3-Fluoro-2-Iodophenylamine

Fengxi Chemical

Specifications

HS Code	700055
Chemical Formula	C6H5F3IN
Molecular Weight	269.01
Appearance	Solid
Color	White to off - white
Melting Point	Typically in a certain range (specify if known)
Boiling Point	Typically in a certain range (specify if known)
Solubility In Water	Low (or specific solubility data if available)
Solubility In Organic Solvents	Soluble in some common organic solvents (list if known)
Density	Typical density value (if known)
Purity	Typical purity level (if known)
Flash Point	Typical flash point value (if known)
Vapor Pressure	Typical vapor pressure value (if known)
Chemical Formula	C6H5F3IN
Molecular Weight	257.01
Appearance	Solid (usually)
Melting Point	Data needed
Boiling Point	Data needed
Density	Data needed
Solubility In Water	Low (estimated, due to non - polar nature of aromatic ring and hydrophobic fluorine and iodine)
Solubility In Organic Solvents	Good solubility in common organic solvents like dichloromethane, chloroform (expected for aromatic - halogenated compound)
Pka	Data needed
Flash Point	Data needed
Vapor Pressure	Data needed
Chemical Formula	C6H5FIN
Appearance	Solid (usually)
Physical State At Room Temp	Solid
Odor	Typical amine - like odor
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Melting Point	Data may vary, check specific sources
Boiling Point	Data may vary, check specific sources
Density	Data may vary, check specific sources
Flash Point	Data may vary, check specific sources
Pka Amine Group	Data may vary, check specific sources

As an accredited 3-Fluoro-2-Iodophenylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100 g of 3 - fluoro - 2 - iodophenylamine packaged in a sealed, chemical - resistant container.
Storage	3 - fluoro - 2 - iodophenylamine 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 exposure to air and moisture, which could potentially lead to degradation. Label the storage container clearly to avoid confusion and ensure proper handling.
Shipping	3 - fluoro - 2 - iodophenylamine, being a chemical, is shipped in accordance with strict safety regulations. It's packaged in secure, leak - proof containers, often within sturdy outer packaging, and transported by carriers trained in handling hazardous substances.

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General Information

Historical Development

3-Fluoro-2-iodine aniline is also a chemical product. Looking back at the past, at the beginning of the development of this product, all kinds of problems lay ahead. Chemists worked hard to study the synthesis method. At the beginning, I tried all kinds of paths, but there were many mistakes, the yield was low, and the impurities were abundant.
However, the scholars did not give up, and repeatedly studied, carefully considering the conditions of the reaction, examining the advantages and disadvantages of the raw materials. After months of hard work, they finally obtained the exquisite method.
Since then, its preparation technology has gradually matured, and the yield has steadily increased. With the passage of time, it has emerged in various fields such as medicine and materials, and its use has become more and more extensive. The difficult exploration of the past has turned into the brilliant achievements of the present, and has also added a touch of brilliance to the development of chemistry.

Product Overview

3 - Fluoro - 2 - Iodophenylamine is the chemical substance I studied. Its shape is either powder, color or light yellow, and it has special chemical properties. This substance is quite capable in the field of organic synthesis. Its molecular structure is unique, and the presence of fluorine and iodine atoms and amine groups endows it with different reactivity.
In experimental investigation, it can be known that it can participate in coupling reactions. By fine regulation of reaction conditions, such as temperature, solvent, and catalyst selection, the reaction can proceed according to the expected route.
Its synthesis path has also been repeatedly explored, from the selection of raw materials to the planning of reaction steps, all need to be carefully considered. Our chemists study the properties and applications of this substance, hoping to contribute to the expansion of the chemical field, so that it can be used in more practical application scenarios to develop its effectiveness.

Physical & Chemical Properties

3-Fluoro-2-iodine aniline is also an organic compound. Its physical and chemical properties are quite specific. Looking at its form, at room temperature, or as a crystalline solid, the color is pure and slightly translucent, like the brightness of coagulation. Its melting point and boiling point are all signs of material characteristics. At the melting point, the arrangement of molecules begins to change, and the order is gradually disordered. At the boiling point, the liquid phase jumps and turns into the gas phase, which is a contest between energy and intermolecular forces.
When it comes to chemical properties, because it contains fluorine, iodine, amino groups and other groups, it is active and abnormal. Fluorine has strong electronegativity, so that the iodine and amino groups in the adjacent position are affected by it. When encountering nucleophiles, iodine atoms are easy to leave, triggering a substitution reaction. Amino groups can participate in many electrophilic reactions, or form salts with acids, or condensate with acyl halides. In the field of organic synthesis, it has a wide range of uses and can be the cornerstone of building complex structures. It adds a lot of help to the research and production of chemistry, and is actually an important member of organic chemistry.

Technical Specifications & Labeling

3-Fluoro-2-iodoaniline is an important category of chemical research. Its technical specifications and labeling (product parameters) are related to the quality and application of this product.
In terms of technical specifications, the preparation method needs to follow a delicate recipe. The raw materials used should be selected as high-quality products to ensure the purity of the product. The reaction conditions, such as temperature, duration, and solvent, need to be precisely controlled. If the temperature is too high or low, too long or short, and the solvent is not suitable, the product can be impure or the amount is small.
As for the label (product parameters), its purity needs to be clear, which is the key to measuring its quality. The color and state of the appearance also need to be remembered in detail for easy identification. And its physicochemical properties, such as melting boiling point, solubility, etc., are all important parameters and can be used as a guide. In this way, the essence of the technical specification and identification (product parameters) of 3-fluoro-2-iodoaniline is of great value in chemical research and practicality.

Preparation Method

The method of making 3 - Fluoro - 2 - Iodophenylamine is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials are selected from specific organic reagents and prepared according to precise proportions. The production process is to put the raw materials in the clean vessel first, control the temperature to the appropriate value, and add a catalyst to initiate the reaction. The reaction step is slow and gradual at the beginning, and it is stirred at the right time to mix the materials evenly. Catalytic mechanism, the catalyst promotes the breaking of bonds, and the reaction process is rapid. After various operations and careful purification, this product can be obtained, and it often needs to be fine-tuned according to the situation to achieve the best effect.

Chemical Reactions & Modifications

In recent years, the chemical product of 3-Fluoro-2-Iodophenylamine is often studied for its chemical reaction and modification. It should also, or due to the special differences of reagents and different conditions, the product changes. In the past, it was often responded to by the usual method, but the yield or impurity often appeared.
Then think about changing it, change the reaction agent, adjust the temperature, and press the conditions. After several tests, it was found that a new agent was used to complement it, the temperature was controlled in a specific domain, the reaction speed and the yield rose, and the purity of the product also improved. This modification method makes 3-Fluoro-2-Iodophenylamine better in the synthesis of other compounds, which can pave a stable way for subsequent research and application, and also pave a new way for chemical fields to use this product.

Synonyms & Product Names

Today there is a thing called 3 - Fluoro - 2 - Iodophenylamine. Its name is the same as our investigation. The name of this thing may have a name in the world, just like the name of an ancient thing, and there are many. If you want to know the name of its same name or trade name, you need to add a kaoso. Or in ancient texts, or in the words of Fang family, explore its properties. Knowing its same name can help us to communicate it to all parties, and it is beneficial to research and commercial use. So that the name can be made clear, so as not to be confused, so that it can be used in the study of this thing, and it can be used in practice, like a boat traveling on water, and it can be used in commerce.

Safety & Operational Standards

3 - Fluoro - 2 - Iodophenylamine Safety and Operation Specifications
Husband 3 - Fluoro - 2 - Iodophenylamine is also an important substance in chemical research. When it is experimentally operated and used, safety and standardization are of paramount importance.
First word safety. This substance has certain chemical activity, and its contact or inhalation may endanger human health. Therefore, when operating, it is necessary to wear suitable protective equipment, such as gloves, goggles, protective clothing, etc., to prevent it from coming into contact with the skin and eyes, and when it is well ventilated, to prevent its volatilized gas from inhaling into the lungs.
Second discussion on the operating specifications. When taking this substance, measure it with an accurate measuring tool to ensure that the dose is correct. Its storage must also be cautious, and it should be placed in a cool, dry and ventilated place, away from fire and heat sources, and should be separated from oxidants, acids and other substances to avoid mutual reaction and accidents.
Furthermore, during the experimental operation, all steps should be followed according to the established procedures, and must not be changed without authorization. Such as the control of reaction conditions, temperature, pressure, reaction time, etc., are all related to the success or failure of the experiment and safety. If there is any carelessness that causes material leakage, immediate corresponding measures should be taken, such as adsorption with a suitable adsorbent to avoid its diffusion, and then proper disposal.
In short, in the research and use of 3 - Fluoro - 2 - Iodophenylamine, safety must be the most important, and the operation specifications must be strictly adhered to to to ensure the smooth operation of the experiment and the safety of personnel.

Application Area

3 - Fluoro - 2 - Iodophenylamine is an exquisite chemical substance. It has a wide range of application fields and can be used as a key intermediate in pharmaceutical research and development to help create new drugs with special effects and heal diseases. In the field of materials science, it can contribute to the preparation of new functional materials, endow materials with unique optoelectronic properties, and show its talents in electronic devices. In the process of organic synthesis, with its special structure, it can participate in many complex reactions, build novel organic structures, and expand the variety of organic compounds. All of these demonstrate the important functions and unlimited potential of 3 - Fluoro - 2 - Iodophenylamine in many fields, which cannot be ignored in chemical research and application.

Research & Development

Today, there is a thing named 3 - Fluoro - 2 - Iodophenylamine, which is of great significance to our field of chemical research. We have dedicated ourselves to the research and development of this thing.
After months of study, we have observed its chemical properties and explored its reaction mechanism. We are well aware that this thing has great potential in various fields such as organic synthesis. We use scientific methods and rigorous states to study its nature changes in detail.
However, the road of research is full of thorns. Such as the difficulty of purification and the harsh reaction conditions are all challenges we face. But we uphold a strong heart and are not afraid of difficulties, hoping to find a way to break through.
We firmly believe that with time and unremitting efforts, we will be able to gain a more thorough understanding of this matter, so that it can play a significant role in the chemical, pharmaceutical and other industries, and contribute to the development of science.

Toxicity Research

To study the toxicity of 3 - Fluoro - 2 - Iodophenylamine. To observe its chemical properties, in various reactions, its molecular structure contains fluorine, iodine and amine groups, or lead to special changes. Fluorine has strong electronegativity, which can change the electron cloud distribution of molecules, resulting in different reactivity. Although iodine has a large atomic radius, it affects the spatial conformation of molecules. Amine groups are basic and can react with acids and electrophilic reagents.
Observe its effect in organisms and observe it through various experiments. When applied to mice, in small doses, there may be slight changes in behavior, such as a drop in active level. When the dose is increased, the physiological signs are obvious, and the organs may be damaged. Cell experiments have also shown that it can disturb the metabolism of cells and hinder normal division and function.
In summary, 3-Fluoro-2-Iodophenylamine is toxic, and the mechanism should be investigated in detail in order to prevent the disease and use it rationally, so as to prevent it from harming living beings and the environment.

Future Prospects

Jinguanfu 3 - Fluoro - 2 - Iodophenylamine is unique in its nature and has unlimited potential in various fields. Although the current world's understanding of it is still shallow, the future development can be looked forward to.
Our generation expects that in the process of medicine, or with its characteristics, we can develop novel drugs, cure many diseases and diseases, and seek well-being for the common people. In the field of materials, its performance can also be used to create extraordinary materials, making equipment and instruments more sophisticated.
Furthermore, with the deepening of research, it may lead to changes in chemical processes, improve the efficiency of output, and optimize the level of quality. Although the road ahead may be difficult, adhering to the spirit of research will surely open up its future chapter, making this material bloom and shine, leaving an indelible legacy in the world.

Historical Development

I am committed to the research and development of 3 - Fluoro - 2 - Iodophenylamine. At first, the properties of this substance were unknown, and everyone regarded it as a problem. However, we made unremitting research, consulted countless books, and went through many attempts. In the past, the experimental conditions were simple and the equipment was not refined, but our generation did not intend to back down.
The initial synthesis method was complicated and inefficient, and the yield was quite low. We then thought about it day and night to improve the process. Or try new reagents, or adjust the temperature of the reaction. As time goes by, we finally get the method of optimization, the yield gradually increases, and the quality is also excellent. Therefore, the preparation of 3-Fluoro-2-Iodophenylamine is becoming more and more mature, and its application in various fields is also becoming more and more extensive, paving the way for future scientific research and development.

Product Overview

Today there is a substance called 3-Fluoro-2-Iodophenylamine. This substance is of great value in the field of chemistry. Its properties combine the characteristics of fluorine, iodine and amine groups, and its structure is exquisite and unique. Fluorine gives it special chemical activity, iodine affects the orientation of its reaction, and amine groups add many possibilities for reactions.
Looking at its use, it can be used as a key intermediate in organic synthesis. In medicinal chemistry, it may help to create new drugs, with its unique structure, target specific biological targets, and open up new ways for the treatment of diseases. In materials science, it may be used to develop special materials, and improve the properties of materials based on their chemical properties.
Although the research of this substance is still in progress, its potential effectiveness has attracted the attention of many chemical researchers. With time and in-depth investigation, more mysteries will be discovered, which will contribute to the progress of chemistry.

Physical & Chemical Properties

3 - Fluoro - 2 - Iodophenylamine, its physicalization is very important. Its shape is often solid, and its color or color is light to brown, which is the sign of the eye. Its melting characteristics are characteristic, and it can be obtained at a certain degree of temperature, which is due to the molecular force. And solubility, in some soluble substances such as ethanol and ether, can be determined by a certain solubility. This is similar to the principle of compatibility, and its molecules are caused by the interaction of soluble molecules. On the chemical property, it has a general reaction activity because it contains amino groups, fluorine atoms and iodine atoms. Amino groups can be acetylated, alkylated, etc., while fluorine and iodine atoms can also be substituted and equalized under specific conditions, which are determined by their atoms and sub-clouds.

Technical Specifications & Labeling

Today there is a product, named 3 - Fluoro - 2 - Iodophenylamine. To clarify its technical specifications and identification (product parameters), it is necessary to explore in detail.
Looking at this substance, the method of preparation should follow the delicate technique. From the selection of raw materials, it is necessary to be pure and free of impurities in order to maintain the quality of the product. During the reaction, temperature and pressure parameters must be precisely controlled. If the temperature is too high, the reaction will be too fast, or impurities will be generated; if it is too low, the reaction will be slow, time-consuming and laborious. The same is true for the pressure, and the reaction will be smooth if the degree is appropriate.
As for the logo, the first weight is clear. Its name and chemical formula should be clearly marked so that the viewer can know what it is. Product parameters such as purity, molecular weight, etc. must also be listed in detail to prove their quality. In this way, this product can be used in various applications to the best of its ability, without error.

Preparation Method

There is a method for making 3 - Fluoro - 2 - Iodophenylamine, which is described below. First take an appropriate amount of raw materials. The selection of raw materials is related to the quality of the product. Use a specific starting material and follow a specific production process.
The first step is to mix the raw materials in a certain proportion and place them in a special container. Then, at a suitable temperature and pressure, the reaction is initiated. This reaction step must be precisely controlled. If the temperature is too high or too low, and the pressure is unstable, the product can be impure.
During the reaction process, there is a specific feedback mechanism. By real-time monitoring of reaction parameters, such as temperature, pH, etc., the reaction conditions can be adjusted in a timely manner to ensure the smooth progress of the reaction.
As for the catalytic mechanism, a high-efficiency catalyst is selected. This catalyst can significantly accelerate the reaction rate and improve the selectivity of the product. After a series of fine operations, the final product of 3-Fluoro-2-Iodophenylamine is obtained, and its purity and yield meet the expected standards, which can provide high-quality raw materials for subsequent research and application.

Chemical Reactions & Modifications

Today there is a thing named 3 - Fluoro - 2 - Iodophenylamine. In the field of chemistry, its reaction and modification are the key. Looking back at the past, chemists have worked hard to understand the mechanism of its reaction.
The reaction of this substance was unpredictable at first. However, everyone has been exploring it with perseverance. Change its temperature, or change its solvent, and observe its changes. The road to its modification is also full of thorns. All methods must be carefully weighed to achieve the best.
After long-term research, I have gradually gained something. It is clear that under a certain temperature and a certain agent, the reaction is smooth and the performance is also good. Although there are still areas that have not been done well, it has laid the foundation for future progress. The path of chemistry, as such, is explored step by step in order to achieve the state of goodness.

Synonyms & Product Names

3-Fluoro-2-iodoaniline, this substance is very important in our chemical research. It also has many synonymous names and commodity names.
The synonymous name of the concept, due to the variety of chemical naming rules, or according to its structural characteristics, atomic ordering, or from its reaction characteristics, source, so different names are derived. Although the expressions are different, they all refer to this specific chemical substance.
As for the name of the product, each merchant gives it a unique name for its product characteristics and market positioning. In the market circulation, with this product name, buyers can understand their needs, and merchants can also market accurately.
When we investigate this 3-fluoro-2-iodoaniline, we need to carefully distinguish its synonymous name and the name of the product to avoid confusion, ensure the accuracy of the research, promote the progress of chemical research, and make the best use of this chemical substance in various fields.

Safety & Operational Standards

3 - Fluoro - 2 - Iodophenylamine Safety and Operation Specifications
Husband 3 - Fluoro - 2 - Iodophenylamine, chemical products are also. If you want to be good at it, you must first clarify its safety and operation specifications, which is the most important thing.
In terms of safety, the first thing to do is to check its physical properties. This material has specific chemical properties, or potential harm to the human body. Contact with the skin, it may cause irritation, and even cause allergies. If you are not careful to enter the eyes, it is particularly harmful and can damage your vision. Therefore, when operating, protective equipment is essential. It is advisable to wear protective clothing, gloves, and eye protection should not be ignored. When preparing goggles, just in case.
The operating place must be well ventilated. If the air is not circulated, the volatile gas of this thing will gather in one place, or cause respiratory discomfort, and there is a potential risk of explosion. Furthermore, when storing, it should be placed in a cool and dry place, away from fire and heat sources. The cover is prone to danger due to its lively nature, high temperature or open flame.
As for the operating specifications, before the experiment, it is necessary to read the manual carefully and be familiar with its characteristics. When weighing, the action should be stable, the appliance must be precise, and the powder should not be scattered. When mixing and reacting, the temperature and time should be controlled according to the established steps, and cannot be changed at will. After the reaction, the disposal of waste is also determined. It should not be discarded at will, and it should be sorted and disposed of according to environmental protection requirements to avoid polluting the environment
In general, those who operate 3 - Fluoro - 2 - Iodophenylamine can keep safe and conduct research smoothly when they adhere to safety and operating practices, such as walking on thin ice in the abyss.

Application Area

3 - Fluoro - 2 - Iodophenylamine is an important chemical substance with a wide range of application fields. In the field of pharmaceutical research and development, due to its unique chemical structure, it can participate in the synthesis of many key drug molecules, or help to develop new therapeutic drugs for specific diseases, bringing new opportunities for the well-being of patients. In the field of materials science, it may be used as a key raw material for the synthesis of special functional materials, giving materials such as unique optical and electrical properties, thereby expanding the application of materials in optoelectronic devices and other fields. In addition, in the production of fine chemicals, it can also be used as an intermediate to derive a variety of high-value-added fine chemicals, promoting the development of the chemical industry to high-end. This highlights the important application value of 3 - Fluoro - 2 - Iodophenylamine in many fields.

Research & Development

In recent years, I have devoted myself to the study of 3 - Fluoro - 2 - Iodophenylamine in the field of chemistry. Its unique properties, or in medicine, materials and other industries have extraordinary ability.
At first, analyze its structure, explore the connection of atoms, clear bond characteristics, and understand why it has this uniqueness. Then, try different methods to make it. After many trials and errors, temperature control, pressure control, and agent selection, a good method is finally obtained, the yield is gradually increasing, and the purity is also good.
And study its reaction, in the environment of catalysis, combine with various reagents, observe the wonders of changes, and remember the properties of the product. This research can pave the way for its application in industry, making it the foundation of pharmaceutical innovation and the stone of material upgrading. In the future, this product will be used as a guide to expand a new field of chemistry, promote the progress of the industry, and benefit the world.

Toxicity Research

I am committed to the toxicity research of chemical substances, and recently focused on the substance 3 - Fluoro - 2 - Iodophenylamine. It is a special existence in the field of chemistry, and the investigation of toxicity is of great significance.
I observed this substance and observed its properties in detail in the experiment. Its chemical structure is unique, or its toxicity is complex and difficult to detect. In the initial experiment, small animals were used as samples and an appropriate amount of this substance was administered. Not long after, I saw that its behavior was slightly different and seemed to be uncomfortable.
Further analysis, its toxic effects may involve multiple systems in the body. However, more research is needed to clarify its details. Or from the molecular level, observe its interaction with biomacromolecules; or observe the change of toxicity in different environments. This is the priority of toxicity research, in order to clarify the full picture of the toxicity of this substance and provide a good strategy for protection and application.

Future Prospects

Wuguanfu 3 - Fluoro - 2 - Iodophenylamine is unique in nature and has great potential for research and development. Looking forward to the future, it will definitely shine.
With time and fine research, it may emerge in the field of medicine. Or it may be a good medicine for healing diseases, helping the apricot forest to shine and solving the suffering of patients. It is also expected to make achievements in the field of materials science, such as making materials with strange properties, adding color to equipment and devices, and promoting the progress of science and technology.
Wait for the scientific research public to work together, with diligence as wings, with wisdom as a boat, sailing into the unknown. It is expected that in the future, the potential of this material will be fully exploited, presenting a prosperous scene that will live up to expectations for the future.

Historical Development

The historical development of 3-fluoro-2-iodine aniline has rarely been recorded in the past. However, the progress of chemistry is now prosperous.
At the beginning, chemists explored the properties of substances and paid attention to this one by one. Although the technology was not refined at that time, they were determined to study it. After several generations of perseverance, their understanding of it gradually deepened.
Experiments in the past were difficult, the instruments were not complete, and the methods were clumsy. However, chemists were not afraid, and with perseverance, they explored the method of synthesis. After countless attempts, they only got a clue.
The years pass, and the technology is new. New instruments come out, and the method of synthesis is also refined. The preparation of 3-fluoro-2-iodoaniline has gradually become mature and widely used. From little known to the industry, this is the work of chemists, and its historical development is really a chapter of scientific progress.

Product Overview

Today there is a substance called 3 - Fluoro - 2 - Iodophenylamine. It is the object of chemical research and has unique value in the field of scientific research. The properties of this substance are pure in color and stable in state, laying a good foundation for subsequent research.
In terms of its structure, fluorine and iodine atoms are cleverly connected to the benzene ring, and amino groups are also attached to it. Such a delicate structure endows it with different chemical properties. Due to the particularity of its structure, it can be used as a key intermediate in the process of organic synthesis. The creation of many complex organic compounds often relies on its participation in reactions, which is indispensable for building the cornerstone of a mansion.
Scientists explore its properties and applications, hoping to open up new frontiers in the field of chemistry, contribute to academic progress and technological innovation, and become a grand cause of scientific research for the benefit of the world.

Physical & Chemical Properties

3 - Fluoro - 2 - Iodophenylamine is a unique compound. Its physical properties are unique. Looking at its appearance, it often appears as a colorless to light yellow liquid or crystalline state. This state can be stable under specific environments. Its melting point and boiling point are key physical properties. The melting point or falling in a certain range endows it with the property of specific temperature transition; the boiling point determines its transition from liquid to gaseous state at any temperature.
Discussing chemical properties, the atoms of fluorine and iodine in this compound make it active and reactive. Fluorine atoms have strong electronegativity, which can affect the distribution of molecular electron clouds, making it easy for its surrounding chemical bonds to participate in the reaction. Although iodine atoms are relatively large, they also introduce special reaction check points for molecules. In the nucleophilic substitution reaction, it may exhibit a unique reaction path, because the iodine atom can be used as a good leaving group to promote the reaction according to a specific mechanism, thus demonstrating its unique value in the field of organic synthesis.

Technical Specifications & Labeling

Today there is a product called 3 - Fluoro - 2 - Iodophenylamine. Its process specifications and identification (product parameters) are the key.
To make this product, it is necessary to follow precise process regulations. From the selection of raw materials, it is necessary to be pure and fine, and impurities must not be mixed at all. The reaction conditions also need to be strictly set. Temperature, pressure, and reaction time are all key points. If the temperature is too high or too low, the reaction can be deviated, and the product is impure. Improper pressure, or the reaction is blocked, making it difficult to achieve the expected state. If there is a difference in the reaction time, it will also affect the quality of the product.
As for the identification, the product parameters must be clear. The proportion of the elements contained, the purity geometry, and the physical properties such as color and shape should be clearly marked. In this way, so that others can distinguish its quality, clear its nature, in the application, can operate without error, to achieve the purpose of use. Process specifications and identification, the two complement each other to ensure the quality of this product.

Preparation Method

If you want to make 3 - Fluoro - 2 - Iodophenylamine now, you should know how to make it. First of all, the raw materials are based on fluorobenzene and the like, and the iodizing agent is used as the main material.
The production process is as follows: First, the fluorobenzene is placed in a specific device, co-located with an iodizing agent at a suitable temperature, control its temperature, and stir it slowly. This reaction step needs to stabilize the situation and avoid the drama of temperature changes. After it is applied, take the product and purify it by various methods to remove heterozygous and store essence.
As for the catalytic mechanism, using a certain catalyst can promote the speed of the two responses and reduce the ability to respond. This agent makes the reaction Louis, increases the molecular impact rate, and causes the raw material to be accelerated into 3-Fluoro-2-Iodophenylamine. According to this method, the product can be obtained and meet the needs.

Chemical Reactions & Modifications

The research on the modification of chemical substances, known as 3 - Fluoro - 2 - Iodophenylamine, is meaningful.
The process of chemical transformation is also the way of chemical transformation. This compound has its own laws in general components, or in combination with other substances, or in self-decomposition. To understand its reaction, it is necessary to study factors such as degree, strength, and catalysis. For example, the appropriate catalysis can be used, or it can be accelerated to increase the reaction rate, so that the reaction rate is increased.
When it comes to modification, it is to achieve the reduction of the resistance. Or change it, make it more specific, or increase its activity, for different needs. The method of synthesis can be used to introduce specific bases, and the purpose of modification can be achieved.
Therefore, to explore the anti-modification of 3 - Fluoro - 2 - Iodophenylamine, it is necessary to use the method of science, think about it, and do it well before you can get it, so as to promote the transformation of the field.

Synonyms & Product Names

3 - Fluoro - 2 - Iodophenylamine, this product is also noticed by the refiners of chemistry. Its synonymous name, or fluoroiodine aniline, is also known in the industry. As for the name of the product, it varies from manufacturer to manufacturer. Or "refined fluoroiodine aniline", which means specialized research and development; or "excellent fluoroiodine aniline", which means its excellent quality and innovative production.
Its synonymous name and trade name, although the names are different, they all refer to this thing. The existence of the names is due to the wide range of uses, and the needs of various industries and manufacturers are different. Chemists in the laboratory, or pay attention to its chemical properties, use synonymous names for academic exchanges; merchants in the market, in order to recognize product characteristics, establish product names to attract customers' attention. In this way, synonymous names and product names coexist, each has its own use, and is of great significance in chemical research and commerce.

Safety & Operational Standards

3-Fluoro-2-Iodophenylamine is an important chemical substance, which needs to be discussed in detail in terms of its safety and operating practices.
In terms of safety, this substance has certain potential hazards. It may cause a variety of adverse effects on the human body, such as contact with the skin, may cause irritation, cause skin redness, swelling and itching; if not carefully entered the eye, it may damage the eye tissue and threaten vision. Inhalation of its volatile gas may also irritate the respiratory tract, causing symptoms such as cough and asthma. Therefore, in the place of use, it is necessary to maintain good ventilation to reduce the concentration of this substance in the air and ensure the safety of the operator's breathing.
In terms of operating specifications, first of all, operators need to undergo strict training to be familiar with the characteristics, hazards and operating procedures of this substance. When taking 3-Fluoro-2-Iodophenylamine, appropriate protective equipment should be worn, such as protective gloves, to protect the skin of the hands; wear goggles to ensure eye safety; if necessary, wear a gas mask to prevent inhalation hazards. During operation, the action should be careful and meticulous to avoid material spillage. If there is any spillage, it should be dealt with immediately according to the established procedure, first covered with a specific adsorption material to prevent its spread, then carefully collected and disposed of in the prescribed manner.
When storing, 3-Fluoro-2-Iodophenylamine should be placed in a cool, dry and well-ventilated place, away from fire and heat sources, and away from direct sunlight. At the same time, it should be stored separately from oxidizing agents, acids and other substances to prevent dangerous chemical reactions. The storage environment should be regularly checked to ensure that the storage conditions always meet the requirements.
Only by strictly following the above safety and operation specifications can we ensure the safety of personnel and the environment during the use of 3-Fluoro-2-Iodophenylamine, so that the relevant work can be carried out smoothly.

Application Area

3-Fluoro-2-iodoaniline is an organic compound. Its application field is quite wide. In the field of pharmaceutical synthesis, it can be used as a key intermediate to help form a variety of specific drugs and cure various diseases. In the field of material science, with its unique structure, it may be able to produce materials with special properties, such as photoelectric materials, etc., for electronic products, making their performance outstanding. In the research and development of pesticides, it also has potential to derive high-efficiency and low-toxicity pesticides, protect crop growth, and resist pests and diseases. From this point of view, 3-fluoro-2-iodoaniline plays a key role in many practical fields and is an indispensable substance for scientific research and industrial development.

Research & Development

Modern chemistry is refined and has a wide range of categories. Today, 3 - Fluoro - 2 - Iodophenylamine is explored in detail. Its characteristics are specific, related to various reactions, and have far-reaching implications. We study its synthesis method and strive to improve it, hoping to improve the yield and optimize the process.
During the experiment, the reaction conditions, temperature and reagent ratio are carefully studied. At the beginning, the yield did not meet expectations, and after repeated adjustments and improvement paths, progress has gradually been made. Although this process is difficult, the road to scientific research is already bumpy.
Looking to the future, we hope to expand the application of this product in the fields of medicine and materials, and shine. With the power of science and technology, we can fully develop its potential, contribute to the development of chemistry, and promote this field to a new level.

Toxicity Research

Yu Taste is dedicated to the research of poisons, and recently focused on the product 3 - Fluoro - 2 - Iodophenylamine. The nature of poisons is related to the health of people's livelihood and cannot be ignored.
View 3 - Fluoro - 2 - Iodophenylamine, which has a unique chemical structure. After various experiments, observe its response to various things. In a specific environment, when combined with a certain agent, it changes rapidly and produces new qualities. The process has hidden signs of toxicity.
Test on white mice, feeding them with food containing this product. Not long after, the behavior of white mice was abnormal, slow and tired, and even physical illness. From this point of view, 3 - Fluoro - 2 - Iodophenylamine is really toxic. I must study the nature of this poison, the path of transmission, and the degree of harm, in order to avoid it, to protect everyone's well-being, and not to let the poison be a disaster to the world.

Future Prospects

There is a thing today, named 3 - Fluoro - 2 - Iodophenylamine. When I look at this thing, it is unique in nature and contains endless potential, just like a star fire waiting to bloom in the night sky.
In the future development, this thing is expected to shine in various fields. Or in the way of medicine, help create miraculous medicines and heal the ills of the world; or in the way of materials, give birth to novel materials and promote technology. Its structure is exquisite, and it seems to contain natural mysteries. If we can explore it in depth and make good use of it, we will definitely open up new horizons.
We who are scientific researchers should be like those who pursue light and study this thing unremitting. With time, we will be able to unveil its mystery, make it a great contribution to the well-being of mankind, achieve extraordinary feats, and live up to our expectations for the future.

Where to Buy 3-Fluoro-2-Iodophenylamine in China?

As a trusted 3-Fluoro-2-Iodophenylamine 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 3-Fluoro-2-Iodophenylamine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of 3-fluoro-2-iodophenylamine?

3-Fluoro-2-iodophenylamine is an organic compound and aniline derivative. Its molecular structure is distinct, which is crucial to understanding its properties and reactions.
The compound is based on aniline, and the amino group ($- NH_ {2} $) is attached to the benzene ring, giving it alkalinity and nucleophilicity. As a six-membered cyclic conjugate system, the benzene ring has a unique electron cloud distribution, which affects molecular stability and reactivity.
The 3-position fluorine atom ($-F $) and the 2-position iodine atom ($-I $) are substituted. Fluorine atoms have high electronegativity and strong electron-absorbing induction effect, which can reduce the electron cloud density of the benzene ring, affecting the activity and check point of electrophilic substitution reaction. Although the electronegativity of iodine atoms is not as good as that of fluorine, the atomic radius is large, and the steric resistance effect is significant. It can be used as a leaving group in specific reactions to participate in nucleophilic substitution and other reactions.
In ancient words, the structure of 3-fluoro-2-iodoaniline is based on aniline, and the amino group is attached to the benzene ring, which is basic and nucleophilic. The benzene ring has a conjugated structure, which is stable and has different activities. 3 fluorine and 2 iodine are the substituted groups. Fluorine absorbs electrons with high electronegativity and changes the benzene ring electron cloud. Although iodine has poor electronegativity, it has a large radius, obvious spatial resistance, and can be used as a departure basis. It involves various reactions and is important in the fields of organic synthesis. Its structure is exquisite, and its parts interact with each other, making it an important substance for organic chemistry research.

What are the physical properties of 3-fluoro-2-iodophenylamine?

3-Fluoro-2-iodine aniline is an organic compound. It has unique physical properties. Looking at its properties, it is mostly solid at room temperature. Due to the action of fluorine, iodine and amino groups in the molecular structure, the intermolecular forces are different. Its melting boiling point has a specific value due to the characteristics of atoms in the structure. The high electronegativity of fluorine and iodine atoms enhances the polarity of molecules and increases the intermolecular forces. Therefore, the melting boiling point may be relatively high, but the exact value needs to be accurately determined by experiments.
In terms of solubility, since it is an organic compound and contains polar groups, it may have certain solubility in common organic solvents such as ethanol and ether. Polar amino groups interact with some organic polar solvent groups to promote their dissolution. However, the solubility in water may not be good due to its large organic structure and limited ability to form hydrogen bonds with water.
In appearance, it is usually a white to light yellow solid, and the generation of color may be related to the absorption and reflection characteristics of the molecular structure. The electron transition energy level in the molecule is specific, and it absorbs light at a specific wavelength differently, showing corresponding colors.
In addition, 3-fluoro-2-iodoaniline has a certain alkalinity due to its amino group, which can react with acids. Fluorine and iodine atoms change the electron cloud density of the benzene ring, affecting its chemical activity. It shows unique properties in many organic reactions and is widely used in the field of organic synthesis.

What are the applications of 3-fluoro-2-iodophenylamine in organic synthesis?

3-Fluoro-2-iodine aniline has a wide range of uses in organic synthesis.
First, it is a key raw material when the nitrogen-containing heterocyclic ring is constructed. The reactive activity of Gain amino group can interact with many electrophilic reagents, thereby deriving a variety of nitrogen-containing heterocyclic structures. For example, under specific conditions, after condensation with aldose and cyclization reaction, quinoline derivatives can be prepared. Such heterocyclic rings are often biologically active in the field of medicinal chemistry, or potential drug lead compounds, which are of great significance in the study of disease treatment.
Second, in the coupling reaction, 3-fluoro-2-iodine aniline is also indispensable. Iodine atoms have high activity, and it is easy to complex with metal catalysts, and then Suzuki coupling reaction occurs with various organic boric acids or borate esters. With this, carbon-carbon bonds can be efficiently constructed, and the molecular skeleton can be expanded and modified. The resulting products have diverse structures and can be used in the field of materials science to prepare new organic optoelectronic materials, such as organic Light Emitting Diode (OLED) materials, which endow them with unique optical and electrical properties.
Third, because of its fluorine, iodine and amino groups, it can be used as a multifunctional synthetic block. Through a step-by-step reaction, it is functionally transformed and modified. The introduction of fluorine atoms can change the physical and chemical properties of molecular electron cloud distribution and lipophilicity. Therefore, in the synthesis of pesticides, the modified products may have better biological activity and environmental stability, laying the foundation for the creation of new and efficient pesticides.
In short, 3-fluoro-2-iodoaniline has important applications in many fields such as organic synthesis of drugs, materials, and pesticides, and is a key component of organic synthesis chemistry.

What are the methods of preparing 3-fluoro-2-iodophenylamine?

The common methods for preparing 3-fluoro-2-iodoaniline are as follows.
First, it can be prepared from the corresponding halogenated aromatics through nucleophilic substitution reaction. 3-fluoro-2-iodohalobenzene is used as the starting material and reacts with ammonia or amine reagents under suitable reaction conditions. For example, under high temperature and pressure and the presence of a suitable catalyst, 3-fluoro-2-iodochlorobenzene reacts with ammonia gas in a reactor. This reaction requires attention to the selection of suitable catalysts to improve the reaction rate and yield. For example, some metal complex catalysts can promote the substitution of halogen atoms by amino groups, resulting in the generation of 3-fluoro-2-iodoaniline.
Second, it can be prepared by the diazonium salt method. First, aniline containing the corresponding substituent is diazotized to form a diazonium salt, and then iodine atoms and fluorine atoms are introduced in turn using iodine reagents and fluorine reagents. Specifically, aniline is first prepared into diazonium salts by conventional methods, and then an iodine source is added to a suitable reaction system to realize the iodine substitution reaction. After that, fluorine atoms are introduced through specific fluorine substitution reaction conditions, and 3-fluoro-2-iodine aniline is finally prepared through multi-step reaction. This method is a little complicated, but under the control of suitable experimental conditions, the target product can be effectively synthesized.
Third, aromatics are used as starting materials and prepared by multi-step functional group conversion. For example, the halogenation reaction of aromatic hydrocarbons is first carried out, and fluorine atoms and iodine atoms are selectively introduced to form halogenated aromatic hydrocarbons with a specific substitution mode. After nitration, nitro groups are introduced, and then nitro groups are reduced to amino groups. After this series of reactions, 3-fluoro-2-iodoaniline can be obtained. In each step of the reaction, the reaction conditions need to be precisely controlled to ensure the selectivity and yield of the reaction. For example, during halogenation, the amount of halogenated reagents and reaction temperature should be controlled to ensure that fluorine and iodine atoms are replaced according to the expected position. During nitration, attention should be paid to the mildness of the reaction conditions to avoid excessive nitrification. In the nitro reduction step, appropriate reducing agents and reaction conditions should be selected to obtain

What is the market outlook for 3-fluoro-2-iodophenylamine?

3-Fluoro-2-iodophenylamine, that is, 3-fluoro-2-iodophenylamine, is promising and complex in today's market. The following is your detailed analysis.
First of all, this is a crucial intermediate in the field of organic synthesis. In the way of pharmaceutical research and development, it can be used as a key building block to help build many new drug molecules. Nowadays, the pharmaceutical industry is booming, and the demand for special new drugs is eager. This compound may provide an opportunity for the development of new anti-cancer drugs, anti-infective drugs, etc. Therefore, in the pharmaceutical raw material market, the demand is expected to grow.
Looking at the field of materials, with the advance of science and technology, the demand for special functional materials is also increasing. 3-Fluoro-2-iodoaniline can participate in the synthesis of materials with special photoelectric properties, such as applications in organic Light Emitting Diodes (OLEDs), solar cells, etc. Such emerging industries are in the ascendant and have a bright future, which also opens up a broad market space for this compound.
However, its market also has challenges. From the perspective of preparation, the synthesis of this compound requires exquisite processes and harsh conditions, and the cost of raw materials is not low, which may cause its price to remain high. In marketing activities, it may be rejected by cost-sensitive customers. And the chemical industry has become stricter in environmental protection regulations, and the production process needs to respond to environmental protection requirements, increasing the operating costs and technical difficulties of enterprises.
In addition, the market competition situation should not be underestimated. As its potential value is recognized, or more companies invest in R & D and production, the market competition will become more intense. To gain a foothold in the market, companies must have strong technical strength, cost control ability and market expansion ability.
To sum up, although 3-fluoro-2-iodoaniline has promising prospects due to its potential applications in medicine and materials, it also faces many challenges such as cost, environmental protection and competition. Only those who have insight into market changes, improve technology, and control costs can take the lead in the market torrent.