Ethyl 3-Iodobenzoate

Fengxi Chemical

Specifications

HS Code	574261
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Typically a solid or liquid
Boiling Point	Varies depending on purity, but generally high
Melting Point	Specific value depends on purity
Density	Density data is substance - specific
Solubility In Water	Poorly soluble in water
Solubility In Organic Solvents	Soluble in common organic solvents
Odor	May have a characteristic odor
Stability	Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Typically a solid or viscous liquid
Physical State At Room Temperature	Solid (usually)
Odor	May have a characteristic organic odor
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, acetone
Boiling Point	Approximately 275 - 280 °C
Melting Point	Around 36 - 38 °C
Density	~1.73 g/cm³
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Flash Point	Relatively high, around 120 °C
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Colorless to pale yellow liquid
Boiling Point	~273 - 275 °C
Density	1.656 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Flash Point	119.4 °C
Odor	Characteristic odor
Cas Number	610-37-7
Stability	Stable under normal conditions, but light-sensitive

As an accredited Ethyl 3-Iodobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	Ethyl 3 - iodobenzoate in 100 - gram glass bottles, well - sealed for safe storage.
Storage	Ethyl 3 - iodobenzoate should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames to prevent potential fire or decomposition due to its flammability. Keep it in a tightly sealed container to avoid exposure to air and moisture, which could lead to degradation. Store separately from incompatible substances like strong oxidizing agents.
Shipping	Ethyl 3 - iodobenzoate is shipped in well - sealed, corrosion - resistant containers. It's transported under regulated conditions to prevent breakage and exposure, following strict chemical shipping safety protocols due to its nature.

Free Quote

Competitive Ethyl 3-Iodobenzoate prices that fit your budget—flexible terms and customized quotes for every order.

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General Information

Historical Development

Ethyl 3 - Iodobenzoate is also an organic compound. At the beginning, chemists studied the properties of substances and wanted to make new substances to expand the field of chemistry. In the past, scholars have gradually advanced in the art of organic synthesis. Everyone explored different methods to find a way to make this thing. At the beginning, I tried many paths, or because the conditions were not suitable, or because the raw materials were difficult to find, the results were not obvious. However, the sages were not discouraged, and they continued to study.
Later, the understanding of organic chemistry became better, and the technology became more refined. Chemists started with benzoate, supplemented by iodide, and finally obtained Ethyl 3 - Iodobenzoate through ingenious reactions. Since then, Ethyl 3-Iodobenzoate has been gradually used in the field of chemistry, either as a raw material for synthesizing other substances or in scientific research to help solve problems. Its development process has also witnessed the progress of chemistry.

Product Overview

"Ethyl 3 - Iodobenzoate Product Overview"
Ethyl 3 - Iodobenzoate is a valuable chemical in the field of organic synthesis. Its chemical structure is derived from ethyl benzoate, and iodine atoms are introduced at the 3rd position of the benzene ring. This unique structure gives it special chemical activity.
In preparation, a delicate organic synthesis path is often required. Benzoic acid is used as the starting material, ethyl benzoate is obtained by esterification reaction, and then under specific reaction conditions, the iodine atom is precisely connected to the 3rd position of the benzene ring by electrophilic substitution reaction.
This product is widely used in organic synthesis and can be used as a key intermediate to build more complex organic molecular structures. It may provide a key structural unit for the development of new drugs in the field of medicinal chemistry, and may also participate in the creation of high-performance materials in the field of materials science. Due to its unique chemical properties, it plays an indispensable role in many chemical reactions and is of great significance to the development of organic synthetic chemistry.

Physical & Chemical Properties

"Rationalization of Ethyl 3 - Iodobenzoate"
Ethyl 3 - Iodobenzoate is an important chemical product. Its physical properties are low, and the outer color is often yellow to light white, which has a special taste. Low melting temperature, often at low temperatures, it is liquid, this characteristic makes it easy to flow in normal environments.
As far as the chemical properties are concerned, due to the presence of iodine atoms in the molecule, it has a certain chemical activity. Its benzene content also makes it a typical reaction of polyaromatic compounds. Under specific conditions, it can generate nuclei to replace the reaction, and the iodine atom is easily replaced by other nuclei. And its ester group part can generate hydrolysis reaction under acid or catalysis to generate benzoic acid and ethanol. Therefore, the rationalization of Ethyl 3 - Iodobenzoate determines its important use in chemical synthesis and other fields.

Technical Specifications & Labeling

There is now a chemical substance called Ethyl 3-Iodobenzoate. To clarify its technical specifications and labels (product parameters), you should study it in detail.
This Ethyl 3-Iodobenzoate should be pure in quality, correct in color, and free of clutter. Looking at its properties, it should be a specific state, in line with the established standards. The proportion of the elements it contains should also be accurate and in line with the specified technical specifications.
On the label, the product parameters must be detailed. Such as molecular weight geometry, melting point, boiling point, all need to be clear. And on its packaging, it should be marked with a prominent note, so that the viewer knows it as Ethyl 3-Iodobenzoate, and its key parameters are clearly stated to comply with the technical specifications and labels, so that the user does not have the risk of misuse.

Preparation Method

The product of Ethyl 3-Iodobenzoate is made today, when the raw materials and production process, reaction steps and catalytic mechanism are clear.
The raw materials are benzoic acid and ethyl iodide. The production process is based on esterification reaction. Prepare an appropriate amount of benzoic acid in the reactor, add an appropriate amount of sulfuric acid as a catalyst, and heat it up to a suitable degree, about 60-80 degrees Celsius. Slowly drop iodoethane, and continue to stir in the meantime to make the two fully contact.
The reaction steps are as follows: The carboxyl group of benzoic acid and the ethyl group of iodoethane are dehydrated and condensed through the action of a catalyst. The mechanism of sulfuric acid catalysis is that it provides protons to enhance the positive electricity of carbonyl carbon of benzoic acid carboxyl group, and ethyl nucleophilic attack of iodoethane to form Ethyl 3-Iodobenzoate. After the reaction is completed, the temperature is lowered, the sulfuric acid is neutralized in sodium bicarbonate solution, the organic phase is separated from the liquid, distilled and purified to obtain pure Ethyl 3-Iodobenzoate.

Chemical Reactions & Modifications

Ethyl 3 - Iodobenzoate is an organic compound of great importance in the field of chemical synthesis. Its chemical properties and reactions are often the key to our chemical researchers' investigation.
In the past, the reaction of this compound was mostly focused on conventional routes, but the purity and yield of the obtained product could be improved. In order to make breakthroughs, we have repeatedly studied and experimented to change the reaction conditions. For example, adjusting the ratio of reactants to accurately measure to make the reaction more complete; selecting new catalysts to accelerate the reaction process and optimize the product structure with their unique activity; adjusting the reaction temperature and time to create a suitable reaction environment.
With these many improvements, the reaction yield of Ethyl 3-Iodobenzoate has been significantly improved, and the product purity has also been greatly improved. These results may provide new ideas and methods for the organic synthesis industry, laying a good foundation for the subsequent research and production of related compounds.

Synonyms & Product Names

Ethyl 3-Iodobenzoate is an organic compound. Although its name is the same, the synonymous name is also different from the trade name.
This compound, viewed from a chemical perspective, is an iodine derivative of ethyl benzoate. In the academic world, it may be called ethyl 3-iodobenzoate, which is based on its chemical structure and naming rules, and is synonymous with Ethyl 3-Iodobenzoate.
As for the trade name, between the market circulation, different manufacturers may have their own names. However, its essence refers to this specific compound. In the field of organic synthesis, it is often used as an intermediate and can participate in many chemical reactions to prepare more complex organic molecules. Knowing its synonymous names and trade names is of great significance in chemical research, industrial production, and academic exchanges, allowing all parties to communicate accurately and avoid ambiguity.

Safety & Operational Standards

Safety and Practice of Ethyl 3 - Iodobenzoate
Ethyl 3 - Iodobenzoate is a common compound in chemical research. Safety and practice are of paramount importance during research and operation.
This compound has certain latent risks. First, it may have an impact on human health. Contact with the skin may cause irritation, so protective gloves are required during operation. If you are inadvertently exposed, you should immediately rinse with plenty of water. Second, inhaling its volatile gaseous substances may damage the respiratory tract. The experimental environment must be well ventilated or operated in a fume hood.
Furthermore, the operating practices should not be underestimated. When weighing, a precise balance should be used to ensure that the dosage is correct. During the reaction process, the reaction conditions, such as temperature and reaction time, are strictly controlled. Reactions involving Ethyl 3-Iodobenzoate, or sensitive to temperature, too high or too low temperature can cause deviation in reaction results. At the same time, the reaction instrument should be clean and dry to prevent impurities from interfering with the reaction.
For storage, Ethyl 3-Iodobenzoate should be placed in a cool, dry place, away from fire sources and oxidants. Due to its active chemical properties, improper storage or potential safety hazards.
In addition, after the experiment is completed, the waste containing Ethyl 3-Iodobenzoate must be properly disposed of in accordance with regulations and should not be discarded at will to avoid polluting the environment.
Adhering to the above safety and operation practices can effectively avoid risks in the study of Ethyl 3-Iodobenzoate, ensure the smooth progress of the experiment, and ensure the safety of the researchers and the safety of the environment.

Application Area

Ethyl 3-Iodobenzoate is also an organic compound. Its application field is quite wide, in the field of pharmaceutical chemistry, it can be a key raw material for the synthesis of many special drugs. Through delicate reactions, specific groups can be introduced to give drugs unique curative effects.
In the field of materials science, it also has important uses. It can be chemically modified to prepare materials with special photoelectric properties, or optimize the properties of polymer materials, contributing to the research and development of new materials.
Furthermore, in the fine chemical industry, Ethyl 3-Iodobenzoate can be used to produce high-end fragrances, pigments and other fine chemicals to improve the quality and characteristics of products, in order to meet the market demand for high-quality fine chemical products. From this perspective, it has significant application value in various fields, promoting the development and progress of related industries.

Research & Development

In recent years, I have devoted myself to the research of Ethyl 3 - Iodobenzoate. At the beginning, I analyzed its chemical properties, but there were many unknowns in the classics. Experiments were set up to explore its changes.
At the beginning, the choice of raw materials, careful, must seek pure quality. The temperature, time and proportion of the reaction agent were all carefully observed and fine-tuned. At the beginning, the effect was not obvious, and the yield was quite low. I was worried. However, I was not discouraged, and I repeatedly studied and improved the method.
In the end, in the catalysis of the reaction and the control of the environment, I got a delicate method. The yield gradually increased, and the quality was also excellent. This research is also not only the preparation of Ethyl 3 - Iodobenzoate, but also the way of understanding research. It is important to be constant and careful, and not discouraged by setbacks. Only then can we make progress. In the future, I also expect its expansion and contribution to the world.

Toxicity Research

Recently, Yu Wu's chemical research focused on the toxicity analysis of Ethyl 3-Iodobenzoate. The main point of this research is to clarify its potential impact on living beings and rings.
Ethyl 3-Iodobenzoate has the structure of halogenated benzoate. After various experiments, it can be observed that it may lead to a series of reactions in living beings. In cell-level experiments, it can be seen that it disturbs the colonization and work of certain types of cells. And in animal tests, it is also found that if it is involved in this substance, there may be changes in physiological characteristics.
Furthermore, considering its feelings in the ring. If this substance enters the ring, it will be transferred and transformed, or it will affect both water, soil and living beings. Although the current research has not fully understood its toxic mechanism and shadow process, the available evidence shows that its toxicity research cannot be ignored. In the future, we should use a more detailed method and a wider dimension to explore its nature, as the basis for prevention and control, to avoid its unpredictable harm to the world's living beings and the environment.

Future Prospects

Ethyl 3-Iodobenzoate is also an organic compound. In today's chemical research, the method of its preparation has become more and more refined, and the yield has also improved. Looking at its future prospects, it will have a wider range of uses. In the field of pharmaceutical research and development, it may be the basis for the creation of new agents, and with its unique structure, it is expected to become a cure for diseases. In the field of material science, it may also emerge, providing key raw materials for the research and development of new materials. Although the current knowledge is limited, over time, scholars who explore its properties and widely study its applications will surely be able to uncover its endless potential, such as pearls emerging from clams, shining in the scientific world of the future, adding luster to the well-being of mankind, and becoming an unlimitable cause.

Historical Development

Ethyl 3-Iodobenzoate is also an organic compound. Tracing back its historical development, the chemists of the past have worked tirelessly in the field of organic synthesis. In the early years, when organic chemistry was still in ignorance, scholars explored various reaction paths.
At that time, the research on benzoic acid derivatives was gradually emerging, and people tried to introduce benzene rings with different halogenates. After repeated experiments and scrutiny, attempts were made to react with ethyl benzoate with iodine-substituted reagents. After countless adjustments to the reaction conditions, such as temperature and catalyst selection, the synthesis of Ethyl 3-Iodobenzoate was gradually obtained.
The evolution of its synthesis is the result of continuous breakthroughs and accumulation in the chemical community. From the initial vague concept to the clear reaction steps, the birth of this compound has witnessed the development process of organic synthetic chemistry from simple to complex and from shallow to deep, paving the way for subsequent organic chemistry research and related industrial applications.

Product Overview

About Ethyl 3-Iodobenzoate Product Overview
Ethyl 3-Iodobenzoate, Chinese name ethyl 3-iodobenzoate, is a crucial compound in the field of organic synthesis. Its chemical structure is derived from ethyl benzoate, and iodine atoms are introduced at the 3-position of the benzene ring, giving it unique chemical activity.
The appearance of this compound is often colorless to light yellow liquid, with a specific odor. Physical properties such as melting point and boiling point are stable, providing convenience for practical applications. In organic synthesis reactions, with the activity of iodine atoms, it can participate in many reactions such as nucleophilic substitution and coupling, and is a key intermediate for the construction of complex organic molecules.
There are various methods for synthesizing Ethyl 3-Iodobenzoate, which can be obtained by halogenation of ethyl benzoate, or esterification of 3-iodobenzoic acid and ethanol. Each method has its own advantages and disadvantages, and it needs to be carefully selected according to actual needs and conditions.
In view of its unique chemical properties and wide application prospects, Ethyl 3-Iodobenzoate is increasingly popular in the fields of medicine, pesticides, materials science and other fields, and continues to promote technological innovation and development in related fields.

Physical & Chemical Properties

Ethyl 3-Iodobenzoate is an organic compound, and its physical and chemical properties are worth studying. Looking at its physical properties, under normal conditions, Ethyl 3-Iodobenzoate is colorless to light yellow liquid with a specific odor. Its boiling point depends on the intermolecular force, which is about a certain temperature range. This temperature causes it to change from liquid to gaseous. The melting point determines the transition temperature between solid and liquid states, which has a great impact on storage and use conditions.
In terms of its chemical properties, the iodine atom in Ethyl 3-Iodobenzoate is highly active and can participate in many substitution reactions. The presence of benzene rings gives it aromatic properties and can undergo electrophilic substitution reactions. Ester groups also have unique reactivity, such as hydrolysis and alcoholysis, and are widely used in the field of organic synthesis. They are important raw materials for the preparation of various compounds.

Technical Specifications & Labeling

There is a thing today, named Ethyl 3 - Iodobenzoate. The technique of its manufacture is the first technical specification and identification (commodity parameters). To make this thing, you need to follow certain rules. Take an appropriate amount of ethyl benzoate and use a specific method to make it encounter the iodizing reagent. In the meantime, control its temperature and time, do not make it too high or too low.
After making it, be careful about the logo. List its quality, quantity, sex and other commodity parameters in detail. Looking at its color, it should be a colorless to light yellow liquid; smell its smell, when there is no odor. Measure its melting and boiling point, remember it accurately, and take it as evidence of the logo. Check its purity, and do not exceed a certain number of impurities. In this way, according to the technical specifications, with accurate identification as evidence, we can get a good product Ethyl 3 - Iodobenzoate.

Preparation Method

To prepare Ethyl 3-Iodobenzoate, prepare the raw materials. 3-Iodobenzoate and ethanol are required as the base. In the reaction kettle, sulfuric acid is used as the catalyst, and temperature is heated. Mix 3-Iodobenzoate and ethanol in an appropriate proportion, and the sulfuric acid catalyzes its esterification. Slow down the temperature to about 60-80 degrees Celsius to make the initial reaction between the two. During this period, closely observe, until the reaction is stable, gradually raise the temperature to 90-110 degrees Celsius to accelerate the reaction process.
After the reaction is completed, pour the product into the separation funnel, wash with saturated sodium carbonate solution to remove residual sulfuric acid and unreacted acid. Then polyester with distilled water to remove salt impurities. The organic phase is dried with anhydrous magnesium sulfate, and the desiccant is filtered off to obtain a crude product.
To obtain a pure product, perform reduced pressure distillation. The temperature is controlled within a specific range, and the fraction is collected according to the boiling point of Ethyl 3-Iodobenzoate. After these steps, pure Ethyl 3-Iodobenzoate can be obtained.

Chemical Reactions & Modifications

Ethyl 3-Iodobenzoate is also an organic compound. In the field of chemistry, we often study its experimental methods and reaction properties.
Looking at its chemical reaction, the activity of halogen atom iodine, often leads to various reactions. When it encounters nucleophiles, iodine is easily replaced, such as with alkoxides, amines, etc., novel compounds can be generated, which is one end of its important reactions.
And its modification method, or by changing the substituent group, adjusts the distribution of its electron cloud to change its physical and chemical properties. If the electron group is added to the benzene ring, it can increase its electron cloud density and affect its reactivity.
or change the reaction conditions, temperature, solvent, can cause the reaction rate and product differences. Good research on the reaction and modification of this compound will be of great benefit to the organic synthesis industry. It can open up new paths and produce more useful substances.

Synonyms & Product Names

Ethyl 3-Iodobenzoate is also a compound of organic chemistry. Its synonymous name, or ethyl 3-iodobenzoate. The name of the market commodity, also known as such. This compound is widely used in the field of organic synthesis. It can be used as an intermediate to participate in various chemical reactions to produce other organic substances. Chemists often explore its reaction characteristics and synthesis methods in the process of research. Ethyl 3-Iodobenzoate can be obtained from different raw materials according to appropriate steps. The study of its properties, related to melting point, boiling point, solubility, etc., is the main point of chemical research, in order to clarify its performance in different environments, and then provide rationale for its practicality.

Safety & Operational Standards

"Ethyl 3 - Iodobenzoate Product Safety and Operation Specifications"
Ethyl 3 - Iodobenzoate is also a chemical product. When preparing, using and storing it, it is necessary to follow safety and operation specifications to ensure that everything goes smoothly and does not worry about people and the environment.
When preparing, all utensils must be cleaned and dried to prevent impurities from mixing in and messing with the reaction. The raw materials used must be taken in accurate quantities and operated precisely without deviation. The temperature and time of the reaction should also be strictly monitored and controlled according to the established schedule. If the temperature is too high, the reaction may be accelerated and unexpected changes will occur; if the time is not appropriate, the product will be impure.
In the operating room, ventilated equipment must be good to drain harmful gases and protect the health of the operator. Everyone should be in front of protective equipment, such as gloves, goggles, protective clothing, etc., to avoid direct contact with the product. If you accidentally touch it, you should quickly rinse it with plenty of water and seek medical attention as appropriate.
When storing, it should be placed in a cool, dry and ventilated place to avoid fire and heat sources. Keep away from strong oxidants, strong alkalis, etc., to prevent severe reactions. The container must be well sealed and marked with a clear name, sex and harm.
When handling, handle it with care and do not damage the container. If there is a leak, quickly cut off the fire source, isolate the scene, and strictly prohibit unrelated people from approaching it. Small leaks can be swept in a clean, covered container and then dealt with according to regulations; if there is a large leak, it needs to be blocked by a dike, collected with an appropriate adsorbent, and handed over to a professional.
Ethyl 3 - Iodobenzoate's safety and operating standards are related to everyone's safety and endanger the safety of the environment. All practitioners should follow them carefully and not slack off.

Application Area

Ethyl 3-Iodobenzoate is an important chemical substance with a wide range of application fields. In the field of organic synthesis, it is often used as a key intermediate. With its unique structure, it can participate in many chemical reactions to build more complex organic molecular structures.
In the field of pharmaceutical research and development, Ethyl 3-Iodobenzoate also has certain value. It may be used as a structural unit of lead compounds to help develop new drugs and contribute to human health. For example, the construction of compounds with specific pharmacological activities often depends on their participation in reactions.
In addition, in the field of materials science, this substance also shows potential applications. Or through specific reactions, materials with special properties can be prepared, which adds to the development of the material field. All of these highlight the important position and broad prospects of Ethyl 3-Iodobenzoate in many application fields.

Research & Development

In recent years, Yu dedicated himself to the research of Ethyl 3-Iodobenzoate. This compound has unique properties and wide application, and has potential in the fields of medicine and materials.
At the beginning, there were many obstacles to the synthesis method. If the ratio of raw materials and reaction conditions are slightly different, the product is impure. Yu and his colleagues repeatedly experimented, adjusting the temperature, pressure, and catalyst dosage. After several months, a stable synthesis path was obtained, and the yield gradually increased.
Next, explore its properties. Analyze its structure and characteristics in detail by spectroscopy and chromatography. Also observe its stability in different solvents and environments to clarify its scope of application.
At present, we are seeking its industrialization expansion. Optimize the process, reduce costs and increase efficiency, and Ethyl 3-Iodobenzoate can be used more widely, contributing to the progress of the industry.

Toxicity Research

Since modern times, chemical refinement, all kinds of products have emerged in an endless stream. Today's research on the toxicity of Ethyl 3-Iodobenzoate is quite important.
Examine this substance in detail. Its molecular structure is unique, and the iodine atom is connected to ethyl benzoate. After various experiments, it has been observed that it may interfere with the normal metabolism of cells in vivo. Looking at its effect on mice, if you consume a small amount, you can also see abnormal behavior or a state of depression.
To explore its mechanism of action, or because the iodine atom is active, it is easy to react with biomolecules in the body, destroy the structure and function of proteins, and cause cell damage. And this substance degrades slowly in the environment, which may accumulate in the ecosystem and endanger all organisms. Therefore, we should treat it cautiously, study its toxicity in depth, and seek preventive measures to protect the safety of life and the environment.

Future Prospects

I am committed to the research and development of Ethyl 3 - Iodobenzoate. This substance is also unique in nature and has a wide range of uses, and has its potential in various fields. In the future, it is expected to shine in the field of medicine. Or it can open up a new path for the production of new drugs and save patients from pain. Or in the field of materials, emerge, create extraordinary quality, and meet the needs of the times.
We should be diligent in our hearts, investigate it carefully, explore its subtleties, and tap its potential. With time, we will be able to make the advantages of Ethyl 3 - Iodobenzoate fully apparent, use it for the world, and benefit all people. This is our future ambition and prospect.

Historical Development

Ethyl 3 - Iodobenzoate is an important compound in the field of organic synthesis. Tracing its historical development, chemists in the past explored the synthesis of organic compounds, and achieved this result through many attempts and research. At the beginning, the synthesis technology was still immature, and the yield was quite low. However, with the passage of time, the chemical technology has improved, and many new synthesis methods have emerged. In the past, the synthesis conditions were harsh, and the raw materials were rare. Nowadays, with the development of the chemical industry, the acquisition of raw materials has become easier, and the synthesis process has become simpler and more efficient. Many scholars have deeply explored its reaction mechanism, laying the foundation for optimizing the synthesis path. In this way, Ethyl 3 - Iodobenzoate has gradually become a commonly used and important substance in the field of organic synthesis from a niche compound that was difficult to synthesize in the early days. Its development process reflects the progress and leap of the chemical discipline.

Product Overview

"Ethyl 3 - Iodobenzoate"
Ethyl 3 - Iodobenzoate is an organic compound. It is formed by the esterification reaction of benzoic acid and ethanol, and the introduction of iodine atoms under specific conditions. The structure of this compound is that on the benzene ring of benzoic acid, there is an iodine atom at position 3, and the carboxyl group is esterified with ethanol to form an ethyl ester group.
Looking at its physical properties, Ethyl 3 - Iodobenzoate is often colorless to light yellow liquid at room temperature, with a certain volatility and a special smell. Its density is greater than that of water, and it is difficult to dissolve in water. It can be soluble in most organic solvents, such as ethanol, ether, etc.
When it comes to chemical properties, its chemical activity is quite high because it contains iodine atoms and ester groups. Iodine atoms can undergo nucleophilic substitution reactions, while ester groups can be hydrolyzed to benzoic acid and ethanol under the catalysis of acids or bases. In the field of organic synthesis, Ethyl 3-Iodobenzoate is often used as a key intermediate, which can be used to prepare a variety of iodine-containing drugs, fine chemicals and functional materials. It is of great value in organic chemistry research and industrial production.

Physical & Chemical Properties

Ethyl 3 - Iodobenzoate is also an organic compound. Its physical properties are mostly liquid at room temperature, transparent in color, and have a slightly special smell. The boiling point is quite high, about a certain temperature range, due to the force between molecules. The melting point also has a specific value, which is related to its lattice structure.
On its chemical properties, the iodine substitute of ethyl benzoate, the iodine atom on the benzene ring can participate in the nucleophilic substitution reaction. In the case of nucleophilic reagents, the iodine atom is easily replaced, because the iodine atom has good departure properties. Its ester group part can undergo hydrolysis reaction. Under acid-base conditions, the hydrolysis rate is different from that of the product. In acidic medium, 3-iodobenzoic acid and ethanol are hydrolyzed; in alkaline environment, 3-iodobenzoic acid and ethanol are generated. This is due to the functional group characteristics in its molecular structure, which is an important direction of chemical research.

Technical Specifications & Labeling

Ethyl 3 - Iodobenzoate is an important organic compound. Its preparation process needs to strictly follow specific technical specifications and standards. When preparing, the selection of raw materials is extremely critical, and its purity and quality must be guaranteed. The reaction conditions also need to be precisely controlled, and parameters such as temperature, pressure, reaction time, etc. will all affect the quality and yield of the product.
For the product index of Ethyl 3 - Iodobenzoate, the purity should reach a specific high standard, and the impurity content should be strictly controlled at a very low level. The appearance needs to show specific properties, and there is no visible foreign matter. In addition, the relevant physical and chemical parameters, such as melting point, boiling point, etc., must also conform to the established specifications, which are all key elements to ensure product quality and performance, so as to obtain high-quality Ethyl 3-Iodobenzoate products.

Preparation Method

Ethyl 3 - Iodobenzoate is an important organic compound. The preparation method involves raw materials, production processes, reaction steps and catalytic mechanisms.
Preparation of raw materials requires ethyl benzoate and iodizing reagents. Ethyl benzoate comes from a wide range of sources and can be prepared by esterification of benzoic acid and ethanol. Iodizing reagents, such as a mixture of potassium iodide and iodine, are the key to introducing iodine atoms.
In the production process, ethyl benzoate is first placed in a reactor at a moderate temperature, such as 50 to 60 degrees Celsius, to create a suitable reaction environment. Then slowly add iodizing reagents and stir at the same time to make the reaction sufficient. During the reaction step, the iodine atom nucleophilic attacks the benzene ring of ethyl benzoate and undergoes a substitution reaction.
Catalytic mechanism, an appropriate amount of copper salt can be introduced as a catalyst. Copper ion complexes with iodine ion to enhance the nucleophilicity of iodine ion, speed up the reaction rate, and increase the yield of Ethyl 3-Iodobenzoate. In this way, the target product Ethyl 3-Iodobenzoate can be obtained through delicate regulation of raw materials, processes, steps and catalysis.

Chemical Reactions & Modifications

In the study of modern chemistry, the chemical reaction and modification of Ethyl 3-Iodobenzoate are quite important in the academic community. In order to make Ethyl 3-Iodobenzoate, ethyl benzoate is often used to react with iodine substitution reagents. However, the yield of the initial reaction is not ideal, and the side reactions are frequent.
After being studied by many people, the reaction conditions have been improved. Choose the right temperature and control the temperature to make the molecule active moderately, which not only promotes the progress of the reaction, but also inhibits the interest of the side reaction. And the catalyst is selected, which has strong catalytic power and can guide the reaction in a directional manner, increasing the yield of the main product.
After this change, the yield of Ethyl 3-Iodobenzoate has been greatly improved, and the quality is also good. The beauty of chemistry lies in constantly innovating, exploring the mystery of material changes between reactions and modifications, and paving the way for various applications. This is also the unremitting pursuit of the academic community.

Synonyms & Product Names

Ethyl 3-Iodobenzoate is also an organic compound. Its synonymous name, in the academic community or called ethyl 3-iodobenzoate. This substance is an important raw material in the field of chemical industry. Merchants in the city, or marked with the name Ethyl 3-Iodobenzoate, in recognition of its chemical characteristics; or use the common name of ethyl 3-iodobenzoate, so that everyone can know. It is often a key material in the process of organic synthesis, and can participate in various reactions to produce a variety of products. Whether it is academic research or industrial production, there is a clear distinction between its synonymous name and trade name to ensure correct communication, orderly operation, and great contribution to the advancement of chemistry.

Safety & Operational Standards

"Code of Safety and Operation of Ethyl 3 - Iodobenzoate"
Ethyl 3 - Iodobenzoate, this chemical substance is related to the safety and operation of the experiment and should not be ignored.
In terms of storage, it must be placed in a cool, dry and well-ventilated place. Because of its certain chemical activity, if the environment is humid or the temperature is too high, it may cause chemical reactions, resulting in deterioration or danger. When storing, it should be separated from oxidants, reducing agents, etc. to prevent interaction and cause accidents.
When operating, the experimenter needs to be fully armed, wearing protective clothing, protective gloves and goggles. If this substance comes into contact with the skin or eyes, it may cause burns or irritation. The operation should be carried out in a fume hood to avoid inhalation of its volatile aerosols. If inhaled accidentally, it should be quickly moved to a fresh air place. If the symptoms of discomfort persist, immediate medical attention is required.
When weighing and transferring Ethyl 3-Iodobenzoate, the action should be precise and gentle to prevent spillage. If there is a spill, it should be cleaned up immediately. Cover with suitable adsorption materials first, then collect it carefully, and dispose of the waste according to regulations. Do not discard it at will to avoid polluting the environment.
Furthermore, in the experiment using Ethyl 3-Iodobenzoate, the reaction conditions need to be strictly controlled. Factors such as temperature and reaction time are slightly poor, which not only affects the quality of the product, but also may bring potential safety hazards. The reaction device should be well sealed to prevent leakage.
In short, Ethyl 3-Iodobenzoate should be treated with rigor and prudence, and safety and operating standards should be strictly followed, so as to ensure the smooth progress of the experiment, as well as the safety of the experimenter and the safety of the environment.

Application Area

Ethyl 3-Iodobenzoate is an important compound in organic synthesis. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate to assist in the synthesis of drug molecules with specific biological activities. With its structural properties, it can participate in many chemical reactions, achieve precise construction and modification of drug molecular structures, and then lay the foundation for the development of new drugs.
In the field of materials science, Ethyl 3-Iodobenzoate can be used to prepare functional materials with special properties after conversion through specific reactions. For example, it can impart unique optical, electrical or mechanical properties to materials through polymerization reactions or blending with other compounds to meet the diverse needs of material properties in different fields.
In addition, it is also an indispensable raw material in the production of fine chemicals. It can be used to synthesize various fine chemicals, such as fragrances, dyes, etc., with its unique chemical properties, giving the product unique quality and characteristics.

Research & Development

In recent years, Yu dedicated himself to the research of the organic compound Ethyl 3 - Iodobenzoate. 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. After repeated experiments, I tried to react with ethyl benzoate and iodizing reagents, but the yield was not as expected. After careful study, I adjusted the reaction conditions, such as temperature, solvent, and catalyst. After repeated trials, a method was finally obtained, which can significantly improve the yield.
Study its properties, and observe its physical and chemical properties in detail. Observe its solubility in different solvents, measure its melting point and boiling point, and explore its spectral characteristics. It also studies the chemical reactions in which it participates, observes its reaction mechanism, and hopes to expand its application scope.
Looking to the future, it is expected to further develop new uses of Ethyl 3-Iodobenzoate in medicine, materials and other fields based on this research, promote the development of organic chemistry, and contribute to the progress of science.

Toxicity Research

About the toxicity study of Ethyl 3-Iodobenzoate
Today's investigation of the toxicity of Ethyl 3-Iodobenzoate is an urgent matter, which is related to the health of everyone and the safety of the environment.
Looking at this substance, its molecules contain iodine and ethyl benzoate structures. After experiments, it has been observed that at a specific concentration, it has an impact on the tested organisms. At the cellular level, it may interfere with the normal metabolism of cells, damage their membrane structure and function, and cause cell physiological abnormalities.
In animal experiments, at low doses, there may be slight behavioral changes and fluctuations in physiological indicators; high doses can cause damage to organs, especially liver and kidney, because liver and kidney are important for detoxification and metabolism.
Furthermore, considering the environmental impact, if it enters the environment or enriches through the food chain, it endangers the ecological balance. Although Ethyl 3-Iodobenzoate has its use in industrial and other fields, toxicity studies warn that it must be used with caution to prevent its escape and avoid irreversible harm, in order to ensure the safety of human beings and the environment.

Future Prospects

Ethyl 3-Iodobenzoate is the best product of transformation. In today's world, the research and development of this product is in progress, and the use of this product is not good. The prospect of the future, can be improved. Its method may be exquisite, and the quantity can also be increased. It can be used in many fields, such as research and development, hoping to help develop a good recipe and cure diseases. Or in the research and development of materials, to promote the development of new materials, so as to meet the needs of the world. It can also be transformed into the needs of the reverse, and the exploration of the theory can be promoted, so that the realm of transformation can be updated. In this way, Ethyl 3-Iodobenzoate has not been developed, full of hope, and must be used in the field of transformation, and it will be greatly colorful.

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Frequently Asked Questions

As a leading Ethyl 3-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 3-iodobenzoate?

Ethyl 3-iodobenzoate is an important raw material for organic synthesis. In the field of organic synthesis, it has a wide range of uses.
First, it can be used to prepare a variety of benzoate ester derivatives. After various chemical reactions, such as nucleophilic substitution, its iodine atom can be replaced with other functional groups, and then complex compounds can be constructed. This is of great significance in the field of medicinal chemistry, because it can be modified by structure to create new drug molecules with unique pharmacological activities.
Second, it is also used in materials science. After a specific reaction, it can be introduced into the structure of polymer materials to change the physical and chemical properties of the materials, such as improving the thermal stability and solubility of the materials, to meet the special needs of material properties in different fields.
Third, in the multi-step reaction sequence of organic synthesis, ethyl 3-iodobenzoate often acts as a key intermediate. By ingeniously designing the reaction path, complex carbon skeleton structures can be constructed through it, laying the foundation for the synthesis of natural products, functional organic molecules, etc.
Furthermore, in organometallic catalytic reactions, it can be used as a substrate to participate in the reaction, synergize with metal catalysts, achieve precise chemical bond construction and conversion, and assist in the synthesis of high-purity, high-stereoselectivity organic compounds, promoting the development and progress of organic synthesis chemistry.

What are the physical properties of Ethyl 3-iodobenzoate?

Ethyl 3-iodobenzoate, ethyl 3-iodobenzoate, is an organic compound. Its physical properties are as follows:
Viewed at room temperature, this compound is a colorless to pale yellow liquid with a clear texture. This color and properties are quite common in organic liquids, and also conform to the general characteristics of this class of halogen-containing benzoates.
Smell, it has a special aromatic smell, which is derived from the structural characteristics of benzene rings and ester groups. The existence of aromatic smell is also common to many benzoic acid ester compounds.
Its boiling point is within a certain range, and it boils at a higher temperature due to intermolecular forces. Among them, the presence of ester groups and iodine atoms increases the intermolecular forces, resulting in an increase in the boiling point. The melting point of
is relatively low, and it is liquid at room temperature, which is closely related to the spatial structure of the molecule and the interaction between molecules. The molecular structure does not form a close and regular arrangement, so the melting point is not high.
The density is greater than that of water, and when mixed with water, it will sink to the bottom. This is due to the large relative atomic weight of iodine atoms in the molecule, resulting in an increase in the overall density.
In terms of solubility, it is slightly soluble in water, but soluble in common organic solvents such as ethanol, ether, chloroform, etc. This is because the compound is an organic molecule and follows the principle of "similar miscibility". Water molecules are polar molecules, and the polarity of the organic molecule is relatively weak, so it is difficult to dissolve in water and easily soluble in non-polar or weakly polar organic solvents.

What are the synthesis methods of Ethyl 3-iodobenzoate?

There are several ways to make ethyl 3-iodobenzoate.
First, it can be obtained by esterification of 3-benzoic acid and ethanol, and then by the action of iodizing reagents. First, take an appropriate amount of 3-benzoic acid and place it in a reactor, add an appropriate amount of ethanol and a catalyst amount of concentrated sulfuric acid, heat it to a certain temperature, and maintain the reflux state for a period of time. This is the esterification process, and ethyl benzoate can be obtained. After that, ethyl benzoate and iodizing reagents, such as sodium iodide, potassium iodide, etc., are heated in an appropriate organic solvent, such as acetone. After a series of separation and purification operations, ethyl 3-iodobenzoate can be obtained.
Second, react with 3-iodobenzoyl chloride with ethanol. First prepare 3-iodobenzoyl chloride, take 3-iodobenzoic acid and react with thionyl chloride to obtain 3-iodobenzoyl chloride. Slowly drop it into a reaction vessel containing ethanol, control the reaction temperature, and after the reaction is completed, remove impurities through washing, drying, and distillation to obtain pure ethyl 3-iodobenzoate.
Third, use the Grignard reagent method. First prepare Grignard reagent from 3-iodobromobenzene, and react 3-iodobromobenzene with magnesium chips in anhydrous ether. Then the Grignard reagent is reacted with carbon dioxide, and then acidified and esterified. That is, 3-iodobenzoic acid is first reacted with carbon dioxide, and then esterified with ethanol. According to the previous method, ethyl 3-iodobenzoate can also be obtained.
These methods have their own advantages and disadvantages, and they need to be used according to the actual situation, such as the availability of raw materials, cost, and difficulty of reaction conditions.

What are the precautions for Ethyl 3-iodobenzoate during storage and transportation?

Ethyl 3 - iodobenzoate is an organic compound. When storing and transporting, there are several precautions to be taken.
First, it is related to storage. This compound should be placed in a cool, dry and well-ventilated place. Since it is more sensitive to heat, it is easy to decompose or deteriorate due to heat, so it should be avoided in a high temperature environment and must not be near fire or heat sources. In addition, it must be sealed and stored to prevent contact with air, moisture, etc. Because moisture may cause hydrolysis reactions, its purity and stability should be affected. When storing, it should be separated from oxidants, acids, bases, etc. to prevent chemical reactions.
Second, about transportation. During transportation, ensure that the packaging is complete and tightly sealed to prevent leakage. This substance may be dangerous in the event of vibration, collision, etc., so proper fixing and buffering measures need to be taken to ensure smooth transportation. The means of transportation should also be clean and dry, and no substances that can react with it should remain. In addition, the transporter needs to be familiar with its characteristics and emergency treatment methods, and can respond quickly and correctly in case of leakage.
In short, when storing and transporting Ethyl 3-iodobenzoate, it is necessary to strictly follow the relevant safety regulations and operating procedures, so as to ensure its quality and safety, and avoid potential dangers and losses.

What is the market price of Ethyl 3-iodobenzoate?

Ethyl 3-iodobenzoate is an organic compound, the Chinese name is ethyl 3-iodobenzoate. Its market price varies due to a variety of factors, and it is difficult to determine exactly.
First, the preparation method will affect the price. If ethyl benzoate is used as the starting material and iodine atoms are introduced into the halogenation reaction to prepare, the cost of raw materials and reaction conditions will be related to the price. If the raw materials are easily available and the reaction conditions are mild, the cost may be reduced; conversely, if special reagents and harsh reaction conditions are required, the cost will be high and the price will rise accordingly.
Second, the purity has a great impact on the price. High-purity Ethyl 3-iodobenzoate is in high demand in scientific research and high-end chemical industries, because it has few impurities and can ensure the accuracy and stability of experiments and production. In order to achieve high purity, finer separation and purification processes are required, which will undoubtedly increase costs and lead to high prices; while those with lower purity are suitable for scenarios with low requirements, and the price is relatively cheap.
Third, the market supply and demand relationship determines the price. In the fields of pharmaceutical research and development, materials science, etc., if the demand for Ethyl 3-iodobenzoate suddenly increases, and the production supply is difficult to keep up in time, the price will rise; if the market demand is weak and the supply is sufficient, merchants may reduce prices for promotional sales.
Fourth, the scale of production also has an impact. In large-scale production, due to the scale effect, the unit production cost may be reduced, and the price is more affordable; in small-scale production, the unit cost is high, and the price is naturally higher.
In summary, the market price of Ethyl 3-iodobenzoate is in dynamic change, ranging from tens of yuan per gram to hundreds of yuan or even higher. For the exact price, please consult the chemical product supplier in detail, and the real-time market conditions shall prevail.