Methyl O Iodobenzoate
Iodobenzene

Methyl O-Iodobenzoate

Fengxi Chemical

Specifications

HS Code

561006

Chemical Formula C8H7IO2
Molar Mass 264.04 g/mol
Appearance White to off - white solid
Melting Point 45 - 48 °C
Boiling Point 260 - 262 °C
Density 1.725 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 110 °C
Stability Stable under normal conditions, but may react with strong oxidizing agents

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

Packing & Storage
Packing 100 g of Methyl O - iodobenzoate packaged in a sealed, labeled chemical - grade bottle.
Storage Methyl O - iodobenzoate should be stored in a cool, dry place away from heat sources and ignition sources. Keep it in a tightly - sealed container to prevent exposure to air and moisture, which could potentially lead to decomposition. Store it separately from incompatible substances like strong oxidizing agents and bases to avoid chemical reactions.
Shipping Methyl O - iodobenzoate is shipped in well - sealed, corrosion - resistant containers. Special care is taken to ensure stability during transit, adhering to all chemical shipping regulations to prevent any potential leakage or hazard.
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Methyl O-Iodobenzoate
General Information
Historical Development
Methyl O-Iodobenzoate is also an organic compound. Its historical development can be traced back to the past. In the early years, the chemists studied the way of organic synthesis, and they worked hard on the exploration of benzoic acid derivatives. At that time, the synthesis method was still simple, and it was quite difficult to obtain this product.
After the years, the chemical technology improved day by day. All kinds of new reagents and new methods emerged, and the method of synthesizing Methyl O-Iodobenzoate became more and more refined. Chemists analyzed its reaction mechanism, improved the process, and the yield and benefit were all improved.
Looking at its development path, it is due to the unremitting research of chemists of all ages. With wisdom and hard work, Methyl O-Iodobenzoate has been synthesized in a difficult situation. As for the state that can be used for scientific research, industry, etc., it has left a strong trace in the field of organic chemistry.
Product Overview
Product Overview of Methyl O - Iodobenzoate
Methyl O - Iodobenzoate is a crucial chemical in the field of organic synthesis. Its properties are colorless to light yellow liquid with a unique odor.
From the perspective of chemical structure, this compound is derived from the structure of methyl benzoate and introduces iodine atoms at the ortho position. This unique structure gives it special chemical activity. In organic synthesis reactions, it is often used as a key intermediate.
Preparation of this product, often follows a specific chemical path, using benzoic acid and iodine substitutes as raw materials, and is carefully synthesized through multi-step reactions. The synthesis process requires precise control of reaction conditions, such as temperature, pH, and reaction time. A slight deviation will affect the yield and purity.
In the field of application, due to its special structure and activity, it can be used as a lead compound in the field of medicinal chemistry to construct key structural fragments and help the development of new drugs. In the field of materials science, it may participate in the synthesis of functional materials, giving materials special optical or electrical properties.
In short, although Methyl O-Iodobenzoate is a chemical, it has significant value in many fields and has a significant role in promoting chemical research and industrial production.
Physical & Chemical Properties
Methyl O - Iodobenzoate is an organic compound, and its physical and chemical properties are particularly important. Looking at its physical properties, at room temperature, this substance is in a liquid state, with a clear and transparent color and a special odor. Its boiling point is quite high, about [X] ° C, due to strong intermolecular forces. The melting point is about [X] ° C, reflecting the molecular arrangement characteristics.
On its chemical properties, it has unique reactivity because it contains ester groups and iodine atoms. Ester groups can be hydrolyzed, and can react with water to form o-iodobenzoic acid and methanol under the catalysis of acids or bases. Iodine atoms are active and can participate in nucleophilic substitution reactions. If they interact with nucleophiles, iodine atoms can be replaced to derive various compounds. These physical and chemical properties provide a solid foundation for their application in organic synthesis and other fields.
Technical Specifications & Labeling
Methyl O-Iodobenzoate is also used to transform things. The method of its quality is to follow the technique. First take the amount of raw materials, according to a certain proportion, and put them in the container. With the measurement of precision, determine the quality of the material.

Of the Only in accordance with this technology can we obtain a good Methyl O-Iodobenzoate for general use.
Preparation Method
To prepare Methyl O-Iodobenzoate, the raw materials and production process, reaction steps and catalytic mechanism are the key. First take o-iodobenzoic acid as raw material, take an appropriate amount of methanol as solvent, and mix the two in a certain proportion. In the reaction vessel, sulfuric acid is added as a catalyst, which is to promote the reaction by taking advantage of its acidity. When heated to a suitable temperature, generally about 60-80 degrees Celsius, the esterification reaction is initiated.
The reaction steps are as follows: After the raw materials are mixed evenly, slowly heat them, and continue to stir during the process to make the reaction sufficient. This reaction is a reversible reaction. In order to improve the yield, the amount of methanol can be appropriately increased, and the balance can be shifted to the right by using the principle of Le Chatelier.
The catalytic mechanism is that the hydrogen ion provided by sulfuric acid interacts with the carboxyl group of o-iodobenzoic acid, making it easier to undergo nucleophilic substitution reaction with methanol to generate Methyl O-Iodobenzoate. After the reaction is completed, the pure product can be obtained through subsequent operations such as separation and purification.
Chemical Reactions & Modifications
In this study, the chemical and reverse modification of methyl ortho-iodobenzoate is studied. This chemical is also attractive for its high-quality, anti-chemical properties.
The anti-chemical properties of methyl ortho-iodobenzoate are often involved in esterification, esterification, etc. Esterification requires high temperature and low temperature, in order to promote its formation. However, its anti-chemical rate is often blocked. To increase the rate of growth, it can be more catalytic, or anti-chemical environment.
As for modification, it aims to improve its properties. Or add groups, change its properties, and improve its solubility and anti-chemical properties. The method of modification is to synthesize and synthesize according to its purpose, which is just right.
>, the chemical and anti-chemical modification of methyl ortho-iodobenzoate, the weight of chemical research, to be further explored in order to expand its use and promote chemical.
Synonyms & Product Names
Methyl O-Iodobenzoate, also known as methyl o-iodobenzoate. Its synonym is a common thing in chemical naming. In my way of chemical research and exploration, I know that this thing has a variety of names, all due to differences in naming rules and habits.
Methyl o-iodobenzoate is a commonly used raw material in organic synthesis. Its preparation method depends mostly on chemical principles and processes, and can be obtained through multi-step reactions. This product is obtained from the esterification reaction of o-iodobenzoic acid and methanol under suitable catalysts and conditions.
In the chemical industry, its synonym or is related to the reaction path and raw materials. However, no matter what the name is, its chemical essence and properties remain unchanged. In experimentation and production, knowing its synonyms can avoid confusion, and accurate use is of great significance for promoting chemical research and industrial production.
Safety & Operational Standards
Rest and Handle Methyl O - Iodobenzoate is also a product of transformation. Its preparation, handling and storage should follow the order of safety and regulation.
At the beginning of preparation, all utensils must be clean and clean to prevent defilements from messing with the process. The amount of various medicines should be weighed accurately, with no difference in the millimeter, in order to be able to obtain what is reasonably desired. On the contrary, temperature and pressure are both important and cannot be ignored. The height of temperature can be adjusted to the speed and direction, so it should be adjusted with a thermostat to make it constant at the appropriate value. The same is true for pressure regulation, which is the basis for safety and formation.
When handling, the operator must be cautious and careful. The hands must be clean to prevent fouling. Wear protective gear, such as rubber gloves, goggles, etc., to prevent the medicine from hurting the body. When taking and taking medicine, use adapters, do not touch it with your hands. When pouring medicine, be slow and steady to avoid its splashing. If there is air coming out of the middle, use a pass device to guide it, so as not to cause danger if the gas gathers.
When in use, there are also rules. Methyl O-Iodobenzoate should be placed in a cool and dark place, protected from heat and light, to prevent it from changing. The memory must be sealed to prevent the entry of air and moisture. When using it, use the amount you need, do not spend extravagantly. After use, the quick sealer returns to its place. If there is a waste medicine, it should not be discarded indiscriminately, but it should be dealt with in accordance with regulations to ensure the cleanliness of the environment.
All these are the regulations of Methyl O-Iodobenzoate safety and management. Follow them, and things can be done without risk; otherwise, they will suffer and regret late. Operators must not ignore it.
Application Area
Methyl O-Iodobenzoate is also an organic compound. Its application field is quite wide. In the field of pharmaceutical synthesis, it is often a key intermediate. Because of its unique structure, it can react ingeniously with many reagents to facilitate the preparation of specific drugs, which contributes to the treatment of diseases.
In the field of materials science, it also has its uses. Or it can participate in the synthesis of special materials, giving materials different properties, such as enhancing the stability of materials and improving their optical properties, making materials suitable for multiple scenarios.
Furthermore, in the field of fine chemicals, methyl o-iodobenzoate can be used as a special additive. Adding to specific products can optimize product quality and enhance its market competitiveness, which is an indispensable ingredient in fine chemicals. From this point of view, it has important value in various application fields.
Research & Development
Today, researchers are studying the product of Methyl O-Iodobenzoate. This product is quite important in the chemical industry and has a wide range of uses.
At the beginning, the method of its synthesis was studied. After various attempts, select suitable materials and methods, control temperature, time and other conditions, and hope to obtain high-purity products.
Then, study its properties. Measure its degree of melting and solubility, etc., and observe its chemical properties in different agents and environments to clarify its reaction rules.
Furthermore, think about its extension. Thinking that it can develop new paths in the fields of medicine, agriculture, etc., then explore its ability to combine with other things, hoping to create more excellent yields.
After many studies, the understanding of Methyl O-Iodobenzoate has gradually deepened, and it will be widely used and promoted in the future, paving stones and building roads, expecting to shine in the chemical industry, developing new looks, and promoting its research and advancement.
Toxicity Research
Taste the essence of medical science, distinguish the good and evil of medicine, and detect its toxicity, which is related to human life. Today's research on Methyl O-Iodobenzoate, the study of toxicity, is a top priority.
Detailed examination of its properties, Methyl O-Iodobenzoate has a unique structure. After various experiments, under specific circumstances, it comes into contact with other substances, or produces strange changes. In animal experiments, when this substance is administered, it can be seen that the physiological appearance of the subject has changed, and the behavior and behavior are abnormal. It may damage the function of the organs, cause poor qi and blood, and block the meridians.
However, the appearance of toxicity is also restricted by many parties. The size of the dose and the way of applying the medicine are all key. Use it in small amounts, or only cause minor diseases. If it is done in excess, it will cause disaster. And different species have different tolerances to it, and human conditions need to be carefully observed.
If you want to understand its harm and protect the well-being of all living beings, you should investigate it carefully. Use scientific methods to explore the secret of its toxicity, and provide clear evidence for medical medicine to prevent the scourge from being invisible.
Future Prospects
I have tried to study Methyl O-Iodobenzoate, observe its properties, and explore its preparation method. Its quality is also pure and stable in nature. In various reactions, it often shows wonderful changes, making it a treasure of organic synthesis.
Looking at the future prospects of this thing, it will be widely used. In the field of medicine, it may help to create new drugs and cure human diseases; in materials science, it may inspire the development of new materials and create extraordinary qualities. Although the road ahead is long, I believe its potential is infinite.
The way of scientific research, although there are many thorns, we researchers should have the determination to be tenacious, and with a fearless heart, explore its mysteries and explore its secrets. Over time, Methyl O-Iodobenzoate will surely shine brightly, adding luster to human well-being, and painting a magnificent picture in the scientific world of the future.
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Frequently Asked Questions

As a leading Methyl O-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 physical properties of Methyl O-iodobenzoate?
The physical properties of methyl o-iodobenzoate are as follows: This substance is mostly liquid at room temperature. It is clear and transparent in appearance, and its color is close to water and slightly yellowish. If it is placed under light, its luster can be seen. It has a specific smell. Although it is not pungent or intolerable, it is also clearly distinguishable. It is similar to the mixed smell of some xyfonyl esters, and has a faint sweet smell. Methyl o-iodobenzoate has a density greater than that of water. If it is dropped on water, it can be seen that it slowly sinks and accumulates at the bottom of the water. Its boiling point is quite high, and it requires strong heat to make it boil and vaporize. This characteristic is due to the strong interaction between molecules. Under normal temperature, its volatilization rate is relatively slow, and it can maintain a relatively stable state in the air. Furthermore, this substance exhibits good solubility in most organic solvents, such as ethanol, ether, etc., and can be uniformly mixed with it to form a uniform solution. However, its solubility in water is very small. Due to the large proportion of hydrophobic groups in its molecular structure, the interaction with water molecules is weak, making it difficult to dissolve in water. In terms of melting point, it is in a relatively low temperature range, and it is easy to change from solid state to liquid state when it encounters a little warmth. The characteristics of this physical transformation make it unique in specific processing and application scenarios. Convenience and performance.
What are the chemical properties of Methyl O-iodobenzoate?
Methyl o-iodobenzoate is one of the organic compounds. It has unique chemical properties and is quite important. In this compound, the ester group is connected to the o-iodophenyl group. In terms of chemical activity, the ester group can undergo hydrolysis reaction. Under acidic or alkaline conditions, the hydrolysis process is different. In acidic media, hydrolysis is a reversible reaction, which will gradually generate o-iodobenzoic acid and methanol; in alkaline environments, the hydrolysis reaction is more thorough, resulting in o-iodobenzoate and methanol. This reaction is often used in organic synthesis to prepare corresponding carboxylic acid compounds. Furthermore, the iodine atoms on its benzene ring can participate in nucleophilic substitution reactions due to the characteristics of iodine atoms. If there is a suitable nucleophilic reagent, the iodine atom can be replaced to derive a series of different compounds, which provides a rich path and possibility for organic synthesis. In addition, due to the conjugate structure of the benzene ring, the compound can also undergo electrophilic substitution reaction under certain conditions, introducing other functional groups at specific positions of the benzene ring, thereby expanding its chemical properties and application range. Due to the interaction of different functional groups contained in it, methyl iodophthalate has shown unique reactivity and application value in the field of organic synthesis.
What are the common synthesis methods of Methyl O-iodobenzoate?
The common synthesis methods of methyl o-iodobenzoate generally include the following. First, o-iodobenzoate and methanol are used as raw materials to form an esterification reaction. This reaction requires acid as a catalyst, common such as sulfuric acid. Put o-iodobenzoate and methanol in a reaction vessel in an appropriate ratio, add an appropriate amount of sulfuric acid, and heat to reflux. Under the catalysis of sulfuric acid, the carboxyl group of o-iodobenzoate and the hydroxyl group of methanol undergo esterification reaction, removing a molecule of water to form methyl o-iodobenzoate. After the reaction, neutralize the sulfuric acid in alkali solution, and then purify the product through separation and distillation. Second, react with o-iodobenzoyl chloride and methanol. First, the chlorination reagents such as o-iodobenzoic acid and thionyl chloride are used to convert the carboxyl group into an acyl chloride to obtain o-iodobenzoyl chloride. After that, the o-iodobenzoyl chloride is dropped into the methanol and the reaction is moderately stirred. This reaction is relatively rapid, and the acid chloride group reacts with the hydroxyl group of methanol to form methyl o-iodobenzoate and hydrogen chloride. After the reaction is completed, the pure product can be obtained by alkali washing, water washing, drying and distillation. Third, the o-iodobenzonitrile is used as the starting material. First, the o-iodobenzonitrile is hydrolyzed to iodobenzoic acid, and then the methyl o-iodobenzoate is reacted with methanol according to the above esterification reaction method. The hydrolysis process is usually carried out at an appropriate temperature with an After alkali-catalyzed hydrolysis, it needs to be acidified to precipitate o-iodobenzoic acid, and the subsequent esterification steps are the same as those using o-iodobenzoic acid as raw material.
Where is Methyl O-iodobenzoate used?
Methyl-o-iodobenzoate has a wide range of uses and is widely used in the field of pharmaceutical and chemical industry. In the field of pharmaceutical creation, it is often a key raw material. Because of its unique chemical structure, it can be prepared through a series of reactions. Or for the synthesis of compounds with specific curative effects, it can participate in the construction of drug molecules, help develop new drugs, treat various diseases, and add a sharp tool for doctors to cure diseases and save people. In the field of chemical production, it is also indispensable. It can be used to synthesize special organic materials, giving unique properties to chemical products. For example, in the preparation of fine chemicals, as an important intermediate, it can promote the smooth progress of the reaction, generate materials with special purposes, or be used in the production of paints, fragrances, etc., to increase its quality and expand its function. Furthermore, in the process of scientific research and exploration, methyl o-iodobenzoate is of great importance to researchers. Because of its structural properties, it can be used as a model compound to assist students in exploring the mechanism of organic reactions, clarifying reaction pathways, and gaining insight into the mysteries of intermolecular interactions. This is important for the improvement of organic chemistry theory and the development of new reactions and new synthesis methods. In summary, methyl o-iodobenzoate plays an important role in many fields such as medicine, chemical industry, and scientific research, promoting progress and development in various fields.
What are the storage conditions for Methyl O-iodobenzoate?
Methyl o-iodobenzoate is one of the organic compounds. The most important storage conditions are in a cool and dry place. A cool cover can prevent its chemical properties from changing due to high temperature, and drying can avoid reactions such as hydrolysis due to water vapor. Store it in a well-ventilated place. With good ventilation, harmful volatile gases can be dissipated, and the risk of explosion and fire can be reduced. Furthermore, keep away from fire and heat sources. Both of these can cause it to burn or explode, endangering safety. When stored, it should also be isolated from oxidants, acids, bases, etc. Because methyl o-iodobenzoate and them are prone to chemical reactions, its quality is damaged, or even dangerous. The packaging must also be in good condition. If the packaging leaks, not only the material is fragile, but also the environment may be polluted and the surrounding area may be endangered. In short, in order to properly store methyl o-iodobenzoate, it must be cool, dry, well ventilated, away from fire heat sources, isolate other chemicals and ensure that the packaging is intact in order to ensure its stability and avoid disasters.