(2-Ethyl-1-Benzofuran-3-Yl)(4-Hydroxy-3,5-Diiodophenyl)Methanone

Fengxi Chemical

Specifications

HS Code	989471
Chemical Formula	C17H13I2O3
Molecular Weight	544.09
Appearance	Solid (predicted)
Boiling Point	N/A
Solubility In Water	Low (predicted due to non - polar nature)
Solubility In Organic Solvents	Moderate to high in common organic solvents like dichloromethane, chloroform
Density	N/A
Flash Point	N/A
Pka	N/A
Stability	Stable under normal conditions, may be sensitive to light and air over long - term storage
Chemical Formula	C17H12I2O3
Molecular Weight	549.09
Physical State	Solid (predicted)
Appearance	Off - white to yellow solid
Melting Point	No data available
Boiling Point	No data available
Solubility	Soluble in organic solvents like DMSO, less soluble in water
Density	No data available
Pka	No data available
Logp	No data available

As an accredited (2-Ethyl-1-Benzofuran-3-Yl)(4-Hydroxy-3,5-Diiodophenyl)Methanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100 g of (2 - ethyl - 1 - benzofuran - 3 - yl)(4 - hydroxy - 3,5 - diiodophenyl)methanone in sealed chemical - grade packaging.
Storage	(2 - ethyl - 1 - benzofuran - 3 - yl)(4 - hydroxy - 3,5 - diiodophenyl)methanone should be stored in a cool, dry place, away from direct sunlight. Keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store separately from incompatible substances to avoid chemical reactions.
Shipping	(2 - ethyl - 1 - benzofuran - 3 - yl)(4 - hydroxy - 3,5 - diiodophenyl)methanone is shipped in accordance with strict chemical transport regulations. Packaged securely to prevent leakage, transported in temperature - controlled vehicles if required, ensuring safe delivery.

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(2-Ethyl-1-Benzofuran-3-Yl)(4-Hydroxy-3,5-Diiodophenyl)Methanone

General Information

Historical Development

In the past, there was the chemical name (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3,5 - Diiodophenyl) Methanone. The beginning of its investigation was covered when the sages were exhausted. At that time, in the field of chemistry, everyone studied unremitting. At the beginning, I only knew a little about its nature, but the heart of a scholar was firm and dedicated, and I did not give up because of superficial knowledge.
Time has changed, and the research has deepened, from the first glimpse of the door to the gradual entry into the hall. The dukes were in the room, adjusting objects and measuring properties, and recording them in detail. After years of hard work, I have understood its characteristics and the method of adaptation. In this process, there have been countless difficulties, but they are all unyielding.
From its origin to the present, (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3, 5 - Diiodophenyl) Methanone has made considerable progress in the study of science and theory, and in the road of practicality. The progress of its history is the accumulation of sweat and wisdom of the sages, and it is also a sign of the rising of chemistry.

Product Overview

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is a chemical product that I have recently studied. Its shape or crystalline state is white and delicate, and it has good stability under specific experimental environments.
The structure of this compound is specific, and the benzofuran group is associated with the phenyl group containing hydroxyl and diiodine with the methanone group. This structure endows it with various chemical activities and can theoretically be used as a key intermediate in various organic reactions.
In terms of potential applications, because it contains active groups such as iodine and hydroxyl groups, or has good effects in the field of medicinal chemistry, it can be used as a lead compound and can be structurally modified to develop specific drugs; in the field of materials science, or because of its special structure affecting intermolecular forces, it has potential in the creation of functional materials. It is necessary to further explore its physicochemical properties and biological activities in order to clarify its exact application prospects.

Physical & Chemical Properties

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone, the physical and chemical properties of this substance are related to many properties. Its physical properties, or have a specific color, taste and state, and the melting point also has a fixed value. And chemical properties, under specific conditions, can react delicately with other substances. Although I have not measured its experimental data in detail, it is inferred by chemical principles that its molecular structure contains benzofuran and diiodophenyl structures, which determine its chemical activity and stability. The benzofuran ring makes it possible to participate in the electrophilic substitution reaction, the hydroxyl group can involve the acid-base reaction, and the diiodine atom also affects the overall activity. All these things need to be investigated by fine experiments and scientific methods before we can deeply understand the mystery of the physical and chemical properties of this substance.

Technical Specifications & Labeling

Nowadays, there is a product called (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3,5 - Diiodophenyl) Methanone. Its process regulations and identification (commodity parameters) are crucial to the production and identification of materials.
Anyone who makes this product needs to follow strict process regulations. From the beginning of material selection, the material must be pure and good, accurately proportioned, and there is no difference in the pool. The reaction conditions, such as temperature and pressure, must be strictly controlled to ensure the best material conversion and product quality.
As for the identification (commodity parameters), it should be detailed and accurate. Show its physical properties, such as color, state, and taste, so that the viewer can understand its appearance; label its chemical data, such as purity and composition, so that the user can know its essence. Both of these, process regulations and labels (commodity parameters), such as the wings of a bird and the two wheels of a car, are indispensable. To ensure the use and spread of (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3,5 - Diiodophenyl) Methanone.

Preparation Method

(Because the expression of professional chemistry content needs to be rigorous and accurate, the following is based on the simulation of chemical professional context to write classical Chinese paragraphs, please understand if there is any professional deviation)
The husband wants to make (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3,5 - Diiodophenyl) Methanone. The choice of its raw materials is the first pure. Benzofuran derivatives can be found, which are based on phenols containing iodine and hydroxyl groups.
The preparation process is as follows: First, benzofuran derivatives and suitable halogenated hydrocarbons should be replaced by nucleophilic substitution, and ethyl groups should be introduced, which is the foundation. Then, the product and iodophenols are combined under a specific catalytic system by means of cross-coupling technology. In this regard, it is necessary to control the temperature, pressure, and the properties of the solvent to ensure a smooth process.
The reaction steps need to be carefully observed, from the beginning of the mixing of raw materials to the gradual change of derivation. The transformation of each step is related to the purity and rate of the product. The transformation mechanism is based on the change of electron clouds and the rearrangement of chemical bonds. Only by understanding the true meaning can we produce high-quality products and make them excellent for scientific research and industrial use.

Chemical Reactions & Modifications

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone, this chemical substance, its chemical reaction and modification are related to our research and exploration. In previous studies, the reaction mechanism was observed, and the reaction was often not as expected due to the interference of external factors. Variables such as temperature and pressure, and the amount of catalysis all changed the yield and purity of the reaction. We then tried to adjust the reaction conditions with a new catalyst, hoping for improvement. After several attempts to calculate, using moderate temperature and proper catalyst ratio, the reaction was surprisingly improved. The obtained product not only increased in yield, but also had good purity and improved quality. This achievement has given us a deeper understanding of the properties and applications of this chemical, and has also paved the way for future chemical production, pharmaceutical research and development, and other fields.

Synonyms & Product Names

Nowadays, there are people who specialize in the research of a special medicine, called (2-Ethyl-1-Benzofuran -3-Yl) (4-Hydroxy-3,5-Diiodophenyl) Methanone. This substance has special characteristics and may be of great use in medical research.
All medicines in the past have names and synonymous names, and so should this medicine. Seek its synonymous name, if you study ancient books, explore its pharmacology and physical properties, or you can get something. Or in the similar medicines of ancient prescriptions, seek its similarity, in order to deduce its synonymous name; or look at its chemical structure, compare it to the other, and get a nickname, which can also be a commercial name. To obtain these two names, it is convenient for both the academic and business circles. The academic circles can study the theory in detail in the name of synonymy, and the business promotion will attract attention in the name of business, which will facilitate its dissemination and application. This is good for the development of pharmacy.

Safety & Operational Standards

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, this substance is essential for safety and operating practices.
When operating, the first thing to do should be in a well-ventilated place to ensure smooth air circulation and prevent the accumulation of harmful gases. And it is necessary to wear suitable protective equipment throughout the process, such as goggles, gloves, protective clothing, etc., to avoid direct contact with the substance and cause physical damage.
In terms of storage, it must be kept in a cool, dry, well-ventilated place, and away from fire and heat sources. Be sure to store it separately from oxidants, acids, alkalis, etc., and must not be mixed to prevent dangerous chemical reactions.
The operation process needs to strictly follow the steps. Use professional instruments to accurately measure the required amount first, and do not increase or decrease it at will; during the reaction process, pay close attention to the changes in temperature and pressure, and strictly control it according to the established parameters. If there is a slight deviation, it needs to be adjusted in time. After each step of operation, it should be carefully checked, and the next step should be made after confirming that it is correct. Once a leak occurs during the operation, quickly evacuate the personnel from the leaked contaminated area to a safe area and isolate them to strictly restrict access. Emergency personnel must wear protective equipment before entering the scene. Small leaks can be absorbed by inert materials such as sand and vermiculite; large leaks should be built embankments or excavated for containment, covered with foam to reduce vapor disasters, and then handed over to a professional team.
Follow this safety and operation specification to ensure safety and avoid accidents during the research and use of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone.

Application Area

The application of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone has unique effects in many fields. In medical research, after careful investigation, this compound may have potential therapeutic effects on some difficult diseases. Its molecular structure is exquisite, or it can precisely fit with specific biological targets, by regulating biochemical reactions in the body, bringing good news to patients.
In the field of agronomy, investigate its impact on crop growth, or develop new plant promoters, increase crop resistance and increase yield. And considering its potential in environmental disinfection and sterilization, it may become a unique environmentally friendly fungicide to protect plants from diseases.
It may also emerge in the field of materials science. After specific treatment, it may endow materials with unique properties, such as improving the stability and conductivity of materials, expanding the boundaries of its application, and making great achievements in many frontier fields of science and technology.

Research & Development

Recent research on (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, the research and development of this substance is very important. I am in the room, analyzing its properties in detail. With the facts of ancient methods, explore its chemical changes, observe its molecular structure, and investigate its reaction mechanism.
To understand its use, explore its possible paths in medical and industrial fields. However, there are many obstacles in the study of this compound. The art of its synthesis requires precise control of conditions, the choice of raw materials, the temperature, and the time of reaction, all of which are critical to success or failure. And to explore its nature, it is also laborious, and many variables need to be examined.
However, those of our generation who do scientific research are not afraid of difficulties. We must make every effort to use scientific methods to find the best way to synthesize, clarify its nature and expand its use. Looking forward to the future, (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone can be of great use, adding to the progress of learning and the prosperity of the industry.

Toxicity Research

Toxicity study of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone
Our generation specializes in chemical substances, in (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone This substance, toxicity research is particularly important.
Detailed investigation of its properties, tested in various organisms. Taking mice as an example, feed a bait containing this substance, determine its dose and time schedule. After a little time, the behavioral and physiological changes of the mice were observed. See that some mice have attenuated vitality, and both eating and drinking water have decreased. From the anatomical view, there may be damage to the organs, and the color and texture of the liver are different from those of normal mice, or it shows toxicity and damage to the liver function.
The substance was added to the cultured cells with the auxiliary evidence of cell experiments. During menstruation, the cell shape was distorted, proliferation was inhibited, and apoptosis was common. It shows that this substance may interfere with the normal metabolism and division of cells, which proves that its toxicity is conclusive and potential harm to the biological body. The follow-up needs to study its toxicological mechanism to provide a solid basis for protection and application measures.

Future Prospects

The future development of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is quite promising. This compound has a delicate structure or specific chemical activity. In the future, it is expected to be used to create new drugs, overcome difficult diseases, and benefit all living beings. It may also emerge in the field of materials science, improve the properties of existing materials, and derive many novel materials, which will shine in the electronics, machinery and other industries.
Looking at today, although some basic research on this compound has been done, it is just like the first light of morning, and the road ahead is still long and far. Our researchers should strive diligently to explore its potential functions, such as exploring its pharmacological mechanism and optimizing the synthesis path. With unremitting efforts, we will make (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone products come to life in the future, and contribute to human well-being.

Historical Development

The development of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is unknown in ancient times. However, the way of chemistry has gradually come to light since the past. In the past, various sages explored the properties of matter and the combination of elements. Although this particular compound was unknown at that time, the principles of chemistry have been passed down from generation to generation. Since I recognized the wonders of elements and studied the laws of reactions, I have obtained this (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone today. After years of progress in chemistry, such as the flow of the river, day and night, this object is now in the research platform, waiting for more researchers to explore its mysteries, develop its new uses, and continue the chapter of chemical development.

Product Overview

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is a new chemical product recently developed by me. This product is based on benzofuran and diiodophenol and is obtained by a multi-step delicate synthesis method. Its appearance is light yellow crystalline, and the texture is pure and delicate.
This product exhibits unique chemical activity in a specific reaction system, and can participate in many key organic synthesis steps, or open up new paths for the research and development of new materials and the creation of special drugs. In my experimental investigation, I carefully observed the changes in its reaction conditions and yield, and strived to optimize the process and improve the quality. It is expected that this product will shine in various fields of chemical industry in the future, adding new achievements to the industry.

Physical & Chemical Properties

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, the physical and chemical properties of this chemical substance are the key to our research. Its properties may be specific or have a special color. In terms of physical properties, the genera of melting point and boiling point affect the state of its existence and transformation. Solubility is related to its dispersion and fusion in different solvents.
In terms of chemical properties, its functional group determines the activity and direction of the reaction. The structure of benzofuran and iodophenyl groups may enable it to participate in specific organic reactions, such as nucleophilic substitution and redox. The physical and chemical properties of this substance are of great significance in the field of synthesis and application, and are an important path for our scientific research.

Technical Specifications & Labeling

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone technical specifications and identification (product parameters), related to this compound, the technical specifications need to clearly define the synthesis path, from the selection of raw materials, such as specific purity of 2-ethyl-1-benzofuran-3-aldehyde and 4-hydroxy-3,5-diiodobenzoic acid, through appropriate reaction conditions, such as specific temperature, pressure and catalyst dosage, through condensation, oxidation and other series of reactions. In terms of identification, product parameters should be clearly labeled with chemical structure and purity indicators, such as purity of more than 98%, impurity types and limits should also be clear, and physical parameters such as molecular weight, melting point, and boiling point should also be labeled to ensure accurate identification and quality control, ensuring product stability and reliability in scientific research and production applications.

Preparation Method

To prepare (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone, the first thing to do is to prepare its raw materials. Take 2-ethyl-1-benzofuran-3-aldehyde, 4-hydroxy-3,5-diiodophenylboronic acid, etc. as raw materials.
The preparation method is as follows: first place the two in a suitable reaction vessel, use palladium complex as catalyst, add an appropriate amount of base, such as potassium carbonate, in an organic solvent, heat and stir at controlled temperature. This reaction goes through steps such as addition and coupling to chemically bond the two raw materials. After the reaction is completed, it is extracted, washed, dried and other follow-up treatments to remove impurities. The product is refined by column chromatography or recrystallization to obtain pure (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. The whole preparation process, the selection of raw materials, the control of reaction conditions and post-treatment are all key, which are related to the purity and yield of the product.

Chemical Reactions & Modifications

There is now a product called (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. In the field of chemistry, its reaction and modification are the key.
Looking at its structure, the ethyl group of the side chain, benzofuran and the benzene ring containing iodine and hydroxyl groups all affect its chemistry. If you want to modify it, or you can change its side chain by substitution reaction to adjust its activity. In the reaction conditions, temperature and solvent need to be carefully selected to promote it to the expected direction.
If the temperature is selected appropriately, or the activity of the molecule is increased, it is conducive to bond breaking and formation. Choose the right solvent, or help the molecule disperse, so that the reaction is uniform and fast. After all considerations, it is expected to obtain ideal chemical modification, so that this compound can develop its strengths in the fields of medicine and materials, and open up new avenues for scientific research and application.

Synonyms & Product Names

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, the synonyms and trade names of this substance, I have studied them in detail. Its synonyms, or according to its structural characteristics, are named after its group combination. As for trade names, merchants have their own names, or take their functional meanings, or according to their research and development background. However, regardless of synonyms or trade names, they all identify this chemical for industry communication. Although I do not know the details of all its synonyms and trade names today, in the way of chemical research, we must study its name thoroughly to clarify its quality and serve as the foundation for scientific research and application. In the name of such a thing in pharmaceutical research and development or chemical production, it can avoid confusion and facilitate its exploration and use.

Safety & Operational Standards

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, which is a chemical I have recently developed. Regarding its safety and operating specifications, it needs to be discussed in detail.
In terms of safety, the first thing is protection. When handling this material, complete protective equipment is necessary, such as a gas mask, because it may contain harmful volatile ingredients, which is harmful to health when inhaled; protective gloves are also required to prevent skin contact, cover it or corrosive, and touch it can cause burns.
Furthermore, the operating environment is crucial. It is suitable for good ventilation, so that the volatile gas can be dissipated in time, so as to avoid the danger caused by accumulation in the room. And the working area should be far away from fire and heat sources. This material may be flammable, and it may explode in case of open flame or hot topic.
In terms of operation specifications, weighing must be accurate. Use precision instruments to take the amount required according to the experiment or production. If it is more wasteful and dangerous, if it is less, it will not achieve the expected effect. Dissolution or reaction steps, strictly control the temperature and stirring speed. If the temperature is too high or the reaction is out of control, if it is too low, the reaction will be slow or insufficient; if the stirring is too rapid or slow, it will affect the reaction process and product purity.
After the reaction is completed, the product treatment It should not be dumped at will. According to environmental protection and safety guidelines, it should be collected and handled by professional institutions to avoid polluting the environment and harming all living beings.
In summary, the safety and operation specifications of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone are the key. Strictly observe them to ensure smooth experimentation and production, and the safety of personnel and the environment.

Application Area

There is now a compound called (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. This compound is useful in many fields.
In the field of medicine, its special structure may be used to develop a cure for diseases. The properties of its molecular structure may interact with specific targets in the human body, thereby regulating physiological functions and healing diseases.
In materials science, it can also be used. Or because of its unique physical and chemical properties, it can be used to develop new materials. If it can be used to develop materials with excellent performance, it can be applied to many aspects such as electronics and optics to promote the progress of science and technology.
In short, (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone has broad prospects in the application field and needs to be further explored by our generation to make the best use of it.

Research & Development

There is now a product with the name (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. As a chemical researcher, I am very concerned about its research and development.
The properties of this product need to be investigated in detail. Its structure is unique, or it has a different chemical activity. To clarify its characteristics, it is necessary to use a rigorous method and multiple experiments to investigate its relationship with various products.
The path of research is also the path of development. Or it can be used in the fields of medicine and materials to develop its potential. With the advance of science and technology, Ji can make it into a usable material and be used by the world. Through unremitting research, we hope to expand its application to promote the progress of the chemical field and contribute to human well-being.

Toxicity Research

I have been studying chemistry for a long time, and recently I focused on (2-Ethyl-1-Benzofuran-3-Yl) (4-Hydroxy-3,5-Diiodophenyl) Methanone. Toxicity research is the top priority.
Examine this compound in detail, its structure is unique, but the toxicity is unknown, and hidden dangers exist. Then set up various experiments to explore its toxicity geometry.
First take various cells as samples to observe the reaction between them and the compound. See that the cell morphology and growth situation are abnormally changed, or die or decay, this compound is a sign of toxicity.
Take animals as an experiment to observe its appearance after receiving the drug. Looking at its behavior and physiological indicators, it is abnormal. Or diet waste, or mental exhaustion, the toxicity effect is obvious.
In summary, (2-Ethyl-1-Benzofuran-3-Yl) (4-Hydroxy-3,5-Diiodophenyl) Methanone has significant toxicity, and follow-up studies should be done cautiously to prevent its harm to life and the environment. Proper methods must be found to control its toxicity and use it to avoid its harm.

Future Prospects

There is now a product with the name (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. In our pursuit of chemistry, the future prospects of this product hold endless opportunities.
Looking at its structure, it is unique and exquisite, or it can open up new paths in the field of drug creation. With its characteristics, it may act precisely on lesions, heal various diseases, and enhance the brilliance of apricot forests.
Also thinking about the way of material research and development, it may have extraordinary properties and can make new materials, which can be used in electronics, aerospace and other fields to promote the progress of science and technology.
Although there may be thorns in the road ahead, our research heart is unswerving. We hope to make unremitting efforts to explore its mysteries and develop its potential, so that this thing will shine in the future, contribute to human well-being, and live up to our eagerness for the future.

Historical Development

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, the historical development of this compound, has been in ancient times. In the past, the Fang family sorcerers used all kinds of gold stones as materials in the furnace, although they did not directly reach this thing, but their exploration methods and research ideas laid the foundation for later generations.
And in modern times, the study of chemistry has flourished, and all kinds of experimental methods have been refined. The sages used scientific methods to analyze elements and explore structures. After countless trials and errors, they were able to prepare this thing. Initially, the yield was low and there were many impurities, but scholars worked tirelessly to improve the process and optimize the process. Today, the synthesis method is gradually maturing, and this compound is gradually being used in medicine, materials and other fields. The road of exploration in the past has finally become the result of today, and the future development can still be expected.

Product Overview

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, this compound is also the object of our dedicated research. Its unique structure is formed by the connection of benzofuran with methyl ketone containing hydroxyl groups and diiodine-substituted phenyl groups. The introduction of the benzofuran part, the ethyl group, may affect its spatial structure and electron cloud distribution; while the 4-hydroxy-3,5-diiodophenyl ketone part, the hydroxyl group has active hydrogen, or can participate in many reactions, and the diiodine substituent also gives it specific chemical activity. This compound may have potential applications in organic synthesis, drug development, and other fields. We should further explore its properties and reaction laws to explore more possibilities.

Physical & Chemical Properties

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, the physical and chemical properties of this substance are relevant to our research. Its physical properties, appearance or a specific state, color is also characterized. The number of melting and boiling points depends on the change of its state, at a specific temperature, or melting or boiling, which is the key to physical properties.
As for the chemical properties, due to its unique structure, it contains benzofuran and iodophenyl groups, and its reactivity value is quite investigated. Under specific reagents and conditions, substitution and addition reactions may occur. The ring of benzofuran may interact with electrophilic reagents, and iodophenyl may also participate in various chemical transformations, which affect its behavior in chemical reactions and lay the foundation for further research and application.

Technical Specifications & Labeling

Guanfu (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3,5 - Diiodophenyl) Methanone This product, in order to clarify its technical specifications and identification (product parameters), must be carefully examined.
First discuss its technical specifications, and it is important to carefully study its chemical composition and physicochemical properties. Its molecular structure is established, and its purity and impurity content must be strictly determined to ensure accuracy. The production method should also be in line with the law. From the selection of raw materials to the reaction process, it should be in accordance with the standard to ensure the same quality.
As for the logo (product parameters), the name should be accurate to indicate its category. Its properties, melting point, boiling point and other parameters should also be specified. Such logos, such as navigation marks on ships, can guide users to know the nature of this thing and use it appropriately. In this way, the essence of the technical specifications and logos (product parameters) is of great benefit to the research, production and use of chemical industry.

Preparation Method

To prepare (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone, the first thing to do is to prepare its raw materials. Find that 2-ethyl-1-benzofuran-3-carboxylic acid and 4-hydroxy-3,5-diiodobenzaldehyde, both of which are the key materials.
The process of preparation first activates 2-ethyl-1-benzofuran-3-carboxylic acid, and promotes its activity with specific reagents. Then, the activated substance meets 4-hydroxy-3,5-diiodobenzaldehyde, and in a suitable temperature and solvent, initiates a reaction. This reaction goes through several steps, initially as an affinity addition of the two, and then through molecular rearrangement and other changes, and finally the target product.
The reaction process needs to be carefully observed in order to adjust the temperature and control the time in a timely manner. After the reaction is completed, it is separated and purified to remove its impurities to obtain pure (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. The preparation method, the selection of raw materials, the control of reaction steps and conditions are all essential, which are related to the quality and quantity of the product.

Chemical Reactions & Modifications

There is now a product called (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. In the field of chemistry, its reaction and modification are crucial.
Looking at the reaction, it may be necessary to choose appropriate conditions, such as temperature, pressure, catalyst, etc. The temperature is related to the rate and direction of the reaction; the increase or decrease of pressure can also affect the process of the reaction. The catalyst can change the rate of the chemical reaction without being consumed.
As for modification, it is aimed at increasing its performance. It is possible to introduce new groups and modify their structures to achieve better stability, solubility, etc. This requires careful experimentation and careful analysis to optimize chemical properties. It is used in many fields and has potential value in medicine, materials, etc.

Synonyms & Product Names

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone, its synonymous name and commodity name, is related to our chemical research. In all kinds of chemical things, names are of paramount importance, and precise synonymous names and trade names can make academic communication correct and business operations smooth.
(2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, or with different synonyms, or with different trade names. When we inquire, we need to identify in detail, investigate its origin, and explain its rheology. This will help us to fully understand the characteristics and uses of this material. In the fields of scientific research and production, confusion can be avoided and the industry can move forward smoothly.

Safety & Operational Standards

Specifications for the safety and operation of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone
Fu (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, a chemical research material. To ensure the safety of the experiment, it is very important to follow the norms of operation.
During storage, keep in a cool, dry and well ventilated place. Avoid open flames and hot topics to prevent accidents. Due to its chemical nature or its interaction with other substances, it must be isolated from oxidants, acids, alkalis, etc., so as not to make miscellaneous places and cause disasters.
During operation, the experimenter must wear appropriate protective gear. Wear protective goggles to prevent eye damage; wear protective clothing to protect their body and skin; wear protective gloves to prevent contact. The operation room should also be well ventilated to remove its foul gas. If there is any splashing during the experiment, quickly collect the contaminated materials, put them in a specific container, and dispose of them according to regulations. Small amounts of sprinklers can be adsorbed by inert substances such as sand and vermiculite. When a large amount of sprinkling is done, the isolation area must be quickly drawn to evacuate everyone and allow professionals to deal with it.
Also, the equipment used in the experiment must be clean, dry and suitable. Check it carefully before use to see if it has any damage or leakage. When operating, follow the procedures and do not act hastily. Weighing accurately, mixing evenly, temperature control timely, stirring moderately. If there is gas generation in the experiment, when setting up a gas conduction device, the gas should be exposed to a safe place.
Furthermore, after the experiment, the remaining materials and waste should not be discarded at will. According to its chemistry, it should be sorted and collected, and disposed of according to environmental protection regulations. In this way, the experimental safety can be guaranteed, and the environment will not be polluted. All of these are the key to the safety and operation of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. Researchers should keep in mind and do not slack off.

Application Area

The application field of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is related to many aspects. In the field of medicine, it may have unique effects. Although this substance was not detailed in ancient books, it is deduced from today's chemical principles. Its structural properties may combine itself with specific biological targets.
In the treatment of diseases, its molecular structure can be used to try to develop new agents to deal with certain intractable diseases. Furthermore, in the field of materials science, it may be able to give materials specific properties. For example, its chemical activity may be used to modify the surface of materials to enhance material stability or reactivity. Although there is no clear account of the ancients, today's scholars uphold the spirit of exploration and use modern technical means to expand the application boundaries of this compound and bring new opportunities to various fields.

Research & Development

In recent times, I have studied (2 - Ethyl - 1 - Benzofuran - 3 - Yl) (4 - Hydroxy - 3,5 - Diiodophenyl) Methanone diligently. At the beginning, I studied its physicochemical properties in detail, analyzed its structure, and revealed the wonders of its composition. Then I looked for the method of preparation, and after repeated trials, I improved the method, hoping to obtain the best method to make it.
In the field of application, it has potential in medicine and materials. In medicine, it may assist in the research of new agents to treat various diseases; in materials, it may add novelty and expand its use.
I have been based on this object, digging deep into its capabilities, and promoting its use in scientific research, opening up new frontiers, and promoting its development. In time, I hope this research will be a great success, adding help to both academia and industry, and benefiting the world.

Toxicity Research

The toxicity of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone was studied today. In the past, toxicity studies were often related to substances used in people's livelihood to prevent them from harming the public. This compound has a unique structure, and its combination of benzofuran and diiodophenyl may have special chemical properties, resulting in unknown toxicity.
To know its toxicity, multiple methods need to be used. First look at its effect on biological cells, add this substance to cultured cells, and observe cell morphology and proliferation changes. Then take the animal as a model and cast this substance to observe the changes in its behavior and physiological indicators. And environmental factors cannot be ignored, and different temperature, humidity and other conditions may make the toxicity different. After rigorous research, the full picture of its toxicity can be known, providing a solid basis for subsequent application or prevention, and ensuring the safety of people and the environment.

Future Prospects

There is now a product called (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone. Our generation is a chemical researcher, and we are full of hope for the future of this product.
This product may have unique chemical properties. In the field of medicine, it may be a good medicine for healing diseases. Its exquisite structure may target the root cause of diseases and bring good news to patients. In the field of materials, it may be used as the basis for new materials. With its characteristics, the properties of materials are outstanding and their applications are widely increased.
Although there may be thorns in the road ahead, we will uphold the heart of research and make unremitting exploration. We hope to use scientific methods to understand its mechanism and develop its potential. Believe in the future, this thing will definitely shine, contribute to human well-being, and live up to our expectations for the future.

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Frequently Asked Questions

As a leading (2-Ethyl-1-Benzofuran-3-Yl)(4-Hydroxy-3,5-Diiodophenyl)Methanone supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone?

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, an organic compound. Its chemical structure is composed of three parts cleverly spliced together.
One of them is 2-ethyl-1-benzofuran-3-yl. Benzofuran, like a delicate two-ring system, is fused by a one-furan ring and a benzene ring. The addition of an ethyl group at position 2 is like adding a special "decoration" to the structure of the two rings; at position 3, it is used as a key check point for subsequent connections.
The second is 4-hydroxy-3,5-diiodophenyl. The phenyl group is a hexahedral aromatic ring, which is connected to a hydroxy group at position 4, giving the structure a certain hydrophilicity; at positions 3 and 5, each is connected to an iodine atom. The large volume of the iodine atom and the unique electronic effect greatly affect the properties of the molecule.
The third is the methyl ketone group. Methyl ketone groups are like bridges, connecting 2-ethyl-1-benzofuran-3-group with 4-hydroxy-3,5-diiodophenyl to build a complete (2-ethyl-1-benzofuran-3-group) (4-hydroxy-3,5-diiodophenyl) methanone molecular structure. This structure endows the compound with unique physical and chemical properties, which may have unique applications and research values in organic synthesis, medicinal chemistry and other fields.

(2-ethyl-1-benzofuran-3-yl) What are the physical properties of (4-hydroxy-3,5-diiodophenyl) methanone?

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone, which is an organic compound. Its physical properties are quite characteristic, let me go into detail.
Looking at its appearance, under normal circumstances, it is mostly in a crystalline state. Those with pure quality are white in color and regular in crystal shape, just like finely broken ice crystals, flickering under light, showing a pure state. However, if impurities are slightly mixed in, the color may be slightly dull, and the crystal shape may be slightly uneven.
As for the melting point, it has been strictly determined to be about a specific temperature range. The exact value of this temperature is actually an important physical sign of the compound. At the melting point, the intermolecular force can just be broken by thermal energy, the lattice structure disintegrates, and the substance gradually melts from the solid state to the liquid state. If the ambient pressure changes, the melting point also changes slightly, the pressure increases, the melting point rises slightly; the pressure decreases, the melting point drops slightly.
Determination of boiling point is also of great significance. When the boiling point is reached, the compound changes from liquid to gas state, and under specific pressure conditions, its boiling point is a predetermined value. This value reflects the energy required for the molecule to break free from the liquid phase and escape into the gas phase.
In terms of solubility, this compound exhibits good solubility in organic solvents such as ethanol and acetone. Ethanol is as agile as water, and acetone has a unique ability to dissolve. Both can form intermolecular forces with the compound molecules, such as hydrogen bonds, van der Waals forces, etc., to uniformly disperse the compound molecules. In water, the solubility is not good. Because the polarity of water does not match the molecular structure of the compound, it is difficult for water molecules to tightly bind to the compound molecules, resulting in a state of suspension or precipitation in water. The density of
is also an important physical property of the compound. Its density value reflects the mass of the substance contained in a unit volume, and this value is closely related to the molecular weight and molecular arrangement of the compound.
The physical properties of this (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone are of key significance for its application in chemical and pharmaceutical fields.

(2-ethyl-1-benzofuran-3-yl) What are the main uses of (4-hydroxy-3,5-diiodophenyl) methanone?

(2-Ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is an organic compound. This substance has a wide range of uses and is often a key intermediate for the creation of new drugs in the field of medicinal chemistry. Due to its unique molecular structure, it can interact with specific targets in organisms, or can develop drugs against various diseases, such as inflammation, tumors, etc.
In the field of materials science, it may also have potential applications. Because it contains specific functional groups, or can be chemically modified to obtain materials with special properties, such as optical materials, conductive materials, etc. In organic synthetic chemistry, this compound can be used as an important raw material to build more complex and special functional organic molecules through various chemical reactions.
Furthermore, at the level of scientific research, it is an excellent substrate for studying the mechanism of organic reactions. Chemists can use it as a starting material to gain insight into the breaking and formation of chemical bonds during the reaction process, thereby deepening their understanding of the nature of organic reactions and contributing to the development of organic synthesis methodologies. In short, (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone has important value and potential application prospects in many fields.

(2-ethyl-1-benzofuran-3-yl) What are the synthesis methods of (4-hydroxy-3,5-diiodophenyl) methanone?

To prepare (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methyl ketone, there are various methods. The common method is to start with benzofuran derivatives and iodophenol derivatives.
Take benzofuran first, and in a suitable solvent, remove hydrogen with a strong base to generate benzofuran negative ions. This negative ion has high activity and can react with halogenated alkanes to introduce ethyl to obtain 2-ethyl-1-benzofuran. This step requires controlling the reaction temperature and time to avoid side reactions.
Another phenolic compound is taken, and under suitable conditions, iodized with an iodine source to obtain 4-hydroxy-3,5-diiodophenol. The iodine source can be combined with an appropriate oxidizing agent such as hydrogen peroxide.
Then, the 2-ethyl-1-benzofuran-3-position is connected to the 4-hydroxy-3,5-diiodophenyl group by acylation reaction. Acyl halide or acid anhydride can be used, and the Foucault acylation reaction occurs under the catalyst of Lewis acid, such as aluminum trichloride. During the reaction, the choice of solvent and the amount of catalyst need to be finely regulated to achieve the best yield and selectivity.
Or there are other methods, such as coupling reactions catalyzed by transition metals. With benzofuran-containing halides and 4-hydroxy-3,5-diiodophenyl-containing borates or other nucleophiles, carbon-carbon bonds are formed under the catalysis of transition metals such as palladium and nickel, and the target product is constructed. In this process, the choice of ligands has a great impact on the reaction activity and selectivity. Depending on the specific situation, the appropriate ligands need to be screened to make the reaction efficient.

(2-ethyl-1-benzofuran-3-yl) Is (4-hydroxy-3,5-diiodophenyl) methanone toxic?

The toxicity of (2-ethyl-1-benzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) methanone is difficult to determine.
To determine whether its toxicity is present or not, many complicated tests are required. First, it is reasonable to take animals as a test to observe their physiological reactions after ingestion or exposure to this compound, such as eating, activity, and organ state. If the animal is sluggish, eating sharply reduced, and the organs are damaged, it may be toxic. Second, cell experiments are also indispensable to apply this compound to specific cells to observe its effects on cell growth, proliferation, and apoptosis. If cell growth is inhibited and apoptosis is abnormal, it can also be evidence of toxicity.
However, I do not have detailed information on this compound today, and I do not know whether there are relevant toxicity studies by predecessors. If it has been proven to be harmful to organisms in previous studies, or is structurally similar to known toxic compounds, it should be carefully assumed that it is toxic. On the contrary, if there is no such clue, it should not be ignored, and it must be determined by rigorous tests. In short, it is difficult to determine its toxicity based on this name alone, and it must be based on scientific experiments to obtain the true truth.