1-(3-Iodophenyl)Ethanone

Fengxi Chemical

Specifications

HS Code	950143
Name	1-(3-Iodophenyl)ethanone
Molecular Formula	C8H7IO
Molecular Weight	246.045 g/mol
Cas Number	49669-27-8
Appearance	Yellow to orange solid
Melting Point	37 - 41 °C
Boiling Point	140 - 142 °C at 1.5 mmHg
Density	1.674 g/cm³
Solubility	Soluble in organic solvents like dichloromethane, chloroform
Flash Point	113.8 °C
Storage Condition	Store in a cool, dry place, away from heat and ignition sources
Chemical Formula	C8H7IO
Molar Mass	248.044 g/mol
Appearance	Solid
Melting Point	61 - 64 °C
Boiling Point	132 - 134 °C at 11 mmHg
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Name	1-(3-Iodophenyl)Ethanone
Molecular Formula	C8H7IO
Molecular Weight	246.045 g/mol
Cas Number	39581-27-4
Appearance	Solid
Melting Point	36 - 38 °C
Solubility	Soluble in organic solvents like dichloromethane
Purity	Typically high - purity for laboratory use

As an accredited 1-(3-Iodophenyl)Ethanone 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)ethanone packaged in a sealed, labeled chemical - grade bottle.
Storage	1-(3 - Iodophenyl)ethanone should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and evaporation. Due to its potential reactivity and toxicity, it should be separated from incompatible substances, preferably in a dedicated chemical storage cabinet.
Shipping	1-(3 - iodophenyl)ethanone is shipped in well - sealed, corrosion - resistant containers. Adequate cushioning is used to prevent breakage. Shipment follows strict regulations for handling chemicals, ensuring safety during transit.

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General Information

Historical Development

In the field of chemistry, this thing also has a past. At the beginning, people did not know its nature, but only briefly observed its shape. However, as time went by, the wise men dedicated themselves to studying it in the laboratory, using exquisite methods to explore its mysteries. Or they used new techniques to create this thing, and after repeated trials, they either failed or succeeded. Gradually understand the way of its synthesis, and can use suitable raw materials to make this product according to specific regulations. In the past, the method of synthesis was not good, the yield was meager, and the quality was not yet perfect. Today is different from the past, the technique of synthesis has advanced day by day, the output has gradually increased, and the quality has also been improved. Its use is also gradually known to everyone, and it can make a difference in medicine and chemical industry. This is the development process of 1- (3-Iodophenyl) Ethanone since it was obscure at the beginning, and it has gradually shown its ability today.

Product Overview

1- (3-iodophenyl) ethyl ketone is a key compound in organic synthesis. Its properties are solid or liquid with a specific melting boiling point, and its appearance may be colorless to light yellow. This substance has a wide range of uses in the field of organic chemistry.
In the synthesis path, specific benzene derivatives are often used as starting materials and obtained through various reactions such as halogenation and acylation. During the reaction process, it is necessary to precisely control the reaction conditions, such as temperature and catalyst dosage, to obtain the ideal yield.
It can be used as a key intermediate in the field of medicinal chemistry to prepare drug molecules with specific biological activities. In the field of materials science, or helpful for the synthesis of some functional materials. Chemists study this compound with the hope of expanding its application boundaries and contributing to the development of many fields.

Physical & Chemical Properties

1- (3-iodophenyl) ethyl ketone is an organic compound. Its physical and chemical properties are related to many chemical studies. Looking at its physical properties, at room temperature, this substance may be in a solid state and have a specific color and taste. This is the intuitive image of the substance. Its melting and boiling point is the key to its morphological transformation under different conditions.
In terms of chemical properties, the presence of iodine atoms and carbonyl groups in 1- (3-iodophenyl) ethyl ketone gives it special reactivity. Iodine atoms can participate in nucleophilic substitution reactions, while carbonyl groups are susceptible to attack by nucleophiles and can undergo reactions such as addition. These reactive activities are used in the field of organic synthesis or as an important foundation for the construction of new compounds, assisting chemists in creating a variety of organic molecules for use in various industries such as medicine and materials.

Technical Specifications & Labeling

1- (3-Iodophenyl) ethyl ketone is an important compound in organic synthesis. Its process specifications and standards (product parameters) are crucial.
In terms of process specifications, the synthesis of this compound requires precise control of the reaction conditions. For example, the reaction temperature should be maintained at a certain range to promote the smooth progress of the reaction and increase the yield. The proportion of reactants also needs to strictly follow the established standards to prevent side reactions from occurring.
When it comes to standards (product parameters), the purity must reach a specific value, and the impurity content must be strictly controlled. Its physical properties such as appearance, melting point, and boiling point are clearly defined. After accurate determination and strict control of these process specifications and standards (product parameters), the quality of 1- (3-iodophenyl) ethyl ketone can be ensured to meet the needs of various applications.

Preparation Method

The method of making 1- (3 - Iodophenyl) Ethanone is related to the raw materials and production process, reaction steps and catalytic mechanism. Take an appropriate amount of 3 - iodobenzene and mix it with the acetylation reagent in a certain ratio. This is the choice of raw materials. In the reaction kettle, controlling the temperature, pressure and reaction time is the key to the production process. First, heat up to a moderate level to make the two contact the reaction initially. This is the first step of the reaction. Then, a specific catalyst is added to accelerate the reaction process. This is the catalytic mechanism. After fine regulation, the reaction is gradually completed, and the product is separated and purified to obtain pure 1- (3 - Iodophenyl) Ethanone. This preparation method requires precise control of all links to achieve good results.

Chemical Reactions & Modifications

Recently, 1- (3-Iodophenyl) Ethanone has been studied for the modification of this material. The method of the past has many inconveniences, and the efficiency has not been ideal. The reverse parts are harsh, and the side effects are generated, and the resulting product is not good.
We thought deeply and changed it. We have integrated the reverse solution, and used special catalysis to make the reverse solution and easy to implement. And we have also refined the reverse solution, avoiding its multiplication, and improving the way. With this improvement, the reverse effect rate has been greatly increased, the side effects are less, and the quality of the product is also good. This is one of the first steps in the research of this transformation, and we hope to use it together to promote the development of this field.

Synonyms & Product Names

1- (3-iodophenyl) ethyl ketone, this substance is also known as iodoacetophenone. According to its naming, it is derived from its chemical structure. In the course of my chemical research, it is common for the same substance to have different names, which are due to different naming rules or habits.
m-iodoacetophenone, or 1- (3-iodophenyl) ethyl ketone, all refer to the same chemical entity. The change of this name is just like the name of an ancient object, which varies with the passage of time and the ease of geography. The field of chemistry, the only reference to a definite substance, is often based on a rigorous system of nomenclature. However, in daily research and application, common names also go hand in hand. The
substance has a wide range of uses in the field of organic synthesis, or is a key intermediate, participating in various chemical reactions and derived a variety of products. Our chemistry researchers need to know its various names, and can communicate and explore accurately in the literature study and experimental operation.

Safety & Operational Standards

1 - (3 - iodophenyl) ethyl ketone, this chemical substance is related to safety and operation standards, and it is extremely important to be cautious.
At the beginning of preparation, all kinds of raw materials and reagents required must be carefully selected to check their quality and ensure that they are pure and free of impurities before they can be used. When taking it, use it according to precise measurements and special equipment, and be sure to check it, and there should be no mistakes.
The experimental site must be well ventilated to remove foul gas and prevent the accumulation of harmful gas. And all kinds of fire and first aid equipment should be placed in a prominent and convenient place to use for emergencies.
When operating, the experimenter should wear special protective clothing and tough gloves to resist the erosion of chemicals; eye protection glasses are also indispensable to prevent eye damage. The heating steps should be especially cautious. Use suitable equipment to control the heat, and do it slowly. Don't be too hasty, causing sudden temperature changes and causing accidents.
During the reaction process, pay close attention to its changes, and record phenomena and data with scientific methods. If there is any abnormality, stop it immediately, check the reason in detail, and don't move forward rashly.
When the reaction is over, the treatment of the product should not be underestimated. Or purify it according to a specific method, or store it properly, it should be done according to the specifications. Waste and debris should not be discarded at will, but should be collected and disposed of according to environmental protection requirements to avoid polluting the environment.
In short, the preparation and use of 1 - (3 - iodophenyl) ethyl ketone should be safety-first, and the operation should be in accordance with regulations to avoid disasters, ensure the smooth operation of the experiment, and ensure the safety of people and the environment.

Application Area

1- (3 -iodophenyl) ethyl ketone, in various chemical products, has a unique use. Its application field is quite wide.
In the field of pharmaceutical development, it can be used as a key intermediate. Based on this, chemists can prepare many drugs with special curative effects. Because of its structural properties, it can lead to a series of chemical reactions and help to build the active ingredients of drugs.
In the field of materials science, it can also be seen. By participating in specific reactions, or materials with special properties can be prepared, such as some optical materials with unique responses to specific wavelengths of light.
Furthermore, in the field of fine chemicals, 1- (3 -iodophenyl) ethyl ketone is also an important raw material. With its chemical activity, it can synthesize various fine chemicals, such as special fragrances or key components of high-performance coatings. This highlights its important value in various application fields.

Research & Development

Recently researched 1- (3-Iodophenyl) Ethanone, its nature is very different, and it is related to its research and progress. It is our priority.
At the beginning, choose the right one among all kinds of materials and combine it with a delicate method. In the meantime, temperature and time are the main factors, and if there is a slight difference, the result will be different.
Try several times, observe its changes, and record them in detail. Or color change, or quality change, all of them are carefully investigated. Although it is difficult to encounter obstacles, it has not been abandoned.
Today, it has gained a little bit, and its shape and nature are gradually becoming clear. In the future, we should explore its use, hoping to make progress in the fields of medicine and chemical industry. With unremitting research, this thing can be used by the world and become a great achievement.

Toxicity Research

Studies on the toxicity of 1- (3-iodophenyl) ethanone
Today's research on the toxicity of 1- (3-iodophenyl) ethanone is the key to chemical research. In the past, the knowledge of these compounds was still shallow. In recent years, scientific research has advanced, and the toxicity of this substance has gradually been carefully observed.
After various experiments, its effect on organisms was observed. Taking mice as a model, an appropriate amount of 1- (3-iodophenyl) ethanone was administered to observe its physiological changes. It can be seen that the mice have abnormal eating and activity, and the organs also show signs of disease.
To explore its effect on cells, the compound was added to cells cultured in vitro. The cell growth is inhibited, the morphology is also different, and some cells even apoptosis. From this point of view, 1- (3-iodophenyl) ethyl ketone is quite toxic. The follow-up should study its toxicological mechanism in detail to find an effective way for protection and treatment, to ensure the well-being of all living beings and to protect the tranquility of the environment.

Future Prospects

The future development is related to the (1 - (3 - Iodophenyl) Ethanone) thing, and the prospect is promising. The nature of this thing has special ability, and it may bloom in various fields.
Looking at the current research path, although there are still obstacles, scholars are all determined. With time, advanced technology may be used in the field of medicine as a sharp blade for healing diseases and helping to heal diseases; in the world of materials, it will become a novel material and explore new ways to use it.
The road ahead is long, but we believe that it will be able to break through barriers and move forward, shine brightly, add brilliance to the future, create a new situation, and develop endless possibilities.

Historical Development

The origin of 1- (3-iodophenyl) ethyl ketone originated from the research of chemical experts in the past. At that time, many sages diligently explored the field of organic synthesis, hoping to open up new substances. At the beginning, the road of synthesis was full of thorns, and many attempts were frustrated due to the difficulty of introducing iodine atoms and the strict requirements for reaction conditions.
However, the wise are not discouraged. After repeatedly considering the reaction mechanism and adjusting various conditions, they gradually achieve success. From the initial occasional production of a small amount of product to the stable preparation after the process is refined. It has added luster to the organic synthesis technique in the development of chemistry and laid the foundation for subsequent related research. With the passage of time, this product has emerged in the fields of medicine, materials, etc., and has become a key imprint in the development of chemistry.

Product Overview

1- (3-iodophenyl) ethyl ketone is a crucial compound in the field of organic synthesis. It has a unique chemical structure, with iodine atoms and acetyl groups attached to the benzene ring.
The preparation of this compound depends on the organic reaction path determined by Chang Lai. In many organic synthesis experiments, the desired yield and purity can be achieved by carefully adjusting the reaction conditions, such as temperature, reactant ratio and catalyst use.
1- (3-iodophenyl) ethyl ketone can act as a key intermediary in organic synthesis. The activity of its iodine atom and acetyl group can participate in diverse reactions, such as nucleophilic substitution, coupling reactions, etc., and then derive rich organic compounds.
And because of its unique structure, it also has potential application value in the fields of medicine and materials science. In pharmaceutical research and development, it may provide key structural fragments for the construction of new drug molecules; in materials science, it may be helpful for the performance improvement of some functional materials.

Physical & Chemical Properties

1- (3-iodophenyl) ethyl ketone is an organic compound. It has specific physical and chemical properties. Looking at its physical properties, it is either solid or liquid at room temperature, depending on environmental conditions. The values of its melting point and boiling point are the keys to characterize its physical properties. As for its chemical properties, it is active because it contains carbonyl and iodine atoms. Carbonyl can cause nucleophilic addition reactions, and iodine atoms can also participate in substitution and other reactions. In the field of organic synthesis, this compound has a wide range of uses and can be used as an intermediate to participate in the construction of many complex organic molecules. The exploration of its physical and chemical properties is the basis for organic synthesis and related research, and helps researchers understand its reaction laws, so as to achieve the purpose of precise synthesis and effective application.

Technical Specifications & Labeling

1- (3-iodophenyl) ethyl ketone is an important compound in organic synthesis. Its process specifications and standards (product parameters) are extremely critical.
In process specifications, the raw materials must be pure, and the reaction conditions must be precisely controlled. If the reaction temperature should be maintained in a specific range to ensure efficient reaction and few side reactions. The reaction time is also strictly required. Too long or too short will affect the purity and yield of the product.
In terms of product standards, the purity should reach a very high level, and the impurity content must be strictly controlled. The appearance should show a specific color and shape for easy identification. The accuracy of relevant parameters is the basis for ensuring that the product can be effectively used in many fields, so as to meet the strict requirements of different scenes for its quality.

Preparation Method

The method of preparing 1- (3-iodophenyl) acetone is related to the raw materials and production process, reaction steps and catalytic mechanism.
To prepare this product, prepare raw materials, such as 3-iodobenzene and acetylation reagent. Using acetyl chloride as acetylation agent and anhydrous aluminum trichloride as catalyst, 3-iodobenzene is slowly poured into a reaction bottle containing acetyl chloride and anhydrous aluminum trichloride in a low temperature environment. This is a Fu-g acylation reaction. During this time, aluminum trichloride activates acetyl chloride, making it easier to react with 3-iodobenzene.
When reacting, pay close attention to the temperature and reaction process. After the reaction is completed, it is quenched with ice water, followed by organic solvent extraction, and then purified by column chromatography or recrystallization to obtain pure 1- (3-iodophenyl) ethyl ketone. The whole preparation, the selection of raw materials, the control of reaction conditions and the purification steps are all key to the purity and yield of the product.

Chemical Reactions & Modifications

Taste the science of chemistry, heavy reaction and change. For 1- (3-Iodophenyl) Ethanone, its transformation is wonderful, and it is worth studying.
The method of the past, the reaction may be inconvenient, and the yield is not perfect. And the conditions are harsh, time-consuming and laborious. However, today's scholars are thinking hard and want to change its shape.
Some researchers have created new agents, adjusted their corresponding conditions, so that the reaction is fast and pure. Moderate temperature and pressure, few impurities. Also think about the method of catalysis, change its activity, make the molecule easy to combine, so that the yield increases significantly.
Such changes are all progress of transformation. I hope that in the future, the research of this thing will be deeper, and more wonderful uses can be obtained. It is necessary for the world to develop and change.

Synonyms & Product Names

1- (3-iodophenyl) ethyl ketone, the same trade name is important in chemical research. It is now described in ancient Chinese.
This compound is also known by its name. To observe its manufacture, the iodine atom is attached to the three digits of the phenyl group, and the ethyl ketone phase. Or there is 3-iodoacetophenone, which is named because of its functional position. As for the trade name, the market or according to its characteristics and uses. However, any name refers to this specific chemical. In the study and communication, it is clear that the same trade name is known, so as to avoid confusion and to achieve the refinement and depth of research.

Safety & Operational Standards

1- (3-Iodophenyl) ethyl ketone is a common chemical compound in chemical research. In the field of experimentation, safety and standard operation are the key.
In terms of safety, this compound may have a certain chemical activity. When handling this substance, the first protection. Experimenters must wear suitable protective clothing, such as lab clothes and gloves, to prevent contact with the skin and prevent skin invasion and adverse reactions. It is also advisable to wear protective goggles to protect the eyes from possible splashing damage.
Furthermore, the operating environment cannot be ignored. When it is done in a well-ventilated fume hood, the volatile substances that may escape are discharged in time to avoid their accumulation in the experimental space and endanger the health of the experimenter. If it is accidentally touched, if it is stained on the skin, it should be rinsed with a large amount of water immediately, followed by an appropriate cleaning agent; if it enters the eye, it is even more necessary to rinse with flowing water immediately and seek medical attention immediately.
In terms of operation specifications, when weighing, use a precise weighing instrument, and take the amount required by the experiment. There should be no slight difference. When dissolving, choose a suitable solvent, and control the temperature and stirring rate according to its solubility characteristics to promote uniform dissolution. During the reaction process, strictly observe the reaction conditions, such as temperature, time, and the proportion of reactants. When heating, it is advisable to use a suitable heating device to control the temperature accurately and prevent the reaction from getting out of control due to overheating.
After the reaction is completed, the treatment of the product also follows the norms. Or through separation and purification, the pure product is obtained; the waste is classified and disposed of according to the chemical waste treatment rules, and must not be dumped at will to avoid polluting the environment.
In short, the research operation of 1- (3-iodophenyl) ethyl ketone is as safe and standardized as the two wheels of a car and the wings of a bird. Only by strictly observing these two can we ensure the smoothness of the experiment, protect the well-being of the experimenter, and maintain the tranquility of the environment.

Application Area

The application field of 1- (3-iodophenyl) ethyl ketone is the key to chemical research. In the field of organic synthesis, it can be an important intermediate. Due to its unique structure, the synergy between iodine atoms and acetyl groups can initiate a variety of chemical reactions.
Through nucleophilic substitution, iodine atoms can be replaced by many nucleophilic reagents, thereby forming novel carbon-carbon and carbon-heteroatom bonds, paving the way for the synthesis of complex organic molecules. In the field of medicinal chemistry, this is used as a starting material, which can be skillfully derived, or can create lead compounds with specific biological activities, opening the possibility for the development of new drugs.
Furthermore, in the field of materials science, products derived from 1- (3-iodophenyl) ethyl ketone may endow materials with unique photoelectric properties and thermal stability, providing opportunities for the development of new functional materials. In short, its application fields are wide and it has potential significant value in many scientific research fields.

Research & Development

Recently, it has been a lot of effort to study 1- (3-Iodophenyl) Ethanone. We use the ancient method as the basis and the new technique as the supplement to explore its nature and study its system. At the beginning, we encountered many difficulties, and the purity of the raw materials and the control of the heat were all difficult things. However, we were not discouraged, so we tried it again and again, and carefully observed and changed it.
After months of work, its properties gradually became clear. Its color is slightly yellow, the quality is relatively stable, and it has a unique application in specific reagents. The preparation method has also been refined, optimizing the process and improving its yield.
Looking at it now, although we have gained something, the road ahead is still far away. Want to use it widely, explore new paths, and add new colors to the industry. We must study it diligently, with the hope of making greater progress, so as to promote the development of this thing and benefit everyone.

Toxicity Research

Yu Taste is dedicated to toxicological research, and recently focused on the toxicity of 1- (3-iodophenyl) ethanone. This substance has attracted more and more attention in the field of chemistry, but there are still few studies on its toxicity.
This 1- (3-iodophenyl) ethanone has a unique structure. Iodine atoms are connected to phenyl and ethanone groups, or affect its chemical activity and biological effects. Experiments have shown that it has a significant impact on specific cell lines and can change cell morphology and metabolism. In animal experiments, changes in physiological indicators are also seen, suggesting its potential toxicity.
However, toxicity studies need to be cautious, and many factors such as dose, exposure route, and duration are all relevant to the conclusion. In the follow-up, when the research dimension is expanded, the mechanism of action is carefully investigated, and the full picture of its toxicity is expected to be revealed, providing a solid basis for safe use and prevention of harm.

Future Prospects

Looking at the research of chemistry today, 1- (3-iodophenyl) ethanone has a promising future. In the field of medicine, it may be able to contribute to the creation of new drugs. Looking at the current scientific research progress, it is expected to accurately optimize the synthesis path in the future, improve yield and purity, reduce costs, and lay the foundation for large-scale production.
Furthermore, in the field of materials science, 1- (3-iodophenyl) ethanone may be able to give birth to new functional materials. By in-depth exploration of its chemical properties and reaction mechanisms, materials with excellent performance may be developed for cutting-edge fields such as electronics and optics.
Although there may be thorns in the road ahead, researchers should be enthusiastic and determined. With time and careful study, 1- (3-iodophenyl) ethyl ketone will be able to bloom and make extraordinary contributions to human well-being and scientific and technological progress. The future is truly promising.

Historical Development

1- (3-Iodophenyl) ethyl ketone is also an organic compound. At the beginning of its origin, all the wise men tried their best to understand and explore its nature, and sought the truth in the end. In the past, the art of chemistry was not as prosperous as it is today, but the public was determined to study it, and through difficulties and obstacles, they finally achieved something.
At that time, the experimental equipment was simple, and the materials were not as pure as they are today. However, everyone held on to their dedication and observed its changes between the little reactions. When I first got this thing, I didn't know its details, and then I pondered it over and over again, analyzed its structure, and studied its characteristics. After years of delay, many chemists have continued to expand their understanding, enabling 1- (3-iodophenyl) ethyl ketone to gradually demonstrate its capabilities in the fields of medicine and materials, paving the way for the development of future generations.

Product Overview

1- (3-iodophenyl) ethyl ketone is an important compound in the field of organic synthesis. Its appearance is white to light yellow crystalline powder, with specific physical and chemical properties.
This compound is often used as a key intermediate in organic synthesis. It can be prepared by a variety of chemical methods, such as through a specific substitution reaction, by interacting a suitable halogenated benzene with an acetylating agent to achieve the synthesis of the target product.
In the vast world of organic synthesis, 1- (3-iodophenyl) ethyl ketone, with its unique molecular structure, can participate in many reactions, such as carbon-carbon bond formation reactions, providing the possibility to construct more complex organic molecular structures. Chemists continue to explore its novel synthesis methods and application fields to expand its value and use in the field of organic synthesis chemistry, and contribute to the development of organic chemistry.

Physical & Chemical Properties

1- (3-Iodophenyl) ethyl ketone, this material has unique physical and chemical properties. Its shape is either solid under normal conditions, color or yellowish, and it has a specific crystalline state. The melting point is fixed, and it melts at a certain temperature, and the liquid is fluent. The boiling point is also characteristic. It boils at a certain high temperature, and the air rises in the air.
In terms of solubility, it is soluble and miscible in organic solvents such as ethanol and ether, but it is difficult to dissolve in water, because its molecular structure is very different from water affinity. In terms of chemical activity, iodine atoms are active and easily involved in nucleophilic substitution reactions. Carbonyl groups are also important reaction sites, capable of chemical transformation with many reagents, and the derivation of a variety of new compounds. They are widely used in the field of organic synthesis. They are the key raw materials for the preparation of other fine chemicals and have important chemical value.

Technical Specifications & Labeling

Today there is a thing called 1- (3 - Iodophenyl) Ethanone. To make this thing, its technical specifications and identification (product parameters) are the key.
To make this thing, first clarify its material ratio, all kinds of raw materials must be accurately weighed, and no difference must be made. The reaction vessel must also be clean and dry, so as not to be disturbed by other things. During the reaction, the temperature and duration are fixed, and a little more than a moment may cause the product to be impure.
As for the label, the properties of this thing must be specified in detail, and the color, taste, and state should be clear. Its purity is certain, and the geometry of impurities must also be marked correctly. In this way, 1- (3 - Iodophenyl) Ethanone, which is suitable for technical specifications and identification (product parameters), can be used in various ways.

Preparation Method

To prepare 1- (3-iodophenyl) ethyl ketone, the method is as follows: First take the raw material, use acetophenone as the starting material, and prepare an appropriate amount of iodine reagent. During the reaction, it is necessary to control the conditions, and at a suitable temperature, use a catalytic agent to help it, so that it can fully respond.
The reaction step is to first make acetophenone and iodine react with electrophilic substitution under the action of a catalyst. In a mild environment, let the iodine atom just fit into the interposition of the benzene ring to obtain the product.
Preparation process, choose the best solvent, keep the reaction smooth, and pay attention to the reaction situation, and adjust it in time. At the time of separation and purification, a suitable method is used to remove heterogeneous sperm and obtain high-purity 1- (3-iodophenyl) ethyl ketone. In this way, it can be prepared.

Chemical Reactions & Modifications

The modification of 1 - (3 - iodophenyl) ethyl ketone is an important issue in chemical research. In the past, in order to obtain this compound, it was often necessary to develop a specific reaction path. Its initial reaction was mostly started with the acetylation of iodobenzene derivatives, and it was obtained in the same way.
However, the reaction is inherent in its shortcomings. If the reaction is harsh, it requires high performance, high performance or special catalysis, and the yield is not ideal, and the side effects are generated, resulting in improved performance.
Today's chemists are innovating. With the improvement of catalysis, high efficiency and a new type of catalysis, the reaction effect is improved, the efficiency is improved, and the side effects are reduced. In addition, the synthesis of 1 - (3-iodophenyl) ethyl ketone is more complete, and it is also more difficult for the future of chemical engineering.

Synonyms & Product Names

1 - (3 - iodophenyl) ethyl ketone, the synonym and trade name of this substance, is really clear in chemical research. Its synonyms or aliases containing specific chemical names vary according to different chemical contexts and research focuses. Trade names show their effectiveness in commercial circulation and chemical product identification. In the process of our chemical inquiry, we can accurately recognize the synonyms and trade names of this substance, which is related to experimental design, raw material procurement and result communication. By knowing its synonyms, we can avoid naming confusion and ensure the accuracy of academic research. Knowing its trade name is beneficial to the acquisition of raw materials in the chemical market and makes the research process smooth. Therefore, a detailed examination of the synonyms and trade names of 1 - (3 - iodophenyl) ethyl ketone is the cornerstone for further chemical research.

Safety & Operational Standards

1 - (3 - iodophenyl) ethyl ketone, this chemical is related to safety and operating standards, and we should treat it with caution.
In terms of safety, the first toxicity awareness. 1 - (3 - iodophenyl) ethyl ketone may be toxic to a certain extent. When exposed, do not let it touch the skin or eyes. If it is accidentally contaminated with the skin, rinse it with a lot of water immediately, and then seek medical treatment. If it enters the eye, open the eyelids immediately, rinse it with flowing water or normal saline, and seek medical treatment immediately. Its volatile gas may also be harmful, so the operation must be carried out in a well-ventilated place to prevent physical damage caused by inhalation.
Discuss the operating specifications. When taking it, use clean and accurate utensils. Weighing should be strictly operated on the balance to ensure accurate dosage and avoid experimental deviations due to errors. During the dissolution process, choose a suitable solvent according to its solubility, and the stirring speed is moderate to prevent splashing. During the reaction process, pay close attention to temperature, pressure and other conditions, strictly follow the established process, and do not change the reaction parameters without authorization. If the reaction involves heating, pay special attention to temperature control to prevent danger caused by overheating.
For storage, 1 - (3 -iodophenyl) ethanone should be stored in a cool, dry and well-ventilated warehouse, away from fire, heat sources, and avoid direct sunlight. At the same time, it needs to be stored separately from oxidants, acids, bases, etc., and should not be mixed to prevent chemical reactions.
Only by strictly observing safety and operating standards can 1 - (3 - iodophenyl) ethyl ketone be properly used to ensure the smooth operation of the experiment and ensure the safety of personnel and the environment.

Application Area

1- (3-iodophenyl) ethyl ketone is also a chemical substance. Its application field is quite wide. In the field of medicinal chemistry, this substance may be a key raw material for the synthesis of specific drugs. With its special structure, it can help chemists make drugs that are effective for specific diseases to treat diseases. In materials science, it also has its place. With its unique chemistry, it may be used to develop new functional materials, such as materials with specific optical or electrical properties, for material innovation. And in the field of organic synthesis, 1- (3-iodophenyl) ethyl ketone is often used as an important intermediate, helping organic synthesizers to construct complex and delicate organic molecular structures and promoting the progress and development of organic chemistry.

Research & Development

In recent years, I have been studying 1- (3-Iodophenyl) Ethanone in the field of chemistry. The properties of this substance are related to many chemical reactions, and are valued by the industry.
At the beginning, the method of its preparation was studied. Numerous trials were made to explore the importance of raw material preparation, temperature and time control. Or there are ancient methods to follow, but new ways are sought, hoping to improve production and reduce consumption. After repeated tests, the best method was obtained, and the yield increased.
Times, study its properties. In different media, observe its stability and inverse activity. Knowing that it encounters a certain agent, it is particularly responsive, which can be the basis for new material research and pharmaceutical preparation.
And think about its use. In medicine, or for the precursor of new drugs; in materials, to assist in research and development of special materials. We should exhaust our wisdom, expand its use, promote the progress of this product, and contribute to the development of industry and the world, so that it can continue to move forward in the way of research and progress, and develop infinite possibilities.

Toxicity Research

Today's study of poisons is based on 1- (3 - Iodophenyl) Ethanone. The toxicity of this substance is related to everyone's health and cannot be ignored. To study its properties in detail, we need to start from multiple ends. Observe its chemical structure, the position of iodine atoms, or it is related to toxicity. Also observe its reaction in different media, and the toxicity of the product may change. After various experiments, it can be known that the way it enters the body, it can be caused by respiration, or through the skin. What it does in the body disrupts the ability of the organs and damages the structure of cells. Therefore, the study of the toxicity of this substance is an urgent task today, aiming to understand its harm, in order to find preventive measures, and ensure everyone's well-being.

Future Prospects

Wuguanfu 1- (3-Iodophenyl) Ethanone This material has extraordinary quality and contains endless future prospects. It may open a new chapter in the field of chemical industry.
Viewed from its characteristics, it may be the cornerstone of new materials. In the way of medical research and development, it is also expected to become a key key to help physicians solve difficult diseases. Although the current cognition is still limited, its potential is like a abyss. With time and careful study, it will surely shine.
It is expected that in the future, this material may shine like a star in the sky, shining brightly in various fields, leading the progress of science and technology, contributing to human well-being, becoming an unfinished cause, and meeting the expectations of everyone.

Where to Buy 1-(3-Iodophenyl)Ethanone in China?

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Frequently Asked Questions

As a leading 1-(3-Iodophenyl)Ethanone 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 chemical properties of 1- (3-iodophenyl) ethyl ketone?

3 - Borosilicate-based materials have special properties. Borosilicate-based materials have high properties and high resistance, and their properties also have high properties.
Borosilicate-based materials are mostly used in general resistance equipment, such as glass devices used in high-quality rooms. The characteristics of borosilicate-based materials can be reduced by strong strength. Because the borosilicate-based materials are solidified, they can resist the invasion of high temperature.
And its performance, in the reaction of the reaction is often very active. It can be neutralized by multiple acids, and the reaction of raw water and phase is difficult. This neutralization and inverse reaction, following the basic law of chemistry, the reaction of the oxygen radical of the acid and the oxygen radical of the acid, then form a water molecule.
In addition, it can also cause some gold particles to react and generate sediments. This property is often used in chemical analysis to determine the existence of a specific gold particle. For example, when a red particle meets, it can generate a red sediment, which can be deduced from the red particle.
In addition, the water solution of the water is of high quality, which can make the indicator appear a specific color. In the case of phenolphthalein indicator, it can be changed from yellow to yellow, which is a common means of quality.
In addition, the chemical properties of 3-borosilicate-based materials, including both the definite resistance of borosilicate-based materials and the active and reactive characteristics of borosilicate-based materials, play an important role in the field of chemical engineering and general engineering, and provide the basis for the application of various processes and materials.

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

The common synthesis methods of 3-hydroxypropyl ether are as follows:
First, the Williamson synthesis method. This is a classic method, which reacts halogenated hydrocarbons with sodium alcohol or sodium phenol to prepare ether compounds. Taking the synthesis of 3-hydroxypropyl ether as an example, haloethane can be reacted with 3-hydroxypropyl alcohol. First, 3-hydroxypropyl alcohol is reacted with sodium metal or sodium hydroxide to generate 3-hydroxypropyl alcohol, and then it is reacted with haloethane in a suitable solvent (such as ethanol, acetone, etc.) at a certain temperature. The reaction conditions are relatively mild and the operation is relatively simple. However, there may be side reactions of halogenated hydrocarbons, such as elimination reaction, which in turn affects the yield and purity of the product. The reaction process is as follows: 3-hydroxypropyl alcohol reacts with sodium to form 3-hydroxypropyl alcohol sodium, and the oxygen negative ions in 3-hydroxypropyl alcohol nucleophilically attack the carbon atoms in haloethane. The halogen atoms leave to form 3-hydroxypropyl ether.
Second, the ethylene oxide method. Let ethylene oxide react with ethanol under the action of a catalyst to obtain 3-hydroxypropyl ether. This reaction has high atomic utilization rate, few side reactions, and good product purity. Commonly used catalysts include acidic catalysts (such as sulfuric acid, p-toluenesulfonic acid, etc.) or basic catalysts (such as sodium hydroxide, potassium hydroxide, etc.). Under acidic conditions, ethylene oxide is protonated to enhance its electrophilicity. The oxygen atom in the ethanol molecule nucleophilically attacks the carbon atom of ethylene oxide and opens the ring to form 3-hydroxypropyl ether; under alkaline conditions, ethanol first interacts with alkali to generate ethanol negative ions, and ethanol negative ions nucleophilic attack ethylene oxide, which also forms the target product. The raw material of this method is relatively active and has high reactivity, but ethylene oxide is flammable and explosive, which requires strict storage and operating conditions.
Third, transesterification method. The transesterification reaction between 3-hydroxypropionate and ethanol can be carried out under the action of catalyst. The advantage of this method is that the raw materials are relatively easy to obtain and the reaction conditions are relatively mild. The catalysts used are mostly titanates, tin compounds, etc. During the reaction, the acyl group of 3-hydroxypropionate is exchanged with the ethoxy group of ethanol to form 3-hydroxypropyl ether and the corresponding carboxylic acid ester. However, the reaction is usually reversible, and in order to increase the yield of 3-hydroxypropyl ether, the carboxylic acid ester generated by the reaction needs to be continuously removed or excess ethanol is used.

What are the applications of 1- (3-iodophenyl) ethyl ketone in organic synthesis?

1 - (3 -cyanopyridine) acetaldehyde has many applications in organic synthesis.
First, in the field of pharmaceutical synthesis, it can be used as a key intermediate to participate in the preparation of many drugs. For example, some drugs used in the treatment of cardiovascular diseases, in their synthesis path, 1 - (3 -cyanopyridine) acetaldehyde can be combined with other organic compounds through specific chemical reactions to construct molecular structures with specific pharmacological activities. Due to its own unique chemical structure, the aldehyde group and cyanopyridine part can participate in various reactions, introducing necessary functional groups for drug molecules, thereby giving the drug corresponding therapeutic efficacy.
Second, it also has important value in pesticide synthesis. It can be converted into pesticide ingredients with insecticidal, bactericidal or herbicidal activities by means of a series of organic reactions. For example, in the development of some new insecticides, 1- (3-cyanopyridine) acetaldehyde is used to react with other compounds containing nitrogen and sulfur to form pesticide products with high biological activity and environmental friendliness. The cyanyl and aldehyde groups in its structure can interact with specific biomolecules in pests or pathogens, interfering with their normal physiological and metabolic processes, and achieving the purpose of preventing and controlling pests.
Third, in the field of materials science, 1- (3-cyanopyridine) acetaldehyde can be used to prepare polymer materials with special properties. By polymerizing with different types of monomers, polymers with unique optical, electrical or mechanical properties can be obtained. For example, polymerization with monomers containing conjugated structures can obtain materials with good photoelectric properties, which are expected to be used in optoelectronic devices such as organic Light Emitting Diodes (OLEDs) to improve the luminous efficiency and stability of the devices. The active groups in its structure can initiate polymerization reactions and have a significant impact on the properties of the polymers.

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

3-Nitrofuryl acetamide is an organic compound with the following physical properties:
Viewed at room temperature, it is a yellow crystalline powder with bright color and high recognition. This morphology is conducive to observation and processing in many chemical and industrial scenarios.
Smell it, almost odorless, and the smell is weak. This characteristic makes it not cause olfactory discomfort or adverse effects to the environment and people due to strong odor when applied.
Touch it, its melting point is about 198-203 ° C, and the physical state changes at a specific temperature, which is of great significance for its processing and use under different temperature conditions. And its solubility in water is small, it is a slightly soluble substance in water, and it has slightly better solubility in organic solvents such as ethanol and acetone. This determines that when selecting a solvent to dissolve or react, it is necessary to choose a suitable organic solvent according to its solubility characteristics to ensure the smooth progress of the relevant chemical process.
In addition, the stability of 3-nifuryl acetamide is very important. Under normal storage and use conditions, the properties are relatively stable, and in case of high temperature, open flame or strong oxidant, it may cause dangerous reactions. Therefore, when storing and transporting, it is necessary to strictly follow safety regulations to ensure a suitable environment and avoid dangerous factors to ensure the stability of its physical properties and prevent accidents.

What are the storage conditions for 1- (3-iodophenyl) ethyl ketone?

In "Tiangong Kaiwu", the preparation of arsenic is as follows: "Where the arsenic is burned, the soil kiln is lowered, the stone is placed on it, and the curvature is built on the top, and the iron kettle is hung upside down. The coal is burned under it to raise the fire. The smoke is fumigated from the curvature and attached to the kettle." That is, the stone containing arsenic is placed in the soil kiln, and the coal fire is burned under it, and the arsenic smoke is fumigated along the curvature and attached to the upside-down iron kettle. This is the method of its preparation.
The conditions for the storage of arsenic, although not detailed in "Tiangong Kaiwu", are deduced according to common sense and ancient experience. First, it needs to be placed in a dry place. Because arsenic is soluble in water, if the environment is humid, it is easy to cause deliquescence, which not only affects its properties, but also may evaporate with water vapor, increasing the risk of poisoning. Second, when hidden in airtight containers. Arsenic is highly toxic. If exposed to the air, its tiny particles are easy to disperse, which is harmful to human and animal environments. Airtight containers can prevent it from escaping. Third, it should be placed in a place that is difficult for children and ordinary people to reach. Because of its severe toxicity, accidental ingestion can cause serious consequences, so the storage place should be carefully selected to prevent accidents. In short, arsenic is highly toxic, and storage should be extremely careful to ensure safety.