing, to clarifying the reaction mechanism and optimizing the process, every step is the wisdom and sweat of chemists.
From the past to the present, its use in medicine, materials and other fields has become increasingly widespread. The history of chemical evolution is also a witness to the development of Ethyl 2-Iodobenzoate. In the future, it may have a wider development, adding luster to the well-being of mankind.

Product Overview

Ethyl 2 - Iodobenzoate is an organic compound. It is a colorless to pale yellow liquid with a special odor. This compound is obtained by the chemical reaction of benzoic acid and iodoethane.
Ethyl 2 - Iodobenzoate is widely used in the field of organic synthesis. It is often an important intermediary and can participate in many organic reactions to prepare other types of organic compounds. For example, it can react with metal-organic reagents to form carbon-carbon bonds, and then synthesize compounds with more complex structures.
Its physical properties are also worthy of attention. The characteristics of boiling point and melting point determine its existence and form under different conditions, and the characteristics of solubility also affect its behavior in the reaction system. In the chemical industry and laboratory research, in-depth investigation of the properties and applications of Ethyl 2-Iodobenzoate can provide assistance and support for the development of the field of organic synthesis.

Physical & Chemical Properties

Ethyl 2-Iodobenzoate is an organic compound. Its physical and chemical properties are particularly important. Looking at its physical properties, under room temperature, it is a colorless to light yellow liquid with a special odor. Its boiling point is quite high, about [X] ° C, due to the force between molecules. The melting point is about [X] ° C.
In terms of its chemical properties, it has a specific reactivity because it contains iodine atoms and ester groups. Iodine atoms can undergo nucleophilic substitution reactions, and ester groups can be hydrolyzed in contact with acids or bases. In the field of organic synthesis, Ethyl 2-Iodobenzoate is often an important raw material, and its properties are used to construct complex organic molecules. Knowing the physical and chemical properties of this compound, it can be used in the chemical, pharmaceutical and other industries to create endless possibilities.

Technical Specifications & Labeling

"Technical Specifications and Labels of Ethyl 2 - Iodobenzoate (Commodity Parameters) "
Ethyl 2 - Iodobenzoate is an important item in chemical research. Its technical specifications are related to the quality. Looking at its properties, it should be a colorless to slightly yellow liquid, and the smell should be pure and free of impurities. Its boiling point and melting point are fixed, with a boiling point of about [X] ° C and a melting point of about [X] ° C. These two are key markers, which can be used to verify its authenticity and purity.
Then discuss its purity, it should reach more than [X]%, and the impurity content must be strictly controlled. The amount of impurities is directly related to the effect of this substance in experimental or industrial applications. On the logo, in addition to the name of "Ethyl 2 - Iodobenzoate", the molecular formula C H IO ², molecular weight 262.07, and the production batch, date and other product parameters must be indicated, so that it can be a complete technical specification and logo.

Preparation Method

To prepare Ethyl 2-Iodobenzoate, the raw materials and production process are the key. First take o-Benzoic acid and ethanol (Ethanol) as raw materials, and use sulfuric acid as a catalyst to carry out esterification reaction. The reaction steps are as follows: put o-benzoic acid and an appropriate amount of ethanol in a flask, slowly add sulfuric acid, heat and stir to promote the full reaction of the two. This is because sulfuric acid can accelerate the esterification process.
After the reaction is completed, it needs to be separated and purified. Wash with a saturated sodium bicarbonate solution to neutralize the sulfuric acid and remove the unreacted acid. Then use a separation funnel to separate the liquid and take the organic phase. Then dry with anhydrous sodium sulfate to remove residual water.
This preparation method, based on the principle of esterification reaction, can obtain Ethyl 2-Iodobenzoate through fine steps, which is of great significance for chemical research and production.

Chemical Reactions & Modifications

Ethyl 2 - Iodobenzoate is an organic compound, and it is of great value to investigate its chemical reaction and modification.
In the past, the reaction of this compound was studied by traditional methods and common reagents and conditions. However, this method is often limited, and the yield and selectivity are difficult to achieve the ideal. We then thought about changes, hoping to find a better way.
After repeated trials and thinking, it was found that changing the reaction solvent and catalyst had a wonderful effect. Using a specific polar solvent instead of the usual one, and complemented with a new catalyst, the reaction activity was greatly improved. This change allowed Ethyl 2 - Iodobenzoate to exhibit different chemical behaviors in the reaction, with a significant increase in yield and more accurate selectivity.
Such chemical modification not only optimizes the synthesis process of Ethyl 2-Iodobenzoate, but also paves the way for its application in more fields. Follow-up research should be carried out in this direction, hoping to expand its application scope and explore more potential values.

Synonyms & Product Names

Ethyl 2-Iodobenzoate, this thing also has many other names. Among merchants, there may be other names for it. Because of the complexity of the world, the names are different and the same is true.
In the past, the names of all things often changed with different regions and industries. Ethyl 2-Iodobenzoate, or scientific name, is rigorous and standardized, in line with scientific standards. However, it is a trader in the market, or take its easy-to-remember and easy-to-call name, so as to facilitate circulation.
Although the names are different, their properties are the same. This chemical substance has specific qualities and uses. Either it is a raw material for pharmaceuticals, or it plays an important role in chemical processes. Its many aliases all refer to the same substance, just as all roads return to the sect, and all streams return to one. Although the names are mixed, when exploring its essence, it can be clearly identified as Ethyl 2-Iodobenzoate.

Safety & Operational Standards

Ethyl 2-Iodobenzoate is an organic compound that is essential for its safety and handling practices.
This substance has certain chemical activity. During operation, the experimenter must wear appropriate protective equipment, such as laboratory clothes, gloves and goggles, to prevent it from coming into contact with the skin and eyes. In case of inadvertent contact, rinse with plenty of water immediately and seek medical assistance according to the actual situation.
Ethyl 2-Iodobenzoate may have potential impact on the environment. Waste after use should be properly disposed of in accordance with relevant regulations. It must not be discarded at will to avoid polluting the environment.
For storage, it should be stored in a cool, dry and well-ventilated place, away from fire sources and oxidants, to prevent dangerous reactions. When taking it, it is necessary to operate in strict accordance with the experimental procedures, precisely control the dosage, and avoid waste and unnecessary risks.
The place where Ethyl 2-Iodobenzoate is operated must be equipped with complete ventilation facilities to eliminate possible harmful gases and ensure the safety of the experimental environment. If a leak occurs during operation, emergency measures should be taken immediately, such as quickly evacuating unrelated personnel, isolating the leakage area, and selecting suitable materials for adsorption and cleaning.
Only by strictly following safety and operating standards can we ensure that the research and use of Ethyl 2-Iodobenzoate minimizes risks and protects the safety of personnel and the environment from damage.

Application Area

Ethyl 2-Iodobenzoate is also an organic compound. Its application field is quite wide, in the field of medicinal chemistry, it is often a key intermediate for the synthesis of special drugs. With the activity of iodine atoms in its structure, it can be bonded with other molecules by chemical reactions to construct substances with specific pharmacological activities.
It also has its uses in materials science. It can be chemically modified to participate in the construction of polymer materials, so that the materials acquire special physical and chemical properties, such as changing the solubility and thermal stability of the materials.
In the field of organic synthetic chemistry, Ethyl 2-Iodobenzoate, as an important raw material, can initiate a variety of chemical reactions, such as nucleophilic substitution reactions, etc., assisting chemists in the preparation of organic molecules with complex structures and unique functions, providing a material basis for the development of many fields.

Research & Development

Taste the wonders of chemical industry, is related to the change of all things. Today there is Ethyl 2-Iodobenzoate, which is quite meaningful in our research.
We have painstakingly studied and explored the method of its synthesis. At the beginning, we tried many times but failed to find the way, and we seem to be lost in all kinds of attempts. However, the road of scientific research has been bumpy, so why should we abandon it because of small setbacks? Then we unremitting search, repeated deduction, and finally obtained the exquisite method.
To observe its properties, under different media and conditions, changes vary. This is the key to in-depth understanding of its application. We also observe its role in the reaction process, whether it is to initiate or promote, all of which are related to the success or failure of the reaction.
As for the development prospects, it is indeed broad. In the field of medicine, it may help the research and development of new agents; in materials science, it is also expected to open up new paths. We should persevere and move forward with determination, hoping to explore more of its potential, contribute to the progress of scientific research, and benefit the world with the great achievements of Zhang Chemical Engineering.

Toxicity Research

The industry of chemical industry is related to people's livelihood, but the investigation of poisons in it cannot be ignored. Now on Ethyl 2-Iodobenzoate, the study of its toxicity is quite important.
Ethyl 2-Iodobenzoate may be potentially harmful. In the experiment, observe its impact on various things. Take small animals as a test and observe their state after ingesting this thing. It may show signs of slow movement, poor diet, and even abnormal changes in the organs.
And explore its role in the environment. If this thing enters the water body and soil, it may cause ecological turbulence. Aquatic species may be poisoned by it, and their reproduction and growth will be hindered. The microorganisms in the soil may also be harmed by them, and the nature of the soil changes accordingly.
Therefore, the study of toxicity should not be taken lightly. It is necessary to carefully observe its nature and understand its harm, so as to avoid disasters and protect people's livelihood and the safety of the environment.

Future Prospects

Ethyl 2-Iodobenzoate is also a chemical product. It has not been developed yet, and there is no way to do it. We expect that, with the refinement of chemical research, the method of improvement may be more subtle, and the improvement rate will also be improved significantly.
Furthermore, this product may be exposed in the field. Based on its chemical properties, it may be used as a raw material for the synthesis of special effects, providing a new way to solve common diseases.
And in the field of materials, Ethyl 2-Iodobenzoate may also be released. It may be able to research new materials, so that the materials have special properties such as better quality and reliability, etc., and expand the new use of materials. After all, its undeveloped, full of possibilities, is waiting to be seen.

Historical Development

Ethyl 2 - Iodobenzoate is an organic compound. Its origin can be traced back to the development of chemical research. In the past, chemists studied the way of organic synthesis and unremitting exploration of the preparation of various compounds. In many attempts and experiments, the synthesis method of this substance was gradually obtained.
At the beginning, it was quite difficult to synthesize Ethyl 2 - Iodobenzoate, because the chemical technology was not mature at that time, and the understanding of the reaction mechanism was limited. However, chemists adhered to the spirit of research, constantly optimizing the reaction conditions and adjusting the proportion of reactants.
With the passage of time, chemical technology has advanced, and the control of its synthesis has become more accurate. The application of this compound in the field of organic synthesis has also become increasingly widespread, providing a key foundation for the construction of many complex organic molecules, witnessing the development process of chemical synthesis technology from simple to complex, from shallow to deep.

Product Overview

Description of Ethyl 2-Iodobenzoate
Ethyl 2-Iodobenzoate is a crucial chemical in the field of organic synthesis. Its properties are colorless to light yellow liquid with a special odor, which has a significant impact on many chemical reactions.
From a structural perspective, the iodine atom on the benzene ring is cleverly connected to the ethyl benzoate group, giving it unique chemical activity. The presence of iodine atoms makes it excellent in nucleophilic substitution reactions, and it is often used as a key intermediate to participate in the construction of complex organic compounds.
Preparation of this product often follows a specific organic synthesis path. Ethyl 2-Iodobenzoate is obtained by using benzoic acid as the starting material, esterification reaction to form ethyl benzoate, and then halogenation reaction to precisely introduce iodine atoms. However, in the preparation process, the control of reaction conditions is particularly critical, and factors such as temperature, catalyst type and dosage have a profound impact on the purity and yield of the product.
Ethyl 2-Iodobenzoate is widely used in the fields of pharmaceutical chemistry and materials science. In pharmaceutical research and development, it can be used as a key building block for the synthesis of specific drug molecules to help create new drugs; in materials science, it participates in the synthesis of functional materials to give unique properties to materials. In conclusion, although Ethyl 2-Iodobenzoate is an organic chemical, its importance in many fields cannot be underestimated, and it is of great significance to promoting scientific research and industrial development.

Physical & Chemical Properties

Ethyl 2-Iodobenzoate is an organic compound, and its physical and chemical properties are particularly important. Looking at its physical properties, it is mostly liquid at room temperature, with a specific color and smell. Its boiling point is related to the intermolecular force, which is the key temperature for the gasification of substances. The melting point also characterizes the transformation of solid and liquid states.
On its chemical properties, because it contains iodine atoms and ester groups, it can participate in a variety of chemical reactions. Iodine atoms have certain activity and can undergo nucleophilic substitution reactions. Ester groups can be hydrolyzed, and the path is different under acid-base conditions. When catalyzed by acids, hydrolysis is a reversible process; when catalyzed by bases, hydrolysis is more complete. In addition, Ethyl 2-Iodobenzoate can also participate in some reactions related to aromatic rings. Under the influence of substituents, the electron cloud density of aromatic rings changes, which affects its reactivity and selectivity. This is the key point to explore the properties of this compound.

Technical Specifications & Labeling

Ethyl 2 - Iodobenzoate is an organic compound. The preparation process is as follows: In a clean reactor, ethyl benzoate and iodine are used as raw materials, and in the presence of suitable catalysts such as iron powder, heated to a certain temperature and maintained for several hours, so that the two can fully react. After the reaction is completed, the product is separated and purified by distillation, extraction, etc.
Its product specifications and labels (commodity parameters): The appearance is colorless to light yellow liquid, with a specific odor. The purity needs to reach more than 98%, which is a key indicator, which is related to its application effect. The impurity content is strictly controlled, such as moisture should not exceed 0.1%, so as not to affect the product performance. When storing, it should be stored in a cool, dry place, protected from light, to prevent decomposition and deterioration, to ensure product quality stability.

Preparation Method

Ethyl 2-Iodobenzoate is an important compound in organic synthesis, and its preparation method is very crucial. The raw materials should be selected ethyl benzoate and iodine elemental. The preparation process is as follows:
First take an appropriate amount of ethyl benzoate and place it in a clean reactor, add an appropriate amount of catalyst, this catalyst can speed up the reaction process. Subsequently, slowly add iodine elemental. During this process, the reaction temperature needs to be closely monitored to maintain its stability within a specific range. This is because temperature has a great influence on the reaction. Too high or too low will affect the purity and yield of the product.
The reaction steps are as follows: Ethyl benzoate and iodine are substituted under the action of catalyst, and iodine atoms replace hydrogen atoms at specific positions of ethyl benzoate to gradually generate Ethyl 2-Iodobenzoate.
To improve the purity of the product, a purification mechanism is set up. After the reaction, the unreacted raw materials and by-products are separated by distillation according to the boiling point difference of each component. After that, recrystallization is used to further purify and obtain high-purity Ethyl 2-Iodobenzoate. This preparation method is stable and efficient, which can meet the needs of many experiments and production.

Chemical Reactions & Modifications

In the field of chemistry, the reaction and modification of Ethyl 2-Iodobenzoate are the key to our research.
In the past, the reaction path has been established, but it is not easy to seek the changeability of its properties. We have tried our best to observe the temperature, time, and proportion of the agent in the reaction, hoping to obtain new properties.
Or adjust the temperature and observe the response. If the temperature is high, it will be fast, and then the side will also be produced; if the temperature is low, it will be slow, and the yield will drop. The amount of reagent is also changed, and the reaction results vary between increases and decreases.
As for the modification, the method is to add other agents and change its structure. Try adding a certain agent, hoping to improve its solubility and stability. Although it has been difficult, every slight gain is an improvement. We will not give up studying, hoping to get better properties of Ethyl 2-Iodobenzoate, so as to benefit the chemical industry.

Synonyms & Product Names

Ethyl 2-Iodobenzoate is also a chemical product. It has the same name, and it also has the same name as ethyl iodobenzoate. In the market, there may be products sold under this name. This name is derived from its chemical manufacture, and ethyl is connected to the carboxyl group of iodobenzoic acid, so there is this.
This product is used in the field of chemical research and development. There can be synthetic raw materials, multi-chemical and anti-chemical, to help the chemical industry to obtain the product they want. The research and analysis, or the manufacturing, are all identified by the same name and trade name, so as to be able to use it and cause confusion, so as to facilitate the work of chemical engineering.

Safety & Operational Standards

Ethyl 2-Iodobenzoate is an important chemical product that is essential for its safety and handling practices.
This compound has certain chemical activity and potential hazards. For storage, it should be placed in a cool, dry and well-ventilated place, away from fire, heat and strong oxidants. Due to its exposure to heat or contact with strong oxidants, it may cause violent reactions and even explosions.
When operating, it is necessary to strictly follow established procedures. Experimenters should wear appropriate protective equipment, such as protective gloves, goggles and lab clothes, to avoid skin contact and eye splashing. If you accidentally touch the skin, you should immediately rinse with a large amount of water and seek medical treatment according to the specific situation; if you splash into the eyes, you need to rinse with a large amount of water quickly, and then send it to the hospital for urgent treatment.
When using Ethyl 2-Iodobenzoate for reaction, it should be operated in a fume hood with good ventilation conditions to prevent the accumulation of harmful gases. The reaction process should be closely monitored, and key parameters such as reaction temperature and pressure should be controlled to ensure the smooth progress of the reaction and avoid accidents.
The disposal of waste should not be taken lightly. Waste containing Ethyl 2-Iodobenzoate must be properly collected, marked and treated in accordance with relevant environmental regulations, and should not be discarded at will to prevent pollution to the environment.
Only by strictly adhering to the above safety and operation standards can we ensure that the safety of personnel and the environment are not endangered during the research and application of Ethyl 2-Iodobenzoate, and promote the smooth development of relevant scientific research work.

Application Area

Ethyl 2-Iodobenzoate is also a chemical substance. Its use is very important, and in the field of, it can be used as a raw material for the synthesis of general materials. With its special properties, it can multiply and reverse, and help to form chemical molecules, or increase efficiency, or change the physicochemical properties of materials. In the field of materials science, it also has its uses. It can be used as a starting material for the synthesis of functional materials, giving specific properties of materials, such as light properties, performance, etc. It is often important in the synthesis of materials. From the generalization, many compounds with different properties are derived, and the research of chemical phase is promoted.

Research & Development

Taste the industry of chemical industry, explore endless, the research of matter, is related to the road of development. In today's words, Ethyl 2 - Iodobenzoate, its research and progress, is quite important.
From the beginning, study its synthesis method, all kinds of raw materials, exquisite proportions, reaction temperature, and time control are all key. After several trials, a feasible path can be obtained. And observe its physical and chemical properties, in different media, the properties are different, which is the basis for subsequent application.
Then, think about the extension of its use. In the field of medicine, or as a raw material, to help the production of new drugs and cure diseases; in the world of materials, it may also have the ability to increase its quality and develop different properties.
Our researchers should persevere and conduct in-depth research, so that the research and progress of Ethyl 2-Iodobenzoate can reach a higher level, be used by the world, and benefit all living beings.

Toxicity Research

The industry of chemical industry is very important to people's livelihood, but the study of poisons is also a top priority. Now on Ethyl 2-Iodobenzoate, the study of its toxicity should not be ignored.
Ethyl 2-Iodobenzoate has a different appearance or state. If you want to study its toxicity, you must carefully observe its response to things and its response to life. Try it in various ways and observe how it changes after entering the body or touching the object. For living beings, observe how their body signs and behaviors are different after eating or receiving this thing.
After research, it can be obtained that Ethyl 2-Iodobenzoate may have a certain toxicity, but its intensity and wide harm still need to be further explored. Chemical researchers should be careful again and again, to understand its harm and prevent its danger, so as to ensure public safety and promote the prosperity of the industry.

Future Prospects

I have studied Ethyl 2-Iodobenzoate, and I deeply feel that it has great potential for future development. Its unique structure and specific reactivity can be used in many organic synthesis routes.
In today's chemical field, there is a growing demand for new materials and efficient synthesis methods. Ethyl 2-Iodobenzoate may be a key raw material for the synthesis of novel functional materials. With its unique properties, it may be able to prepare materials with special optical and electrical properties, which will shine in the field of optoelectronics.
And it is also expected to open up new avenues in drug synthesis. After rational design of reactions, compounds with unique pharmacological activities may be constructed, providing more possibilities for the development of new drugs.
In the future, we will further study its reaction mechanism, optimize the synthesis process, and improve the yield and purity. We also hope to join hands with colleagues to explore more application potential of Ethyl 2-Iodobenzoate, so that it can play an important role in future scientific and technological development and seek more benefits for human well-being.

Where to Buy Ethyl 2-Iodobenzoate in China?

As a trusted Ethyl 2-Iodobenzoate manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.

Frequently Asked Questions

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

What are the main uses of Ethyl 2-iodobenzoate?

Ethyl 2-iodobenzoate (ethyl 2-iodobenzoate) is also an organic compound. It has a wide range of uses and is an important intermediate in the field of organic synthesis.
First, it can be used to prepare various benzoate derivatives. Through nucleophilic substitution reaction, its iodine atom can be replaced by many nucleophilic reagents, such as alcohols, amines, etc., to construct esters or amides with rich structures, which is of great significance in the fields of medicinal chemistry and materials science. When drugs are developed, benzoate derivatives with specific structures may have unique biological activities and can be used as lead compounds to develop new drugs.
Second, in material synthesis, Ethyl 2-iodobenzoate participates in the reaction and can give materials specific properties. For example, introducing its structural units into the main or side chains of the polymer can change the solubility, thermal stability, and optical properties of the polymer.
Third, it is also useful in the preparation of fine chemical products. For example, in the synthesis of fragrances, it can be used to participate in the reaction to construct compounds with special aromas, adding new products to the fragrance industry. In addition, in the preparation of some functional coatings and inks, Ethyl 2-iodobenzoate can participate in the reaction to optimize product performance and enhance its market competitiveness. In short, Ethyl 2-iodobenzoate is an indispensable raw material in organic synthesis and related industrial production.

What are the physical properties of Ethyl 2-iodobenzoate?

Ethyl 2-iodobenzoate (ethyl 2-iodobenzoate) is an organic compound. Its physical properties are as follows:
Looking at its properties, it is usually a colorless to light yellow oily liquid. Due to the conjugated system of benzene ring in the molecular structure, it also contains ester groups and iodine atoms, resulting in this appearance.
When it comes to boiling point, it is about 280-285 ° C. Due to the existence of van der Waals force between molecules, and the conjugation between ester groups and benzene rings enhances the intermolecular force. A higher temperature is required to overcome this force and realize the transition from liquid to gaseous state.
In terms of melting point, it is about -12 ° C. The relatively low melting point is due to the fact that the molecular structure is not tightly arranged, and the intermolecular forces are not sufficient to fix the molecules in the lattice position at the lower temperature.
The density is about 1.665 g/cm ³, which is greater than the density of water. This is due to the large relative atomic weight of iodine atoms, which increases the weight of the whole molecule, resulting in an increase in density.
In terms of solubility, it is slightly soluble in water, but soluble in organic solvents such as ethanol and ether. Due to the fact that the ester group in the molecule is a lipophilic group and the water molecule is a polar molecule, according to the principle of similarity and miscibility, its interaction with water is weak, so it is slightly soluble in water; while organic solvents such as ethanol and ether can interact with ethyl 2-iodobenzoate molecules through van der Waals forces, etc., so it is soluble.
In addition, the substance has a certain refractive index, which is about 1.587-1.591 under specific conditions. The characteristics of refractive index are related to molecular structure and electron cloud distribution. This value reflects its ability to refract light.

What are the chemical properties of Ethyl 2-iodobenzoate?

Ethyl 2-iodobenzoate (ethyl 2-iodobenzoate) is an organic compound with specific chemical properties. Its appearance is often colorless to pale yellow liquid or crystalline solid, and it is widely used in the field of organic synthesis.
In terms of physical properties, it has a certain melting point and boiling point, and the melting point and boiling point values vary according to specific conditions. It is insoluble in water, but soluble in common organic solvents such as ethanol and ether. This solubility makes it convenient to participate in many organic reaction systems.
From the perspective of chemical properties, the iodine atom in ethyl 2-iodobenzoate is highly active and prone to substitution reactions. For example, when it meets a nucleophilic reagent, the iodine atom can be replaced by a nucleophilic group to form a new carbon-heteroatom bond, and then a variety of organic compound structures can be constructed. Its ester group is also active, and under the catalysis of acid or base, hydrolysis can be carried out. In acidic hydrolysis, 2-iodobenzoic acid and ethanol are formed; in alkaline hydrolysis, 2-iodobenzoate and ethanol are formed. Such hydrolysis reactions are of great significance in organic synthesis and product conversion. In addition, the compound can also participate in reactions such as esterification and addition. By rationally designing the reaction path, many organic compounds with specific functions and structures can be prepared, which have potential applications in many fields such as medicinal chemistry and materials science.

What are the synthesis methods of Ethyl 2-iodobenzoate?

There are several ways to synthesize ethyl 2-iodobenzoate. First, it can be started from 2-benzoic acid. First, introduce iodine atoms at specific positions on the benzene ring of benzoic acid with appropriate halogenating reagents, such as iodizing reagents. This step requires attention to the control of reaction conditions, such as temperature and solvent selection. In the halogenation reaction, select a suitable catalyst, or it can promote the reaction and increase its selectivity. After obtaining 2-iodobenzoic acid, esterification reaction is carried out with ethanol under the condition of acid catalysis. In this esterification process, the acid can promote the reaction equilibrium to move in the direction of ester formation, and the reaction temperature and time should be controlled to avoid side reactions.
Second, benzoic acid and ethanol can be used to form ethyl benzoate first, and then iodine atoms can be introduced into the benzene ring. When introducing iodine atoms, due to the existence of ester groups on the benzene ring, the localization effect needs to be considered in detail. Select an appropriate iodization method, such as using a specific iodine source and activator combination, under mild reaction conditions, so that iodine atoms can selectively connect to the 2-position of the benzene ring. In this approach, the early esterification reaction must be ensured to be complete, and the later iodization step also needs to optimize the conditions to achieve higher yield and purity.
Or there are other synthesis methods, such as using raw materials containing iodine and ester groups, through organic synthesis methods, the structure of the target molecule is gradually constructed. However, no matter what method is used, it is necessary to carefully investigate the reaction mechanism, control the reaction conditions of each step, and fine separation and purification to obtain high-purity ethyl 2-iodobenzoate.

Ethyl 2-iodobenzoate requires attention during storage and transportation

Ethyl 2-iodobenzoate is an organic compound. When storing and transporting it, the following numbers should be paid attention to:
First, because of its certain chemical activity, the storage place should be cool, dry and well ventilated, away from fire and heat sources. If heated, or cause chemical reactions to accelerate, causing danger, such as deterioration, decomposition or even fire.
Second, this compound should be stored separately from oxidants, acids, bases, etc., and must not be mixed. Because of its violent chemical reaction with the above substances, such as meeting with oxidants, or triggering oxidation reactions, resulting in the risk of combustion and explosion.
Third, the storage container must be tightly sealed. Ethyl 2-iodobenzoate may react with components in the air, such as water vapor, oxygen, etc., to cause it to deteriorate. Sealing can effectively avoid excessive contact with air and maintain its chemical stability.
Fourth, during transportation, make sure that the container does not leak, collapse, fall, or damage. Load lightly and unload lightly to prevent damage to the container due to collision and vibration, so that Ethyl 2-iodobenzoate leaks and causes safety problems.
Fifth, relevant transportation regulations must be followed. Transportation vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. In the event of leaks and other accidents, they can be responded to in time to reduce hazards.