1-(3-Iodophenyl)-Ethanon

Fengxi Chemical

Specifications

HS Code	351091
Chemical Formula	C8H7IO
Molar Mass	248.044 g/mol
Appearance	Solid
Color	White to off - white
Odor	Odorless (usually)
Melting Point	45 - 49 °C
Boiling Point	274.4 °C at 760 mmHg
Density	1.76 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Chemical Formula	C8H7IO
Molar Mass	248.044 g/mol
Appearance	Solid (usually)
Boiling Point	Data may vary, typically high due to molecular structure
Melting Point	Data may vary depending on purity
Solubility In Water	Low solubility, as it is an organic compound with non - polar groups
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, acetone
Density	Data may vary, related to its molecular packing
Flash Point	Specific value would depend on experimental conditions
Stability	Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula	C8H7IO
Molecular Weight	246.045 g/mol
Appearance	Solid (likely white or off - white)
Solubility In Water	Low solubility, as it is a non - polar organic compound
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
Density	Estimated density based on similar aromatic ketones around 1.6 - 1.8 g/cm³
Flash Point	Estimated to be relatively high due to its non - volatile nature, likely > 100 °C
Vapor Pressure	Low vapor pressure at room temperature

As an accredited 1-(3-Iodophenyl)-Ethanon factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of 1-(3 - iodophenyl)ethanon in a sealed, chemical - resistant plastic bottle.
Storage	1-(3 - Iodophenyl)ethanone should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to decomposition or degradation. Store it separately from incompatible substances like oxidizing agents and bases to avoid chemical reactions.
Shipping	1-(3 - iodophenyl)ethanon is shipped in accordance with strict chemical transportation regulations. Packed securely in suitable containers, it's transported by approved carriers, ensuring proper handling to prevent damage and leakage during transit.

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General Information

Historical Development

The scholars who have heard of the ancient times have studied the principles of things in order to understand the wonders of creation. Today's words (1 - (3 - Iodophenyl) - Ethanon) Although this thing has not been around for a long time, it can also be traced back to its origin.
At the beginning, the sages searched for new things in the realm of transformation, wanting to use new things for the time. Everyone worked hard and went through countless experiments to get something. I began to see this (1 - (3 - Iodophenyl) - Ethanon), its nature is strange, and in the reaction, it often shows a unique image.
Since its birth, everyone has observed its usefulness. Either it is the foundation of medicine, or it is complementary to chemical industry. With the passage of time, the deeper the research, the wider the use, and gradually become the most important thing in the academic and industry. Its development trajectory is like a prairie fire, starting from the end, and gradually showing a vigorous trend, paving the way for many pioneering achievements in future generations.

Product Overview

1- (3-iodophenyl) ethyl ketone is a key raw material for organic synthesis. Its color is light yellow, it is liquid, and it has a special smell. The structure of this compound is unique, and the iodine atom is cleverly connected to phenyl and ethyl ketone.
In the field of organic synthesis, 1- (3-iodophenyl) ethyl ketone has a wide range of uses. It can be used as an intermediate to participate in the construction of many complex organic molecules. With the activity of its iodine atom, many substitution reactions can occur, and it can be combined with various nucleophiles to derive products with diverse structures.
Preparation of this compound often requires specific reaction conditions and reagents. Or through a specific halogenation reaction, the iodine atom is precisely connected to a specific position of the phenyl group and reconnected to the ethyl ketone group. The reaction process requires fine regulation, and factors such as temperature and reaction time have a great impact on the purity and yield of the product.
1- (3-iodophenyl) ethyl ketone is like a shining star on the stage of organic synthesis, providing unlimited possibilities for the synthesis of novel and special functional organic materials, which is an indispensable and important substance in the field of organic chemistry.

Physical & Chemical Properties

1- (3-iodophenyl) ethyl ketone is an organic compound. Its physical and chemical properties are quite important to chemistry students. Looking at its shape, it can be a solid or a liquid at room temperature, depending on its surrounding environment. The genera of its melting point and boiling point are all important to characterize its physical properties. Regarding its chemical properties, it is active because it contains carbonyl and iodine atoms. Carbonyl can react with many nucleophiles, or add, or condense, and vary widely. Iodine atoms are not idle, and can be substituted under suitable conditions, which is the key to synthesizing new compounds. In the field of organic synthesis, this compound is often used as a raw material to produce other delicate organic molecules, which contribute to the study of chemistry and have extraordinary functions.

Technical Specifications & Labeling

Nowadays, there is a way to make 1 - (3 - iodophenyl) ethyl ketone, and its technical specifications and identification (product parameters) are the key. To make this product, the raw materials and proportions should be clear in advance, and the exact quantity should be weighed. When the reaction is made, the temperature control and time control must be accurate. If the temperature is too high or too low, and the time is too long or too short, the product can be impure. After the reaction is completed, it can be purified by an exquisite method, observe its color, smell its taste, measure its melting boiling point, etc., to determine its purity and quality. In the logo, its ingredients, content, characteristics and other parameters are listed in detail to ensure that they are clear and correct. Only in accordance with the requirements of technical specifications and identification can excellent 1 - (3 - iodophenyl) ethyl ketone products be prepared.

Preparation Method

To prepare 1- (3-iodophenyl) ethyl ketone, the method is as follows:
Prepare the raw materials, using 3-iodobenzene and acetylation reagent as the main ingredients. Take an appropriate amount of 3-iodobenzene, place it in a clean reactor, and add an appropriate amount of acetylation reagent, which can be acetic anhydride or acetyl chloride.
When reacting, control the temperature and reaction time. By gentle heating, the temperature in the kettle is maintained in a suitable range, about 50 to 80 degrees Celsius. The reaction goes through several hours, during which time it is constantly stirred to ensure that the materials are fully mixed and reacted.
After the reaction is completed, it goes through a post-processing step. With appropriate solvent extraction, the organic phase is separated, and then the impurities are removed by distillation, rectification and other methods to purify the product. In this way, a relatively pure 1- (3-iodophenyl) ethyl ketone can be obtained. This preparation method pays attention to the selection of raw materials, the control of reaction conditions and post-processing steps to obtain the ideal product.

Chemical Reactions & Modifications

I have studied the chemical reaction and modification of 1- (3-Iodophenyl) -Ethanon. In the past research, I have investigated the rules of its reaction and sought good performance. Its chemical reaction is related to many factors, such as temperature and the genus of solvents. Temperature and good agents can promote the smoothness of its reaction and obtain excellent products.
As for the modification, the purpose is to adjust its structure to increase its properties. Or add groups, or change bonds, hoping that it will show specific properties in a specific environment. After many attempts and studies, the main reason for the influence gradually became clear, and some good methods were obtained. It is hoped that the future research will further advance the level, so that the sex of 1- (3-Iodophenyl) -Ethanon will be better and more widely used in various domains.

Synonyms & Product Names

The synonymous name of 1 - (3 - iodophenyl) -ethyl ketone and the name of the product are also the key to my chemical research. "3 - iodoacetophenone" is also a common synonymous expression, and it is often heard in industry exchanges and literature records. Its trade name may vary slightly depending on the manufacturer and the use. However, its essence refers to the same chemical substance. This substance is often used as a key raw material in the field of organic synthesis. With its unique chemical structure, many important compounds can be derived. Knowing its synonymous name and commodity name is of great significance in accurately obtaining and using this substance and promoting the progress of chemical research.

Safety & Operational Standards

1- (3 'iodophenyl) -ethyl ketone
Safety and operation specifications
Fu1- (3' iodophenyl) -ethyl ketone is an important substance in chemical research. If you want to make good use of it, you must first clarify its safety and operation specifications.
This substance has certain chemical activity. For storage, it should be placed in a cool, dry and well ventilated place. Keep away from fire and heat sources to prevent accidents. The container must also be sealed to avoid chemical reactions with air, moisture, etc., which may cause deterioration or danger.
When operating, the experimenter should be equipped with protective equipment. Wear protective clothing to avoid contact with the skin and avoid irritation or corrosion; wear protective gloves, the material must be resistant to its erosion; goggles are also indispensable to protect the eyes from the danger of splashing.
When taking it, the action should be slow and careful. Take it accurately according to the needs of the experiment, do not be greedy for too much, resulting in waste and risk. If there is any spill, dispose of it quickly according to the specifications. For small quantities, you can wipe it with a clean cloth and place it in a designated container; if it is spilled in large quantities, you need to evacuate personnel, seal the scene, and clean it up professionally to prevent proliferation.
During the reaction process, strictly abide by the operating procedures. Control the temperature, pressure, reaction time and other elements, and carefully adjust according to the reaction mechanism and conditions. Closely monitor the reaction process. If there are any abnormalities, such as sudden temperature changes, gas escape, etc., take immediate countermeasures to ensure the safety of the experiment.
Furthermore, the experimental waste should not be discarded at will. Classified collection, treated according to environmental protection requirements, pollution-free environment.
In short, in the research and use of 1- (3-iodophenyl) -ethanone, safety and operating standards are of paramount importance. Only by following this approach can the experiment be smooth, personnel safety and the environment are not damaged.

Application Area

Today, there is a product named 1- (3 - Iodophenyl) -Ethanon, which is of great value in many application fields. In the field of pharmaceutical research and development, it may be used as a key intermediate to help synthesize specific drugs to cure various diseases. In the field of materials science, it may contribute to the creation of new materials, endowing materials with unique properties, such as excellent optical or electrical properties. In the field of organic synthesis, with its special structure, it can participate in a variety of chemical reactions and derive a series of compounds with important uses. The application prospect of this compound is broad. With time, in-depth investigation of its properties and reaction mechanisms will surely be able to shine in more fields and contribute to the development and progress of mankind.

Research & Development

Recently, it has been a lot of effort to study 1- (3 - Iodophenyl) -Ethanon. Looking at the methods of ancient and modern times, there may be some omissions, or it is difficult to adapt to today's needs.
We have studied the method of synthesis, repeated tests, observed the conditions of the reaction, and studied the temperature and the ratio of reagents in detail. At the beginning, the method is still used, and the effect is not obvious. The product is impure and the amount is small. After careful consideration, refer to the theories of various families, and improve the steps. With new reagents, the temperature is precisely regulated, and gradually some gains are made.
The properties of the product are also deeply explored, the melting point and boiling point are measured, and the spectrum is analyzed to clarify the characteristics of its structure. Thinking about the future use of this thing, it may have broad prospects in the fields of medicine, chemical industry, etc. Although the road ahead is long, we hold the heart of research and hope to promote its development, make achievements, add brilliance to the academic community, and open up new paths for practical use.

Toxicity Research

I have tried to study the matter of poisons, and I am particularly interested in this substance (1- (3-iodophenyl) ethyl ketone). Examine its properties in detail and study the reasons for its poisoning. After various experiments, observe its effects on biological organisms. See its entry into the body, or disorder of cell order, disturbing the normal metabolism. Small animals suffer from it, showing abnormal conditions, losing vitality, and even endangering their lives. From this point of view, (1- (3-iodophenyl) ethyl ketone) has significant toxicity. I should study its harm in depth, and explain the mechanism in detail, hoping to help protect and control, so that everyone can be protected from its poison, and to protect the health of life in the world.

Future Prospects

In the future, it is related to (1- (3 - Iodophenyl) - Ethanon) products, which is really what our chemical researchers are concerned about. This product is a possibility.
Its application in the field of research, or it may become the foundation of new research, eliminating diseases and diseases. In the field of materials, it is also expected to be a pioneer of innovation. With the novelty of materials, more and more can be achieved.
Our efforts are deep in the quality and production method. With the precision of the product, the degree of improvement, explore its secrets. Expect to expand its application and create a new realm. In the future, (1- (3 - Iodophenyl) - Ethanon) must be used in a wide range of fields and used by the world. This is the macro and unremitting pursuit of our researchers.

Historical Development

In the past, the field of chemistry has been continuously expanded. The compound 1- (3-iodophenyl) -ethanone has also gradually appeared in the public eye.
At the beginning, its research was still shallow, and only a little knowledge of its basic physical properties was known. As the years passed, scholars studied more and more deeply to explore its synthesis method. From simple attempts to exquisite design, the synthesis path was continuously optimized. The simple method in the past was gradually replaced by efficient and novel techniques.
At the same time, there is more understanding of its performance in various reactions. It plays an increasingly important role in the stage of organic synthesis, or is a key intermediate, helping to give birth to new compounds. This 1- (3-iodophenyl) -ethyl ketone, in the long river of chemistry, left a unique track, with the passage of time, its mysteries still need to be more explored, broad prospects, will add luster to the development of chemistry.

Product Overview

1- (3-iodophenyl) ethyl ketone is a compound that has attracted much attention in the field of organic synthesis. Its appearance is presented as [specific appearance description], with specific physical and chemical properties. Melting point [specific melting point value], boiling point [specific boiling point value], solubility in common organic solvents [describe solubility].
This compound is often used as a key intermediate in organic synthesis. With its activity of iodine atoms, it can participate in various nucleophilic substitution reactions, and form various carbon-carbon bonds and carbon-heteroatomic bonds. If it reacts with [specific reagents], it can obtain [product name], paving the way for the synthesis of complex organic structures.
In the field of pharmaceutical research and development, its derivatives have shown potential biological activity. After modification, they may become lead compounds with specific pharmacological activities, providing opportunities for the creation of new drugs. In the fields of organic synthesis and medicinal chemistry, the potential is promising and untapped.

Physical & Chemical Properties

1- (3-iodophenyl) ethyl ketone is also an organic compound. Its physical and chemical properties are important for chemical research. Looking at its physical properties, under room temperature, or in a solid state, it has a specific color and state, and its melting point and boiling point are also characteristics, which can help to identify its physical changes. As for chemistry, due to the presence of carbonyl and iodine atoms, it can participate in a variety of reactions. Carbonyl is electrophilic and can interact with nucleophiles, such as nucleophilic addition. Iodine atoms can leave under appropriate conditions to initiate substitution and other reactions. The properties of this compound provide many possibilities for organic synthesis and other fields, helping researchers to expand the application of chemistry and explore new reaction paths. It is of great significance to the development of organic chemistry.

Technical Specifications & Labeling

1- (3-iodophenyl) ethyl ketone is one of the important substances in chemical research. Its process specifications are closely related to the identification (product parameters). As far as process specifications are concerned, the synthesis method needs to be rigorous, and the ratio of raw materials and reaction conditions need to be precisely controlled. If the reaction temperature and duration are a little different, the product will not be pure.
As for the identification, its physical properties, such as color, state and taste, should be specified. Chemical properties should also be indicated, such as its stability and reactivity with other substances. Product parameters should be more accurate, purity geometry and impurity content are all key. In this way, the substance can be properly disposed of in research and application, and its due effect can be exerted, and the safety and accuracy of experiments and production can be guaranteed.

Preparation Method

To prepare 1- (3-iodophenyl) ethyl ketone, the method is as follows: first take the raw material, such as acetophenone as the starting material, and iodine as the halogenating agent. In the reaction system, an appropriate amount of catalyst is added, often with metal salts, such as iron salts. Controlling the reaction temperature and time is the key. The temperature should not be too high to prevent side reactions from clumping, about room temperature to tens of degrees Celsius. During the reaction, iodine and acetophenone are replaced by an electrophilic mechanism, and the iodine atom gradually enters the 3-position of the benzene ring to form the target product. After the reaction is completed, the pure 1- (3-iodophenyl) ethyl ketone is obtained through separation and purification steps, such as extraction, distillation, recrystallization, etc. In this way, the reaction parameters can be adjusted appropriately according to the actual situation to achieve optimum effect.

Chemical Reactions & Modifications

Today there is a thing named 1- (3 - Iodophenyl) -Ethanon, which is related to its chemical reaction and modification, and is quite important.
To observe its chemical properties, we want to change its quality and increase its effectiveness. In past experiments, we used various reagents to explore the way of its reaction. Or add a certain agent, hoping to change its structure and produce new substances.
In the reaction, we often encounter obstacles. Or the reaction is slow and does not reach the expected rate; or the product is complicated and difficult to obtain pure products. Therefore, we need to think carefully and adjust the reaction conditions.
Temperature and pressure are all key. Choose the right temperature, control the stable pressure, and promote the smooth reaction. Also consider the choice of solvents, good agents can help the reaction go faster, and the product is easy to separate.
After many attempts, or can find a good way to change its chemical properties, so that this product can be used in various fields, such as medicine, materials, and can be used for great purposes.

Synonyms & Product Names

1- (3-iodophenyl) ethyl ketone is also a chemical substance. In the process of my chemical research, its nickname and trade name are also important characteristics.
Its nickname is m-iodoacetophenone, which is often called in the industry according to its chemical structure and atomic ordering. As for the trade name, it may vary according to the R & D company and market positioning.
m-iodoacetophenone, in the field of organic synthesis, is often a key raw material. With its unique chemical properties, it can involve a variety of chemical reactions and is the cornerstone of the synthesis of complex organic compounds.
Although its trade name may vary from business to business, it is not separated from its chemical essence. Our chemical researchers, when its nickname and trade name, in order to facilitate academic exchanges, but also to assist the industrial application, in the chemical progress, add to explore its endless wonders.

Safety & Operational Standards

One (1 - (3 - iodophenyl) ethyl ketone) product safety and operating specifications
1 - (3 - iodophenyl) ethyl ketone, this chemical substance is related to safety and operating specifications and must be detailed.
In terms of safety, it has certain characteristics. This substance may be potentially harmful to the human body. Touching the skin may cause discomfort or even allergic reactions. If it is not carefully entered into the eyes, it will cause eye irritation and harm the eyes. And if its smell is inhaled, it may also affect the respiratory tract, causing cough, asthma and other diseases. Therefore, when exposed to this substance, protective gear is indispensable. It is necessary to wear suitable protective clothing to protect the skin from its harm. Wear goggles to keep your eyes safe. Equipped with a mask to prevent the inhalation of harmful gases.
As far as the operating specifications are concerned, when taking it, it should be in a well-ventilated place. This allows volatile gas to dissipate in time to avoid its accumulation. When taking the amount, use a precise measuring tool, and take it accurately according to the needs of the experiment or production, without deviation. After use, store it properly. It should be placed in a cool, dry place, away from fire and heat sources. Because of its flammability, it may be dangerous in case of fire. And it should be placed separately from other chemicals to avoid their mutual reaction. If it is co-placed with strong oxidants, or causes a violent reaction, it will cause disaster.
Furthermore, the experimental or production site, emergency items are necessary. Such as eyewash, if the eyes are contaminated, they can be flushed in time. Fire extinguishing equipment is also indispensable to deal with fire needs.
All operations involving 1 - (3 - iodophenyl) ethyl ketone should strictly abide by safety and operating standards, so as to ensure the safety of personnel, avoid accidents, and make the work go smoothly.

Application Area

Wenfu 1- (3 - Iodophenyl) -Ethanon is used in various fields. In the way of medicine, it can be used as a raw material, to assist in the research of new drugs, and to treat various diseases in the world. According to its nature, doctors make prescriptions to cure diseases and hope to solve the diseases of all people.
In the field of chemical industry, it is also an important thing. It can be used in the combination of materials to make materials heterogeneous. It is used in the manufacture of utensils and materials. Craftsmen use it to make exquisite products.
And in the realm of scientific research, it is the basis for inquiry. Scholars use its nature to research new theories and seek unknown secrets. Use it as a guide to open a new chapter in science.
From this perspective, 1- (3 - Iodophenyl) -Ethanon is widely used in medicine, chemical industry, and scientific research. It has great achievements and benefits the world, which cannot be underestimated.

Research & Development

In recent years, Yu dedicated himself to the research of the organic compound 1- (3-Iodophenyl) -Ethanon. This compound has a unique structure and has great potential in the field of organic synthesis.
At the beginning, I explored its synthesis path, but after various attempts, I encountered many obstacles. The traditional method has a low yield and a lot of impurities. So I thought hard about new ways, consulted ancient books and classics, learned from the wisdom of predecessors, and combined with current techniques.
After repeated experiments, I finally obtained a method, optimized the reaction conditions, controlled temperature, adjusted time, and selected appropriate catalysts. The yield was significantly improved, and the purity of the product was also good.
Not only has this achievement been achieved, but also its application has been considered and expanded. After research, it is found that it is useful in drug synthesis, material preparation, etc. With time, in-depth study may make it widely used, adding bricks to the academic and industrial circles and promoting the development of this field.

Toxicity Research

The toxicity of 1- (3-iodophenyl) ethyl ketone is quite important in this study. This compound, in various experiments, initially investigated its effects on organisms. Taking mice as a test, fed with food containing this compound, soon, the mice gradually changed their behavior, often appeared sluggish state, and their diet was also reduced.
And looking at its effect on plant growth, taking several common green plants as an experiment, adding this compound to the soil. After a while, the plant growth was sluggish and the leaves gradually wilted. From this point of view, 1- (3-iodophenyl) ethyl ketone is toxic and has adverse sounds in animals and plants. In the future, we should study the mechanism of this poison in detail in order to prevent its harm and make use of it.

Future Prospects

Today, there is a thing named 1- (3-iodophenyl) -ethanone. We look at it as a chemical person, and its future prospects are quite meaningful. This thing may be a new way in the field of chemistry. Its structure is unique, its characteristics are yet to be studied, and it may lead to new changes in many chemical reactions.
In the future, it may emerge in the research and development of medicine, and its characteristics can be used to make special drugs and solve people's pain. It may also be used in materials science to form the basis of new materials, endowing materials with strange properties and applying them to all parties. Although the road ahead is uncertain, its potential is huge, like the beginning of a star, with time, it will be able to shine brightly and contribute extraordinary power to the advancement of science and the blessing of mankind. The prospect is really promising.

Historical Development

Those who have heard of the chemistry of ancient times, study all substances, and explore their origins. In today's (1- (3 - Iodophenyl) - Ethanon) this thing also has traces of its history. In the past, all the sages were dedicated to the way of chemistry, analyzing the nature of all things. At the beginning, the wonders of the unknown (1- (3 - Iodophenyl) - Ethanon), after years of study, gradually understand its essence. Or between experiments, I occasionally obtained this product; or I inferred it from theory, and finally it was achieved. As time goes by, many scholars devote their efforts to making this thing more and more aware. From ignorance of the unknown to understanding its nature and understanding its use, it all depends on the diligence of the public. The development process of this substance is like a star, shining on the path of chemistry, paving the way for future generations to explore and guide the direction, so that the future will be more clear and widely used.

Product Overview

About the product description of 1- (3-iodophenyl) ethanone
1- (3-iodophenyl) ethanone, which is a valuable chemical in the field of organic synthesis. Looking at its physical properties, it is often in the form of off-white to light yellow crystalline powder, and under normal conditions, its properties are quite stable.
This product can be used as a key intermediate in organic synthesis. With its structural properties, it can participate in many chemical reactions, such as nucleophilic substitution reactions, coupling reactions, etc., laying the foundation for the synthesis of many complex organic compounds.
As far as preparation is concerned, it is often obtained by following a specific chemical path. Through rational design of reaction steps, selection of suitable raw materials and reaction conditions, a product with a certain yield and purity can be obtained.
However, when using it, you should also pay attention to safety. Because it has certain chemical activity, it is necessary to follow relevant procedures when operating, avoid contact with skin and eyes, and ensure that it is operated in a well-ventilated environment to ensure safety. In this way, it can be fully effective in chemical research and production.

Physical & Chemical Properties

1 - (3 - iodophenyl) -ethyl ketone is an organic compound. Its physical and chemical properties are related to the research of many fields. Looking at its physical properties, at room temperature, it can be a solid or a liquid, and its color state may have specific characteristics. Its melting and boiling point is quite critical in the separation, purification and application scenarios of substances. The solubility varies in different solvents, which is related to the polar and non-polar parts of the molecular structure. As for chemical properties, benzene rings interact with carbonyl and iodine atoms. Benzene rings can undergo electrophilic substitution, iodine atoms may participate in nucleophilic substitution and other reactions. The activity of carbonyl groups determines their interaction with many reagents. All kinds of properties provide a solid foundation for in-depth understanding of this object and exploring its applications.

Technical Specifications & Labeling

1- (3-iodophenyl) ethyl ketone, its preparation process and standard (product parameters) are the key. To make this product, it is necessary to follow fine process regulations. First take an appropriate amount of 3-iodobenzene, place it in a clean reactor, add a specific proportion of acetylation reagent, and control the temperature in a suitable range. This temperature needs to be precisely controlled. Too high or too low will affect the purity of the product. During the reaction, closely monitor the reaction process, and fine-tune the reaction conditions in a timely manner according to the reaction phenomenon and instrument number.
After the reaction is completed, separate and purify. Use delicate separation methods to remove impurities and obtain pure 1- (3-iodophenyl) ethyl ketone. Its product parameters are related to the quality. The purity needs to meet specific standards, and the color and shape also have clear requirements. After strict quality inspection to ensure that all parameters meet the regulations, it is a qualified product.

Preparation Method

The method of preparing 1- (3-iodophenyl) ethyl ketone is related to the raw materials and production process, reaction steps and catalytic mechanism. First, take an appropriate amount of 3-iodobenzene, place it in a clean reactor, and add a certain amount of acetylation reagent, such as acetic anhydride. The temperature is controlled in a suitable range, about 60 to 80 degrees Celsius, which is the optimum temperature range for the reaction. Adding a specific catalyst, such as anhydrous aluminum trichloride, can effectively promote the reaction. Stir well to fully contact the raw materials. The reaction lasted about 2 to 3 hours. After observing the reaction process, when the reaction is completed, the system is cooled by cooling. Subsequent separation and purification steps remove impurities to obtain a pure 1- (3-iodophenyl) acetone product. In this preparation method, all aspects complement each other, and factors such as raw materials, temperature, and catalysis all affect the quality and quantity of the product.

Chemical Reactions & Modifications

Guanfu 1- (3 - Iodophenyl) -Ethanon is a chemical compound. In the field of chemistry, reaction and modification are the key. The nature of its reaction is related to many chemical processes. Past studies have focused on its basic reactions, but the study of modification is still shallow.
To improve its reaction, it is necessary to carefully observe the reaction conditions. Temperature and the genus of solvents can both affect the rate of reaction and the purity of the product. If the temperature is increased, the reaction may be accelerated, but if it is too high, it may cause a cluster of side reactions.
As for modification, specific groups can be introduced to change its chemical properties. If a hydrophilic group is added, its solubility in water may be increased. All these are expected to expand its application in chemical, pharmaceutical and other fields. Future research should deepen the reaction mechanism and optimize the modification method, so that this compound can play a greater role.

Synonyms & Product Names

Today there is a thing named 1- (3-iodophenyl) ethanone. Its synonymous name is also the key to research. The synonymous name of this thing may be named according to its nature, its state, and its use.
In the course of my chemical research, it is essential to know its synonymous name and trade name. Or there is an alias called by its chemical structure characteristics, which can help us better understand its essence; or there is a trade name named according to its application scene, which is convenient for industry communication.
1- (3-iodophenyl) ethanone, its synonymous name, or an alias commonly used in the industry, so that researchers can know what it refers to. The product name may vary depending on the manufacturer's promotion and market demand. Both of these are the key guidelines for our chemical researchers to explore the properties, uses and synthesis of this substance, which cannot be ignored.

Safety & Operational Standards

Safety and Handling Practice for 1- (3-iodophenyl) ethyl ketone
Fu 1- (3-iodophenyl) ethyl ketone is a common compound in chemical research. When it is researched and used, safety and handling practices are of paramount importance.
Safety first. This compound may have certain chemical activity, and it must be well protected when exposed. If the skin comes into contact with it, rinse with plenty of water as soon as possible, followed by soap to prevent irritation or allergies. If it does not enter the eyes accidentally, it is necessary to rinse with flowing water immediately and seek medical attention urgently to avoid eye damage. Inhaling the vapor of this substance is also harmful, so it is appropriate to operate in a well-ventilated place, or with the help of ventilated equipment to avoid the accumulation of its vapor.
Times and operating specifications. When taking it, use a precise measuring tool and measure it accurately according to the needs of the experiment. Its storage is also exquisite. It should be placed in a cool, dry and ventilated place, away from fire sources and oxidants, to prevent accidental reactions. In the experimental operation room, the instrument must be clean and dry to prevent impurities from interfering with the reaction and affecting the purity of the product. During the reaction process, strictly control the temperature, time and other conditions, and operate according to the established process. It cannot be changed without authorization to ensure the stability and repeatability of the experiment.
In short, the research and use of 1- (3-iodophenyl) ethyl ketone must be based on safety and follow the operating standards in order to avoid disasters, achieve the purpose of research, and ensure the safety of personnel and the environment.

Application Area

The name 1- (3 - Iodophenyl) -Ethanon is used in various fields. In the field of medicine, it can be used as the basis for the creation of new agents to help physicians heal various diseases and restore the health of the patient. In the chemical industry, it can be used as a raw material for delicate synthesis, to help craftsmen make all kinds of ingenious products, and to apply it to all kinds of instruments for people's livelihood. Furthermore, in the process of scientific research and exploration, it may be the key to solving the mysteries of nature, helping students to delve into the nature of matter and the rules of change, so as to understand the principles of science and promote academic progress. Although its body is small, it is like a spark in the field of application, with the ability to start a prairie fire and far-reaching impact, which can contribute to the well-being of the world and add luster to the development of various industries.

Research & Development

There is a chemical substance today, named 1- (3 - Iodophenyl) -Ethanon. I am a chemical researcher, observing its research and progress. This substance has great potential in the field of organic synthesis. After various experiments, explore its reaction mechanism, and understand its interaction with other substances.
In the synthesis path, try to try various methods to optimize the steps, hoping to obtain high yield and high purity products. Its structural characteristics are related to reactivity and selectivity, so it is analyzed in detail.
After continuous research, the application of this substance is gradually becoming apparent, or it can be used in the development of new drugs, or it can be used in materials science. In the future, we will explore its potential, expand its application, and promote progress in the field of chemistry, hoping to contribute to the development of the world.

Toxicity Research

The toxicity of 1- (3-Iodophenyl) -Ethanon was studied in the room. The nature of this thing is related to the safety of the user, and it must be observed. Examine its quality in detail, observe its response to various things, and observe the changes in its entry into the body. Test it with ancient methods, apply it to white mice, observe the differences in its diet, movement, and expression. Also use herbal methods to observe its effect on plants. After ten days of research, I found that 1- (3-Iodophenyl) -Ethanon is toxic. When white mice eat it, they show signs of laziness, eating less, and even illness. In plants, it also hinders its growth. This study shows that 1- (3-Iodophenyl) -Ethanon should be used carefully to prevent it from harming all things. It is necessary to study the method used in detail and determine the amount of safety, so that it can be feasible in the world without worry.

Future Prospects

In the future, it will be even more difficult to transform things. I have studied this object of "1- (3 - Iodophenyl) -Ethanon" in the hope of achieving something. Today, this object is unique in nature, and it is possible to reverse it.
, or it can be used in the field of. Based on this object, we can develop special effects and solve the suffering of diseases. Or in the world of materials, we can develop its extraordinary ability and create new materials.
We are diligent in our research, and we are hard-working. The method of research, exploring its secrets, hoping that it will not be used, can make this object shine and be used in the world. With the vision of the future, I will study the macros of.

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Frequently Asked Questions

As a leading 1-(3-Iodophenyl)-Ethanon supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of 1- (3-iodophenyl) ethyl ketone?

(3-Piperyl) pentanal, its main use is in the scope of "Tiangong Kaiwu", and it is mostly used in the preparation of fragrances and medicines.
Together with fragrances, (3-piperyl) pentanal has a unique aroma and can be added to many incense prescriptions. The ancient fragrance is very particular about the matching and fusion of all kinds of fragrances. This substance can add luster to the fragrance with its unique fragrance. Or in incense, burning it, the aroma is pervasive, which can create a quiet and elegant atmosphere, which is good for the daily living and elegant gatherings of the ancients; or used to make incense powder, wear it with you, and emit an elegant aroma, which has the effect of removing filth and leaving fragrance.
As for the preparation of medicines, in traditional herbal medicine, spices often have certain medicinal value. (3-Piperonyl) valeraldehyde or because of its special chemical properties, can be used as adjuvant in some prescriptions to assist the main medicine to play its role. Or it has the functions of activating qi and opening orifices, helping to regulate the flow of human qi and blood and dredge meridians. Although "Tiangong Kaiqi" does not detail its exact application in medicines, it is not difficult to infer that it should have a place in the field of medicine according to the ancient cognition and usage habits of spices and medicines.

What are the synthesis methods of 1- (3-iodophenyl) ethyl ketone?

To prepare 1 - (3-pyridyl) ethanolamine, there are many methods for synthesis, which are outlined below.
First, 3-pyridyl formaldehyde is used as the starting material. Shilling 3-pyridyl formaldehyde and nitromethane are condensed to obtain 3- (pyridyl-3-yl) -2-nitropropene. This reaction needs to be carried out in a suitable alkaline environment. Bases such as potassium carbonate can be used as catalysts. In organic solvents such as ethanol, heat is refluxed to promote the smooth occurrence of the reaction. Then, the resulting product is reduced with a suitable reducing agent, such as hydrogen as a reducing agent, in the presence of catalysts such as palladium and carbon, a catalytic hydrogenation reaction is carried out, the nitro group is then reduced to an amino group, and the double bond is also reduced to obtain 1 - (3-pyridyl) ethanolamine.
Second, 3-pyridyl acetonitrile can also be used as a raw material. First, 3-pyridyl acetonitrile is hydrolyzed to convert the cyano group into a carboxyl group to obtain 3-pyridyl acetic acid. This hydrolysis reaction can be carried out under the catalysis of an acid or a base. If it is catalyzed by a base, a sodium hydroxide solution is often used and heated to reflux to promote complete hydrolysis of Subsequently, the esterification reaction of 3-pyridyl acetic acid is carried out, and ethyl 3-pyridyl acetate is heated with ethanol under the catalysis of concentrated sulfuric acid. Finally, ethyl 3-pyridyl acetate is reduced with a strong reducing agent such as lithium aluminum hydride to reduce the ester group to an alcohol hydroxyl group. At the same time, the ester group derived from the carboxyl group formed by cyanide reduction is also reduced, and the target product 1 - (3-pyridyl) ethanolamine is finally obtained.
Third, the Grignard reagent method can also be used. The Grignard reagent is prepared by the reaction of 3-halogenated pyridine with magnesium. For example, 3-bromopyridine reacts with magnesium in anhydrous ether to generate 3-pyridyl After that, the Grignard reagent is reacted with ethylene oxide, the Grignard reagent attacks ethylene oxide, undergoes a ring-opening reaction, and then hydrolyzes under acidic conditions to obtain 1- (3-pyridyl) ethanolamine.
All synthesis methods have advantages and disadvantages. In practical application, the optimal method should be selected according to the availability of raw materials, the difficulty of reaction conditions, the yield and cost.

What are the physical properties of 1- (3-iodophenyl) ethyl ketone?

3-Hydroxymethylglutaric acid, its physical properties are as follows:
3-Hydroxymethylglutaric acid is usually white to off-white crystalline powder. Its melting point is relatively high, generally around 160 ° C - 163 ° C, which indicates that its intermolecular force is strong and its solid structure is relatively stable.
It is soluble in water and can dissolve to a certain extent in water, thanks to the polar groups such as hydroxyl and carboxyl groups contained in the molecule. These polar groups can form hydrogen bonds with water molecules, so that it has a certain water solubility. At the same time, it can also dissolve in some polar organic solvents, such as ethanol, acetone, etc. In ethanol, 3-hydroxymethylglutaric acid can interact with ethanol molecules to dissolve by virtue of the principle of similar phase dissolution.
From the appearance morphology, its crystalline characteristics make it appear regular crystal shape, fine powder, with a certain gloss. Under normal temperature and pressure, it exists stably in solid form and has relatively stable chemical properties, but under extreme conditions such as high temperature, strong acid, and strong base, its molecular structure may change. Its density is moderate, compared with some heavy metal salts, which is related to its molecular composition and structure. Organic molecules composed of atoms such as carbon, hydrogen, and oxygen have such density characteristics determined by the accumulation method. Due to its unique physical properties, 3-hydroxymethylglutaric acid has an important application basis in the fields of chemical industry and medicine, providing a material basis and characteristic support for the development of related industries.

What are the chemical properties of 1- (3-iodophenyl) ethyl ketone?

3-Cyanopyridine is an organic compound with multiple chemical properties. Its structure contains cyano (-CN) and pyridine rings, giving it unique chemical activity.
From the perspective of nucleophilic substitution reactions, cyanyl groups have strong electron-absorbing properties, which reduce the electron cloud density of pyridine rings, especially the ortho and para-positions of carbon atoms connected to cyanyl groups, which are more susceptible to attack by nucleophiles. For example, under suitable conditions, it can react with nucleophiles such as sodium alcohol to form corresponding substitution products. This reaction is often a key step in the construction of new carbon-carbon bonds or carbon-hetero bonds in organic synthesis.
In terms of alkalinity, the nitrogen atom of the pyridine ring contains lone pair electrons and has a certain alkalinity. Although the alkalinity is slightly weaker than that of pyridine due to the electron-withdrawing conjugation effect of cyanyl, it can still protonate with strong acids to form pyridine salts. This property is widely used in the field of medicinal chemistry and catalysis. For example, when preparing some pharmaceutical intermediates or as a specific reaction catalyst, its alkalinity can be adjusted to optimize the reaction conditions.
Cyanyl groups can participate in a variety of reactions, and hydrolysis reactions are an important class. Under acid or base catalysis, the cyanyl group of 3-cyanopyridine can be gradually hydrolyzed to amide groups, and then hydrolyzed to carboxyl groups to form 3-pyridinecarboxylic acid. This reaction is a common method for the preparation of pyridine carboxylic acid compounds. 3-pyridinecarboxylic acid has a wide range of uses in the fields of medicine, pesticides and materials science.
In addition, 3-cyanopyridine can also participate in the reduction reaction, and the cyano group can be reduced to an amine group. If treated with a suitable reducing agent, 3-aminomethylpyridine can be formed. Such nitrogen-containing compounds are key intermediates in organic synthesis and drug development, and can be used to construct more complex molecular structures.
3-cyanopyridine has important application value in many fields such as organic synthesis, medicinal chemistry, and materials science due to its unique chemical structure and active chemical properties, providing rich possibilities for chemical research and industrial production.

What are the precautions for 1- (3-iodophenyl) ethyl ketone during storage and transportation?

1 - (3 - Poria cocos) caramel should pay attention to many matters during storage and transportation.
When storing, the first environment. A dry place must be selected, because the caramel is hygroscopic, if it is in a humid place, it is very susceptible to moisture, causing its properties to change, or sticking and agglomeration, which affects the quality and use. And the temperature also needs to be controlled, and it should be stored in a cool place to avoid high temperature. High temperature is easy to melt the caramel, spoil and deteriorate. In addition, the choice of container is also critical, and a well-sealed container should be used to prevent air from invading, breeding microorganisms, and causing deterioration.
During transportation, there are also important points. Make sure that the packaging is strong to prevent it from being damaged or leaking during handling and bumping. At the same time, the temperature and humidity of the transportation environment also need to be paid attention to, and the caramel should not be exposed to severe temperature and humidity conditions for a long time. In case of high temperature weather, corresponding cooling measures should be taken; in humid climate, moisture protection should be done. And the means of transportation must be clean and odor-free, so as not to contaminate the caramel.
In short, whether it is storage or transportation, it needs to be carefully operated and strictly follow suitable conditions, so as to ensure that the quality of 1 - (3 - Poria) caramel is not damaged, and its effective use and characteristics are maintained.