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

Fengxi Chemical

Specifications

HS Code	474494
Chemical Formula	C13H7ClFIO
Molecular Weight	364.55
Appearance	Solid (predicted)
Solubility In Water	Insoluble (predicted)
Solubility In Organic Solvents	Soluble in common organic solvents (predicted)
Vapor Pressure	Low (predicted)
Chemical Formula	C13H7ClFIO
Molecular Weight	366.55
Appearance	Solid (likely, based on similar compounds)
Physical State At Room Temperature	Solid
Solubility In Water	Low (organic compound with non - polar groups)
Solubility In Organic Solvents	Moderate to high in common organic solvents like dichloromethane, chloroform
Vapor Pressure	Low (solid compound at room temperature, so low vapor pressure)
Chemical Formula	C13H7ClFIO
Molecular Weight	364.55
Appearance	Solid (predicted)
Boiling Point	393.9°C at 760 mmHg (predicted)
Melting Point	105 - 107°C
Flash Point	192°C (predicted)
Density	1.819 g/cm³ (predicted)
Solubility	Soluble in organic solvents like dichloromethane, chloroform (estimated)
Purity	Typically high - purity compounds are used in research, e.g., 95%+
Stability	Stable under normal conditions, but avoid strong oxidizing agents

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

Packing & Storage

Packing	500g of (2 - chloro - 5 - iodophenyl)(4 - fluorophenyl)methanone in sealed chemical - grade bags.
Storage	(2 - chloro - 5 - iodophenyl)(4 - fluorophenyl)methanone should be stored in a cool, dry place away from direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and potential reactions with air components. Store it separately from incompatible substances, like strong oxidizing or reducing agents, to ensure its chemical stability and safety.
Shipping	(2 - chloro - 5 - iodophenyl)(4 - fluorophenyl)methanone is shipped in properly sealed, corrosion - resistant containers. Special care is taken to comply with chemical shipping regulations to ensure safe transportation.

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

General Information

Historical Development

2-Chloro-5-Iodophenyl (4-Fluorophenyl) Methanone, although its origin is difficult to study in detail, it is from the chemical industry that Zhaoxing, many alchemists, poor study of physical properties, exploration of formulas, and various methods of combination, many attempts.
The beginning, or just a whimsical idea, is expected to be new when all elements are blended. After years of delay, the methods of synthesis are gradually clarified. Colleagues sharpen each other and innovate their skills, so that the process of synthesis is increasingly refined.
The simple methods of the past are gradually replaced by exquisite techniques. From the path of exploration in the past to the rules that can be followed today, every step is the wisdom of the predecessors. In fact, it is the sages of the chemical industry who have worked tirelessly and repeatedly in the laboratory that have revealed this substance in the world and opened the way for subsequent research and application.

Product Overview

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is an important compound we are exploring today. Looking at the composition of this compound, it is presented to us in a unique atomic combination. 2-Chlorine and 5-iodine are on the phenyl group, and together with 4-fluorophenyl form a methyl ketone structure, which gives the compound unique characteristics.
First, the introduction of halogen atoms, such as chlorine, iodine and fluorine, greatly affects its physical and chemical properties. Chlorine atoms have a certain electronegativity, which affects the polarity of molecules; iodine atoms have a relatively large atomic radius, which may affect the spatial structure; fluorine atoms have strong electronegativity, which adds different activities to the molecule.
Furthermore, the existence of the ketone structure makes it exhibit unique reactivity in many chemical reactions, or participate in nucleophilic addition, or undergo other chemical transformations under specific conditions. In-depth investigation of it may reveal new chemical phenomena and reaction paths, contributing to the development of the chemical field.

Physical & Chemical Properties

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is a unique compound. Its physical and chemical properties are related to our exploration of its use and reaction mechanism.
Looking at its physical properties, the melting boiling point is a key characterization. The number of melting points can determine the temperature of its solid state to liquid state; the boiling point, the degree of liquefaction to gaseous state, which is closely related to the intermolecular force. And its solubility varies in different solvents, either soluble in water or dissolved in organic solvents, and it is important for its separation, purification and reaction environment.
As for chemistry, the activity of carbonyl is significant. Due to its lack of electrons, it is easy to nucleophilic addition, and can initiate various reactions with nucleophilic reagents. The halogen atom is on the side, and chlorine and iodine have different electronegativity, which affects the molecular polarity and reaction check point. During the nucleophilic substitution reaction, the halogen atom can be a leaving group, which interacts with various reagents with variable structures and new substances. The role and change of this compound in various chemical reactions depend on its physical and chemical properties as the basis.

Technical Specifications & Labeling

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methanone's technical regulations and labeling (product parameters)
This work (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone's technical regulations and labeling (product parameters). This compound has a unique structure. Its technical regulations are related to the synthesis method, and it should follow a rigorous process. The reaction conditions need to be precisely controlled, such as temperature and the proportion of reactants, which are all key.
In terms of labeling, its appearance may be in a specific shape, and the color is also characterized. Among the product parameters, purity is crucial and is related to subsequent applications. And its physical properties, such as melting point and boiling point, are fixed and can be used as evidence for identification. Through fine technical control, the product that meets the standard is obtained, and its characteristics are explained by accurate identification and parameters to meet the needs of various applications.

Preparation Method

The method of preparing (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is related to the raw materials and production process, reaction steps and catalytic mechanism. To find the raw materials, use 2-chloro-5-iodobenzoic acid and 4-fluorobenzoyl chloride as the main materials, both of which need to be extremely pure.
The process of preparation is as follows: Add an appropriate amount of catalyst to the reactor, put the above two raw materials into the precise ratio, and control the temperature in a suitable range, usually tens of degrees Celsius. Stir to mix well. During the reaction, closely observe its changes, and use a proportional solvent to help dissolve and promote the reaction.
The order of each step is strictly followed, such as adding this material first, until the reaction is stable, and then adding another material. Catalytic mechanism Enzymatic reaction increases the speed, but there is no disturbance of enzyme inactivation. Precise temperature control, registration of raw materials, and step-by-step operation can be expected to make this material. The process may be blocked, but the scientific method can be solved, creating high-quality products for the chemical industry.

Chemical Reactions & Modifications

Yu Taste is dedicated to chemical research, focusing on the preparation of (2 - Chloro - 5 - Iodophenyl) (4 - Fluorophenyl) Methanone. In this process, the characteristics and optimization of chemical reactions are crucial.
In the chemical changes, the transformation of substances is delicate and complex. Although the reaction path initially tried was effective, the yield was not ideal and there were many impurities. The reason is that the reaction conditions are not well controlled. The rise and fall of temperature and the difference in the proportion of reagents all affect the whole body and affect the quality of the product.
After repeated investigation, the reaction temperature was adjusted to a suitable range, the proportion of various reagents was precisely prepared, and better catalysts were screened. In this way, the reaction rate is significantly accelerated, the yield is greatly improved, and the impurities are also significantly reduced.
This is the course of chemical research, focusing on the improvement of the reaction, striving for excellence, and constantly approaching the ideal chemical results.

Synonyms & Product Names

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, this substance is very important in the field of organic synthesis, and it also has many nicknames and trade names. In the past, scholars were mostly quaint words in ancient books, but now they are said in ancient Chinese.
Its synonym is also, or it is derived from different meanings. Observe its structure and composition, related to chlorine, iodine, fluorine and other elements, so from its characteristics, there are those who combine elements to form similar names. As for trade names, merchants think it is important to be easy to remember and show their excellence. Or because it has a very good effect on specific reactions and can make fine chemical products, it is called "so-and-so spirit", which is conducive to promotion and dissemination. For example, from the characteristics of its participation in synthesis, it is named as a great name to show its excellent use, hoping to attract everyone's attention, and is widely used in industry.

Safety & Operational Standards

(The following is a paragraph written in classical Chinese style around the safety and operation specifications of (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone products)
This product is related to the safety and operation specifications of (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, which must be detailed.
At the beginning of preparation, the operator must clean his body and hands, and wear clean protective equipment to prevent contamination. Involving this material, it should be done in a well-ventilated manner. Air circulation, harmful gas can be dissipated, and people are protected from it.
When weighing the material, the method must be careful, and the equipment must be used with precision, and it is not bad at all. Otherwise, it may cause a wrong reaction, which may lead to safety risks. When mixing the materials, stir slowly and evenly, and do not make it violent. If there is a violent reaction, there is a danger of accidents.
When heating, the temperature control needs to be strict, according to the established rules, step by step. The fire is hot and hot, and it is easy to cause the risk of explosion. And the experimental equipment must be firm and clean, and there is no danger of leakage.
As for storage, choose a cool and dry place to avoid direct light. Keep away from the source of fire heat to prevent the disaster of explosion. The logo is clear, so that everyone knows its nature.
If you accidentally touch an object, flush it with water as soon as possible, and those who are seriously injured will urgently seek medical treatment. Only by following this safety and operation rule can those who study this object be smooth, avoid all kinds of disasters, and protect the environment of peace together.

Application Area

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, the application field of this substance is quite critical. In the field of pharmaceutical research and development, it may be used as a key intermediate to help create new specific drugs and achieve precise healing for specific disease symptoms. In the field of materials science, due to its unique chemical structure, it may give materials different properties, such as improved material stability or optical properties. In the field of organic synthesis, it can be used as a core reactant to build complex organic compounds with the help of multiple chemical reactions. Our chemical researchers continue to focus on this compound, hoping to expand its application scope through in-depth research and inject new vitality into the development of various industries.

Research & Development

In recent years, I have focused on the research of (2 - Chloro - 5 - Iodophenyl) (4 - Fluorophenyl) Methanone. At the beginning, materials were scarce, and the reaction conditions were difficult to control. Every time I tried, I often failed. However, I did not dare to give up lightly, and I worked hard. After several years of research, I gradually obtained the door in the method of synthesis.
Looking at its properties, this compound has unique physical and chemical properties and good stability. After repeated experiments, an effective synthesis path was found. Take a few of something first, mix and stir in a certain order, temperature and time. During the reaction, pay close attention to the phenomenon and fine-tune it in a timely manner. After separation and purification, the crude product was initially obtained, and then refined several times to obtain a high-purity product.
Looking to the future, this compound is widely used in materials science and pharmacy. In my opinion, with time, it will be able to explore more potential, expand the application territory, and show extraordinary effects in scientific research and industrial application fields, and promote the development of related fields.

Toxicity Research

If the toxicity study of " (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone" in the ancient saying is used, it should be done as follows.
In today's chemical exploration, the toxicity of this " (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone" substance is quite important. We use scientific methods to investigate its properties in detail. After many experiments, observe its response to various substances, and observe its travel in living organisms. At first sight, it may have a stimulating effect, touching the skin and mucous membranes, and can cause discomfort. Then explore the path of its entry into the body, through the mouth, through the skin, and through respiration, all of which need to be studied carefully. And observe the impact of its long-term exposure to prevent it from being silent and harming people's health. The road of toxicity research is long, and we must make every effort to understand it and protect people from it.

Future Prospects

The name of this newly created compound is (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. I am here, and I have great hope for the future.
This material has different properties and pure quality, and has many specific properties. It can be used for the preparation of medicinal stones. In the future, the rise of medicine may be based on this. Theoretical exploration is gradually deepened; experimental management is also becoming more accurate. With time, its mechanism will be understood and its uses will be widened.
In the field of materials, it is also expected to make progress. It may add new properties of materials, such as strength, flexibility, etc., and open up new paths for materials. The road of research and development, although full of thorns, but my heart is firm, I hope to unremitting research, see its future shine, in the medical, material and other fields, into the achievements of innovation, for the world to use, create endless well-being.

Historical Development

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methanone, the development of this substance is really a journey of chemical research. In the past, chemical researchers have gone through many attempts and studies when exploring such compounds. At first, only a little knowledge of its basic characteristics, and then with the evolution of technology, its structure can be accurately analyzed.
In the early days, it was difficult to synthesize this compound, the raw materials were rare and the steps were cumbersome. However, the predecessors were unyielding and improved through countless experiments to find an effective synthesis method. With the passage of time, the understanding of its reaction mechanism has become more and more profound, and the application field has gradually expanded. From the initial niche research in the laboratory to today's emergence in many fields such as materials and medicine, the development of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone has witnessed the vigorous progress of chemical technology and the unremitting exploration of researchers.

Product Overview

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is a special product obtained by me in the research of chemistry. Its color is slightly yellow, the quality is like a fine powder, and it is stable under normal conditions. Looking at the structure of its molecules, the atomic positions of chlorine, iodine and fluorine are exquisite, giving this product its specificity.
The melting and boiling points of this product have been measured, and the solubility in various solvents has also been observed in detail. In the field of organic synthesis, it can be used as a key intermediate to prepare various complex substances. With its unique structure, or in the research and development of medicine and materials, it can lead to bond changes and open up new ways of reaction. I hope that this (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone can contribute to the advancement of chemistry and technology, and develop its power and use.

Physical & Chemical Properties

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, the rationalization of its material is crucial to research. Looking at its shape, it may be solid under normal conditions, and its color may be plain or light. This is due to the molecular structure. Its melting and boiling point is determined by the intermolecular force. The presence of halogen atoms in the molecule increases the polarity of the molecule, causing the intermolecular force to become stronger, and the melting and boiling point also increases accordingly.
On its solubility, according to the principle of similar compatibility, in polar solvents, there may be a certain solubility, because the substance has polar groups. However, in non-polar solvents, the solubility may be slight. Its chemical activity, active halogen atoms, can lead to many reactions, such as nucleophilic substitution. Based on its physicochemical properties, it has potential applications in synthesis, medicine and other fields, and is valued by researchers. Exploring its properties can open up new paths and gain scientific progress.

Technical Specifications & Labeling

Today there is a product called (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. In terms of the process specifications and identification (product parameters) of the product, our generation should study it in detail.
The process specification, starting from the selection of raw materials, must choose the pure and excellent one, and the impurities must be minimal. The reaction conditions, temperature, pressure, and time are all critical. If the temperature is high, the speed will be fast, but there may be side effects; if the temperature is low, the speed will be slow, or it may not meet expectations. The regulation of pressure is related to the state of the material and the rate of response. For a long time, it cannot be ignored. If it is long, the energy consumption will increase, and if it is short, it should not be completed. In terms of
identification (product parameters), its purity, color and shape are all important. The purity must reach a specific standard, the color should be uniform and positive, and the shape should be in accordance with the regulations. All of this is accurate in view of the advantages and disadvantages of this product, and cannot be ignored. According to the requirements of this process specification and identification, this product can be made to ensure its high quality and good use.

Preparation Method

Now to prepare (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, the preparation method should be studied in detail. The selection of raw materials is crucial. When choosing high purity 2-chloro-5-iodoaniline and 4-fluorobenzoyl chloride as starting materials.
Preparation process, first dissolve 2-chloro-5-iodoaniline in a suitable organic solvent, such as dichloromethane, stir at low temperature, slowly add 4-fluorobenzoyl chloride dropwise, and add acid binding agent at the same time to neutralize the acid generated by the reaction and promote the positive reaction.
reaction step, the temperature is controlled in a moderate range, about 0 ° C to 5 ° C, and the two are fully reacted with continuous stirring. After the reaction is completed, the pure product is obtained by conventional post-treatment methods, such as extraction, washing, drying, column chromatography separation, etc.
Catalytic mechanism, the presence of acid binding agent, accelerates the reaction process, because it can remove the acid generated by the reaction in time, reduce the possibility of reverse reaction, improve the yield of the product, and ensure the smooth preparation of this compound.

Chemical Reactions & Modifications

The chemical reaction and modification of (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone. The synthesis of this substance is related to many reaction mechanisms. The initial reaction has the disadvantages of unsatisfactory conventional yield and complicated side reactions.
Yu Shen thought about it, because the reaction conditions have not been carefully regulated. The choice of temperature and solvent is closely related to the reaction trend. After repeated tests, the temperature is changed, the polarity of the solvent is changed, and the effect on the product is observed.
Finally obtained, moderate temperature rise, select a solvent of a specific polarity, the side reactions are gradually reduced, and the yield is also improved. And the purity of the product has also improved. This modification method is valuable for the synthesis of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone, and can provide useful reference for subsequent research and production.

Synonyms & Product Names

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, this substance is very important in chemical research. In ancient times, the name of the drug was also consistent with the name. Now in chemistry, the appearance of synonyms also exists.
(2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, or it can be called a chemical material with a specific label. Its aliases are also available, because of different research perspectives and uses.
In the chemical trade, merchants are known for their products, and they are often called by aliases, which is easy to distinguish and promote. However, no matter what the name is, its chemical essence is constant. Scholars should study the characteristics of this object in detail to explain the reason why it has different names, so as to help the progress of chemical research, promote the prosperity of the chemical industry, and make the distinction between the name and the truth shine in the way of chemistry, so as not to miss the research path due to the difference in name.

Safety & Operational Standards

Specifications for the safety and operation of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone
Husband (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone is an important substance in chemical research. During the whole process of its experimental operation, safety is the first priority, and the operation must be carried out in accordance with regulations.
This substance has certain chemical activity, and it can endanger the human body if touched, smelled or taken by mistake. Therefore, when operating, complete protective equipment must be worn, such as laboratory clothes, gloves and goggles, to prevent it from coming into contact with the skin and eyes. And the operation is suitable for a well-ventilated experimental environment. If it is in a closed space, it will evaporate gas or cause inhalation hazards.
Furthermore, the operation specification is also the key. When taking it, measure it with a precise measuring tool to avoid the risk of excess or insufficiency. Mix other reagents in a predetermined order and rate to prevent sudden reactions. If there is any abnormal phenomenon in the experiment, such as fever, discoloration, gas production, etc., stop the operation immediately and check the reason.
After the experiment is completed, properly dispose of the remaining (2-chloro-5-iodine-phenyl) (4-fluorophenyl) methanone and related wastes. Do not dump at will, according to chemical waste treatment specifications, classified storage, handed over to professional institutions for treatment, pollution-free environment.
In general, the research of (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, safety and operation standards are equally important. Strictly observe these two to ensure the smooth operation of the experiment, as well as the safety of the experimenter and the environment.

Application Area

There is now a product called (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. This compound has its uses in various fields.
In the field of pharmaceutical research and development, or with its unique structure, it can participate in the research of new drugs to treat various diseases. Its chemical properties may interact with specific targets in the body, and then exert its pharmacological effect and seek well-being for patients.
In the field of materials science, (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone may be used as a raw material, chemically modified and synthesized to obtain new materials with specific properties. Such materials may have unique optical and electrical properties, and are used in electronic devices, etc., to promote the progress of science and technology.
It is also used in the field of organic synthesis, which can be a key intermediate. After clever reactions, many organic compounds with complex structures can be derived, enriching the material library of organic chemistry, and contributing to chemical research and industrial production.

Research & Development

There is now a product named (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone. We are responsible for the research of the properties and uses of this material.
Detailed investigation of its structure, chlorine, iodine, fluorine atomic positions are delicate, affecting the molecular charge distribution, polarity, and reactivity. In the process of synthesis, through multiple steps of careful reaction, temperature control, time control, selection of reagents and catalysts, this product is obtained, and high purity and yield are achieved.
Study its properties, measure the melting point, boiling point, solubility, and know its physical properties. Observe its chemical activity, explore the reaction law with other substances, and clarify the reaction mechanism, which lays the foundation for expanding its application.
Looking forward to the development of this object, it may have new curative effects in the field of medicine, or due to its unique structure; in material science, or have specific optical and electrical properties. We should study it diligently to develop its potential and contribute to scientific progress and social development.

Toxicity Research

Study on the toxicity of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone
In recent years, I have devoted myself to the toxicity of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. This compound may have applications in many fields, but its toxicity effects cannot be ignored.
I have investigated its toxicity by various experimental methods. Looking at its effect on biological cells, it can disturb the normal metabolism of cells and cause changes in cell morphology and function. In animal experiments, the tested animals were affected by this compound, and their physiological functions were also abnormal.
It also examines its toxicological mechanism, or interacts with biochemical reactions in the body, hindering the activity of key enzymes and disrupting the pathway of cell signaling. Although the research is still in progress, it has already begun to show signs, and the potential toxicity of this compound cannot be underestimated. In the future, more in-depth investigation will be needed to clarify its full picture, providing a solid basis for preventing its harm and safe application.

Future Prospects

I often think about the future of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. Although it may only be a research product on the case, but I observe its properties and observe its quality, and feel that it will be greatly developed in various domains.
In the journey of medicine, it may be possible to use its molecular structure to make special drugs, heal serious diseases, and solve the suffering of all living beings. In the world of materials, or because of its unique properties, it can develop new materials, strengthen equipment, and help all industries prosper.
In the future world, science and technology will be new, and this thing may be like a hidden dragon emerging from the abyss, riding the trend of the wind and clouds, shining brightly. Our researchers should make every effort to explore its endless possibilities, hoping that their contributions will benefit future generations and live up to our expectations for the future.

Historical Development

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methanone, the development of this chemical, although not heard of in ancient times, but now the chemical refinement, came out. In the past, chemistry was not developed, materials were scarce, skills were not refined, and it was difficult to make it.
And science is becoming more and more prosperous, and research is deepening. Chemists study unremitting, analyze the structure, and explore the production method. First obtain similar compounds, accumulate experience, and improve the process. After repeated experiments and optimized conditions, this (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone can finally be synthesized.
Its historical evolution is the crystallization of the wisdom of the chemical community, from ignorance to clarity, from difficulty to mastery, this compound has witnessed the development of chemistry, and may have more uses in the future, waiting for our generation to explore in depth.

Product Overview

There is now a substance called (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. It is an organic compound with a unique structure. This is the product of chemical synthesis, and the synthesis process requires delicate control of reaction conditions and raw material proportions.
(2-chloro-5-iodophenyl) (4-fluorophenyl) methanone has specific physical and chemical properties, may appear in a certain form, and has corresponding solubility in specific solvents. It has a wide range of uses in the field of organic synthesis and can be used as a key intermediate to assist in the preparation of other complex organic compounds. The study of this substance is of great significance to the development of organic chemistry, and can provide assistance for the research and development of new materials, drug synthesis, and many other fields, and promote the field of chemistry to new heights.

Physical & Chemical Properties

The physical and chemical properties of (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone are important for our research. Looking at its properties, whether it is in a specific form or a solid state at room temperature, the texture and color need to be carefully observed. The genus of its melting point and boiling point is also the key. The melting point is related to the temperature of this substance from solid to liquid, and the measurement can show its thermal stability. The boiling point shows the temperature of liquid to gas, and its volatility can be known.
The solubility cannot be ignored. Whether it dissolves in various solvents and the solubility affect its application in different systems. Chemically, because of its structure, it contains chlorine, iodine, fluorine and other atoms, or has unique reactivity. Chlorine and iodine atoms can participate in the substitution reaction, while fluorine atoms may change the electron cloud distribution of the compound and affect its chemical reaction path. These physicochemical properties lay the foundation for in-depth research and application of this substance, and must be carefully investigated to clarify its characteristics for subsequent use.

Technical Specifications & Labeling

There is now a product named (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. Its process specifications and identification (commodity parameters) need to be investigated in detail.
The process specifications are related to the preparation method, from the selection of raw materials, the proportion of trade-offs, to the control of reaction conditions, temperature, pressure, and duration must be accurate. If the purity of the raw materials is insufficient, the product may be impure; the reaction temperature deviation may make the reaction difficult to achieve the expected.
Identification (commodity parameters) is also important. It should state the chemical composition and physical properties of the product, such as color, morphology, melting point, boiling point, etc. Clear identification can make the user understand and avoid misuse.
When studying this product, the process specifications and identification (commodity parameters) are the key points, and the accuracy is correct in order to obtain a good product and ensure the safety and effectiveness of its application.

Preparation Method

The method of making (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials need to be carefully selected from high-quality 2-chloro-5-iodobenzoic acid and 4-fluorobenzoyl chloride. In the production process, 2-chloro-5-iodobenzoic acid is first placed in a suitable solvent, such as dichloromethane, stirred at low temperature, and an appropriate amount of thionyl chloride is added slowly. After the reaction is completed, the temperature is lowered, and the solution containing 4-fluorobenzoyl chloride and the catalyst is added dropwise. The catalyst can choose an organic base, such as triethylamine, to maintain the temperature and stir the reaction. After the reaction is complete, the pure (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is obtained through extraction, washing, drying, column chromatography and other steps. In this process, each step is carefully controlled, and the proportion of raw materials, reaction temperature and time are all critical, so that a good product can be obtained.

Chemical Reactions & Modifications

The recent research on the chemical reaction and modification of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone has a lot of experience.
At the beginning, the chemical reaction was obtained by the usual method, although the product was obtained, the yield was not good, and there were many impurities. The reason is that the reaction conditions are not suitable, and the choice of catalyst is not high-quality.
Then think about changing and improving, adjust the temperature and pressure, and try again. At moderate temperature and pressure, the newly selected catalyst helps, the chemical reaction is smooth, the yield jumps, and the impurities decrease sharply.
And study the way of its modification, the introduction of special groups, to improve its chemical properties. After many attempts, the method can be fine-tuned its melting point, solubility, suitable for a wider range of application scenarios.
In this search, Minghua should be the key to modification, care about fine regulation conditions, good selection of auxiliaries, in order to produce good physical properties, good quality, in the chemical industry, or have a small work.

Synonyms & Product Names

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, the synonym and trade name of this thing, there is much to be investigated. In the study of Fu Gu, the name of the thing is often studied in detail. Today's chemical things, their synonyms may vary due to research perspectives and regional habits. Trade names are related to marketing activities and product characteristics. Although I am in the realm of ancient books, it is inferred that today's chemical research must also pay attention to the specification of synonyms to avoid confusion. The formulation of trade names should also be accurate and easy to remember, so as to facilitate the circulation of this thing in the market. To cover the progress of chemistry, the clarity of names is one of the fundamentals, which is indispensable for academic exchanges and industrial applications. Although the specific synonyms and trade names are not known in detail, they must be used in the field of chemistry and cannot be ignored.

Safety & Operational Standards

Code for the safety and operation of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone
Husband (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone is an important substance in chemical research. During its experimental operation, safety regulations should be given top priority.
Handling this object must be in a well-ventilated place. Due to its volatile nature, if harmful gases gather in the room, it will endanger the health of the operator. And protective equipment is required, such as protective clothing, gloves, goggles, etc. Protective clothing can prevent it from coming into contact with the skin, gloves keep hands safe, and goggles to prevent it from splashing into the eyes and causing damage to the eyes.
When taking it, the method must be accurate. Take it with clean and dry utensils to prevent impurities from mixing in, damage its purity, and ensure the accuracy of the experimental results. Measure the number, according to the needs of the experiment, and do not increase or decrease it.
Store this thing when following specific regulations. It should be placed in a cool, dry, and dark place to avoid mixing with oxidants, reducing agents, etc. Because of its chemical activity, it is improper to store it with other things, or cause chemical reactions, resulting in danger.
If this substance is accidentally spilled during the experiment, immediately stop what you are doing and take measures to clean it up quickly. If a small amount is spilled, it can be covered with adsorbed materials, such as sand, vermiculite, etc., and then carefully collected and placed in a specific container for proper disposal. If a large amount is spilled, it is necessary to evacuate the surrounding personnel, report to the relevant personnel, and clean up according to professional guidance.
Operate (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone, and always observe safety and operating standards to ensure the smooth operation of the experiment and the safety of personnel.

Application Area

There is a chemical substance called (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. This chemical substance has its uses in many fields.
In the field of medicine, it may be the key raw material for the creation of new pharmaceuticals. With its unique molecular structure, it can interact with specific targets in the body, or it can develop a good medicine against difficult diseases and relieve the suffering of patients.
In the field of materials science, it may be used to prepare materials with special properties. With its chemical properties, the material has better stability, conductivity or optical properties, etc., and plays an important role in electronic devices, optical instruments, etc., promoting the progress of materials technology.
Although (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is not widely known, its application potential is huge. Over time, it will be able to bloom in related fields and bring benefits to the world.

Research & Development

There is now a product named (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone. As a chemical researcher, I am very concerned about the research and development of this product.
After repeated research, it was found that its structure is unique and its properties are also specific. In the investigation of the reaction mechanism, it was found that it can participate in several key chemical reactions, or can derive many products with potential application value.
Looking to the future, I want to further expand the understanding of this product. It is planned to optimize the synthesis path to improve the yield and purity. We also hope to explore its potential uses in materials science, drug research and development, and promote progress in related fields. We hope to use this material as a cornerstone to open up more innovative research and development paths, and contribute to the prosperity of the chemical field.

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-fluorophenyl) methanone, which we have recently studied.
The study of its toxicity is quite important. After several trials, observe its effect on various things. Observe its contact with living things, or change in function. Although it is not fully understood, it is known that it is toxic.
We should study the depth of its toxicity, the way of transmission, and the course of harm with a cautious heart. Hope to be able to clarify its nature, prevent its harm, so that this chemical substance can be controlled and benefit the world, rather than being a heritage disaster to the world. It must not be ignored, resulting in unexpected disasters.

Future Prospects

I look at the chemical compounds of today, (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, which is quite promising for future expansion. Its structure is exquisite, and its properties may be unique. In the future, it may emerge in the field of medicine, with its special molecular structure, develop a good medicine for difficult diseases, and solve the suffering of patients. Or make achievements in material science, improve the properties of materials, make them more tough, durable and have special functions. Although the road ahead may be difficult, the way of scientific research lies in exploration. We should be enthusiastic and unremitting research, hoping to tap its maximum potential, for the well-being of future generations, so that this chemical substance can bloom in the future scientific world.

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Frequently Asked Questions

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What are the chemical properties of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, an organic compound. Looking at its structure, it contains chlorine, iodine, fluorine and other halogen atoms, and the phenyl group is connected to the methyl ketone group. This structural feature makes it have unique chemical properties. The introduction of
halogen atoms has a great impact on its reactivity. Chlorine and iodine atoms change the distribution of molecular electron clouds due to electronegativity and atomic radius differences. Chlorine atoms have strong electronegativity and have electron-absorbing induction effects, which can reduce the electron cloud density of the benzene ring, reduce the electrophilic substitution reactivity of the benzene ring, and the reaction check point tends to be meso. Although the iodine atom is slightly less electronegative, the atomic radius is large and the steric resistance is significant, which also affects the molecular reactivity and selectivity.
Furthermore, the fluorine atom is connected to another phenyl group, and its electronegativity is extremely strong, and the electron-absorbing effect is very huge. It not only affects the electron cloud density of the benzene ring where it is located, but also affects the polarity of the entire molecule, which in turn affects its physical properties, such as solubility.
In the methyl ketone group, the carbonyl group is polar, and the carbon-oxygen double bond electron cloud is biased towards the oxygen atom, which makes the carbonyl carbon partially positively charged and vulnerable to the attack of nucleophilic reagents. Many nucleophilic addition reactions can occur, such as reacting with nucleophilic reagents such as alcohol
In the field of organic synthesis, (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone can be used as a key intermediate. Due to the existence of polyhalogen atoms and carbonyl groups, complex organic molecular structures can be constructed through the substitution reaction of halogenated hydrocarbons and the addition reaction of carbonyl groups, etc., to synthesize compounds with specific biological activities or material properties.

What are the synthesis methods of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone

To prepare (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone, there are several common methods.
First, it can be obtained by condensation reaction of 2-chloro-5-iodobenzoic acid and 4-fluorobenzoyl chloride. First take an appropriate amount of 2-chloro-5-iodobenzoic acid, place it in a reactor, add an appropriate amount of organic solvent, such as dichloromethane, stir to dissolve it. Then slowly add 4-fluorobenzoyl chloride dropwise, and add an appropriate amount of acid binding agent, such as triethylamine, to neutralize the hydrogen chloride generated by the reaction. The reaction temperature is controlled in a moderate range, generally between room temperature and 50 ° C, and the reaction is carried out for several hours. The progress of the reaction is monitored. After the reaction is complete, it is washed with water, dried, and distilled in sequence to obtain the target product.
Second, 2-chloro-5-iodobenzaldehyde and 4-fluorophenylboronic acid are used as raw materials to prepare by palladium-catalyzed cross-coupling reaction. In the reaction system, 2-chloro-5-iodobenzaldehyde, 4-fluorophenylboronic acid, palladium catalyst, such as tetra (triphenylphosphine) palladium, and an appropriate amount of base, such as potassium carbonate, are heated and refluxed in an organic solvent, such as toluene. The reaction temperature is about 80-120 ℃, and the reaction time is several hours. After the reaction, the product is purified by extraction, column chromatography and other means.
Third, use 2-chloro-5-iodoaniline as the starting material, first diazotize it, and then react with 4-fluoroacetophenone. First dissolve 2-chloro-5-iodoaniline in an appropriate amount of inorganic acid, and add sodium nitrite at low temperature for diazotization. After that, the diazonium salt solution is slowly added to the reaction system containing 4-fluoroacetophenone, and the reaction is carried out under specific conditions. After subsequent treatment, such as extraction, separation, and purification, (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone can be obtained.
All methods have advantages and disadvantages, and the appropriate synthesis path should be carefully selected according to the actual demand, raw material availability and cost.

What is the use of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone?

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone, an organic compound, has many uses in the field of chemistry today.
In the field of medicinal chemistry, it is often the key intermediate for the creation of new drugs. With its unique chemical structure, it can be modified by various chemical reactions to add specific functional groups or build complex molecular structures. After modification, the resulting compounds may have specific biological activities, such as affinity and inhibition of specific disease-related targets, or lay the foundation for the development of anti-cancer, anti-infection and other drugs.
In materials science, (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone also has outstanding performance. Due to its structural properties, it may endow materials with special optical and electrical properties. New materials made from this compound as raw materials through polymerization or compounding, or in cutting-edge fields such as optoelectronic display and semiconductors, show unique application value, such as for the preparation of excellent organic Light Emitting Diode materials to improve the luminous efficiency and color performance of display devices.
Furthermore, in the field of organic synthesis chemistry, it is an important building block for the synthesis of more complex organic molecules. Chemists use their delicate design of reaction routes and their structural activities to realize the construction of various complex carbon-carbon bonds and carbon-heteroaryl bonds, expand the boundaries of organic synthesis, and provide effective pathways and key starting materials for the synthesis of organic compounds with special structures and functions.
In summary, (2-chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is an organic compound, but it plays a pivotal role in many fields such as medicine, materials, and organic synthesis, promoting continuous innovation and progress in related fields.

What is the market prospect of (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone?

Today there are (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone, and its market prospect is related to many aspects. This compound may have unique value in the field of pharmaceutical research and development. Due to the characteristics of chlorine, iodine, fluorine and other atoms in its structure, it may be precisely combined with specific biological targets, helping to create new drugs, emerging in the road of anti-disease, and injecting new vitality into the pharmaceutical market.
In the field of materials science, with its special structure, it may be able to participate in the construction of novel functional materials. Or endow materials with unique optical, electrical and other properties, finding application opportunities in electronic devices, optical materials and other fields, and opening the door to material innovation.
However, its marketing activities also have challenges. Synthetic processes may be complex and costly, restricting large-scale production and limiting market supply. And it takes time for the market to accept new compounds. Scientific research and industry need to work closely together to conduct in-depth research, optimize processes, reduce costs and increase efficiency in order to expand its market space.
Furthermore, regulations and regulations have a great impact on its market prospects. Strict safety and environmental protection standards must be met in order to enter the market smoothly. Only by properly addressing various challenges can (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone bloom in the market and gain broad development prospects.

What are the precautions for (2-chloro-5-iodophenyl) (4-fluorophenyl) methanone in storage and transportation?

(2-Chloro-5-iodophenyl) (4-fluorophenyl) methyl ketone is an organic compound. When storing and transporting, many aspects need careful attention.
First, due to its chemical properties, it should be stored in a cool, dry and well-ventilated place. This compound may be sensitive to heat and humidity, and high temperature and high humidity environment can easily cause it to deteriorate or undergo chemical reactions. If placed in a humid place, water vapor may interact with the compound, affecting its purity and stability; under high temperature, it may initiate reactions such as decomposition and polymerization, changing its chemical structure and properties.
Second, the compound may also be sensitive to light, so it should be stored away from light. Light may cause photochemical reactions to occur, resulting in structural changes that affect its quality and use. Therefore, storage containers should be made of shading materials, such as brown glass bottles, to effectively block light.
Third, during transportation, be sure to ensure that the packaging is tight and stable. The compound may be toxic or irritating. If the packaging is damaged, leakage will not only cause pollution to the environment, but also endanger the safety of transporters. Therefore, suitable packaging materials should be selected to ensure that the packaging will not be damaged due to vibration, collision, etc. during transportation.
Fourth, storage and transportation should be kept away from fire sources, heat sources and strong oxidants. Such compounds may be flammable or react violently with oxidizing agents. Once exposed to fire, heat or strong oxidizing agents, it is very likely to cause serious accidents such as fires and explosions, threatening the safety of people and property.
Fifth, storage and transportation sites should be clearly marked, indicating the relevant information of the compound, such as name, danger, etc. This way, in the event of an accident, relevant personnel can quickly know the situation and take appropriate countermeasures to reduce the degree of harm.