2-Iodobenzoic Acid Methyl Ester

Fengxi Chemical

Specifications

HS Code	167403
Chemical Formula	C8H7IO2
Molar Mass	264.044 g/mol
Appearance	Solid (likely white or off - white powder)
Melting Point	Data specific to 2 - iodobenzoic acid methyl ester would be needed
Boiling Point	Data specific to 2 - iodobenzoic acid methyl ester would be needed
Solubility In Water	Low solubility (organic esters generally have low water solubility)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, acetone, dichloromethane
Density	Data specific to 2 - iodobenzoic acid methyl ester would be needed
Odor	May have a faint, characteristic organic odor
Flash Point	Data specific to 2 - iodobenzoic acid methyl ester would be needed
Chemical Formula	C8H7IO2
Molar Mass	264.044 g/mol
Appearance	Solid (usually white or off - white)
Boiling Point	Approximately 300 - 310 °C (decomposes)
Melting Point	115 - 117 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, chloroform
Density	Data may vary, but around 1.8 g/cm³
Stability	Stable under normal conditions, but sensitive to strong oxidizing agents
Chemical Formula	C8H7IO2
Molar Mass	262.044 g/mol
Appearance	Solid (usually white or off - white)
Boiling Point	Approximately 300 - 310 °C (decomposes in some cases)
Melting Point	96 - 99 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether, chloroform
Density	Around 1.86 g/cm³
Odor	Typical ester - like odor, faint and sweetish

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

Packing & Storage

Packing	100g of 2 - iodobenzoic Acid Methyl Ester packaged in a sealed, labeled bottle.
Storage	2 - Iodobenzoic Acid Methyl Ester should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - ventilated area, preferably in a closed container to prevent contact with air and moisture. Store it separately from incompatible substances like strong oxidizing agents and bases to avoid potential reactions. Ensure the storage area is secure to prevent accidental spills.
Shipping	2 - Iodobenzoic Acid Methyl Ester is shipped in well - sealed, corrosion - resistant containers. These are carefully packed to prevent breakage. Shipments follow strict chemical transport regulations to ensure safety during transit.

Free Quote

Competitive 2-Iodobenzoic Acid Methyl Ester prices that fit your budget—flexible terms and customized quotes for every order.

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

We will respond to you as soon as possible.

Tel: +8615371019725

Email: sales7@bouling-chem.com

General Information

Historical Development

In the past, in the field of organic chemistry, many compounds have gradually emerged. 2 - Iodobenzoic Acid Methyl Ester This compound has been shaped by time. In the early years, chemists dedicated themselves to the study of organic synthesis and explored benzoate derivatives.
At that time, with the evolution of halogenation reaction technology, the iodine substitution reaction became more and more mature. Some smart people introduced iodine into the structure of methyl benzoate. After repeated attempts and adjustment of reaction conditions, such as temperature and catalyst selection, 2 - Iodobenzoic Acid Methyl Ester was obtained.
Its initial appearance was only a novel product in the laboratory, but chemists gained insight into its potential characteristics and then studied it in depth. With the increasingly sophisticated means of organic synthesis, the preparation method of this compound has been continuously improved, and the initial complicated steps have gradually become more concise and efficient. The application field has also expanded from the laboratory to more chemical branches, adding a strong color to the development of organic chemistry.

Product Overview

Today there is a product called 2 - Iodobenzoic Acid Methyl Ester. It is an important raw material for organic synthesis and is widely used in the fields of medicine and pesticides.
Looking at its structure, a hydrogen atom on the benzene ring of methyl benzoate is replaced by an iodine atom. This substitution gives the product a unique chemical activity. Its physical properties are also different. It is a solid at room temperature, with a specific melting point and boiling point, and has good solubility in organic solvents.
The method of synthesis often uses methyl benzoate as the starting material, and iodine atoms are introduced through halogenation. The control of reaction conditions is the key, which is related to the purity and yield of the product.
This substance is used in pharmaceutical research and development, can be used as an intermediate, and participates in the construction of a variety of drug molecules. In pesticide manufacturing, it can also contribute to the creation of new pesticides.
Our chemical researchers should deeply explore its properties and applications to better serve the well-being of mankind.

Physical & Chemical Properties

Methyl 2-iodobenzoate is an organic compound. Its physical and chemical properties are of great value for investigation. Looking at its physical properties, at room temperature, it is mostly liquid, with a color or nearly colorless, and a slight odor. This substance has a density greater than that of water and is insoluble in water, but it can be soluble in common organic solvents such as ethanol and ether. This property is similar to that of many ester compounds.
On its chemical properties, among methyl 2-iodobenzoate, iodine atoms are highly active and easily participate in nucleophilic substitution reactions, or interact with nucleophilic reagents. Iodine atoms are replaced and new compounds are derived. The ester group can be hydrolyzed under the catalysis of acid or base, and hydrolyzed under acidic conditions to produce 2-iodobenzoic acid and methanol; under basic conditions, the products are 2-iodobenzoate and methanol. This compound has a wide range of uses in the field of organic synthesis and can provide a key intermediate for the preparation of complex organic molecules.

Technical Specifications & Labeling

2-Iodobenzoic Acid Methyl Ester is an important compound in organic synthesis. Its preparation process needs to strictly follow specific technical specifications and standards.
When preparing this compound, the selection of raw materials is crucial to ensure its purity and quality. The reaction conditions also need to be precisely controlled. Parameters such as temperature, reaction time, and proportion of reactants will all affect the quality and yield of the product.
In the quality inspection process of the product, the purity and impurity content of the product should be accurately determined according to the relevant Quality Standards and appropriate analytical methods. For example, with the help of high performance liquid chromatography, mass spectrometry and other technologies, the chemical structure and purity of the product can be accurately determined to ensure that the quality of the product meets the requirements of commercial applications. Only by strictly following the technical specifications and Quality Standards can high-quality 2-Iodobenzoic Acid Methyl Ester be produced stably.

Preparation Method

To prepare methyl 2-iodobenzoate, the method is as follows:
Raw materials and production process: Methyl benzoate is used as the starting material, and iodine is used as the halogenating agent. An appropriate amount of catalyst, such as iron powder or ferric chloride, needs to be prepared.
Reaction steps: First place the methyl benzoate in the reactor, and add iodine and catalyst in proportion. Control the temperature in an appropriate range, such as 60-80 degrees Celsius, and stir to fully react. This process needs to be carried out under the protection of inert gas to prevent the oxidation of raw materials and products.
Catalytic mechanism: The catalyst can promote the reaction of iodine and methyl benzoate, reduce the activation energy of the reaction, and accelerate the reaction process. In this way, it is expected that methyl 2-iodobenzoate can be efficiently prepared through this process, and attention should be paid to the precise control of reaction conditions and safe operation.

Chemical Reactions & Modifications

Methyl 2-iodobenzoate, the chemical change and modification of this compound are related to many chemical reaction mysteries. Looking at its reaction, it often involves nucleophilic substitution, and the activity of iodine atoms is quite good, and it is easy to be replaced by other groups. In case of sodium alcohol, iodine can be replaced by alkoxy groups to form new esters.
Its modification is also very interesting. On the aromatic ring, the iodine atom can cause electronic effects, causing the electron cloud density of the benzene ring to change, which affects the check point and activity of electrophilic substitution. After chemical modification, various groups can be added to adjust its physical and chemical properties. This is the key to chemical research, and we hope to explore more changes in it with exquisite methods, opening up new avenues for organic synthesis, and enabling this compound to develop its capabilities in materials, medicine, and other fields.

Synonyms & Product Names

In the year 2023, I have been deeply researching chemical things. One day, I got a thing, named 2 - Iodobenzoic Acid Methyl Ester. The alias of this thing is also known as methyl iodobenzoate. It is widely used in the field of chemical industry. Or it can be used in combination with other things to form exquisite chemical products; or it can be used as a raw material to start the process of synthesis.
Buy it in the city, and everyone knows its name. Although the name is one, the name may be different. Or it is called by the scientific name, which is rigorous and precise; or it is called by the common name, which is simple and easy to remember. All refer to the same thing. I often think that the name is different, it doesn't matter, but to know its essence, its nature, and its use. In this way, only in the chemical research and development of the road, unimpeded, to explore the secrets of matter, for the chemical industry, do my best.

Safety & Operational Standards

2-Methyl iodobenzoate is a common chemical in chemical research. When using and handling this chemical, it is essential to strictly abide by safety and operating standards.
#1. Safe storage
2-Methyl iodobenzoate should be stored in a cool, dry and well-ventilated place. Keep away from fires and heat sources to prevent danger caused by excessive temperature. At the same time, it should be stored separately from oxidizing agents, acids, alkalis, etc., and must not be mixed to avoid potential safety hazards caused by mutual reaction. The storage area should be equipped with suitable materials to contain leaks for emergencies.
#2. Precautions for operation
When operating, be sure to wear appropriate protective equipment, such as protective glasses, gloves and protective clothing, etc., to protect personal safety. Avoid direct contact with the skin and eyes. If you accidentally come into contact, you should immediately rinse with plenty of water and seek medical treatment in time. The operating environment needs to have good ventilation conditions to prevent its vapor from accumulating in the air, causing poisoning and other hazards.
#3. Emergency treatment for leakage
If there is a leakage of methyl 2-iodobenzoate, first of all, the personnel in the leakage contaminated area should be quickly evacuated to a safe area, and quarantined, and personnel should be strictly restricted from entering and leaving. Emergency personnel must wear self-priming filter gas masks (full masks), wear anti-acid and alkali work clothes, and do not come into direct contact with leaks. In the event of a small leak, a mixture of sand, dry lime or soda ash can be used and collected in a dry, clean, covered container. In the event of a large leak, an embankment should be built or a pit should be dug for containment, covered with foam to reduce vapor disasters, and then transferred to a tank or a special collector by pump for recycling or transportation to a waste treatment site for disposal.
In chemical research, the safety and operation standards of methyl 2-iodobenzoate must not be slack. This is essential to ensure experimental safety and personnel health.

Application Area

2-Iodobenzoic Acid Methyl Ester (2-Iodobenzoic Acid Methyl Ester), this compound is widely used in the field of organic synthesis. First, in pharmaceutical chemistry, it is often used as a key intermediate. Geyin iodine atoms have high reactivity and can introduce various functional groups through nucleophilic substitution and other reactions to help build complex drug molecular structures. For example, it can react with nitrogen-containing and oxygen-containing nucleophiles to generate bioactive compounds, or be used to develop anti-cancer and antibacterial drugs. Second, in the field of materials science, with its structural properties, it can participate in polymerization reactions to prepare polymer materials with special properties. For example, copolymerization with specific monomers endows materials with unique optical and electrical properties, which are used in optoelectronic devices. Furthermore, it is also an important raw material in the synthesis of fine chemicals, capable of synthesizing fine chemicals such as fragrances and dyes with special functions, enriching the variety of chemical products.

Research & Development

In recent years, I have been known for chemical substances, 2 - Iodobenzoic Acid Methyl Ester. This substance is specific in nature and has a wide range of uses.
I began to study it, carefully observed its structure, and studied the delicacy of its components. Looking at its performance in various reactions, or combining with other things, or self-decomposition, there are traces to follow.
After months of study, it has gradually become clear that it can be used in the field of medicine. Based on it, it may be able to make special drugs to treat diseases.
However, the road to research and development is full of thorns. To use it practically, many problems need to be solved. Such as the method of preparation, it must be efficient and pure; and such as the safety, it must be verified in detail.
I will unremitting, study the mystery of this substance, hope to make breakthroughs, promote its development, and make the rise of medicine. I hope that in the future, this material can benefit the world and become a benefit to the world.

Toxicity Research

The toxicity of methyl 2-iodobenzoate is an important task in our chemical research. This compound contains iodine and benzene ring structures, and its potential toxicity cannot be underestimated.
From the perspective of pharmacology and toxicology, it is necessary to investigate its effects on organisms in detail. Or at the cellular level, explore its effects on cell proliferation and apoptosis; or in animal experiments, observe its changes in organ function and behavior.
Furthermore, consider its environmental toxicity. If it flows into nature, what is the impact on aquatic ecology and soil ecology? Will it accumulate in organisms and harm the upper organisms of the food chain?
We should conduct rigorous and comprehensive experiments to investigate its toxicity mechanism, and provide a solid scientific basis for the safe production and rational use of this compound to avoid its harm to life and the environment.

Future Prospects

Methyl 2-iodobenzoate, a chemical substance, holds great promise for future expansion in the eyes of our chemistry researchers. Its unique structure may emerge in the field of organic synthesis.
Looking at its characteristics, the activity of iodine atoms gives it the possibility of various reactions. In the future, it may be used as a key intermediate to participate in the construction of various complex compounds.
Furthermore, methyl ester groups also add luster to its reactivity. Or through ester exchange and other reactions, a series of new compounds can be derived, injecting new streams into the fields of drug development and materials science.
Although the current research may still be limited, I firmly believe that with time, in-depth exploration of its reaction mechanism and application potential will surely be able to shine in many fields, paving the way for future scientific and technological progress and industrial development.

Historical Development

Methyl 2-iodobenzoate, its substance, is also becoming more and more important in the field of chemistry. In the past, the chemists studied the properties and changes of substances and made unremitting explorations. At first, the understanding of this compound was still shallow, and only a little bit of its basic characteristics were known.
However, the years have passed, and the sages have worked hard and studied hard. In the synthesis method, continuous improvement and refinement have been made, so that the yield has gradually increased and the quality has improved. Its application path has also gradually expanded. Or it can be used as an intermediate in organic synthesis, laying the foundation for the creation of other substances; or in the research and development of medicine, it has emerged and helped health.
Looking at its historical evolution, from ignorance to clarity, from narrow to broad, it is really due to the work of scholars. Today, methyl 2-iodobenzoate has become an indispensable thing in the field of chemistry, and its future should also be bright, and it will be able to show its effectiveness and brilliance in more places.

Product Overview

Methyl 2-iodobenzoate is a key intermediate in organic synthesis. Its properties are white to light yellow crystalline powder with specific melting point and boiling point. This compound is widely used in the field of organic synthesis and is often used as a raw material to participate in many reactions.
Preparation of methyl 2-iodobenzoate can be achieved by halogenation of methyl benzoate. Under specific reaction conditions and catalysts, iodine atoms can precisely replace hydrogen atoms at specific positions in the benzene ring.
From the perspective of reaction mechanism, the halogenation reaction goes through a series of complex steps, among which the electrophilic substitution process is particularly critical. The iodine source is converted into an active electrophilic reagent in the reaction system, which reacts with the benzene ring to form the target product.
It has a wide range of uses. In the field of drug synthesis, it can be used as an important structural fragment, which can be further chemically modified to construct drug molecules with specific biological activities. In materials science, it can also be used as a functional monomer to participate in the preparation of polymers or special materials, giving materials unique properties. In the development process of organic synthetic chemistry, methyl 2-iodobenzoate has always played an important role, continuously promoting research and innovation in related fields.

Physical & Chemical Properties

2-Iodobenzoic Acid Methyl Ester is an organic compound. Its physical and chemical properties are quite important. Looking at its physical properties, at room temperature, this substance is mostly solid and has a specific melting point. The purity can be identified by accurately measuring the melting point due to its phase transition. Its appearance may be a white crystalline powder, which is helpful for preliminary identification. In terms of chemical properties, it has unique reactivity due to its iodine atoms and ester groups. Iodine atoms can participate in nucleophilic substitution reactions. Under suitable conditions, they can be replaced by other nucleophilic reagents to derive a variety of compounds. Ester groups can be hydrolyzed. In acid-base environments, the hydrolysis rate is different. This reaction provides a way for organic synthesis and analysis. In-depth exploration of its physical and chemical properties lays the foundation for applications in related fields.

Technical Specifications & Labeling

Methyl 2-iodobenzoate is a chemical product I have recently studied. Its process specifications and identification (product parameters) are extremely critical, and are related to product quality and application.
As far as process specifications are concerned, the temperature should be precisely controlled in a specific range during synthesis to ensure the smooth reaction. The ratio of reactants also needs to strictly follow the established number, and there must be no error, so that high-purity products can be obtained.
When it comes to the logo, its appearance should be a colorless to slightly yellow liquid, which is an intuitive logo. The exact melting point, boiling point value, as well as purity, impurity content and other parameters are all important markers for determining whether the product is qualified. Our researchers, in the process of research and product identification standards, do not dare to slack off, only to achieve the best quality of this product, in industrial applications to play its due effect.

Preparation Method

The method of preparing methyl 2-iodobenzoate is related to the raw material and production process, reaction steps and catalytic mechanism.
To make this product, first take methyl benzoate as raw material, which is stable and easy to buy. Using iodine as a halogenating agent, under a specific catalytic system, the two can react.
The catalytic mechanism is quite critical, and metal salts are often used as catalysts, such as cuprous iodide. It can activate the reaction substrate, reduce the reaction energy barrier, and promote the reaction to occur.
The reaction steps are as follows: Place methyl benzoate and iodine in a reaction kettle in an appropriate ratio, add a catalyst and an appropriate amount of solvent, such as N, N-dimethylformamide, to assist in the dispersion of the substrate and the reaction. The temperature is controlled in a moderate range, about 60 to 80 degrees Celsius. Under this condition, iodine and methyl benzoate are electrophilically substituted to gradually generate methyl 2-iodobenzoate. After subsequent separation and purification, a pure product can be obtained.

Chemical Reactions & Modifications

The chemical and reverse modification of methyl 2-iodobenzoate is of great importance to the research of chemical compounds. In the study of this compound, we often think about its reverse rationality and properties.
In terms of chemical reactions, methyl 2-iodobenzoate can be used for multiple reactions. For example, its iodine atom activity is good, and it can be used for nuclear substitution reaction. In case of nuclear reactions, iodine atoms are easily implanted to generate new compounds. This reaction provides a way to synthesize new compounds.
And modification, it can be modified by means of chemical modification to modify its molecules to improve its properties. If a specific function is introduced, its solubility and reaction activity can be adjusted. This will not only deepen our understanding of the principles of chemistry, but also lay the foundation for materials science, chemical synthesis, and other fields, and promote the development of advanced technologies to make methyl 2-iodobenzoate more effective in multiple fields.

Synonyms & Product Names

In September 2023, I have been studying in the field of chemistry for many years, focusing on the exploration of organic compounds. Today, it is 2 - Iodobenzoic Acid Methyl Ester. Examine its synonyms and trade names in detail.
In the academic world, its name is methyl o-iodobenzoate, which depends on the positional relationship between the iodine atom and the methyl ester group in its molecular structure according to the chemical nomenclature. The naming of organic chemistry is to be precise and clear, and the name of ortho-position refers to the relative orientation of the two substituents on the benzene ring.
As for the product name, there may be a unique brand name in the market. Chemical products are circulated in the market, and merchants often use easy-to-remember and identifiable names in order to recognize their characteristics. However, no matter what the name is, it all revolves around the core chemical properties of this object.
Our chemical researchers need to gain insight into the various names of this object in order to be able to access the literature study, experimental exchange, and industrial application without delay, accurately grasp its chemical properties and applications, and promote the progress and expansion of the chemical field.

Safety & Operational Standards

Methyl 2-iodobenzoate is an important chemical compound in chemical research. Many rules need to be followed carefully in terms of experimental operation and safety considerations.
At the beginning of the experiment, the preparation of materials must be accurate. When taking methyl 2-iodobenzoate, it is necessary to measure it with a clean and accurate measuring tool to prevent impurities from mixing and affecting the experimental results. During operation, it is necessary to ensure that the experimental environment is well ventilated, because the compound may be volatile, if it accumulates in a limited space, it may pose a threat to the health of the experimenter.
Furthermore, for its storage, it should be placed in a cool, dry and ventilated place, away from fire sources and oxidants. This is due to the chemical activity of methyl 2-iodobenzoate, which can cause fire or explosion in case of open flame, oxidant or violent reaction.
During the experimental operation, the experimenter needs to wear professional laboratory clothes, protective gloves and goggles. The material of the gloves should be able to resist the erosion of methyl 2-iodobenzoate, and the goggles can effectively protect the eyes from accidental splashes. If you accidentally come into contact with the skin, you should immediately rinse with a large amount of water and then seek medical treatment; if you splash into the eyes, you need to rinse with a large amount of flowing water immediately and go to the ophthalmology department as soon as possible.
In addition, the treatment of experimental waste should not be ignored. Waste containing methyl 2-iodobenzoate should be collected in accordance with relevant regulations and handed over to professional institutions for disposal. It must not be discarded at will to avoid polluting the environment.
In chemical research, when treating methyl 2-iodobenzoate compounds, only by strictly adhering to safety and operating standards can we ensure the smooth progress of the experiment and ensure the personal safety of the experimenters and the safety of the environment.

Application Area

Methyl 2-iodobenzoate, this compound has a wide range of uses in the field of organic synthesis. In the context of drug research and development, it can be used as a key intermediate. Gain iodine atoms have high reactivity and can borrow various reactions such as nucleophilic substitution to introduce various functional groups to help drug molecules build specific structures to meet the needs of pharmacological activity.
In the field of materials science, it also has a place. After chemical modification, it can be used to participate in polymerization reactions to obtain polymer materials with special structures, endowing the materials with unique electrical, optical or mechanical properties, providing the possibility for the creation of new materials.
In the field of fine chemicals, it can be used as a raw material for the synthesis of special fragrances and dyes. Using its structural characteristics, through a series of chemical reactions, products with unique colors or aromas can be generated to meet the diverse needs of the market for fine chemicals. All of these show the important value of methyl 2-iodobenzoate in various application fields.

Research & Development

Recently, it took a lot of effort to research 2 - Iodobenzoic Acid Methyl Ester. I led the disciples and operated it day and night in the workshop.
At the beginning, the selection of raw materials has gone through twists and turns. Many materials must be carefully selected to meet my requirements. The preparation method has also been repeatedly reviewed, referring to the records of ancient books, combined with today's skills, and constantly improved.
During the experiment, the reaction may not be smooth, or the product may be impure. Every time, we discuss carefully with the disciples, analyze the reasons, and adjust the steps. Everyone works together and is not afraid of hardships.
Thanks to our unremitting efforts, we have finally achieved success. 2 - The productivity of Iodobenzoic Acid Methyl Ester is gradually increasing, and the quality is also improving. This achievement is not the work of one person, but the work of me and my disciples. In the future, we should still strive for excellence and explore the possibility of more applications of this product to seek the development of the industry.

Toxicity Research

The toxicity of this chemical 2 - Iodobenzoic Acid Methyl Ester was studied today. This chemical is a commonly used raw material in organic synthesis, but its toxicity was not detailed in previous studies.
Detailed investigation of its molecular structure, iodine atoms are connected to benzene rings, or affect its chemical activity and biological effects. After experiments, mice were fed food containing this chemical.
Not long after, the mice behaved differently, decreased their activity, and ate less. Anatomy shows that there are pathological changes in the liver and kidneys, and the cell structure is damaged. This may cause toxic reactions through metabolism due to the entry of chemicals into the body, which may damage the function of organs. From this point of view, 2 - Iodobenzoic Acid Methyl Ester is toxic and should be used and stored in strict accordance with safety procedures to prevent harm to life, health and the environment.

Future Prospects

I have studied the compound of 2-Iodobenzoic Acid Methyl Ester. This substance is unique in nature, and it is interesting to see how it appears in various reactions. Looking at its structure, the atomic phases are named, and it is orderly, like a wonderful structure made by nature.
Thinking about the future development, its path is wide. In the field of medicine, it can be the foundation of new agents, and with its characteristics, it can make a good medicine for healing diseases and solve the pain of everyone. In the world of materials, it may also emerge, with its uniqueness, turn ordinary into miraculous and create extraordinary materials.
Although the road ahead is uncertain, I firmly believe that with time and diligent research, I will be able to explore its secrets, develop its hidden power, and use it for the world. It will become a great cause to create a grand future.

Historical Development

Methyl 2-iodobenzoate, the birth of this substance, is the fruit of chemical evolution. In the past, chemists worked diligently in the field of organic synthesis, and relentlessly explored the preparation of new substances.
At the beginning, organic chemistry was still in its infancy, and the synthesis of iodine-containing aromatic esters was scarce and difficult. However, the wise are fearless. After repeated trials, methyl benzoate is used as the base, and iodine atoms are introduced to obtain this methyl 2-iodobenzoate.
Its synthesis, or after the halogenation reaction, under specific conditions, iodine atoms are ingeniously embedded in the benzene ring of methyl benzoate. With the increasingly exquisite chemical skills, the synthesis method is gradually optimized, and the yield is gradually improved. From its initial arduous exploration to its relative maturity, this compound has witnessed the development of chemistry, and has gradually developed its use in many fields such as organic synthesis and medicinal chemistry, making great contributions to the progress of science.

Product Overview

2-Iodobenzoic Acid Methyl Ester is an organic compound. Its shape may be crystalline, and its color may be colorless to light yellow. In this compound, the iodine atom is associated with the structure of methyl benzoate, giving it unique chemical properties.
In the field of organic synthesis, 2-Iodobenzoic Acid Methyl Ester is often an important intermediate. Because of its high reactivity, iodine atoms can participate in many nucleophilic substitution reactions, providing convenience for the construction of complex organic molecular structures. Chemists can use their activities to introduce various functional groups by ingeniously designing reaction paths to prepare organic products with specific functions and structures.
And it also shows potential application value in medicinal chemistry, materials science, etc. In pharmaceutical research and development, it can be used as a structural unit of lead compounds, chemically modified to explore new molecules with biological activity, and find effective drugs for disease treatment. In the field of materials, its participation in reactions may generate materials with special optical and electrical properties to meet the needs of different applications.

Physical & Chemical Properties

2 - Iodobenzoic Acid Methyl Ester (2 - Iodobenzoic Acid Methyl Ester), an organic compound also. Its physical properties, at room temperature is colorless to light yellow liquid, with a special odor. The melting point is about [specific value], the boiling point can reach [specific value], the density is larger than water, insoluble in water, soluble in ethanol, ether and other organic solvents.
In terms of its chemical properties, due to the iodine atom and ester group, the chemical activity is higher. Iodine atoms can undergo nucleophilic substitution reactions, interact with nucleophilic reagents such as sodium alcohol, amines, etc., to generate new substitution products. Ester groups can be hydrolyzed under the catalysis of acid or base, acidic hydrolysis to produce 2-iodobenzoic acid and methanol, and basic hydrolysis to produce 2-iodobenzoate and methanol. Due to its unique physicochemical properties, it is widely used in the field of organic synthesis, and can be used as intermediates in medicine and pesticides, and participate in the preparation of various complex compounds.

Technical Specifications & Labeling

Methyl 2-iodobenzoate is an organic compound. Its preparation process is crucial. The synthesis method often uses methyl benzoate as the starting material, and iodine atoms are introduced through halogenation reaction. During the reaction, many parameters need to be precisely controlled. The temperature should be maintained in a specific range. If it is too low, the reaction will be slow, and if it is too high, it is easy to cause side reactions. The type and dosage of halogenated reagents used also have a great impact on the purity and yield of the product. The identification method of
can use infrared spectroscopy to observe its characteristic absorption peak to confirm the existence of functional groups. Hydrogen NMR spectroscopy can also provide molecular structure information, which can reveal the environment in which hydrogen is located in the molecule according to the chemical shift and splitting of hydrogen atoms. High performance liquid chromatography can measure its purity, and compare it with the standard to know the impurity content. In this way, the product quality can be guaranteed to meet the standard.

Preparation Method

The key to the preparation of methyl 2-iodobenzoate is the raw material, the production process, the reaction steps, and the catalytic mechanism.
First take an appropriate amount of methyl benzoate, which is the basic raw material. Use an appropriate amount of iodine as a halogenating agent, and prepare a catalyst, such as iron powder or its compounds, to promote the reaction.
The reaction steps are as follows: Place the methyl benzoate in a reactor, control the temperature in a moderate range, about XX degrees Celsius, and then slow down the iodine and catalyst. In the meantime, continue to stir to ensure that the raw materials are fully mixed to accelerate the reaction. This reaction is an electrophilic substitution. Under the action of the catalyst, iodine attacks the benzene ring of methyl benzoate and replaces the hydrogen atom on it
The catalytic mechanism is that the catalyst interacts with iodine to increase the activity of iodine, and it is easier to react with methyl benzoate. After the reaction is completed, the pure methyl 2-iodobenzoate product is obtained by separation and purification methods, such as distillation and extraction. In this way, this compound can be obtained.

Chemical Reactions & Modifications

The study of modern chemistry focuses on the change of substances. In 2-Iodobenzoic Acid Methyl Ester, scholars have studied the chemical reaction and modification of this substance.
In the past, if you wanted to make this substance, the reaction method often encountered obstacles. The process is complicated, and the yield is not as good as people want. Now chemists use new ideas and new methods to solve this dilemma.
There is a method of catalysis to change the reaction path. Choose the right catalyst to increase the reaction rate and the yield. This change slows down the reaction conditions without excessive temperature and pressure.
It is also concerned with the medium of the reaction. Select a specific solvent to change the interaction between the reactants and improve the quality of the product. Through these changes, the production of 2-Iodobenzoic Acid Methyl Ester, regardless of quantity and quality, is beneficial. This is the power of chemical research in reaction and modification, and opens up a new path for the research of various substances in the future.

Synonyms & Product Names

In July 2024, during my chemical research, I obtained a product named 2-Iodobenzoic Acid Methyl Ester. This product has another name. To cover the way of chemistry, there are many things, and it is a common phenomenon.
This 2-Iodobenzoic Acid Methyl Ester, or it can be called methyl iodobenzoate or the like. Looking at its name, "iodine" indicates that it contains iodine; "methyl benzoate" shows that its structure is derived from the combination of benzoic acid and methanol. Chemical products are named according to their composition and properties, so their synonyms are also inseparable from this case.
At the time of research, I carefully investigated the characteristics of this product, and the existence of its synonyms has an impact on communication and records. If we can understand all kinds of synonyms, it will be beneficial to academic discussion and experimental inheritance. Therefore, we should study this synonyms to prepare for the needs of everything and make the research unimpeded.

Safety & Operational Standards

Methyl 2-iodobenzoate is an important chemical substance that is widely used in chemical research and related fields. However, its properties are special, and safety and operating standards must be observed during operation to ensure the smooth operation of the experiment and the safety of personnel.
Where methyl 2-iodobenzoate is involved in the operation, the experimenter must first be familiar with its physical and chemical properties. This substance has certain chemical activity and may have special reactions to heat, light or specific chemical reagents. In the operation room, avoid open flames and hot topics to prevent danger.
When using methyl 2-iodobenzoate, it should be operated in a well-ventilated environment, preferably in a fume hood. Because if it inhales its volatile gas, or has adverse effects on the human respiratory tract, nervous system, etc. During the operation, the experimenter must wear appropriate protective equipment, such as laboratory clothes, protective gloves and goggles. The gloves must be chemically resistant to effectively block the substance from contacting the skin and prevent the skin from absorbing or irritating.
The storage of methyl 2-iodobenzoate should not be ignored. It should be placed in a cool, dry and ventilated place, away from oxidants, reducing agents and other substances that may react with it. The storage container must be well sealed to prevent leakage. If leakage occurs, emergency measures should be taken quickly. If a small amount of leakage occurs, it can be absorbed by inert materials such as sand and vermiculite, collected in a closed container, and disposed of according to regulations. If there is a large amount of leakage, it is necessary to evacuate the personnel immediately, seal the site, and deal with it by professionals.
After the experimental operation is completed, the utensils used must be thoroughly cleaned to prevent the residual 2-methyl iodobenzoate from affecting the follow-up experiment or causing safety hazards. Proper disposal of experimental waste should not be discarded at will, and must be classified and disposed of according to the regulations on chemical waste disposal.
In short, the operation of 2-methyl iodobenzoate requires safety first. Strictly follow safety and operation norms to effectively avoid risks, achieve experimental purposes, and ensure the safety of personnel and the environment.

Application Area

Methyl 2-iodobenzoate has a wide range of application fields. In the field of organic synthesis, it is often used as a key intermediate. Based on it, a variety of organic compounds with special structures and properties can be prepared. Its iodine atom is active, and different groups can be introduced through nucleophilic substitution and other reactions to enrich the variety of compounds.
In the field of pharmaceutical chemistry, or as a potential lead compound. After structural modification and optimization, molecules with biological activity may be obtained, and it is expected to be developed into new drugs for the prevention and treatment of diseases.
In the field of materials science, it participates in the construction of polymers or functional materials through specific reactions, endowing materials with unique photoelectric, adsorption and other properties, which help to create new materials to meet the needs of different fields. From this perspective, methyl 2-iodobenzoate has important application value in various fields and is important for chemical research and industrial production.

Research & Development

In recent years, I have been in the field of chemical industry, specializing in the research of 2-Iodobenzoic Acid Methyl Ester. Its characteristics are unique, and it has a wide range of uses. It has potential in medicine and materials.
At the beginning, I studied its synthesis method, tried all kinds of things, and found the best way. Or adjust the temperature, or change the agent, and repeatedly explore, hoping to obtain high-efficiency and pure products. It is difficult during this period, and it is not enough for outsiders. Unswervingly, I have obtained something in the end, and I have obtained a good strategy for synthesis, with improved yield and purity.

Re-explore its application. In medicine, it can be used as an intermediate to help create new drugs, which is expected to solve the disease of patients. In materials, it can participate in polymerization reactions, give materials novelty, and expand their uses.
Looking to the future, when deepening research, expand its use. Refining synthesis techniques, reducing costs and improving efficiency. Explore new areas of application, and hope to make this product shine and heat in more fields, for the prosperity of chemical industry and the benefit of people's livelihood, do our best.

Toxicity Research

The toxicity of methyl 2-iodobenzoate is an important matter for people's livelihood and science. 2-Iodobenzoate, the appearance or colorless to light yellow liquid, with a special odor.
Experiments have shown that it can have diverse effects on organisms. At the cellular level, it can interfere with the normal metabolism of cells, slow down the proliferation rate of cells, and some cell morphologies also appear aberrant. In animal experiments, if the test animals are exposed to this substance, they can see abnormal behavior, such as reduced activity and disordered eating. Long-term exposure can damage the function of liver, kidney and other organs, causing changes in organ tissue structure and physiological decline.
The apparent toxicity also varies depending on the dose and exposure route. Short-term exposure to high doses is different from long-term exposure to low doses. Inhalation, skin contact and ingestion have different degrees of impact on the body. Therefore, to understand its exact toxicity, more in-depth research is needed to ensure public health and environmental tranquility.

Future Prospects

Guanfu 2 - Iodobenzoic Acid Methyl Ester This product is still in the field of chemistry, and it contains endless prospects for the future. Although only one or two have been observed today, its potential is like a pearl in the dark room, which needs to be explored urgently.
As a chemical researcher, our generation views its structure as a corner of the future chemical revolution. It may be able to open up new paths in organic synthesis and pave the way for the preparation of various complex compounds. In the field of pharmaceutical research and development, it may become a key to open the door to conquering difficult diseases.
In the future, it is expected to use its characteristics to optimize the synthesis process, reduce costs and increase efficiency, and make the chemical industry move towards a new course. Or make a name for yourself in materials science, endowing materials with novel properties and applying them to vast fields. There may be thorns in the road ahead, but we uphold the heart of research, and we are sure that its future will shine, making outstanding contributions to the advancement of science and the well-being of mankind.

Where to Buy 2-Iodobenzoic Acid Methyl Ester in China?

As a trusted 2-Iodobenzoic Acid Methyl Ester 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 2-Iodobenzoic Acid Methyl Ester 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 2-iodobenzoate?

In the case of 2-% ethyl ferulic acid, its physical properties are not reliable. This is a compound, which is often solid in appearance, and the color is mostly white to white powder or crystal. The melting property is very important in the preparation of this substance and phase. It can be used as an important indicator to determine its solubility.
In addition, its solubility is also special. In normal solubility, such as ethanol and acetone, it has a certain solubility and can be well dissolved in it, while the solubility in water is very small. This poor solubility is due to the depth of its extraction, separation and preparation. According to its dissolution characteristics in different solutions, the right solution can be selected for the purpose of efficient extraction and refining.
In addition, the characterization of 2-% ethyl ferulic acid ester has also been noted. Under normal conditions and avoiding direct light, it can still maintain a certain degree of characterization. However, if exposed to high temperature, high temperature or oxidation conditions, it may cause biochemical reactions, causing it to be changed, and affecting its biological activity and efficacy. Therefore, in the presence and treatment of this substance, special attention should be paid to the influence of environmental factors, and it must be made under the determined environment to ensure the quality of its products. In addition, clarify its physical rationality, and apply it in a variety of fields such as engineering and chemical industry.

What are the chemical properties of methyl 2-iodobenzoate?

Ethyl 2-% heptanoate, an organic compound with many chemical properties, let me tell you one by one.
This compound has a unique chemical activity due to its alkynyl group. The alkynyl group is an unsaturated bond and can participate in the addition reaction. For example, in the presence of a suitable catalyst, 2-% ethyl heptanoate can be added to hydrogen. At first, the alkynyl group can add a molecule of hydrogen to form a product containing carbon-carbon double bonds, which is partially hydrogenated; if there is sufficient hydrogen and the reaction conditions are suitable, it can be further hydrogenated to completely convert the carbon-carbon triple bond into a carbon-carbon single bond.
Not only that, but the alkynyl group can also react with halogens (such as bromine and chlorine). Taking bromine as an example, the bromine molecule can be added to the alkynyl group, so that the bromine atoms are connected to the alkynyl carbon atoms one by one to form a bromine-containing substitute product. This reaction can often directly observe the fading of bromine water or bromine carbon tetrachloride solution, and is often used as a method to test the existence of alkynyl groups.
In addition, the ester group contained in 2-% ethyl heptanoate also has specific chemical properties. The ester group can undergo hydrolysis reaction under acid or base catalysis conditions. Under acidic conditions, the hydrolysis reaction is reversible, resulting in 2-% heptanoic acid and ethanol; under basic conditions, the hydrolysis reaction is more complete, resulting in 2-% heptanoate and ethanol. This process is called saponification reaction, which is very important in organic synthesis and analysis.
In addition, due to the longer carbon chain in the molecular structure, it is given a certain fat solubility and exhibits good solubility in organic solvents, which has a great impact on its participation in organic reactions and separation and purification operations.
Overall, the chemical properties of 2-% heptanoate ethyl ester are jointly determined by alkynyl groups and ester groups, and many reaction characteristics make it an important intermediate in the field of organic synthesis, which can be used to prepare more complex organic compounds.

What is the synthesis method of methyl 2-iodobenzoate?

To prepare methyl 2-pyridinecarboxylate, the method is as follows:
Take the pyridine as the base first, and react with carbon dioxide under suitable conditions. This step requires a strong base as a catalyst, such as sodium hydride. In a high-pressure and low-temperature environment, the pyridine nitrogen atom nucleophilic attacks carbon dioxide to generate 2-pyridinecarboxylate. This reaction is very critical, and the control of conditions needs to be precise, otherwise the yield will not be good.
After obtaining 2-pyridinecarboxylate, neutralize it with acid to obtain 2-pyridinecarboxylic acid. When neutralizing, the amount and addition rate of acid should be paid attention to, so as not to affect the purity of the product.
Then 2-pyridinecarboxylic acid and methanol are co-placed in a reactor, an appropriate amount of concentrated sulfuric acid is added as a catalyst, and heated to an appropriate temperature, usually at 60-80 degrees Celsius, for esterification reaction. Concentrated sulfuric acid in this reaction not only serves as a catalyst to accelerate the reaction process, but also absorbs the water generated by the reaction, promoting the balance to move in the direction of ester formation. During the reaction, it is necessary to stir from time to time to ensure that the reactants are fully contacted.
After the reaction is completed, the reaction solution is cooled and washed with a saturated sodium bicarbonate solution to remove the unreacted acid and catalyst. The amount of sodium bicarbonate should be moderate, and excessive amount may lead to the hydro After washing, the organic phase is separated by a separation funnel, and then dried with anhydrous magnesium sulfate to remove residual water. Finally, by distillation, fractions in a specific boiling point range are collected to obtain pure methyl 2-pyridinecarboxylate. During distillation, temperature and pressure control are very important, which are related to the purity and yield of the product.

In which fields is methyl 2-iodobenzoate used?

2-% decylbenzoyl ethyl acetate, which is used in various fields.
In the field of medicine, it is a key raw material for the creation of new drugs. Because of its specific chemical structure and activity, it can be chemically modified and pharmacologically studied to develop drugs with unique curative effects, or used to regulate human physiology, or to treat specific diseases and help human health.
In the field of materials science, it can be used as a starting point for the synthesis of functional materials. By polymerizing or reacting with other compounds, it can generate materials with special properties, such as those with unique optical, electrical or mechanical properties, which play a role in electronic devices, optical instruments and the preparation of high-performance materials.
In the field of organic synthesis chemistry, it is an extremely important class of organic synthesis intermediates. Chemists can use it as a basis to build more complex organic molecular structures with the help of various organic reactions, expand the types and properties of organic compounds, and contribute to the development of organic chemistry.
In the fragrance industry, its unique chemical structure may impart a special smell. After formulation and research, it may become a part of the fragrance formula, adding a unique aroma to various perfumes and flavors to meet people's diverse needs for fragrance.
In summary, 2-% decylbenzoyl ethyl acetate has shown important application value in many fields such as medicine, materials, organic synthesis and fragrances, and is of great significance to promote the development of related fields.

What are the storage conditions for methyl 2-iodobenzoate?

It is necessary to pay attention to the general matters when storing 2-% ethyl acetate. Its properties are easy to burn and flammable, so it is appropriate to store it in a safe room. It should not exceed 37 ° C, and it should be used to prevent fire and gas sources to prevent danger.
In addition, oxidizing, acid, and other substances should be stored separately, and must not be mixed. Because of the connection of this material, or the reaction of intensification, it will cause danger. And the room should have appropriate prevention and fire protection, so as not to be needed.
In addition, the storage container should also be well sealed to prevent loss. When using it, you must also follow the relevant operation procedures and wear necessary anti-damage, such as anti-damage gloves, gas masks, etc., to ensure personal safety. In addition, proper storage can ensure the stability of 2% ethyl acetate, and can also effectively reduce the risk of accidents.