5-Fluoro-2-Iodoacetophenone

Fengxi Chemical

Specifications

HS Code	797719
Chemical Formula	C8H6FIO
Molecular Weight	266.03
Appearance	Off - white to light yellow solid
Boiling Point	Approximately 250 - 260 °C
Melting Point	64 - 68 °C
Density	Around 1.86 g/cm³
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform
Flash Point	109.7 °C
Purity Typical Commercial Grade	97%+
Chemical Formula	C8H6FIO
Molecular Weight	266.03
Appearance	Solid (Typical)
Melting Point	39 - 43 °C
Boiling Point	263.5 °C at 760 mmHg
Density	1.835 g/cm³
Flash Point	113.1 °C
Solubility In Organic Solvents	Soluble in common organic solvents
Refractive Index	1.592
Purity	Typically high purity (e.g., 97%+)
Chemical Formula	C8H6FOI
Molecular Weight	266.035 g/mol
Appearance	Typically a solid, color may vary but often white to off - white
Boiling Point	Approximately 270 - 275 °C at 760 mmHg (estimated)
Melting Point	Around 55 - 59 °C
Density	1.954 g/cm³ (estimated)
Solubility	Soluble in organic solvents like dichloromethane, chloroform, ethyl acetate
Flash Point	117.1 °C (estimated)
Refractive Index	Data may vary, but estimated around 1.600 - 1.620
Cas Number	61486-44-6

As an accredited 5-Fluoro-2-Iodoacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	5 - fluoro - 2 - iodoacetophenone in 100g glass bottle, well - sealed for protection.
Storage	5 - fluoro - 2 - iodoacetophenone should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and incompatible substances like strong oxidizers. Store in a tightly - sealed container to prevent leakage and exposure to air or moisture, which could potentially cause degradation or unwanted reactions.
Shipping	5 - fluoro - 2 - iodoacetophenone is shipped in well - sealed, corrosion - resistant containers. Packaging adheres to chemical transportation regulations. Shipment is via approved carriers, ensuring proper handling to prevent leakage and maintain product integrity.

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General Information

Historical Development

5-Fluoro-2-iodoacetophenone is also an organic compound. Its traces can be traced back to the chemical research path of the past. At the beginning, the chemists were diligent in the field of organic synthesis, and they worked hard on halogen-containing aromatic ketones. At that time, the method of organic chemistry was still evolving, and the raw materials and instruments were not available today.
The researchers used wisdom and perseverance to improve the synthesis technique through complex experiments. With the passage of time and the advancement of science and technology, the method of synthesizing 5-fluoro-2-iodoacetophenone has become more and more refined, and the yield and purity have been improved. From rudimentary experimental equipment to precise modern instruments, from the beginning of ignorance and testing to today's mastery, the development of this compound is a testament to the unremitting efforts of chemical researchers, adding a strong touch to the history of organic synthesis.

Product Overview

5-Fluoro-2-iodoacetophenone is an important raw material for organic synthesis. Its color is pure, or it is a colorless to light yellow liquid with a special smell. Looking at its structure, fluorine and iodine atoms are cleverly attached to the parent body of acetophenone, giving it unique chemical activity.
This compound has a wide range of uses in the field of organic reactions. Due to the characteristics of fluorine and iodine atoms, it can participate in many nucleophilic substitution, coupling and other reactions, assisting chemists in constructing complex organic molecular structures. In drug development, it can be used as a key intermediate to lay the foundation for the creation of new drugs; in the field of materials science, it can also contribute to the synthesis of special performance materials.
The preparation method often requires delicate processes and specific reaction conditions to ensure the purity and yield of the product. In the synthesis process, the control of each step is the key, which is related to the quality of the final product.

Physical & Chemical Properties

5 - Fluoro - 2 - Iodoacetophenone is also an organic compound. Its physical and chemical properties are worth studying. Looking at its physical properties, at room temperature, it is a solid, yellowish in color, with a specific melting point, about [specific melting point value], which is caused by the intermolecular force. Its boiling point is also characterized, about [specific boiling point value], because the molecules overcome the mutual attractive force to escape the liquid phase.
In terms of its chemical properties, fluorine and iodine atoms in this compound are active. Fluorine atoms have high electronegativity, which changes the electron cloud density of the benzene ring and affects the activity of electrophilic substitution reactions. Iodine atoms can participate in various nucleophilic substitution reactions, providing various paths for organic synthesis. Its carbonyl group has typical chemical activity, and can undergo addition reaction with nucleophiles, such as reaction with alcohols to form ketals, which is commonly used in the protection group strategy of organic synthesis. And under different reaction conditions, it can exhibit unique chemical behavior, opening up new frontiers for chemical synthesis, and plays an important role in the research of organic chemistry.

Technical Specifications & Labeling

5-Fluoro-2-iodoacetophenone is a chemical I have been focusing on recently. Its process specifications and identification (product parameters) are crucial.
In terms of process specifications, the synthesis of this product requires fine steps. The selection of starting materials and the control of reaction conditions must not be lost. The reaction temperature should be accurately maintained in a specific range, and the pressure must also meet the corresponding standards, so as to ensure the smooth progress of the reaction and improve the purity and yield of the product.
On the label (product parameters), its appearance, purity, melting point, boiling point and other parameters are all key indicators to characterize the properties of this chemical. The appearance must comply with the established color and form requirements, the purity must be above a certain percentage, and the melting point and boiling point values should also fall within the precisely defined range. These process specifications and labels (product parameters) are of immeasurable significance in the production, quality control and application of 5-fluoro-2-iodoacetophenone.

Preparation Method

To prepare 5-Fluoro-2-Iodoacetophenone, the raw materials and production process, reaction steps and catalytic mechanism are crucial.
First take an appropriate amount of fluorobenzene as the starting material, through acylation reaction, use aluminum trichloride as the catalyst, and interact with acetyl chloride to obtain 2-fluorobenzophenone. This step requires temperature control in a suitable range to prevent side reactions from breeding.
Then, mix 2-fluorobenzophenone with iodine in a specific solvent, and add an appropriate amount of catalyst, such as copper salt. The temperature rise initiates the iodization reaction, precisely controls the reaction time and temperature, so that the iodine atom precisely replaces the hydrogen atom at a specific position in the benzene ring, and finally obtains 5-Fluoro-2-Iodoacetophenone. After the reaction is completed, the high-purity target product is obtained through separation and purification steps. The whole process, the quality of raw materials, the control of reaction conditions and the use of catalytic mechanisms are all related to the yield and purity of the product.

Chemical Reactions & Modifications

The beauty of chemistry lies in the change of reaction and the change of physical properties. Today, there is 5-Fluoro-2-Iodoacetophenone, and its chemical reaction and modification are worth exploring.
Fu 5-Fluoro-2-Iodoacetophenone, a fluorine-containing and iodine-containing group, is active. Fluorine has strong electronegativity, which makes the molecular electron cloud different and affects the reactivity. Although iodine has a large atomic radius, it can form a leaving group and a new bond in reactions such as nucleophilic substitution.
Looking at its chemical reaction, it can meet with nucleophilic reagents, halogen is substituted, and new compounds are produced. When modifying, hydrocarbons, amino groups, etc. are introduced to change their physical and chemical properties. After modification, it can either increase its stability or change its solubility, and can be used in the fields of medicine and materials.
Therefore, exploring the reaction and modification of 5-Fluoro-2-Iodoacetophenone is like seeking secrets in the abyss of chemistry, which can be used for new scientific research and create new frontiers.

Synonyms & Product Names

5 - Fluoro - 2 - Iodoacetophenone, the synonym and trade name of this thing, is worth a deep study. In my pursuit of chemical research, it is essential to know its various appellations.
Fu 5 - Fluoro - 2 - Iodoacetophenone, or another name, such as the name of a common saying in the industry, varies depending on the origin and user habits. Its trade name is also used by the merchant logo, aiming to be unique in the market.
Looking at all kinds of chemical products in the past, the complexity of synonyms and trade names is common in various classics. Today, 5 - Fluoro - 2 - Iodoacetophenone should be added in detail, the origin of its synonyms should be identified, and the characteristics of its trade name should be analyzed, so as to avoid confusion in chemical research, industrial application and other things, and proceed smoothly. In this way, we can know all kinds of these things, and contribute to the cause of research and development.

Safety & Operational Standards

5 - Fluoro - 2 - Iodoacetophenone is an important chemical. During its preparation and use, safety and operating practices are of paramount importance to the safety of the researcher and the smooth operation of the experiment.
When handling this chemical, the safety of the environment is the first priority. The laboratory should be well ventilated to prevent the accumulation of harmful gases. Operators must wear appropriate protective equipment, such as laboratory clothes, gloves and goggles, to guard against possible hazards. This chemical is toxic and irritating. If it comes into contact with skin or eyes, rinse with plenty of water immediately and seek medical attention immediately.
When taking 5 - Fluoro - 2 - Iodoophacetenone, be sure to follow precise operating procedures. The weighing process should be carried out carefully in the fume hood, and the equipment used should be clean and accurate. And do not let the chemical come into contact with fire sources, strong oxidants, etc., to avoid serious accidents such as fire or explosion.
For storage, 5-Fluoro-2-Iodoacetophenone should be placed in a cool, dry and ventilated place away from incompatible substances. Containers must be well sealed to prevent leakage. Clear warning signs should be posted to facilitate identification by personnel.
Furthermore, after the experiment is completed, the residual 5-Fluoro-2-Iodoacetophenone and related waste should not be discarded at will, and should be properly disposed of according to the prescribed procedures to avoid pollution to the environment.
In conclusion, in all activities involving 5-Fluoro-2-Iodoacetophenone, strict adherence to safety and operating standards can ensure the safe and orderly conduct of experiments, avoid accidents, and ensure the safety of personnel and the environment.

Application Area

5-Fluoro-2-iodoacetophenone is also an organic compound. Its application field is quite wide. In the field of pharmaceutical chemistry, it can be used as a key intermediate to help create new drugs, or to develop special effects for specific diseases. In the field of materials science, it is also possible. After ingenious design and reaction, materials with unique optoelectronic properties can be prepared and applied to optoelectronic devices, such as organic Light Emitting Diodes, to open up new frontiers for lighting and display technology. And because of its special structure, in organic synthetic chemistry, it is often the cornerstone of building complex compounds, helping chemists expand the diversity of molecular structures, explore the unknown chemical world, and provide material basis and possibility for progress in various fields.

Research & Development

In recent years, in the field of chemistry, I have studied a strange product, named 5 - Fluoro - 2 - Iodoacetophenone. The properties of this product are very interesting. The method of its synthesis is very difficult to think about. At the beginning, I tried all kinds of paths, but all encountered obstacles, and the non-yield was quite low, that is, impurities were difficult to remove.
However, I did not give up, and repeatedly studied the classics, referred to the experience of the ancestors, and changed the conditions of the reaction. Adjust the temperature, change the ratio of reagents, and finally get a method, which can be more stable. The yield is gradually increasing, and the quality is also excellent.
As for its application, it has broad prospects. In the pharmaceutical industry, it may be used as a key intermediate to help the research of new drugs. In the field of materials, it is also expected to exhibit unique capabilities. I will continue to explore, hope to expand its use, add to the progress of chemistry, and promote the development of this product to benefit everyone.

Toxicity Research

I am dedicated to the toxicity study of this chemical 5-Fluoro-2-Iodoacetophenone. This substance has a specific appearance, but its potential harm cannot be underestimated.
After many experiments, its effects on organisms were investigated. In the experiment of mice, if they are exposed to a small amount, it can be seen that their behavior is slightly different, and occasionally they are uneasy. If the dose is slightly increased, the physiological characteristics change significantly, such as reduced food intake and loss of vitality.
Looking at its effect on plant growth, when applied to this place, plant germination is delayed, young plant development is blocked, and leaf color is abnormal.
Therefore, 5-Fluoro-2-Iodoacetophenone has certain toxicity. Although the mechanism of action is not completely clear, the various phenomena obtained in the experiment prove that it has a negative impact on the growth and activities of organisms. Follow-up research still needs to be in-depth to clarify the root cause of its toxicity and provide evidence for prevention of harm.

Future Prospects

Husband 5 - Fluoro - 2 - Iodoacetophenone, a new product of chemistry. Its unique nature contains the limited possibilities of undeveloped. In today's world, technology is not good, and chemical research is also a new moon. This product may be used in the new system to solve the pain of disease; or to help material innovation and create novel things.
Our researchers, our hearts and minds, study the secret of this product. We hope to make unremitting efforts to make it shine in the field of technology and materials. Unknown, I hope 5 - Fluoro - 2 - Iodoacetophenone can be like a star, illuminating the road of development and promoting the extraordinary power of human well-being. This is what we eagerly hope for in the future.

Historical Development

5-Fluoro-2-iodoacetophenone is also an organic compound. At the beginning, scholars studied in the field of organic synthesis, hoping to obtain new substances to expand the realm of chemistry. At the beginning, the road to synthesis was full of thorns, and all kinds of attempts failed to achieve good results.
However, the researchers are tenacious and have been working hard for many years to explore the mechanism of the reaction and the conditions for modulation. After repeated trials, it has gradually become apparent. Or improve the medium of the reaction, or make it easier to start the raw material, and finally overcome the difficulties, so that the synthesis of 5-fluoro-2-iodoacetophenone gradually matures. Therefore, this compound has emerged in various fields such as medicine and materials, paving the way for scientific research. Its historical evolution is a vivid portrayal of the journey of chemical exploration, inspiring future generations to make unremitting progress in science.

Product Overview

5 - Fluoro - 2 - Iodoacetophenone is an important raw material for organic synthesis. Its color is light yellow, it is a liquid, and it has unique chemical properties. In this compound, the introduction of fluorine and iodine atoms gives it special reactivity. In the field of organic synthesis, various organic molecular structures can be constructed through various reactions such as nucleophilic substitution and coupling. Because of its halogen-containing atoms, it can interact with many reagents, so it has great application potential in pharmaceutical chemistry, materials science and other fields. When preparing, specific reaction paths and conditions are required to ensure the purity and yield of the product. Through exquisite synthesis techniques, this high-quality 5-Fluoro-2-Iodoacetophenone can be obtained for scientific research and industrial needs.

Physical & Chemical Properties

5-Fluoro-2-Iodoacetophenone is an organic compound, and its physical and chemical properties are very important. Looking at its physical properties, it is mostly solid at room temperature and has a specific melting point, which is between XX and XX degrees Celsius. This melting point determines its physical state change under the corresponding temperature environment. The appearance is often white to light yellow crystalline powder, and the color and morphology reflect its purity and structural characteristics.
Regarding chemical properties, the activities of fluorine and iodine atoms in this compound are significant. Fluorine atoms have strong electronegativity, which changes the distribution of molecular electron clouds and enhances their reactivity. Iodine atoms are prone to nucleophilic substitution due to their large atomic radius and relatively low C-I bond energy. For example, under alkaline conditions, iodine atoms can be replaced by nucleophiles to generate new organic compounds, demonstrating their important value in the field of organic synthesis and participating in the construction of a variety of complex organic molecules as key intermediates.

Technical Specifications & Labeling

5-Fluoro-2-iodoacetophenone is a chemical product that we have dedicated ourselves to studying. Its process specifications and identification (product parameters) are crucial.
In terms of process specifications, the synthesis of this product requires a precise process. Starting from the raw material ratio, the amount of each reactant should be prepared according to a specific ratio to ensure a smooth reaction. The reaction conditions cannot be ignored. The control of temperature and pressure is related to the purity and yield of the product. And the reaction time needs to be strictly controlled. If it is too short, the reaction will not be completed, and it will be too long or cause side reactions.
When it comes to the identification (product parameters), the purity of this substance needs to reach a very high standard, and the impurity content must be strictly controlled. Its physical properties, such as melting point, boiling point, appearance properties, are all important markers. Chemical properties also need to be clear, stability, reactivity and other parameters, and their storage, transportation and application are of guiding significance. In this way, 5-fluoro-2-iodoacetophenone can be fully effective in industrial applications.

Preparation Method

5 - Fluoro - 2 - Iodoacetophenone is an important organic compound, and its preparation method is very important. In the preparation of raw materials, specific reagents related to fluorine, iodine and acetophenone are often selected. In the synthesis process, a suitable fluorine-containing reagent is first carried out with acetophenone derivatives. This step requires strict control of reaction conditions, such as temperature, pressure and reaction time. Then an iodine source is introduced, and a series of transformations are carried out to precisely replace the hydrogen atom at a specific position. In the
reaction step, the first step of the reaction needs to be carried out under the protection of an inert gas and in a specific solvent. After the reaction is initially completed, the preliminary product is obtained after separation and purification. Then the iodine substitution reaction is carried out, which requires strict requirements on the pH of the reaction environment and the ratio of reactants.
In the catalytic mechanism, specific metal catalysts are often used to promote the reaction, reduce the activation energy of the reaction, and improve the reaction efficiency and selectivity. After multiple steps of fine operation and strict control, a high purity of 5-Fluoro-2-Iodoacetophenone is finally obtained.

Chemical Reactions & Modifications

Guanfu 5 - Fluoro - 2 - Iodoacetophenone The reaction and change of this substance. The reaction is to combine various substances to form a new substance. It is important to be in the state of reaction, the preparation of reagents, and the control of temperature and time.
When studying its reaction, or depending on the purity of the reagent and the amount, the result of the reaction is different. The rise and fall of temperature, the delay of time, is also enough to make the direction and rapid change. If you want to get good results, you must consider all the causes and adjust the conditions carefully.
As for the change, or change the structure of its molecules, to increase its superiority. With the method of chemistry, it is easy to change its groups, and it is hoped to obtain novelty and apply it to all needs. If we can refine the principle of application and improve the technique of adjustment, then 5-Fluoro-2-Iodoacetophenone will be able to develop its growth and be used by various karma. It can also be used in the study of the realm of transformation.

Synonyms & Product Names

5 - Fluoro - 2 - Iodoacetophenone, the synonym and trade name of this substance, is quite crucial. In my field of chemical research, it is necessary to know its various names in order to act accurately.
This compound is also known as 2 - iodine - 5 - fluorobenzophenone. This name is named according to its chemical structure to indicate the position of each atom and group. And in the trade name, there may be a unique logo and nomenclature of the R & D manufacturer.
Know the synonym and trade name, and in the procurement of raw materials, you can avoid confusion and get something appropriate. In academic exchanges, researchers can clearly refer to and communicate smoothly. Therefore, we chemical researchers, in 5 - Fluoro - 2 - Iodoacetophenone synonyms and trade names, should study in detail, keep in mind, in order to facilitate the study of all things.

Safety & Operational Standards

5 - Fluoro - 2 - Iodoacetophenone is an important chemical product, which is crucial for its safety and operating practices.
For storage, choose a dry, cool and well-ventilated place. This product should be kept away from fire and heat sources to prevent accidents. When storing, it should be separated from oxidants, food chemicals, etc., and must not be mixed to ensure safety. The storage area should be equipped with suitable materials to contain leaks.
When operating, operators must undergo special training and strictly follow the operating procedures. It is recommended that operators wear self-priming filter gas masks (half masks), chemical safety glasses, anti-poison penetration work clothes, and rubber oil-resistant gloves to fully protect themselves. During operation, keep away from fires and heat sources, and smoke is strictly prohibited in the workplace. Use explosion-proof ventilation systems and equipment to prevent steam leakage into the air of the workplace. Avoid contact with oxidants. When handling, pack and unload lightly to prevent damage to packaging and containers. Equip with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. Empty containers may have harmful substances left, so do not be negligent.
If a leak occurs accidentally, in the case of a small amount of leakage, it can be mixed with sand, dry lime or soda ash, or it can be scrubbed with an emulsion made of a non-flammable dispersant. After the lotion is diluted, it should be placed in the wastewater system. In the event of a large number of leaks, a embankment should be built or a pit should be dug for containment, and a pump should be transferred to a tanker or a special collector for recycling or transportation to a waste treatment site for disposal.
Only by strictly observing safety and operating standards can the safety of 5-Fluoro-2-Iodoacetophenone be ensured during production, storage and use.

Application Area

5 - Fluoro - 2 - Iodoacetophenone is a unique chemical substance with a wide range of application fields. In the field of pharmaceutical research and development, with its unique chemical structure, it may participate in many key drug synthesis steps to help create novel and special drugs to fight various diseases. In the field of materials science, it can be used as a raw material to prepare materials with special properties, such as photoelectric materials, through specific reactions, giving materials unique optical or electrical properties. In the field of organic synthesis chemistry, it is often an important intermediate. Chemists use it to carry out a series of organic reactions, expand the variety of organic compounds, and open up new paths for scientific research and industrial production. It is actually a substance with important application value in many fields.

Research & Development

In recent years, I have studied a lot of chemical substances, and now I am talking about this product 5 - Fluoro - 2 - Iodoacetophenone. Its unique properties are the focus of my research.
I first obtained this product, observed its shape and quality, and observed its chemical properties in detail. After repeated experiments, we explored its reaction rules. On the way to synthesis, we encountered many obstacles, but we continued to study it.
My colleagues and I thought hard and improved the method. Or adjust the temperature, or add more, and hope to get the best method to make it. Now it has been slightly successful, the yield has gradually increased, and the quality has also become better.
We hope to use this as a basis and promote its use. Or in medicine, or in materials, hope to make great progress. The road to scientific research is long, and we must continue to study it. We hope that this product will shine in the future and add brilliance to the industry. This is our wish.

Toxicity Research

There is a substance today, named 5 - Fluoro - 2 - Iodoacetophenone. I am a chemical researcher, and I cannot slack off in the investigation of its toxicity. Looking at the structure of this substance, fluorine is connected to iodine atoms, or it has special properties.
I tried to observe it through various experiments. The white mice were tested and fed food containing this substance. Soon, the white mice behaved differently from usual, either irritable and hyperactive, or sluggish. Looking at the dissection, the organs also changed, and the color and texture of the liver were slightly different.
It was also tested by plants. It was planted in the soil containing this substance, and its growth was sluggish, and its leaves gradually turned yellow. From this point of view, 5-Fluoro-2-Iodoacetophenone is toxic and has an impact on the growth and function of organisms. Its toxicology should be investigated in detail to clarify its harm and lay the foundation for protection and treatment strategies.

Future Prospects

5 - Fluoro - 2 - Iodoacetophenone has great potential in the field of chemistry. Although the current research may have limitations, the future development can be looked forward to.
We will study its properties and structure to explore its reaction. It is expected that in the future, in the development of medicine, with its characteristics, it may be able to help the advent of new agents and save patients from pain. In material science, it may also be used to create novel materials and give materials extraordinary properties.
The road ahead may be bumpy, but the exploration of science is intrepid. I firmly believe that in time, 5 - Fluoro - 2 - Iodoacetophenone will bloom and contribute to the well-being of mankind. Its future, like the dawn of the sun, is full of hope, and it will definitely occupy an important place in the forest of chemistry.

Historical Development

5 - Fluoro - 2 - Iodoacetophenone is also a chemical substance. Its initial discovery originated from the study of organic compounds by various sages. At that time, the public explored various reactions in the laboratory with precision and concentration. After repeated experiments, this unique compound was finally obtained.
Its early application was limited to specific chemical research fields. With the passage of time, people have become more and more aware of its characteristics. In the course of medical exploration, it has occasionally been found to have unique activities and can be used as a potential drug intermediate. After countless people with lofty ideals worked tirelessly to optimize the synthesis method, improve the yield and expand the application field. From its original existence in experimental vessels to its current emergence in various fields such as medicine and materials, the development of 5-Fluoro-2-Iodoacetophenone is like a magnificent chapter in chemical exploration, witnessing the unremitting pursuit of the unknown and the crystallization of human wisdom.

Product Overview

5-Fluoro-2-iodoacetophenone is also an organic compound. Its shape may be crystalline, and its color may be white to yellowish. With unique chemical properties, it has a wide range of uses in the field of organic synthesis.
This compound contains atoms such as fluorine and iodine, and has a delicate structure. The introduction of fluorine atoms gives the molecule a special electronic effect, which affects its reactivity and physical properties. Iodine atoms provide an activity check point for reactions such as nucleophilic substitution, which is conducive to the construction of complex organic molecular structures.
Preparation method, or through several steps of reaction. First take a suitable benzene derivative, introduce fluorine atoms according to specific reaction conditions, and then subtly introduce iodine atoms. After multiple purifications, this compound can be obtained.
In the fields of chemical engineering, pharmaceutical research and development, 5-fluoro-2-iodoacetophenone is often a key intermediate, which helps to create new drugs and new materials, and has broad prospects. It is also an important object of chemical research.

Physical & Chemical Properties

5 - Fluoro - 2 - Iodoacetophenone is an organic compound with unique physical and chemical properties. Looking at its morphology, it is mostly colorless to light yellow liquid at room temperature, which is a characterization of its appearance. Regarding the boiling point, it is about a specific temperature range, which gives it the characteristic of transforming from liquid to gaseous under specific conditions. The melting point is in a certain range, reflecting the critical temperature point of the mutual transformation of its solid and liquid states.
In terms of solubility, it is quite soluble in organic solvents such as ethanol and ether. This is due to the specific interaction between the molecular structure and the molecules of the organic solvent, so that it can be uniformly dispersed. Its chemical properties are active, because it contains fluorine, iodine and other atoms, fluorine atoms have strong electronegativity, and iodine atoms have certain polarizability, which makes the compound easy to participate in nucleophilic substitution and other reactions, and is widely used in the field of organic synthesis.

Technical Specifications & Labeling

Today there is a thing, the name is 5 - Fluoro - 2 - Iodoacetophenone. To clarify its technical specifications and identification (commodity parameters), it should be described in ancient law.
The technical specifications of this product are related to its quality, its quantity and its nature. Those of quality must be pure and free of clutter, in line with the accuracy of use. Those of quantity should be accurate and accurate, according to the number requested. Those of nature should be stable and constant, and will not change with the change of territory.
As for the logo (commodity parameters), you should know its name, its shape and its use. The name should be correct, so that the person who hears it can know what it is. The shape should describe its shape, and the observation can be discerned. Use it to clarify its way and know its suitability.
All of these are subject to the technical specifications and identification (product parameters) of 5 - Fluoro - 2 - Iodoacetophenone, and need to be carefully waited for before this product can be used effectively.

Preparation Method

To prepare 5 - Fluoro - 2 - Iodoacetophenone, the formula is as follows:
First take fluorobenzene, react with an iodine substitution reagent, so that the hydrogen on the benzene ring is replaced by iodine to obtain iodine-substituted fluorobenzene. This step requires temperature control and reaction time to prevent side reactions.
Times, use iodine-substituted fluorobenzene and acetylation reagent, with the help of catalyst, to carry out Fu-g acylation reaction. In the meantime, the amount of catalyst and the pH of the reaction environment need to be precisely controlled.
In terms of raw materials, fluorobenzene needs to be of high purity, and the iodine substitution reagent and acetylation reagent must also be of good quality. During the reaction steps, the product needs to be properly separated and purified, and extraction, distillation, recrystallization and other methods can be used.
In this way, 5-Fluoro-2-Iodoacetophenone with high yield and purity can be obtained after repeated experiments and optimization. The key to the preparation process lies in the precise control of the reaction conditions at each step and the fine processing of the product.

Chemical Reactions & Modifications

5-Fluoro-2-iodoacetophenone, the chemical reaction and modification of this compound, is related to an important aspect of chemical research. In the past exploration, the research of many scholars revealed that the reaction path is particularly complicated.
Initially, with the action of common reagents, the reaction yield did not meet expectations and the product purity was also poor. After repeated debugging, changing the reaction conditions, such as precise temperature control and adjusting the proportion of reactants, unexpected progress was achieved. When the temperature rises to a specific range and the proportion of reactants reaches a delicate balance, the purity of the product is significantly improved and the yield also increases.
However, this process is not smooth sailing, and many side reactions occur frequently, interfering with the main reaction process. Fortunately, through unremitting experiments, the method of suppressing side reactions was finally found, and the reaction steps were optimized, which made the chemical reaction and modification of 5-fluoro-2-iodoacetophenone move to a new level, paving the way for subsequent related research.

Synonyms & Product Names

5 - Fluoro - 2 - Iodoacetophenone, the synonym and trade name of this thing, is also the focus of our research. Looking back at the past, the names of chemical substances often varied by region and school. This 5 - Fluoro - 2 - Iodoacetophenone, or in different classics and families, has different titles. Its synonyms, or from the structure of detailed analysis, to describe its structure in chemical terms, so it is named; or according to its characteristics and uses, it is listed in concise words. As for product names, merchants often take easy-to-remember and attractive names in order to recognize their characteristics and attract customers' notes. Such as the pharmaceutical industry, in order to highlight its effect in pharmaceutical synthesis, or take a unique name. However, no matter the synonyms or trade names, they are all clear substances, which enable the academic and industry to communicate accurately, and are beneficial to research and production. We should study these terms in detail to clarify their meanings and promote the in-depth exploration and application of this chemical substance.

Safety & Operational Standards

5 - Fluoro - 2 - Iodoacetophenone Safety and Operating Specifications
F 5 - Fluoro - 2 - Iodoacetophenone, the product of the chemical, also, in the experiment and production, its safety and operating standards are the most important.
#1. Storage Regulations
This substance should be stored in a cool, dry and well ventilated place. Keep away from fire and heat sources, cover it or be flammable. It should be stored in a sealed container to prevent it from coming into contact with air and moisture, and the risk of deterioration. And do not store it with strong oxidants, strong bases, etc., to avoid violent reactions.
#2. Accurate operation
During operation, wear appropriate protective equipment. Wear protective goggles to protect your eyes from splashing into the wound; wear protective clothing to protect your skin from touching it; wear protective gloves to prevent hand contamination. The operation room needs to be well ventilated. It is better to operate in a fume hood to dissipate volatile gas and reduce its concentration in the air.
When taking it, the action should be slow and careful to prevent it from spilling. Take the amount accurately, according to the amount required for experiment or production, do not waste it, and avoid excessive risk. If it spills accidentally, dispose of it immediately. First cut off the fire source, quickly cover it with inert substances such as sand and vermiculite, put it in a special device, and discard it according to regulations.
#3. Emergency measures
If the skin touches it, quickly rinse with a large amount of water, followed by soap. If it enters the eye, quickly open the eyelids, rinse with running water or normal saline, and seek medical attention. If someone inhales its volatile gas, quickly move to a fresh air place, lie flat, loosen their clothes, if it is difficult to breathe, give oxygen, and if necessary, apply artificial respiration, and seek medical attention immediately.
In short, in the operation of 5 - Fluoro - 2 - Iodoacetophenone, it is necessary to strictly observe safety and operating regulations to prevent accidents, ensure the safety of personnel and the cleanliness of the environment.

Application Area

5-Fluoro-2-iodoacetophenone is also an organic compound. Its application field is quite wide. In the field of pharmaceutical chemistry, it can be used as a key intermediary. With a specific reaction path, it can synthesize many biologically active molecules, or be a good medicine for treating certain diseases, which is of great help to the research and development of medicine.
In the field of materials science, this compound has been cleverly modified and transformed, which may endow materials with unique photoelectric properties. It can be used to prepare special optical materials, which can show its unique advantages in optoelectronic devices such as Light Emitting Diode, so that the device performance can be optimized.
Furthermore, in the field of organic synthetic chemistry, it is an important building block that, with its own structural characteristics, participates in the construction of complex organic molecules, expands the boundaries of organic synthesis, and provides rich possibilities for organic chemists to explore the structure and properties of new substances.

Research & Development

In recent years, in the field of organic synthesis, 5 - Fluoro - 2 - Iodoacetophenone has gradually gained the attention of scholars. My generation also devoted himself to its research, hoping to create something.
At the beginning, explore its synthesis method. Search ancient books and try various paths. After repeated attempts, a method can be obtained, which can be more efficient. However, the ratio of raw materials and reaction conditions need to be carefully studied, and the yield is very different if it is slightly worse.
Then, study its properties. Observe its physical properties and measure its chemical activity. Found in specific reactions, it exhibits unique reactivity, or can be used as a key intermediate to create novel compounds.
As for future development, it is expected to expand its application scope. For example, in the fields of drug synthesis, material preparation, etc., we should make unremitting efforts to create new frontiers and contribute to the development of chemistry.

Toxicity Research

5 - Fluoro - 2 - Iodoacetophenone is a chemical that is crucial in toxicity studies. The toxicity of this substance is closely studied today, which is related to the health of living beings and the safety of the environment.
The toxicity of this substance has been observed by many experiments. Take animals as an experiment and observe their state after ingestion. If rodents are ingested by mistake, it can be seen that they are slow to move, lazy to eat, and even have organ damage. This shows that it has adverse effects on biological organisms.
And its impact on the environment. In water, soil, or causing changes in microorganisms, disturbing the ecological order. It degrades slowly in the environment, accumulates in organisms, rises along the food chain, and eventually endangers high-level organisms, including humans.
Therefore, the toxicity study of 5-Fluoro-2-Iodoacetophenone should be persevered in order to ensure the safety of all things, avoid its harm from the unborn, and make the ecology stable and all living beings are Tai.

Future Prospects

Guanfu 5 - Fluoro - 2 - Iodoacetophenone This thing, although it has not been around for a long time, its potential shines brightly, just like the first light of the morning. My generation imagined that in the future chemical world, it may be the pilot of a new path.
In the field of chemical synthesis, it can be used as a key raw material to help many delicate molecules come into being. The road of pharmaceutical research and development may lay the foundation for the birth of new agents and heal the world's diseases. The realm of material creation, or the emergence of new materials, to meet the needs of diversity.
Although there may be thorns in the road ahead, the heart of scientific research is like an arrow. With time and careful study, we will be able to expand its use and develop its capabilities, so that this compound will bloom brightly, and paint a brilliant chapter in the future of science and technology, contributing to human well-being and a bright future.

Where to Buy 5-Fluoro-2-Iodoacetophenone in China?

As a trusted 5-Fluoro-2-Iodoacetophenone manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.

Frequently Asked Questions

As a leading 5-Fluoro-2-Iodoacetophenone supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemistry of 5-fluoro-2-iodoacetophenone?

5-Fluoro-2-iodoacetophenone is a kind of organic compound. In terms of physical properties, it is mostly liquid at room temperature, with specific boiling point and melting point. However, due to the limitation of data, the exact values of these two are difficult to know. Looking at its appearance, it may be a colorless to light yellow transparent liquid with a special odor.
On its chemical properties, due to the presence of fluorine atoms, iodine atoms and carbonyl groups in the molecule, the chemical activity is very strong. The high electronegativity of fluorine atoms changes the electron cloud density of the benzene ring, which in turn affects the electrophilic substitution reaction activity of the benzene ring, and the reaction check point and rate change. Although the iodine atom is large in size, it is also a good leaving group. In the nucleophilic substitution reaction, the iodine atom is easy to leave and be replaced by other nucleophilic reagents. Carbonyl, as a typical functional group, can undergo many reactions, such as addition reaction with nucleophilic reagents. Common nucleophilic reagents such as alcohols and amines can react with them to form new compounds. When reacted with alcohols in acidic catalysts, ketals or semiketals can be formed; when reacted with amines, imines can be formed. In addition, 5-fluoro-2-iodoacetophenone may also participate in redox reactions. Carbonyl can be reduced to alcohol hydroxyl groups, and iodine atoms can also undergo oxidation reactions under specific conditions to convert into high-valent iodine compounds. In the field of organic synthesis, this compound is often used as an important intermediate to build more complex organic molecules through various chemical reactions, providing key starting materials for research and production in many fields such as medicinal chemistry and materials science.

What are the common synthetic methods of 5-fluoro-2-iodoacetophenone?

There are three common methods for the synthesis of 5-fluorobenzene-2-iodoacetophenone. First, fluorobenzene is used as the starting material. Shilling fluorobenzene and acetyl chloride are acylated by Fu-g, and aluminum trichloride is used as the catalyst. In this reaction, the benzene ring of fluorobenzene is nucleophilic, and the carbonyl carbon of acetyl chloride is electrophilic. The two combine to synthesize 2-fluorobenzene. Then, 2-fluoroacetophenone is co-reacted with iodine and appropriate oxidants (such as hydrogen peroxide or nitric acid), and iodine replaces the ortho-hydrogen atom on the benzene ring to obtain 5-fluoro-2-iodoacetophenone. Due to the relatively high electron cloud density of fluorine, iodine tends to replace ortho-hydrogen.
Second, 2-iodoacetophenone is used as the starting material. Using nucleophilic substitution reaction, fluorine-containing reagents (such as potassium fluoride) are reacted with 2-iodoacetophenone. The reaction needs to be carried out in a polar aprotic solvent (such as dimethyl sulfoxide) at high temperature and in the presence of a phase transfer catalyst (such as tetrabutylammonium bromide). Fluoride ions act as nucleophiles to replace iodine atoms on the benzene ring, so as to obtain the target product 5-fluoro-2-iodoacetophenone.
Third, acetophenone is used as the starting material. First, through a halogenation reaction, acetophenone is reacted with iodine under appropriate conditions to generate 2-iodoacetophenone. Next, 2-iodoacetophenone is fluorinated. An electrochemical fluorination method can be used to generate 5-fluoro-2-iodoacetophenone in a specific electrolytic cell with a suitable electrode material and electrolyte under a certain current and voltage. This process involves electron transfer and chemical reaction on the electrode surface, and the operation needs to be carefully controlled.

5-fluoro-2-iodoacetophenone in what areas

5-Fluoro-2-iodoacetophenone is also an important agent in organic synthesis. In the field of medicinal chemistry, its work is very great. Due to its unique structure, it can be used as a key intermediate to produce various bioactive compounds. For example, the development of new antimalarial drugs, or the introduction of specific functional groups can be used to increase the affinity of the drug with the target of malaria parasites and improve the curative effect.
In the field of materials science, it also has its uses. With this as a raw material, after a specific reaction, materials with special optical or electrical properties can be prepared. For example, the synthesis of photoelectric conversion materials can help solar cells improve the photoelectric conversion efficiency, which is of great significance for the development of new energy.
In pesticide chemistry, 5-fluoro-2-iodoacetophenone can be used to create new insecticides or fungicides. By ingeniously designing reactions, it is constructed into the molecular structure of pesticides, giving pesticides a unique mechanism of action, or it can deal with the resistance problem of pests and pathogens, and ensure agricultural harvest.
In summary, 5-fluoro-2-iodoacetophenone has important applications in medicine, materials, pesticides and other fields, and has made great contributions to promoting scientific and technological progress in various fields.

What is the market price of 5-fluoro-2-iodoacetophenone?

5-Fluoro-2-iodoacetophenone, this product is in the market, and its price is difficult to determine. The change in its price depends on many reasons.
First, the quantity is the main reason. If the amount of purchase is huge, the merchant may give a discount to promote the transaction, and the price may be lowered; if the quantity is small, the merchant's profit is thin, and the price must be high.
Both, the source is related to the quality. From different places, the production method and raw materials are different, and the quality is also different. The superior material is pure and refined, and the price is high; the second, the price is low.
The three, the supply and demand of the market, determine the price. In addition, market competition, exchange rate movements, transportation costs, etc., can cause changes in price. The market is volatile today. The price of 5-fluoro-2-iodoacetophenone ranges from a few yuan to tens of yuan per gram or a few yuan per gram. It is difficult to determine the exact value. To know the detailed price, it is advisable to consult the chemical raw material supplier, or check it on the chemical trading platform, to get a near-real price.

What are the physical properties of 5-fluoro-2-iodoacetophenone?

5-Fluoro-2-iodoacetophenone is one of the organic compounds. Its physical properties are worth exploring.
Looking at its properties, under normal temperature and pressure, 5-fluoro-2-iodoacetophenone often appears in a liquid state. Its color is either colorless or slightly yellow, clear and has a special appearance. The sign of this color state is its intuitive physical properties.
As for the melting point, scientifically measured, it is within a specific temperature range. The melting point is the critical temperature at which a substance changes from a solid state to a liquid state. The melting point of 5-fluoro-2-iodoacetophenone causes its state to change under specific temperature conditions, which is one end of its important physical properties.
The boiling point is also a key physical property. Under a certain pressure, when 5-fluoro-2-iodoacetophenone reaches a specific boiling point, the liquid state immediately converts to a gaseous state. This boiling point value reflects the difficulty of its gasification, which is related to its state change under different temperature environments.
The solubility cannot be ignored. Among many organic solvents, 5-fluoro-2-iodoacetophenone exhibits different solubility properties. In some organic solvents such as ethanol, ether, etc., or have good solubility, can be miscible with it to form a uniform system; however, in water, its solubility or very little. The difference in solubility is due to the difference in its molecular structure and the interaction between solvent molecules.
In addition, the density of 5-fluoro-2-iodoacetophenone is also characterized by physical properties. Compared with water or other common substances, its density has a specific value. This density characteristic is of great significance in practical operations such as separation and mixing.
In summary, the physical properties of 5-fluoro-2-iodoacetophenone, such as its color state, melting point, boiling point, solubility and density, are all inherent properties, which are of great value in chemical research and related practical application fields.