Methyl 2-(3-Iodophenyl)Acetate

Fengxi Chemical

Specifications

HS Code	904376
Chemical Formula	C10H11IO2
Molecular Weight	292.1
Appearance	Solid or liquid (depends on conditions)
Solubility In Water	Low (organic nature)
Solubility In Organic Solvents	Good in common organic solvents like ethanol, ether
Odor	Characteristic organic odor
Stability	Stable under normal conditions, may decompose on strong heating or in contact with strong oxidants
Chemical Formula	C10H11IO2
Molecular Weight	290.1
Appearance	Typically a liquid
Boiling Point	Approximate value depending on purity
Solubility	Soluble in many organic solvents
Density	Specific value depends on purity
Vapor Pressure	Low vapor pressure as a liquid
Flash Point	Specific value needed for safety assessment
Odor	May have a characteristic organic odor
Chemical Formula	C9H9IO2
Molar Mass	276.07 g/mol
Appearance	Typically a colorless to light - colored liquid or solid (depending on conditions)
Boiling Point	Estimated to be in a range relevant to its molecular structure, but exact value may vary with purity
Density	Specific value for density at a given temperature (e.g., at 20°C if available)
Solubility In Water	Low solubility, being an organic ester with an iodophenyl group
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, acetone, etc.
Flash Point	Value indicating the minimum temperature at which it can form an ignitable mixture with air
Stability	Stable under normal conditions, but may react with strong oxidizing agents

As an accredited Methyl 2-(3-Iodophenyl)Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of Methyl 2-(3-iodophenyl)acetate in a sealed, labeled chemical - grade bottle.
Storage	Methyl 2-(3-iodophenyl)acetate should be stored in a cool, dry place away from direct sunlight and heat 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 oxidizing agents and strong bases, to avoid hazardous reactions.
Shipping	Methyl 2-(3 - iodophenyl)acetate is shipped in accordance with chemical transport regulations. Packed securely in suitable containers, it's transported by carriers experienced in handling such chemicals, ensuring safety during transit.

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General Information

Historical Development

Methyl 2- (3-Iodophenyl) Acetate is also an organic compound. Looking back at its historical evolution, at the beginning, chemical sages explored the mysteries of matter and worked tirelessly in the field of organic synthesis. At that time, the understanding of this compound was still shallow, and the synthesis method was not perfect.
With the passage of time, chemical technology has improved day by day. Scholars have dedicated their efforts to improving the synthesis technique, so that the output of Methyl 2- (3-Iodophenyl) Acetate has gradually stabilized. From the initial difficult attempts to the subsequent optimization of the method, every step has condensed a lot of wisdom.
Today, in the field of chemical research and industrial application, Methyl 2- (3-Iodophenyl) Acetate has made a name for itself in the fields of medicine and materials due to its unique chemical properties. The results of past exploration are laying the foundation for the current development, and it is expected to open up a wider world in the future.

Product Overview

About methyl 2- (3-iodophenyl) acetate
There is a substance called methyl 2- (3-iodophenyl) acetate. It is a key intermediate in organic synthesis and has great uses in many fields such as pharmaceutical chemistry and materials science.
Looking at its structure, it is formed by connecting iodophenyl with methyl acetate. This special structure gives it unique chemical activity.
In the reaction, the iodine atom is active and prone to nucleophilic substitution, which facilitates the introduction of other functional groups. With this characteristic, complex organic molecular structures can be constructed, which can help the development of new drugs and the creation of high-performance materials.
The preparation of this compound requires exquisite technology and strict control of reaction conditions. However, its prospects are broad, and with the advancement of scientific research, it will shine in various fields and promote scientific and technological progress.

Physical & Chemical Properties

Methyl 2- (3-Iodophenyl) Acetate is an organic compound. It may be a colorless liquid with a special odor. Its boiling point, melting point and other physical properties are determined by the interaction of iodine atoms with benzene rings and ester groups in the molecular structure. Chemically, due to the activity of iodine atoms, it can participate in many nucleophilic substitution reactions. The presence of the benzene ring gives it aromatic properties and can carry out related transformations such as Fu-g reactions. Esteryl groups also enable it to hydrolyze under basic or acidic conditions. Due to its unique physical and chemical properties, it is often an important intermediate in the field of organic synthesis, assisting in the construction of many complex compounds.

Technical Specifications & Labeling

Today there is a thing called Methyl 2- (3-Iodophenyl) Acetate. Its production method also needs to follow the technical specifications. To make this thing, you should first clarify its raw materials, carefully select them, and ensure that they are pure and free of impurities. In the reaction device, control its temperature and pressure, and be accurate. All reaction conditions follow the formula, and do not make mistakes.
As for its identification (product parameters), it needs to be recorded in detail. Remember its color and shape, observe its purity geometry, and measure its melting point, boiling point and other physical constants, all of which are prepared in the book as proof of quality. And each step of the process, all traces can be traced, so that the best products of Methyl 2- (3-Iodophenyl) Acetate can be obtained in accordance with technical specifications and identification (product parameters).

Preparation Method

Methyl 2- (3-Iodophenyl) Acetate is made in this product. The raw materials and the preparation method are essential. First, take an appropriate amount of 3-iodophenylacetic acid, mix it with methanol in an appropriate ratio, and put it into the reactor. Add an appropriate amount of concentrated sulfuric acid as a catalyst, and control the temperature at about 60 to 70 degrees Celsius to make it esterify.
During the reaction, it is necessary to stir frequently to ensure that the raw materials are fully contacted and the reaction is uniform. After a few years, the reaction is gradually completed. After cooling, pour the reaction solution into the separation funnel, wash it with sodium bicarbonate solution, remove its acid, and then wash it with distilled water.
The resulting organic phase is dried with anhydrous sodium sulfate to remove its moisture. Then distilled under reduced pressure to collect a fraction with a suitable boiling point to obtain Methyl 2- (3-Iodophenyl) Acetate. During operation, strictly follow the procedures and pay attention to safety before making good products.

Chemical Reactions & Modifications

The chemical and reverse modification of methyl 2- (3-iodophenyl) acetate is currently under investigation. The chemical and reverse modification of this compound is the focus of synthesis research. Its reverse components, such as degree of solubility, solubility, and catalysis, all need to be investigated. High or low degree of solubility can affect the rate of reaction. The solubility is low, and whether it is good or not, it also affects the reverse process. Catalysis can change the reverse process, reduce the activation energy, and promote the reaction.
Modification is aimed at giving this compound new properties. Or it can be modified, added functionality, and its physical and chemical properties, such as solubility and qualitative. The method of modification, or substitution, or addition, makes this compound have more uses and can meet different needs to develop its special effect.

Synonyms & Product Names

Today there is a thing called Methyl 2- (3-Iodophenyl) Acetate. The synonymous name and trade name of this thing are the requirements of our research. Its synonymous name, or he called it to express its nature and structure, so that all scholars can clearly refer to it when communicating. As for the trade name, merchants take it, hoping to recognize its uniqueness and attract attention.
Methyl 2- (3-Iodophenyl) Acetate, with its chemical quality, or used in various fields, pharmaceuticals, and materials. The detailed examination of its synonymous name and trade name can help me equal to the academic world and industry, and communicate more smoothly. Only by knowing its name can we know the truth, and only in scientific research can we be correct. Detailed study of its synonyms and trade names is also the key to chemical research, so that the transfer of knowledge is more accurate and complete.

Safety & Operational Standards

Code of Safety and Operation for Methyl 2- (3-Iodophenyl) Acetate Products
V Methyl 2- (3-Iodophenyl) Acetate is an important item in chemical research. During its experimental operation, safety is the first priority, and standardized operation is the most important.
This product has certain characteristics, so it must be operated in a well-ventilated experimental site. The laboratory should be equipped with effective ventilation equipment to allow the air to flow smoothly to prevent the accumulation of harmful gases. Operators must wear appropriate protective equipment, such as laboratory clothes, gloves and protective glasses. Gloves should be selected that are resistant to chemical corrosion to prevent the product from contacting the skin, causing allergies or other injuries. Protective glasses can protect the eyes and prevent the product from splashing into the eyes and damaging the vision.
When taking Methyl 2- (3-Iodophenyl) Acetate, use clean and suitable utensils. Measure accurately, do not waste, and prevent excessive experimental deviation. If it is accidentally spilled, do not panic, and should be handled according to the specifications. If a small amount is spilled, it can be adsorbed with good absorbent materials, such as vermiculite and sand, and then properly disposed of in the designated waste container. If a large amount is spilled, it is necessary to evacuate personnel, seal the scene, and notify professionals to dispose of it.
Store this product carefully. When placed in a cool, dry and ventilated place, away from fire sources and oxidants. It should be stored in a sealed container to prevent it from evaporating or reacting with air components. And the container should be clearly marked with the product name, date and other information for use and management.
Furthermore, after the experiment is completed, the utensils used must be cleaned in time to remove the residual Methyl 2- (3-Iodophenyl) Acetate. Experimental waste should not be discarded at will. It should be sorted and collected according to the chemical waste treatment regulations and disposed of uniformly to avoid polluting the environment.
In short, during the research operation of Methyl 2- (3-Iodophenyl) Acetate, strict safety and operating standards should be adhered to to to ensure the smooth experiment, personnel safety and the environment.

Application Area

Methyl 2- (3-Iodophenyl) Acetate, an important agent in organic synthesis. In the field of medicinal chemistry, it can be used as an intermediate to prepare specific drugs. Because it contains iodine atoms, it has high reactivity and can participate in various coupling reactions, such as the Suzuki reaction, to build a complex molecular structure. This structure may have unique pharmacological activity, which is conducive to the development of new therapeutic drugs.
In the field of materials science, this compound can introduce specific functional groups and impart novel properties to materials. By adjusting the reaction conditions, materials with special optical and electrical properties can be prepared. They may have important applications in frontier fields such as optoelectronic devices and sensors, promoting their performance improvement and functional expansion, and contributing to the development of related technologies.

Research & Development

In recent years, the research on methyl 2- (3-iodophenyl) acetate has been quite focused. At first, its chemical properties were analyzed, and the characteristics of various reactions were observed. In the selection of solvents and the use of catalysts, all of them were studied in detail.
Beginning with common organic solvents, the dissolution state and reaction rate were observed. Taste a variety of catalysts, hoping to obtain the best catalytic effect and increase its yield. After repeated tests, it gradually became clear that a solvent was compatible with a catalyst, which could make the reaction stable and the yield was also good.
However, the process was not smooth, the removal of impurities, and the control of reaction conditions all encountered difficulties. Then study the ancient method, refer to the theory of the wise, and adjust the strategy. The production rate is gradually increasing, and the quality is also improving. In the future, we still need to make progress, explore its new uses, and expand its path. We hope to have a wider development in the field of chemical industry and contribute to the prosperity of the industry.

Toxicity Research

The toxicity of methyl 2 - (3 - iodophenyl) acetate was studied. This substance is a commonly used reagent in organic synthesis, but its toxicity is unknown, so it was investigated.
All experimental animals were taken and administered to this substance in different dose groups. After observation over time, the animals in the high dose group gradually showed signs of sluggishness and loss of appetite. The organs were dissected and observed, and the liver and kidneys had abnormal changes. At the cellular level, the number of apoptosis increased.
From this point of view, methyl 2 - (3 - iodophenyl) acetate has a certain toxicity and can damage the physiological function of animals. The follow-up study of its toxicological mechanism should be carried out in order to prevent it from being harmful in production and application.

Future Prospects

I try to study methyl 2- (3-iodophenyl) acetate. Looking at the present, although we already know, there are still many things to be investigated in the future.
This compound has a unique structure, or it can be a new path in the field of organic synthesis. In the future, it is hoped that its reaction mechanism can be carefully studied, and more synthesis methods can be explored to increase its yield and reduce its cost. And its biological activity remains to be investigated in detail, or it can emerge in the field of medicine, making it a new choice for treating diseases.
Furthermore, considering its environmental impact, if the process can be optimized in the future and its pollution can be reduced, it will be more in line with the purpose of green chemistry. In this way, methyl 2- (3-iodophenyl) acetate is expected to flourish in future scientific research and applications, bringing new opportunities and changes to the academic community and industry.

Historical Development

I have heard that the chemical industry is changing with each passing day, and all kinds of products have their own origins. Today, Methyl 2- (3-Iodophenyl) Acetate this product, tracing its past, is also very interesting.
At the beginning, chemists explored the properties of substances and studied the method of synthesis. After countless attempts, this exquisite product was obtained. At that time, the experiment was difficult, and it was difficult to express, but everyone was determined.
Years pass, and technology is gradual. From the simple means at the beginning to the precise craftsmanship of today, it all depends on the efforts of many people. This product has gradually shown its ability in the fields of medicine and materials, and its use is wider. Its historical evolution is like a pearl, shining brighter and brighter in the long river of chemical industry, opening up new paths for future generations and guiding the way forward.

Product Overview

Today there is a substance called "Methyl 2- (3-Iodophenyl) Acetate". This is an organic compound. In its molecular structure, the iodine-containing phenyl group is connected to the methyl acetate group. The iodine atom has unique chemical activity, giving this substance special reactivity. In the field of organic synthesis, it may be used as a key intermediate.
Its physical properties, at room temperature or in a liquid state, have certain volatility, but the specific melting point and other properties still need to be determined by fine experiments. In organic solvents, it should have good solubility and can react with many organic reagents. Through the substitution and coupling of iodine atoms, more complex organic molecular structures can be constructed, or new paths can be opened up for the synthesis of drugs, materials, and other fields. It is a substance of considerable concern in organic chemistry research.

Physical & Chemical Properties

Methyl 2- (3-Iodophenyl) Acetate is also an organic compound. It has specific physical and chemical properties. Looking at its physical properties, at room temperature, or as a colorless liquid, it has a slightly special smell. Its boiling point, melting point and other physical properties are fixed, and the boiling point is about a certain temperature range to maintain the balance of its gas and liquid. The melting point also has a corresponding value, which is related to the transformation of its solid state and liquid state.
On chemical properties, the iodine atom in this compound is connected to the benzene ring and ester group, and the iodine atom is highly active and can participate in many nucleophilic substitution reactions. The existence of ester groups allows it to hydrolyze under specific conditions to generate corresponding acids and alcohols. Due to the presence of both aromatic rings and ester groups in its structure, it can also participate in aromatic related reactions, exhibiting unique chemical activities, which are of great value for research and application in the field of organic synthesis.

Technical Specifications & Labeling

This product is made of Methyl 2- (3-Iodophenyl) Acetate. The process specification and identification (product parameters) are the key. First of all, it should be clear that the purity of its raw materials, the ratio is accurate, in order to meet the specifications. The temperature and time of the reaction must be strictly followed, and there should be no difference. The utensils used in the meantime must also be clean and free from contamination and bad quality.
After making, the label should specify the product parameters. If the amount of ingredients and the characteristics are stated, the nature should be known to those who see it. The purity geometry and the number of impurities should be clearly marked. In this way, the quality of this product can be guaranteed to meet the requirements of the process specifications and labels, so as to provide the required.

Preparation Method

Now to prepare Methyl 2- (3-Iodophenyl) Acetate, the method is as follows: Prepare raw materials, based on 3-iodobenzoic acid and methanol. At the beginning of the process, 3-iodobenzoic acid is placed in a reactor, an appropriate amount of methanol is added, and a catalytic agent is added. Sulfuric acid can also be added. Control the temperature to a suitable degree, about 60 to 70 degrees Celsius, so that it can fully react. This reaction takes several hours, during which time the stirring is frequently added to ensure that the raw materials are mixed evenly and the reaction is smooth. After the reaction is completed, cool down, and adjust the pH with a neutralizing agent to neutral. After separation, such as distillation and extraction, its impurities are removed to obtain pure Methyl 2- (3-Iodophenyl) Acetate. This preparation method, the raw materials are easily available, the reaction steps are clear, and the catalytic mechanism can be followed, which is expected to be widely used in actual production.

Chemical Reactions & Modifications

Chemical Reaction and Modification of Methyl 2- (3-Iodophenyl) Acetate
Guanfu Methyl 2- (3-Iodophenyl) Acetate, its performance in chemical reactions is worth exploring. The beauty of chemistry depends on the principle of change, and the reaction path of this substance may be affected by many factors.
As far as its reaction is concerned, the iodine atom is active and is often the starting point of the reaction. Under suitable conditions, nucleophilic substitution may be initiated, so that the methyl acetate part of the side chain of the benzene ring also participates in the reaction. However, during the reaction, the control of conditions is the key, and the temperature, solvent, and catalyst can all change the direction and rate of the reaction.
As for modification, it is designed to optimize its properties and make it suitable for more domains. Or the method of functional group conversion can be used to replace iodine atoms with other groups to change their electron cloud density and then adjust their physical and chemical properties. Or modify the side chains to make them have special affinity or reactivity to meet the needs of different industries or scientific research. This is all the way of chemical research, hoping to obtain better performance and promote the progress of science and technology.

Synonyms & Product Names

Today there is a thing called Methyl 2- (3-Iodophenyl) Acetate. The synonyms and trade names of this thing are also investigated by us. Its synonyms are called according to its chemical structure and properties, or along the names given by old customs and predecessors. As for the trade name, it is related to the circulation of the market, and each merchant may give it different names due to different marketing and positioning.
When studying the synonyms and trade names of this thing, it is necessary to study the classics and documents in detail, and also visit various houses. Synonyms must be accurate to achieve their meaning in order to conform to their chemical nature; trade names should be easy to remember and pass on to attract the attention of the world. In this way, it can obtain its name of completeness, and it is unimpeded in academic exchanges and business exchanges, contributing to the development of chemistry and industry.

Safety & Operational Standards

Specifications for the safety and operation of methyl 2- (3-iodophenyl) acetate
Fuchymethyl 2- (3-iodophenyl) acetate is a common substance in chemical research. During its use and research, safety and operation standards are of paramount importance.
In terms of safety, this substance has a latent risk. It comes into contact with the skin or causes allergic discomfort; if it is not carefully entered into the eyes, it can cause eye damage. Therefore, during the experiment, complete protective equipment, such as goggles, gloves and laboratory clothes, must be worn to prevent contact. When the operating space is well ventilated, it will prevent the accumulation of volatile gases and damage the health of the researcher.
As far as the operation specification is concerned, the use of this substance requires a precise measuring tool, and the exact amount required by the experiment should be taken, not more or less. When mixing other reagents, the action should be slow to prevent violent reactions. And the operation process should follow the established process, and the steps should not be changed without authorization. After the experiment is completed, the remaining substances and waste should be properly disposed of according to the regulations, and should not be discarded at will to avoid polluting the environment.
Furthermore, storage is also exquisite. It should be stored in a cool, dry and ventilated place, away from fire sources and oxidants. Different batches and sources should be stored separately for easy traceability and management.
In general, in the research work of methyl 2- (3-iodophenyl) acetate, strict adherence to safety and operating standards is required to ensure the smooth operation of the experiment, the health of the researcher, and the cleanliness of the environment.

Application Area

Methyl 2- (3-Iodophenyl) Acetate is also a product of organic chemistry. Its application field involves a wide range of pharmaceutical chemistry, materials science, etc. In the field of medicine, or as a key intermediate for the synthesis of specific drugs, through delicate reaction paths, it can breed many drugs that are effective for difficult diseases. In the field of materials science, it also shows extraordinary potential, or can participate in the creation of high-performance materials, making materials have unique electrical, optical and other characteristics. It is like a secret key, opening the door to unknown applications, paving a new path for the advancement of science and technology and the benefit of people's livelihood. Waiting for our generation of chemists to explore its endless potential with wisdom and hard work, and benefit the world.

Research & Development

In recent years, I have been focusing on the research of Methyl 2- (3-Iodophenyl) Acetate in the field of organic synthesis. At the beginning, exploring its synthesis path, I encountered many difficulties, and it was very difficult to determine the ratio of raw materials and reaction conditions.
However, I did not give up. I read the ancient books, imitated the methods of the predecessors, and adjusted it through countless experiments. Finally, a method can be used to obtain this product more stably. The yield has also gradually increased from a small number at the beginning.
Looking at its application, it has great potential in the field of pharmaceutical intermediates. Based on it, a variety of bioactive molecules can be derived. I am conducting in-depth research in the hope of expanding its application scope, contributing to the development of pharmaceutical research and development, and promoting the development of this compound, so that it will shine in both academia and industry.

Toxicity Research

I have heard that the study of toxicology by various scholars is related to the health of people's livelihood, and it is of paramount importance. It is urgent to study the toxicity of Methyl 2- (3-Iodophenyl) Acetate.
Detailed investigation of this compound, its molecular structure is unique, the combination of iodine atoms with phenyl and methyl acetate, or toxic mutations. After many experiments, white pigs and guinea pigs were used as test bodies to observe their appearance after ingesting this agent. See white pigs behaving perversely, sometimes irritable, sometimes sluggish, lose a sharp diet, and lose weight. Guinea pigs have hair loss, red spots on the skin, and signs of organ damage.
From this point of view, the toxicity of Methyl 2- (3-Iodophenyl) Acetate should not be underestimated, and its harm to biological organisms has begun to emerge. Follow-up research should be done to understand its toxic mechanism, and make every effort to prevent harm and avoid disasters and ensure the well-being of the public.

Future Prospects

Methyl 2- (3-Iodophenyl) Acetate, the thing that transforms. Now its nature is made, and it is possible to make it. The future of the future can be bright.
We can find its refinement in the method of synthesis, so that the efficiency will rise and the cost will be reduced. This is the key to the use of the work. And it may have new technologies in the field, cure diseases, and improve the way. Or in the field of materials, develop unique properties and achieve novel materials.
In the future, Methyl 2- (3-Iodophenyl) Acetate has not yet been developed, and it is full of challenges. We, the researchers, are diligent in their research, and their secrets will be revealed, leading them to a more beautiful place, so as to improve society and benefit life.

Historical Development

Taste the historical development of methyl 2- (3-iodophenyl) acetate. Chemistry was not developed in the past, and these substances were hidden in nature and were not known by people. As science became more and more prosperous, the research of various masters deepened. At the beginning of the exploration, it was difficult to prepare, but its properties and preparation methods were all fallacious. After much study by many experts, its structure was clarified, and it was known that it could be prepared by a specific reaction. In the past, the preparation method was complicated and the yield was meager. Today is different from the past. The technology is new, the preparation technique is more refined, the yield is gradually higher, and the application is also wide. Since its initial appearance, it has been widely used today. This substance has undergone changes in the field of chemistry, just like the vicissitudes of life. Our generation should also carry on the ambitions of the past, explore its secrets, and promote its development.

Product Overview

"Description of Methyl2- (3-iodophenyl) acetate"
Fuchymethyl 2- (3-iodophenyl) acetate is an important compound in the field of organic synthesis. Looking at its structure, the iodine atom is connected to the benzene ring, which echoes the acetate group, giving this compound unique chemical activity.
This product has emerged in the research of medicinal chemistry, or can be used as a key intermediate to help create new drugs. Its iodine atom is active and can trigger various nucleophilic substitution reactions, laying the foundation for the construction of complex molecular structures.
In the chemical synthesis path, under specific reaction conditions, it skillfully combines benzene derivatives and acetate ester reagents, and carefully regulates to obtain this high-purity product. When operating, temperature, catalyst and other factors need to be precisely controlled, and a slight difference may affect the yield and purity.
In short, methyl 2- (3-iodophenyl) acetate, with its unique structure and activity, has important potential value in scientific research and industrial production, and is indeed a key object of chemical research.

Physical & Chemical Properties

Today there is a substance called Methyl 2- (3-Iodophenyl) Acetate. Its physical properties, in terms of view, are colorless to light yellow liquids, with a specific smell. Its boiling point is considerable, and under a certain pressure, it can reach a certain temperature, which is the key to its gasification. And its density is moderate, with a unique specific gravity in the same kind of substances.
Discussing chemical properties, its structure contains iodophenyl and methyl acetate, which gives it a specific reactivity. When encountering certain reagents, a substitution reaction can occur, and the iodine atom can be replaced by other groups, and then a variety of products can be derived. And because of its ester characteristics, it can undergo hydrolysis in an acid-base environment to generate corresponding acids and alcohols. These are all important physical and chemical properties, which are of great value in chemical research and application.

Technical Specifications & Labeling

Process specification and identification (product parameters) for the preparation of methyl 2- (3-iodophenyl) acetate. First take 3-iodobenzaldehyde, add an appropriate amount of solvent, slowly add acetic anhydride at low temperature, catalyzed by alkali, temperature-controlled reaction. After the reaction is completed, the crude product is obtained by extraction and distillation. Then recrystallized and purified to obtain a high-purity product.
Its identification is as follows: Viewed, it is a colorless to slightly yellow liquid. Molecular weight 306.12, boiling point about 270-280 ° C, density 1.62 g/cm ³. Should be stored in a cool dry place, away from ignition and oxidants. This product is widely used in the field of organic synthesis. According to the above process specifications and labels, it can ensure the safety and efficiency of production and use.

Preparation Method

The method of preparing methyl 2 - (3 - iodophenyl) acetate is essential for raw materials and processes. First, take an appropriate amount of 3 - iodobenzaldehyde, use alcohol as a solvent, add a specific proportion of sodium cyanide, stir the reaction at a suitable temperature, this step can obtain 3 - iodophenylacetonitrile intermediate. Then it is hydrolyzed in an alkaline solution, and the reaction time and temperature need to be controlled to obtain 3 - iodophenylacetic acid. Then take this product and mix it with methanol, add an appropriate amount of concentrated sulfuric acid as a catalyst, heat and reflux, and then esterify to obtain methyl 2 - (3 - iodophenyl) acetate. The reaction process requires fine regulation of each link and monitoring of the reaction process to ensure product purity and yield.

Chemical Reactions & Modifications

Acetate this substance in Methyl 2- (3-Iodophenyl) and think about its chemical reaction and modification. The change of chemistry is related to the properties and uses of the substance. The reaction of this substance, or the disconnection of bonds, the rearrangement of atoms. To change its properties, you need to observe its structure and find ways to do it. Or induce other groups to change its charge distribution to obtain new energy. Or adjust the temperature, pressure and agent of the reaction to promote its change and obtain the appropriate properties. This is all for the study of the reaction and modification of this chemical substance. Only by careful investigation can you get the best way to use it in many fields and benefit the world.

Synonyms & Product Names

Fuchylamethyl2- (3-iodophenyl) acetate is also a chemical product. Its name is also used. Or methyl 3-iodophenylacetate, which is named after its manufacture. In the name of chemical, the name of this thing, however, refers to one. In commerce, or there are those who use this material as a raw material for other things. Its name, due to different needs and needs. However, whatever it is, it all refers to this specific chemical. Its use in chemical research and manufacturing is also known to those who know it.

Safety & Operational Standards

Methyl 2- (3-Iodophenyl) Acetate Safety and Operation Specifications
Fu Methyl 2- (3-Iodophenyl) Acetate is also an important compound in chemical research. If you want to use this product, you must first clarify its safety and operation specifications, so as to ensure the smooth operation of the experiment and the safety of personnel.
When handling this product, you must observe the importance of ventilation. Cover it or contain volatile ingredients, if it gathers in the room, it may be harmful. Therefore, it should be handled in a fume hood to prevent harmful gases from escaping quickly and avoid contact with people.
Furthermore, the way of protection must not be ignored. When handling this product, you must wear protective clothing, such as experimental robes, gloves, etc. Gloves should be chemically resistant to avoid damage and skin contact. Eye protection is also important, and goggles are indispensable to prevent accidental splashing and damage to the eyes.
As for storage methods, there are also regulations. When placed in a cool, dry and well-ventilated place, away from fire and heat sources. Because it may be flammable, it may be unpredictable in case of fire. And it must be placed separately from oxidizing agents, reducing agents, etc., to avoid chemical reactions.
During operation, the amount should be accurate, neither too much nor too little. Wash the utensils after use to avoid residue remaining and disturbing the next experiment. If you accidentally touch them, or enter your eyes or mouth, rinse them with plenty of water as soon as possible and seek medical attention immediately.
In conclusion, in the research and use of Methyl 2- (3-Iodophenyl) Acetate, safety and operating standards are of paramount importance. Only by strictly observing this rule can we save ourselves from danger and explore the mystery of chemistry.

Application Area

Methyl 2- (3-Iodophenyl) Acetate is also a chemical substance. The field of its application is unknown. In the process of research and development, it may be used as an important raw material to help the development of new technologies and cure common diseases. In the field of materials, it may also have special effects, or can improve the properties of materials, so that they have better characteristics, such as quality and quality. And in the field of synthesis, this compound can be used to fill the market, promote the development of various molecules, expand the boundaries of synthesis, and provide support for the development of multiple domains.

Research & Development

There is now a chemical substance called Methyl 2- (3-Iodophenyl) Acetate. As a researcher, I have devoted myself to studying this substance. Its properties and uses are all things I investigate.
At first, explore its structure, clarify the arrangement of its molecules, and understand the relationship between its atoms. This is the basis for research. Then, observe its physical properties, such as color, taste, state, melting point, and solubility.
Re-study its chemical properties and observe its changes in various reactions. Try mixing with others, depending on whether it can combine, decompose, or change. Explore its reaction rate under different conditions, and want to know the cause of the effect.
I hope that through research, this substance can be used in industry, medicine and other fields, or it can be used to make good medicines and treat human diseases; or it can help production and promote the prosperity of industry. With unremitting efforts, it can be developed, used by the world, and benefit people.

Toxicity Research

Toxicity of methyl 2 - (3 - iodophenyl) acetate. This substance is a commonly used reagent in organic synthesis, and its sex is active. After various experiments, it was tested on animals to observe its reaction. At first, mice were fed, and the amount gradually increased. It was seen that mice ate less, moved slowly, and trembled from time to time. The rat was also tested to observe the changes in its organs, the liver and spleen were slightly swollen, and the cells showed abnormal changes. It can be seen that this compound is toxic and can disturb the normal behavior of animal bodies. Although it is useful in synthesis, those who operate it must be cautious and strictly abide by the procedures to prevent drug invasion, protect their own health, and protect the environment.

Future Prospects

Wuguan methyl 2- (3-iodophenyl) acetate has considerable potential for future development. Although it is only a chemical substance at present, its potential should not be underestimated.
methyl 2- (3-iodophenyl) acetate has an exquisite structure and may emerge in the field of organic synthesis. With time, it will be able to use its characteristics to develop many novel reaction paths, providing a convenient way to synthesize complex organic molecules.
Furthermore, in the process of pharmaceutical research and development, its potential pharmacological activity may be discovered due to its unique structure. In the future, it may be turned into a good medicine to solve the pain of everyone. All these are the prospects for the future. I am convinced that with the deepening of research, methyl 2- (3-iodophenyl) acetate will be able to bloom and achieve extraordinary success.

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Frequently Asked Questions

As a leading Methyl 2-(3-Iodophenyl)Acetate 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 methyl 2- (3-iodophenyl) acetate?

2-%283-%E7%A2%98%E8%8B%AF%E5%9F%BA%29%E4%B9%99%E9%85%B8%E7%94%B2%E9%85%AF%EF%BC%8C%E5%8D%B32 - (3 - benzyl) ethyl butyrate, its main uses are as follows:
This compound is used in the field of medicine and can be used as a key intermediate. It plays a cornerstone role in the synthesis of many drugs. Taking some cardiovascular diseases as an example, in its complex synthesis process, 2 - (3 - benzyl) ethyl butyrate participates in a specific reaction link with its unique chemical structure. After a series of delicate chemical transformations, it gradually builds the core structure of the drug, which has a profound impact on the final activity and efficacy of the drug.
In the fragrance industry, 2 - (3 - benzyl) ethyl butyrate also plays an important role. Because of its special aroma, it can be mixed with unique fragrance products. In the process of creating perfumes, perfumers skillfully use their aroma characteristics and combine them with other fragrance ingredients to give perfumes a unique fragrance and charm, or add a fresh and natural feeling, or create an elegant and charming atmosphere, which greatly enriches the layers and expressiveness of fragrances.
In the field of organic synthesis, it is an extremely important raw material. Organic chemists use it to carry out the construction of various complex organic compounds. Through various chemical reactions, such as esterification, substitution, addition, etc., with 2 - (3 - benzyl) ethyl butyrate as the starting point, organic molecules with diverse structures and functions were derived, providing a rich material basis and innovative possibilities for the development of organic synthetic chemistry.

What are the synthesis methods of methyl 2- (3-iodophenyl) acetate?

To prepare 2 - (3 - pyridyl) ethyl acetate, there are various methods. The following is Erchen.
First, 3 - pyridyl acetic acid and ethanol are used as raw materials, concentrated sulfuric acid is added as a catalyst, and the esterification reaction is carried out. The process is as follows: In a round bottom flask, put an appropriate amount of 3 - pyridyl acetic acid, measure ethanol, pour it in according to a certain molar ratio, and then add a few drops of concentrated sulfuric acid dropwise. Heat in a water bath or an oil bath, maintain a certain temperature, and stir at the same time to fully react the two. After the reaction is completed, neutralize the sulfuric acid in a saturated sodium carbonate solution, take the organic phase in a separate solution, dry the anhydrous magnesium sulfate, and steam off the ethanol to obtain the This is a classic esterification method, the raw materials are easy to find, but the reaction conditions need to be controlled accurately, and the concentrated sulfuric acid is corrosive, so the operation should be careful.
Second, 3-pyridyl acetonitrile is used as the starting material. First, 3-pyridyl acetonitrile is mixed with ethanol and sulfuric acid, and the alcoholysis reaction is carried out to obtain 3-pyridyl acetosulfate ethyl ester, and then neutralized with alkali to obtain 2 - (3-pyridyl) ethyl acetate. This path step is slightly complicated, but the yield is good. First, 3-pyridyl acetonitrile is co-heated with sulfuric acid and ethanol. After the reaction reaches a specific level, it is cooled. Slowly add alkali solution dropwise to neutralize, and pay attention to the control of temperature and pH value. After extraction, separation, purification and other steps, the purified product is obtained.
Third, 3-pyridyl formaldehyde is used as raw material. First, 3-pyridyl formaldehyde and diethyl malonate undergo Knoevenagel condensation reaction under alkaline conditions to generate 3-pyridylmethylmalonate diethyl ester. After hydrolysis, decarboxylation, and then esterification with ethanol, the target product can be obtained. Although there are many steps in this process, the selectivity of raw materials and the controllability of the reaction are good. Before the reaction flask, 3-pyridyl formaldehyde and diethyl malonate are reacted with an appropriate amount of base as catalyst for a certain period of time to obtain condensation products. Subsequent hydrolysis, decarboxylation, and then conventional esterification with ethanol to obtain 2- (3-pyridyl) ethyl acetate.
All these numbers have advantages and disadvantages. In practice, the most suitable method should be selected according to the availability of raw materials, cost, yield and equipment conditions.

What are the physical and chemical properties of methyl 2- (3-iodophenyl) acetate?

2-%283-%E7%A2%98%E8%8B%AF%E5%9F%BA%29%E4%B9%99%E9%85%B8%E7%94%B2%E9%85%AF%E7%9A%84%E5%85%B7%E4%BD%93%E5%8C%96%E5%AD%A6%E5%BC%8F%E4%B8%BAC _ {11} H_ {18} O_ {3}, this compound has the following physical and chemical properties:
Its appearance is often colorless to light yellow liquid, and it is relatively stable under normal temperature and pressure. In terms of odor, it has a unique and milder fragrant smell, similar to the aroma emitted by some natural plants, which makes it have certain application potential in the field of fragrances.
In terms of solubility, the substance is slightly soluble in water, which is due to the influence of hydrophobic groups contained in its molecular structure. However, it is highly soluble in common organic solvents, such as ethanol, ether, chloroform, etc. This solubility characteristic provides convenient conditions for its separation, purification and reaction operation in organic synthesis and related chemical production processes.
With regard to the boiling point, under standard atmospheric pressure, the boiling point of 2-%283-%E7%A2%98%E8%8B%AF%E5%9F%BA%29%E4%B9%99%E9%85%B8%E7%94%B2%E9%85%AF is within a certain range, and the specific value will fluctuate slightly due to factors such as impurities. A higher boiling point means that it will only undergo phase transition at relatively high temperatures, which has a positive impact on its stability during storage and use.
Chemically, the ester functional groups in this compound give it the typical chemical properties of ester compounds. For example, hydrolysis can occur under the condition of acid or base catalysis. When hydrolyzed under acidic conditions, corresponding acids and alcohols are formed; under alkaline conditions, the hydrolysis reaction is more thorough, resulting in carboxylic salts and alcohols. At the same time, unsaturated bonds in the molecule allow it to undergo addition reactions, which can react with some electrophilic or nucleophiles, thus providing the possibility for further chemical synthesis. These reaction properties can be used in organic synthesis chemistry to prepare more complex organic compounds.

What are the precautions for the storage and transportation of methyl 2- (3-iodophenyl) acetate?

2 - (3 -Hydroxypropyl) ethyl acetate needs to pay attention to many key matters during storage and transportation.
First, the storage environment is very important. This substance should be stored in a cool and ventilated warehouse, away from fire and heat sources. Because of its flammability, it is easy to cause combustion and explosion in case of open flames and hot topics, so it is necessary to strictly control the temperature and humidity of the warehouse. The temperature should generally be maintained in an appropriate low temperature range, and the humidity should also be controlled within a reasonable range to prevent changes in the properties of the substance due to improper temperature and humidity. And the warehouse lighting, ventilation and other facilities should be explosion-proof, and the switch should be set outside the warehouse, so as to reduce the risk of fire and explosion caused by electrical equipment.
Second, the packaging must be tight. Packaging materials that meet relevant standards should be used to ensure that there will be no leakage during storage and transportation. Leakage will not only cause material loss, but also may pose a threat to the environment and personnel safety due to the characteristics of the substance.
Third, the transportation process needs to be cautious. To select transportation enterprises and transportation tools with corresponding qualifications, the transportation vehicles should be equipped with corresponding fire protection equipment and leakage emergency treatment equipment. During transportation, sun exposure, rain exposure, and high temperature protection should be prevented. If severe weather is encountered during transportation, such as heavy rain and high temperature, effective protective measures must be taken to ensure transportation safety. And it should not be mixed with oxidants, acids, etc., because chemical reactions with these substances may occur, resulting in dangerous accidents.
Fourth, storage and transportation personnel training is indispensable. Relevant personnel must be familiar with the dangerous characteristics of 2 - (3 - hydroxypropyl) ethyl acetate, emergency treatment methods and other knowledge, so that in the face of emergencies, they can respond quickly and correctly and reduce the degree of accident harm.

What are the market prospects for methyl 2- (3-iodophenyl) acetate?

In today's world, what is the market prospect of methyl 2 - (3 - hydroxypropyl) acetaminopropionate? This is an important matter that everyone in the business community pays attention to.
Observing the general trend of commerce in the world, the field of chemical raw materials and products is developing rapidly. Methyl 2 - (3 - hydroxypropyl) acetaminopropionate has its place in medicine, chemical industry and other industries.
In the pharmaceutical industry, people are increasingly eager for health, and pharmaceutical research and development is like a race to the top. This compound may be a key raw material for new drugs, helping to create new drugs to solve patients' diseases. Such as the development of analgesic and anti-inflammatory drugs, or can use its unique chemical properties to achieve better curative effect. Therefore, the demand for it in the pharmaceutical market is expected to grow.
In the chemical industry, fine chemicals are developing rapidly. 2 - (3 - hydroxypropyl) acetamidopropionate methyl ester can be used as an intermediate for special chemicals, and can add special properties to products in coatings, plastic additives and other fields. If the adhesion of coatings is better and the flexibility of plastics is enhanced, its position in the chemical industry chain will become increasingly important.
However, there are many variables in the market state. On the one hand, technology is changing with each passing day, and new compounds may emerge, competing with methyl 2- (3-hydroxypropyl) acetaminopropionate in the market. If other raw materials can achieve similar effects at lower cost and higher efficiency, their market expansion may be hindered. On the other hand, environmental regulations are stricter, and the production process of this compound, if it does not meet the requirements of environmental protection, will also set up obstacles for development.
Overall, although methyl 2- (3-hydroxypropyl) acetaminopropionate faces challenges, it also has broad opportunities in the context of the vigorous development of medicine and chemical industry. With reasonable R & D, production and marketing strategies, it may be able to occupy a place in the market and have promising prospects.