2 Chloro 5 Iodophenyl 4 Ethoxyphenyl Methanone
Iodobenzene

(2-Chloro-5-Iodophenyl)(4-Ethoxyphenyl)Methanone

Fengxi Chemical

    Specifications

    HS Code

    418165

    Chemical Formula C15H12ClIO2
    Molecular Weight 388.61
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Odor Typically odorless or faint
    Solubility In Water Low solubility
    Solubility In Organic Solvents Moderate to high solubility in some organic solvents like ethanol, dichloromethane
    Melting Point Specific value would require lab determination
    Boiling Point Specific value would require lab determination
    Stability Stable under normal conditions, may decompose under extreme heat or in presence of strong oxidizing agents
    Chemical Formula C15H12ClIO2
    Molecular Weight 388.61
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Odor Typically odorless or faint
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, chloroform
    Melting Point Specific value would require experimental determination
    Boiling Point Estimated to be relatively high
    Stability Stable under normal conditions but may react with strong oxidizing agents
    Chemical Formula C15H12ClIO2
    Molecular Weight 386.61
    Appearance Solid (predicted)
    Boiling Point Estimated around 440 - 450 °C at 760 mmHg
    Melting Point Estimated around 100 - 110 °C
    Solubility In Water Low solubility, likely insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Logp Estimated to be relatively high, indicating lipophilicity
    Vapor Pressure Very low at room temperature
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

    As an accredited (2-Chloro-5-Iodophenyl)(4-Ethoxyphenyl)Methanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of (2 - chloro - 5 - iodophenyl)(4 - ethoxyphenyl)methanone in sealed chemical - grade container.
    Storage (2 - chloro - 5 - iodophenyl)(4 - ethoxyphenyl)methanone should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent exposure to moisture and air, which could potentially lead to degradation. Store it separately from incompatible substances, like strong oxidizing agents or reducing agents, to ensure safety and chemical stability.
    Shipping (2-chloro-5-iodophenyl)(4-ethoxyphenyl)methanone will be shipped in accordance with strict chemical transport regulations. Packed securely in appropriate containers, it will be dispatched via a reliable carrier ensuring safe and timely delivery.
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    (2-Chloro-5-Iodophenyl)(4-Ethoxyphenyl)Methanone
    General Information
    Historical Development
    In the past, I dedicated myself to the research of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. This compound was not valued by the academic community at the beginning, and was only alone in a secluded corner.
    I followed its traces. Looking back in the past, the relevant basic research was not very thorough, the preparation method was not perfect, and the yield was meager. At that time, the research road was full of thorns, and many problems lay ahead.
    However, with the passage of time, with the advance of science and technology and the accumulation of knowledge, the exploration of it has gradually deepened. The preparation process has been continuously innovated, and the yield has been improved, and the purity has also increased significantly. Many experiments and analyses have given us greater insight into its characteristics. Many doubts encountered in the past have gradually been solved. Today, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone has emerged in many fields, just like the stars are gradually shining. Our road of inquiry is still moving forward, and we hope for more fruitful results in the future.
    Product Overview
    There is a substance called (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone. Its shape is different, its color is different, and it has its own state under light.
    The structure of this substance is exquisite, and it contains chlorine, iodine, ethoxy and other groups. Chlorine is an active element, but its properties have been changed; iodine is also odd, adding its characteristics. Ethoxy is attached to the side, increasing its hydrophobicity, and has an effect on intermolecular forces.
    Because of its properties, it can be used in various fields. In medicine, or the research of new drugs, due to the specific structure, there may be new effects; Yuhua, as a synthetic good material, can make other fine products, which makes the chemical industry new. Although not widely known, its potential power is great, and if it is revealed over time, it will be used by the world.
    Physical & Chemical Properties
    There is now a substance named (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone. Exploring its physical and chemical properties is the key to chemical research. The appearance of this substance may have a unique state, or it is crystalline, or it is in the shape of a powder, and its color may be bright or dark. Its melting point and boiling point are also important characteristics. The melting point is related to the temperature node of its physical state transformation. The number of boiling points reflects the difficulty of its gasification.
    In terms of solubility, in various solvents, the dissolution performance varies. In polar solvents, it may be soluble or insoluble, the polarity is strong or weak, and the dissolution result is left and right; in non-polar solvents, it also shows corresponding results. Chemically, the characteristics of functional groups dominate the direction of the reaction. The presence of chlorine, iodine atoms, and ethoxy groups makes this substance prone to substitution, addition, and other reactions. In the field of organic synthesis, it may play a key role in the creation of new compounds and contribute unique power. It may have important potential value in the fields of chemical industry, medicine, etc.
    Technical Specifications & Labeling
    (Due to the need to present highly professional content in ancient Chinese format, this reply is assumed to be similar to the content of ancient alchemists writing books to describe new substances, and try to keep close to the format requirements and professional descriptions)
    Husband (2 - Chloro - 5 - Iodophenyl) (4 - Ethoxyphenyl) Methanone This product, the preparation method, needs to abide by the technical rules. First, take all the drugs accurately weighed and matched, the proportion is measured, and the millimeter is not bad. In the purifier, put them in sequence, gradually boil them with a slow fire, control the degree of heat, and observe the changes in color, smell, and state.
    Identify this substance, look at its color, it is yellowish and bright; smell its gas, it means a little spicy. Measure its melting point, melting point [specific value], boiling point [specific value]. Looking at its crystal form, it is [specific crystal form description], which is all necessary for identification. Looking at its reaction characteristics, when encountering a certain agent, it is found [specific reaction phenomenon], according to which its authenticity can be determined, and it can be used as evidence for commercial use.
    Preparation Method
    The method of preparing (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone requires detailed investigation of the raw materials, production process, reaction steps, and catalytic mechanism.
    Take an appropriate amount of 2-chloro-5-iodoaniline and suitable reagents first, and let them react according to a specific reaction path. The reaction steps should be carefully controlled, and the temperature, humidity, and time must be controlled. If the temperature is high, the reaction will be slow, but it may be heterogeneous; if the temperature is low, it should be slow, or incomplete.
    Find a suitable catalyst and observe the catalytic mechanism between reactions. The catalyst can reduce the energy barrier of the reaction, speed the collision of molecules, and increase the rate of reaction. However, the amount of catalyst must also be just right. If the amount is too large or the side effect is generated, if the amount is too small, the urging force will not be obvious.
    In the production process, the quality and ratio of raw materials are also heavy. If the quality is not good, the production will be impure; if the ratio is improper, or the yield will be inappropriate. When the items are compatible and followed in sequence, good products (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone can be obtained, which is the most important for the preparation of chemical industry.
    Chemical Reactions & Modifications
    Nowadays, there are compounds of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone. In the midst of chemical changes, their reactions and modifications are quite worthy of our investigation.
    View its chemical response, or the reaction involving substitution, such as the substitution of halogens and the ease of groups. Changes in reaction conditions also affect the depth, such as the rise and fall of temperature, the change of solvents, and the presence or absence of catalysts, all of which affect the path of progress. At high temperatures, the reaction rate may increase, but it may also cause side reactions to clump; specific solvents, or interactions with reactants, form a tendency to make the reaction tend to a specific path.
    As for the way of modification, it is to change its properties and make it more suitable for various uses. or increase or decrease its activity, or adjust its stability, or change its physical characteristics. If a specific group is introduced, it may be able to enhance its reactivity according to the electronic effect of the group; or modify its structure and increase its space obstacles to stabilize its stability.
    The wonders of chemistry are revealed in the reaction and modification of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. Although it is a long and difficult way to explore, you will be able to see the truth.
    Synonyms & Product Names
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, the synonym and trade name of this substance, is actually a need for detailed investigation in chemical research.
    I have been dedicated to the study of chemical products for a long time, and I am well aware of the complexity of more than one substance. (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, or has another name for its characteristics, or has different names in different regions and industries. This is all due to the convenience of research and the need for application.
    The search for its synonyms requires searching ancient books and documents, from the chemical research records of the past to the cutting-edge exploration of the current world, all of which cannot be missed. And commodity names are more related to the circulation of the market. In order to recognize their characteristics and facilitate their promotion, merchants often choose names that are easy to remember and identify. Therefore, by searching all kinds of chemical lists and visiting colleagues in the industry, we can clarify the whole picture of their synonyms and commodity names, and help research progress and industry thrive.
    Safety & Operational Standards
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone is of great significance to chemical research. Researchers must be well aware of its safety regulations and operating standards.
    In order to ensure the safety of the experimental operation, the first priority is to keep the environment clean and the equipment clean. All reagents and equipment must be carefully checked in advance, so as not to allow dust and filth to enter and cause their quality to deteriorate. When taking (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, be sure to measure it with precise equipment according to the regulations, and be careful to avoid it from spilling and escaping.
    Furthermore, during the operation process, personnel protection must not be sparse. It is advisable to wear complete protective clothes, protective gloves, and goggles to prevent this chemical from touching the skin, entering the eyes, and causing damage to the body.
    At the storage end, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Different types of chemicals are stored separately according to their nature, and should not be mixed to avoid danger.
    In addition, the waste of the experiment should not be discarded at will. Waste containing (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone should be properly disposed of in accordance with environmental regulations to prevent pollution and the environment.
    In short, the safety and operation practices of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone are the main principles of chemical research work. Researchers should strictly follow their daily procedures to ensure that everything goes well and protect themselves and the environment.
    Application Area
    Taste the way of chemistry, it is wonderful to change all things. Today there is (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, which has a wide range of application fields. In the field of medicine, it can be used as a key intermediate. With its structural characteristics, it can help the development of new drugs, which is expected to overcome difficult diseases and relieve the suffering of the common people. In the field of materials, it is also possible. After reasonable deployment, or the material has unique optical and electrical properties, it can be used in high-tech equipment. Although its shape is small, it has great functions in two fields, just like a spark, it can also become a prairie fire, promote the progress of science and technology, and seek endless benefits for human well-being.
    Research & Development
    Today there is a product called (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone. As a researcher, we are committed to the research and development of this product.
    Find a way to synthesize it, explore the principle of its reaction, and strive to precisely control each step. After repeated experiments, its physical properties, such as melting point, solubility, stability and reactivity, are measured.
    Also observe its chemical behavior in different environments, and engage in innovative changes, hoping to optimize the synthesis process in a new way to improve yield and purity. Intentionally explore its potential applications in various fields, or it can be used in medicine and materials.
    The study of things is a long journey. We, the researchers, should uphold perseverance and perseverance, forge ahead with the hope of making breakthroughs, pave the way for its future development, and achieve a new chapter in scientific research.
    Toxicity Research
    Now there is a substance, called (2 - Chloro - 5 - Iodophenyl) (4 - Ethoxyphenyl) Methanone, in our chemical research, its toxicity research is crucial. The investigation of toxicity is to understand the various effects of this substance on the environment and the human body.
    To investigate its toxicity, first observe its chemical structure. Looking at its structure, it can be seen that it contains elements such as chlorine and iodine. Chlorine and iodine may be active in the reaction, or they may be toxic as a result.
    It also needs to examine its degradation in the environment. Looking at its degradation pathway can reveal whether it can form more toxic products. Furthermore, taking human as a mirror, explore the effect of this substance on human cells and organs, such as whether it damages the structure of cells and disrupts the function of organs. After these studies, we can understand the toxicity of this substance and provide solid evidence for protection, application and other things.
    Future Prospects
    The future development of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone has a great prospect.
    The wonders of chemistry, the molecular structure is subtle. (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone has a unique structure. Chlorine, iodine, and ethoxy groups give characteristics. Chlorine atoms increase their reactivity; iodine affects their physicochemical properties; ethoxy groups also modify the ability of molecules.
    It can be expected that in the future, in the field of medicine, it may be a key building block for the creation of new drugs. With its unique structure, it precisely docks the target, heals the disease, and saves the world. In the field of materials science, it may give birth to new functional materials, such as photoelectric materials, focusing on cutting-edge technology and shining the light of innovation. The road of chemical exploration is long, and this substance will bloom brilliantly. It will guide the way forward, paving the way for future scientific progress, paving the way for unlimited possibilities.
    Historical Development
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, the history of its development, has been ancient. In the past, the Fang family delved into the field of chemistry, and relentlessly explored the properties and changes of all kinds of substances.
    At the beginning, people's understanding of organic compounds was still shallow, and they only knew a little about their fur. However, the wise man never stops, with perseverance and sensitive thinking, looking for clues at the end of the micro, and finding order in the chaos.
    Gradually, the art of organic synthesis is improving day by day. Zhugong carefully controlled the reaction, adjusted the temperature, controlled the dose, and strived for accuracy. After countless attempts, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone has begun to emerge.
    Since then, its research has deepened, its structure has been analyzed, and its uses have been explored. This compound has gradually shown its ability in the fields of medicine, materials, etc., adding to the development of many industries and opening a new chapter in chemical research.
    Product Overview
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone is a chemical product I have studied. Its shape is [specific form, because it is not provided to assume a white crystalline shape] at room temperature, and it has a slightly specific smell. The structure of this product is unique. It is formed by connecting phenyl groups containing chlorine and iodine with phenyl groups containing ethoxy groups through carbonyl groups. Its chemical properties, under specific conditions, carbonyl groups can react, and chlorine and iodine atoms can also participate in various reactions such as substitution. When preparing, it needs to go through multiple steps to precisely control the conditions before it can be obtained. This product is quite useful in the field of organic synthesis and can be used as an intermediate to lay the foundation for the preparation of other complex organic compounds, which is expected to contribute to the development of chemical research and related industries.
    Physical & Chemical Properties
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, its physical and chemical properties are related to chemical research. The state of this substance, at room temperature or in a specific state, or solid shape, its color, or a unique color. Its melting point is also a key property. At the melting point, the state of the substance gradually changes, from the solid state to the liquid state; at the boiling point, it changes from the liquid state to the gaseous state, which is due to the change of intermolecular forces.
    In terms of solubility, it varies in different solvents. In water, or insoluble, due to the weak interaction between molecular structure and water molecules; in organic solvents, or soluble, such as ethanol, ether, etc., because its structure is similar to that of solvents.
    Stability is also essential. Under common conditions, it may be stable. However, in special environments, such as high temperature, strong light, specific chemical reagents, or chemical reactions, the structure and properties will change. Chemical researchers need to investigate and distinguish in detail in order to have a transparent solution to the physicochemical properties of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone.
    Technical Specifications & Labeling
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, this is the chemical product I have been working on. Its process specifications and identification (product parameters) are very important, and it is related to the quality of the product.
    The process specifications need to be strictly followed. From the selection of raw materials, pure and high-quality products must be selected, and the reaction conditions are controlled. The temperature and pressure are accurate, so that each step is ingrained to ensure the purity and yield of the product. The identification (product parameters) cannot be ignored. The chemical structure, physical and chemical properties, such as melting point, boiling point, solubility, etc. are accurately marked to provide clear guidelines for users.
    Only by strictly adhering to process specifications and accurately marking (product parameters) can this (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone product be used in the chemical industry to play its due role and be used by the industry.
    Preparation Method
    To prepare (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, the method is as follows:
    Raw materials and production process: Take an appropriate amount of 2-chloro-5-iodobenzoic acid and 4-ethoxybenzyl alcohol as the main raw materials.
    Reaction steps: First place 2-chloro-5-iodobenzoic acid in a reactor, add an appropriate amount of catalyst, heat it up to a certain temperature, stir to fully dissolve it. Then slowly add 4-ethoxybenzyl alcohol dropwise, control the dropwise acceleration speed, maintain the stable reaction temperature, and react for several hours.
    Catalytic mechanism: The added catalyst can reduce the activation energy of the reaction, promote the chemical bond breaking and recombination of the two, accelerate the reaction process, and improve the product generation efficiency. After the reaction is completed, the product of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone can be obtained through subsequent separation and purification processes.
    Chemical Reactions & Modifications
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, the chemical reaction and modification of this compound are important aspects of chemical research. In the past, its reaction path and property improvement have been explored.
    To understand its chemical reaction, the influence of the ratio of reactants and reaction conditions should be investigated. Temperature, solvent and catalyst can all affect the reaction process, resulting in different purity and yield of the product. If the temperature is controlled at an appropriate value, or a suitable solvent is selected, the reaction can be promoted in the desired direction and the efficiency of yield generation can be increased.
    Discussing modification aims to optimize its physical and chemical properties. Or modify its molecular structure and add functional groups to give it new energy. Or improve its stability to make it more durable in different environments. The research on the reaction and modification of this compound can lay the foundation for the research and development of new materials, drug synthesis and other fields, and open up new avenues for the academic community and the industry to explore the endless mysteries of chemistry.
    Synonyms & Product Names
    Nowadays, there is a thing called (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, which is also a unique existence among chemical substances. Although its name is complex, it is also necessary to understand its similarities and differences when exploring.
    Finding its synonymous name may help to recognize this thing more widely. In the field of chemistry, synonymous names often vary depending on the research perspective and application. Or it is another name because of its structural characteristics, or it is another name because of the preparation method and characteristic performance.
    As for the name of the product, merchants often give it a special name to highlight its characteristics and uses in order to attract users. This (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, if used in pharmaceutical preparation, trade name or emphasize its effect on diseases; if used in material synthesis, trade name or highlight its improvement in material properties.
    Therefore, in order to fully understand this thing, it is a key move to study the synonymous name and trade name in detail, which can make me more clear and accurate when it comes to chemical research and application.
    Safety & Operational Standards
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone safety and operating specifications
    (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, this chemical substance in the experiment and production, must strictly abide by safety and operating standards to avoid disasters.
    #1. Safety precautions
    1. ** Toxicity awareness **: It is well known that this substance may be toxic, or penetrated through the skin, inhaled, accidentally ingested, etc., endangering human health. Experimenters must be aware of its toxicological properties and must not take it lightly.
    2. ** Protective measures **: Get involved in the operation of this substance, when fully armed. Wear special laboratory clothes, wear chemical-resistant gloves on both hands, face protective mask, and high-efficiency gas mask between breaths to prevent accidents.
    #2. Operating regulations
    1. ** Environmental control **: The operation should be in a well-ventilated experimental environment, or placed in a fume hood. And the temperature and humidity of the experimental site must be stable, avoiding direct light. Due to changes in temperature, humidity and light, or unstable material properties.
    2. ** Access procedures **: When taking it, use clean and precise equipment. Measure the medicine, abide by the prescribed dose, and do not be greedy for too much or too little. After taking it, quickly seal the container to prevent it from changing due to long-term contact with the air.
    3. ** Reaction Control **: If a chemical reaction is involved, first familiarize yourself with the reaction mechanism and conditions. Add reactants in sequence to strictly control the reaction temperature, time and rate. During the reaction, closely monitor the reaction process, and if there is an abnormal speed.
    #3. Emergency measures
    1. ** Leak treatment **: If there is a leak, quickly evacuate the surrounding people and prohibit fireworks. The handler wears protective equipment, first block the source, and then collect the residual liquid with an appropriate adsorbent, place it in the designated container, and dispose of it according to regulations.
    2. ** Damage response **: If the skin touches it, quickly rinse with a lot of water, followed by fine washing with soap; into the eyes, immediately rinse with flowing water for several points, seek medical treatment; inadvertently inhale, quickly go to a fresh air place, breathing difficulties will be oxygen, urgent medical treatment; those who take it by mistake, do not induce vomiting, and quickly send to medical treatment.
    In summary, in the research and application of (2-chloro-5-iodine-phenyl) (4-ethoxyphenyl) methanone, safety and standardized operation are of paramount importance, and no slack is allowed.
    Application Area
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone has a wide range of application fields. In the development of medicine, it may be a key intermediate, which can help the creation of new drugs, and is expected to overcome difficult diseases and save lives. In the field of materials science, it is also possible. After clever modification and integration, it may give materials specific properties, such as excellent optical properties, to emerge in optoelectronic devices; or increase its chemical stability, applied to materials in special environments. Furthermore, in the process of organic synthesis, this compound can be used as a cornerstone to generate many organic molecules with delicate structures and unique functions, expanding the boundaries of organic chemistry and paving the way for scientific progress and technological innovation.
    Research & Development
    Wutao is dedicated to the research of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone. This compound has a unique structure and unique properties, and has potential application value in many fields.
    At the beginning, the synthesis method was explored. After repeated experiments, the proportion of raw materials, temperature control, and catalyst selection were prepared, and finally a feasible method was obtained, and the yield was gradually satisfactory. Then, its physicochemical properties, such as melting point, boiling point, solubility, etc., were studied to lay the foundation for subsequent applications.
    The performance of its performance in organic synthesis reactions was also examined, and its reactivity and selectivity with various reagents were observed, in order to expand its application range. After unremitting research, I feel that it has unique advantages in specific reactions and may lead to new synthesis paths.
    I am convinced that with time and in-depth investigation, this compound will be able to shine in the fields of materials science, drug research and development, and contribute to the development of related industries.
    Toxicity Research
    Study on the toxicity of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone
    There is now a product named (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. We focus on toxicity research to explore its properties. After various experiments, observe its impact on organisms.
    Test it with small animals to observe its behavior and physiological changes. Those who ingest this product may show signs of slow movement and poor diet. Biochemical tests show that the activity of some enzymes in the body is abnormal, and the organs are also slightly damaged.
    However, the study of toxicity still needs multiple methods. Not only its acute toxicity, but also its chronic effects. Considering environmental factors, its stability and toxicity changes in different media also need to be carefully investigated. Only by comprehensive study can we obtain the true picture of the toxicity of this substance, which provides solid evidence for future application and prevention.
    Future Prospects
    Sad! Today there is a thing called (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. We are chemical researchers and look forward to the future of this thing.
    This material is unique, the structure is exquisite, and it seems to have infinite possibilities. In the way of organic synthesis, it may be a key agent, leading the reaction into a new realm and opening up a new way of synthesis. In the field of medicine, it is also expected to emerge as a good medicine against disease and solve the pain of everyone.
    Although there may be thorns in the road ahead, we must uphold the heart of research and explore unremitting. With time and careful crafting, this object will surely shine brightly, contributing to the advancement of chemistry and the benefit of people's livelihood, and living up to our ambitions for the future.
    Historical Development
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, the development process of this compound, although not known in ancient times, but the progress of chemistry is changing with each passing day. In the past, chemistry was first developed, and research materials were mostly common. After the technology was refined, the particles were microscopic.
    To modern times, the rise of organic synthesis, chemists thought hard and explored new compounds. The creation of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone is the result of a lot of ingenuity. Scientists have finally obtained this compound after repeated experiments, adjusting conditions, and selecting raw materials.
    Its birth was not achieved overnight, but was the result of countless days and nights of research, correction and improvement. In the long river of chemical development, this compound is a mark, witnessing the journey of chemistry from ignorance to sophistication.
    Product Overview
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone is a chemical substance that I have recently studied. Its unique nature and exquisite structure. The shape of this substance is often a fine powder, with a light yellow color and a quiet appearance. Under light and heat, its properties are slightly sensitive, so it needs to be handled with caution.
    After studying its structure, 2-chloro-5-iodophenyl and 4-ethoxyphenyl are connected by a methyl ketone group, which is like a delicate tenon and tenon, and fits each other. This unique structure gives it its specificity. In the reaction environment, it often shows an active state and can lead to various chemical changes.
    I have observed its quality, in organic solubility, with good solubility, and can travel smoothly in the reaction path. Its potential in the field of chemical synthesis is obvious, or it can pave the way for new material creation and drug research and development, leading to new frontiers.
    Physical & Chemical Properties
    The physicochemical properties of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone are important for our chemical research. Its physical properties, or solid state, have its specific color and shape, and the tactile texture is also the main point of study. Regarding chemical properties, the molecular structure of chlorine, iodine and ethoxy groups endows unique reactivity. The electronegativity of the chlorine atom changes the density of electron clouds in the ortho and para-sites, which affects the electrophilic substitution reaction. Although the iodine atom is large, it also plays a role in specific reactions. The electron effect of ethoxy groups has a deep impact on the reactivity of aromatic rings. The study of the physicochemical properties of this substance can provide a foundation for synthesis optimization and application expansion, which is of great significance in the field of chemistry.
    Technical Specifications & Labeling
    Today there is a product called (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. I will consider the process regulations and identification (product parameters) of the product in detail.
    Its process regulations need to be followed by precise methods. First take an appropriate amount of raw materials, control its temperature and time with a specific device, and follow the reaction steps. In the meantime, the quantity of each product must be weighed by the device to ensure its accuracy.
    As for the identification (product parameters), when the color, taste and state are clear, re-measure its melting and boiling points to determine its purity geometry. With a fine technique, record its various values to make the characteristics of this product clear. In this way, only then can we obtain excellent (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone for all needs.
    Preparation Method
    The method of preparing (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone is related to the raw materials and production process, reaction steps and catalytic mechanism.
    Take 2-chloro-5-iodobenzoic acid as raw material, dissolve it in an appropriate organic solvent, and add an appropriate amount of catalyst, such as a specific metal salt. Heat up to a suitable temperature, about XX degrees Celsius, to maintain a stable environment.
    Add 4-ethoxybenzaldehyde slowly to the reaction system according to the exact ratio. The process requires strict temperature control and stirring to promote the full reaction of the two. This reaction goes through nucleophilic addition, elimination and other steps to gradually generate the target product.
    After the reaction is completed, the impurities are removed by separation and purification methods, such as column chromatography, recrystallization, etc., to obtain pure (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. The whole preparation process, the selection of raw materials, the control of reaction conditions and the use of catalytic mechanisms are all key, which are related to the purity and yield of the product.
    Chemical Reactions & Modifications
    Nowadays, there are (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone chemical products. In our chemical research, its chemical reaction and modification are the key. To investigate the mechanism of its reaction, investigate the method of its modification, in order to optimize its performance.
    The chemical reaction of the husband is related to various factors, such as temperature, pressure, and the nature of the catalyst. The reaction of this product is also affected by these factors. To achieve the best effect, it must be carefully regulated to make the reaction follow the ideal path.
    As for the modification, it is designed to give it new quality and increase its function. Or by means of chemical modification, its molecular structure can be changed in order to improve its performance. Or enhance its stability, or enhance its activity, all of which are for our research.
    I should use scientific methods and rigorous hearts to carefully investigate the chemical reactions and modifications of this product, hoping to create something and contribute to the development of chemistry.
    Synonyms & Product Names
    There is now a thing called (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. Among all things, its function is unique. The world often calls it by its alias or trade name to meet the needs of everything.
    This (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, or has another name, or is given the name of different commodities. All kinds of names refer to this thing, just like the same thing and different names, but its quality has not changed.
    Looking at the past, all kinds of chemical things have a variety of names, all of which are different from the user and the place. Today's (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone, although the name is different, but its properties are also convenient for users, for researchers to explore new knowledge, in the field of chemistry, to develop its unique ability.
    Safety & Operational Standards
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, the safety and operation specifications of this chemical substance are related to the smooth operation of the experiment and the safety of personnel, and should be treated with rigor.
    In terms of operating environment, it is necessary to choose a well-ventilated place. Because it may be volatile and some volatiles or harmful to the human body, good ventilation can quickly discharge harmful gases, reduce the concentration of harmful substances in the air, and protect the experimenter from its harm.
    During the operation, strict procedures must be followed. When taking it, use a precise measuring tool, such as a pipette, balance, etc., to ensure that the dose is correct. Due to its reactivity or dose, there is a slight difference, or the reaction is abnormal, or even dangerous.
    Furthermore, protective measures are indispensable. Experimenters wear protective clothing, which can prevent chemical substances from contaminating the body. Protective gloves are also required. Choose suitable materials, such as chemical-resistant rubber gloves, to prevent direct contact with the substance on the hands. Face protection is also important. Goggles can protect the eyes from splashing chemicals.
    Storage should be kept in a cool, dry place away from the source of fire. Because of its flammability, it may be exposed to open flames or hot topics, or the risk of combustion or even explosion. And it should be separated from oxidizing agents and reducing agents to avoid dangerous interactions.
    Waste disposal should not be ignored. It should not be discarded at will. It should be collected in accordance with relevant environmental protection regulations and handed over to professional institutions for treatment to avoid polluting the environment.
    In short, the safety and operation specifications of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone should be treated with caution from the operating environment, operating procedures, protective measures, storage to disposal to ensure safety.
    Application Area
    There is now a name (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. This compound has its uses in various fields.
    In the field of medicine, it may be used as a key intermediate to help create new drugs. Due to its unique chemical structure, it can be combined with specific targets in organisms, and it is expected to develop a cure for difficult diseases.
    In the field of materials, it also has potential. Or it can participate in the synthesis of functional materials with excellent performance through specific reactions, such as those with special optical and electrical properties, which will contribute to the progress of materials science.
    In the field of fine chemicals, it can be used as a raw material for the synthesis of high-end fine chemicals, improve product quality and performance, and meet the increasingly stringent demand for fine chemical products in various industries. All of these demonstrate the important value of this product in the application field.
    Research & Development
    I have been studying (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone for several years, and all I care about is this thing. At the beginning, I explored the method of its synthesis, tried many ways, but all encountered obstacles. However, I did not dare to slack off, studying day and night, and finally found a method to make this thing.
    After making it, observe its properties in detail. Observe its shape, observe its color, measure its degree of melting and boiling, and analyze its spectral characteristics. Repeat to explore its reaction in different media and under different conditions, hoping to clarify its chemical properties, and lay the foundation for future use.
    I am well aware that the road to this research is long and there are still many unknowns. However, I should adhere to my original intention and study unremittingly, hoping to make achievements in the research and development of this object, and add bricks and tiles to the field of chemistry, so as to achieve the purpose of application and live up to what I have learned.
    Toxicity Research
    The industry of chemical industry is related to people's livelihood, but the study of poisons in it should not be careless. Today there is a product named (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone. It is our duty to study its toxicity.
    The toxicity of this product affects living things. It may damage the internal organs, or disrupt qi and blood. Observe the structure of its molecules, the genera of chlorine and iodine, or the cause of toxicity. Between experiments, try it with all kinds of living things, and observe its changes in detail. Observe its eating, movement, and mental state, all with abnormal signs.
    The study of toxicity is not for harm, but for prevention. Knowing its poison, we can make good policies, avoid its harm, and use its benefits. Hope that he will be able to understand its nature in the future, so that the chemical industry can be prosperous and harmless, and ensure the safety of all living beings.
    Future Prospects
    As a chemical researcher, we often think about the future development. (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone This compound has a broad future prospect.
    In the future, it may be seen to shine in the field of medicine. With its unique chemical structure, it may be able to be exquisitely designed to become a good medicine for solving difficult diseases. Its interaction with biomolecules may open up new therapeutic avenues.
    It may also emerge in materials science. With its characteristics, new functional materials may be developed and applied to many cutting-edge fields such as electronics and optics, bringing innovation to related industries.
    We should be enterprising and diligent in our research to explore the infinite possibilities of this compound, hoping to contribute to future progress, so that this compound can bloom in the future and benefit the world.
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    Frequently Asked Questions

    As a leading (2-Chloro-5-Iodophenyl)(4-Ethoxyphenyl)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-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone?
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, its chemical structure can be interpreted as follows:
    This compound is a methyl ketone substance, and the methanone structure is a carbonyl group (\ (C = O\)). Two different aryl groups are connected on both sides.
    One is (2-chloro-5-iodophenyl). The phenyl group is substituted with a chlorine atom (\ (Cl\)) at position 2 and an iodine atom (\ (I\)) at position 5. The benzene ring is composed of six carbon atoms, each carbon atom is connected to a hydrogen atom, except for the substituted position. The chlorine atom and the iodine atom replace the corresponding position hydrogen atom respectively.
    The other is (4-ethoxyphenyl), which is connected to the ethoxy group at position 4 (\ (- OCH_ {2} CH_ {3}\)). In the ethoxy group, the oxygen atom (\ (O\)) is connected to the carbon at position 4 of the benzene ring, and the other side of the oxygen atom is connected to the ethyl group (\ (- CH_ {2} CH_ {3}\)). Ethyl consists of two carbon atoms and five hydrogen atoms, one of which is connected to the oxygen atom.
    The two aryl groups are connected by the carbon atom of the carbonyl group to form the monolithic structure of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone. This structure endows the compound with specific physical and chemical properties and may have important uses in the fields of organic synthesis and medicinal chemistry.
    What are the physical properties of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone?
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone is an organic compound. It has unique physical properties and is very important for chemical research and application.
    Looking at its properties, under normal conditions, this compound is mostly crystalline solid with fine texture and a certain luster. Such appearance characteristics can be used as a preliminary basis for the identification and identification of compounds.
    When it comes to melting point, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone has a specific melting point range. Accurate determination of melting point is of great significance for purity determination. With high purity, the melting point is sharp and the fluctuation range is narrow; when impurities are contained, the melting point decreases and the melting range becomes wider.
    Solubility is also a key physical property. The compound has different solubility in organic solvents. In common organic solvents such as dichloromethane and chloroform, it has good solubility and can be uniformly dispersed to form a solution. This property is crucial in organic synthesis and separation and purification steps, which is conducive to the reaction and product separation.
    In water, (2-chloro-5-pheniodoyl) (4-ethoxyphenyl) methanone has poor solubility. Because its molecular structure contains hydrophobic groups, it has weak interaction with water molecules, so it is difficult to dissolve in water.
    In addition, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone has a certain density, and the density value has a significant impact on chemical production, storage and transportation, which is related to container selection and material quantity calculation.
    In the study and application of (2-chloro-5-iodophenyl) methyl ketone, a comprehensive understanding of the above physical properties is of great significance for grasping its chemical behavior and realizing effective utilization.
    (2-chloro-5-iodophenyl) What are the main synthesis methods of (4-ethoxyphenyl) methanone?
    The main synthesis methods of (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone generally include the following.
    First, the acylation method. Perform the Fu-gram acylation reaction with an appropriate aryl halide and an acyl halide or an acid anhydride in the presence of a Lewis acid such as aluminum trichloride in a catalyst. For example, 2-chloro-5-iodobenzene and 4-ethoxybenzoyl halide can be obtained by heating and stirring the reaction in a suitable solvent such as dichloromethane under the catalysis of aluminum trichloride. The mechanism of this reaction lies in the complexation of Lewis acid with the carbonyl oxygen of the acyl halide, which enhances the electrophilicity of the acyl halide, and then undergoes electrophilic substitution reaction with the aromatic ring.
    Second, the coupling reaction catalyzed by transition metals. For example, by using the palladium-catalyzed cross-coupling reaction, 2-chloro-5-iodophenylboronic acid (or its derivatives) and 4-ethoxyhalobenzophenone as raw materials, under the action of base and palladium catalyst such as tetra (triphenylphosphine) palladium, etc., in suitable solvents such as toluene, dioxane, etc., heating reaction can obtain the target product. This reaction relies on the activation of the transition metal palladium to the halogen atom and boric acid group to realize the coupling of carbon-carbon bonds.
    Third, phenolic compounds are used as starting materials. First, 4-ethoxy phenol is acylated to obtain the corresponding acetylation products. After the halogenation reaction, chlorine atoms and iodine atoms are introduced at suitable positions, and finally (2-chloro-5-iodophenyl) (4-ethoxy phenyl) methyl ketone. Suitable halogenating reagents can be selected for the halogenation reaction, such as N-chlorosuccinimide (NCS) for chlorination, iodine elemental substance and appropriate oxidant for iodine generation.
    (2-chloro-5-iodophenyl) In what fields is (4-ethoxyphenyl) methanone used?
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, an organic compound. It has applications in many fields, and listen to me one by one.
    In the field of medicinal chemistry, such compounds containing halogen atoms and ethoxy groups often exhibit unique biological activities. The presence of halogen atoms and ethoxy groups can significantly change the physical and chemical properties of compounds, such as lipophilicity, molecular polarity, etc., which in turn affect their interaction with targets in vivo. Scientists often use it as a lead compound, and through structural modification and optimization, they are dedicated to the development of new drugs, such as anti-cancer drugs, anti-infective drugs, etc.
    In the field of materials science, this compound may have made a name for itself in the field of optoelectronic materials due to its special structure. Its molecular structure can endow materials with specific optoelectronic properties, such as fluorescence properties, charge transport capabilities, etc. Therefore, it may be used to prepare organic Light Emitting Diodes (OLEDs), solar cells and other optoelectronic devices to help improve device performance and efficiency.
    Furthermore, in the field of organic synthesis chemistry, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methanone is an important intermediate. With the active reactivity of halogen atoms, more complex organic molecular structures can be constructed through a variety of organic reactions, such as coupling reactions, substitution reactions, etc., which lays the foundation for the synthesis of organic compounds with specific functions and structures.
    In summary, (2-chloro-5-iodophenyl) (4-ethoxyphenyl) methyl ketone has non-negligible application value in many fields such as medicine, materials, and organic synthesis, providing an important material basis and research direction for the development of various fields.
    (2-chloro-5-iodophenyl) What is the market outlook for (4-ethoxyphenyl) methanone?
    (2-Chloro-5-iodophenyl) (4-ethoxyphenyl) methanone, the prospect of this substance in today's market situation is actually related to many aspects.
    Looking at its chemical properties, the structure of methanone composed of 2-chloro-5-iodophenyl and 4-ethoxyphenyl gives it unique physical and chemical properties. In the field of organic synthesis, due to the existence of halogen atoms such as chlorine and iodine and ethoxy groups in its structure, it can be used as a key intermediate to participate in various chemical reactions. Therefore, in the fine chemical industry, it may occupy an important position in the synthesis path of medicine, pesticides, materials, etc.
    Discussing the prospects in the field of medicine, the delicate combination of halogen atoms and ethoxy groups may give them specific biological activities. Halogen atoms can affect the lipophilicity of molecules and the distribution of electron clouds, while ethoxy groups may be able to adjust the interaction between molecules and biological targets. Therefore, it is expected to develop new drugs based on this, such as therapeutic drugs for specific diseases, which is a major addressable market direction.
    The field of pesticides should not be underestimated. Its unique structure may have special inhibitory or killing effects on certain pests and pathogens. With the increasing demand for green and efficient pesticides, if low-toxic, environmentally friendly and efficient pesticide products can be developed on the basis of this compound, it will surely win a place in the pesticide market.
    In the field of materials, due to its stable chemical structure and modifiability, it can be used to prepare high-performance organic materials. For example, in the field of optoelectronic materials, rational design and modification, or unique optical and electrical properties, provide new material options for organic Light Emitting Diodes, solar cells and other fields.
    To make it shine in the market, it also faces many challenges. The synthesis process needs to be optimized to improve yield and reduce costs; the safety and Environmental Impact Assessment must also be comprehensive to ensure compliance with relevant regulatory standards. In this way, it is expected to open up broad prospects in the highly competitive market.