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1,3-Difluoro-4-Iodobenzene

1,3-Difluoro-4-Iodobenzene

Hongda Chemical

Specifications

HS Code

975917

Chemical Formula C6H3F2I
Molecular Weight 254.0
Appearance A colorless to light yellow liquid
Boiling Point 190 - 192 °C
Density 1.998 g/cm³
Flash Point 81.4 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, toluene
Stability Stable under normal conditions, but avoid heat, flames, and strong oxidizing agents

As an accredited 1,3-Difluoro-4-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 100g of 1,3 - difluoro - 4 - iodobenzene packaged in a sealed, chemical - resistant bottle.
Storage 1,3 - difluoro - 4 - iodobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be kept in a tightly sealed container to prevent evaporation and exposure to air and moisture. Store it separately from oxidizing agents and reactive chemicals to avoid potential chemical reactions.
Shipping 1,3 - difluoro - 4 - iodobenzene is shipped in sealed, corrosion - resistant containers. It's transported with proper hazard labels, following strict regulations for chemicals. Shipment ensures protection from physical damage and environmental factors during transit.
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1,3-Difluoro-4-Iodobenzene 1,3-Difluoro-4-Iodobenzene
General Information
Historical Development
In the field of chemistry, there is a thing called "1,3 - Difluoro - 4 - Iodobenzene". The rise of things is not achieved overnight. In the past, various sages studied the wonders of chemistry and explored it in the organic world. At the beginning, only a glimpse or two of it, but the properties and uses of this compound were unknown.
As time goes by, many scholars have studied it diligently, using various techniques to explore its structure and analyze its characteristics. After many trials, or considering the reaction conditions, or selecting the raw materials. Gradually, it can be used in various synthesis paths, and can add bricks and mortar to organic synthesis.
Since its inception, it has become known that the development of this compound is like the rise of the stars. From the attention of few people to the awareness of chemists, many hardships have been the cornerstone of chemical progress, and it has also become a chapter in the development of "1,3 - Difluoro - 4 - Iodobenzene".
Product Overview
1,3-Difluoro-4-iodobenzene is also an organic compound. It is a white to light yellow crystalline powder with a unique chemical structure. In the field of organic synthesis, this compound has a wide range of uses. Because of its fluorine and iodine atoms, fluorine atoms can enhance the stability and lipophilicity of compounds, while iodine atoms are active, which is conducive to many chemical transformations such as nucleophilic substitution reactions.
Preparation of this product often requires a delicate synthesis process. Through a specific halogenation reaction, the reaction conditions and reagents are reasonably selected to achieve higher yield and purity. When storing, it should be placed in a cool, dry and well-ventilated place to prevent its deterioration. Due to its important value in scientific research and chemical production, many chemists have investigated its preparation, properties and applications in depth, hoping to expand its use in more fields and promote the progress of chemical science.
Physical & Chemical Properties
1,3-Difluoro-4-iodobenzene is an organic compound. Its physical properties, at room temperature, are colorless to light yellow liquids with a special odor. Its boiling point is quite high, about a certain temperature range, due to the force between molecules. In terms of chemical properties, fluorine and iodine atoms give their unique reactivity. Fluorine atoms have strong electronegativity, which changes the electron cloud density of the benzene ring, resulting in different activities of electrophilic substitution reactions. Iodine atoms can be used as leaving groups in many reactions and participate in reactions such as coupling. Due to its structure and properties, it can be used to prepare various complex compounds containing fluorine and iodine in the field of organic synthesis, and has potential application value in drug research and development, materials science, etc.
Technical Specifications & Labeling
1,3-Difluoro-4-iodobenzene is a chemical product that we have painstakingly studied. Its process specifications and identification (product parameters) are the key to the quality and application of this product.
Looking at its process specifications, the synthesis method needs to be precisely controlled. The choice of raw materials should be pure and free of impurities, and the proportions must be accurate. The temperature, pressure and time of the reaction must be in accordance with scientific regulations, and there should be no slight difference. In this way, high-purity products can be obtained.
As for the label (product parameters), the purity item should reach a very high standard, and the impurity content should be minimal. The appearance is also fixed, and it should show a specific color state. In addition, physical and chemical parameters, such as melting point, boiling point, etc., are important markers that can help users understand their characteristics and apply them to different uses. The two, process specifications and labels (product parameters), complement each other to build the quality foundation of 1,3-difluoro-4-iodobenzene.
Preparation Method
The method of preparing 1,3-difluoro-4-iodobenzene involves raw materials and production processes, reaction steps and catalytic mechanisms. The selection of raw materials is crucial, and suitable materials need to be carefully selected. The production process also requires rigorous planning, from the treatment of starting materials to the control of each reaction stage, which cannot be ignored.
The reaction steps are advanced in sequence, and each step has its own subtlety. The starting material initiates the reaction under specific conditions, or is heated, or supplemented by specific solvents, to promote the ingenious transformation between molecules. And the catalytic mechanism is indispensable. The selection of high-efficiency catalysts can accelerate the reaction process and improve the purity and yield of the product. This catalyst acts precisely on the reaction system, reducing the activation energy of the reaction and making the reaction more prone to occur. In this way, through a series of fine operations, the product of 1,3-difluoro-4-iodobenzene can be obtained.
Chemical Reactions & Modifications
1,3-Difluoro-4-iodobenzene is also an organic compound. In the process of chemical research, its reaction and modification are crucial.
In the past, the reaction followed the conventional method, but the effect was not good. Chemists are trying their best to improve it. Gai wants its reaction to be faster, higher yield, and less by-products.
Today's chemical masters, after repeated trial and error, find the number method. Or change the reaction conditions, such as adjusting the temperature and pressure, to increase the activity of the molecule; or use new catalysts to urge the reaction and change its chemical properties. In this way, 1,3-difluoro-4-iodobenzene is more convenient and efficient in the synthesis of other important compounds, and also adds new possibilities to the field of chemistry, contributing greatly to the great cause of organic synthesis.
Synonyms & Product Names
1,3-Difluoro-4-iodobenzene, which is of great significance in the field of chemical industry. Finding its synonyms and trade names is an important matter for chemical research.
Looking at ancient books, although there is no exact record of it, it is deduced from chemical principles that this compound is cleverly connected by fluorine, iodine and benzene rings. In the current chemical industry, its synonyms are either derived from structural characteristics or named because of similar synthesis paths. Trade names may be chosen by manufacturers according to market and characteristics.
Today's scholars are dedicated to exploring its various titles. After repeated experiments and literature comparison, we hope to be able to accurately find all synonyms and trade names, providing detailed information for chemical research and production, and helping the development of this field. In this way, we can go to the next level in the road of chemistry, so that the effectiveness of 1,3-difluoro-4-iodobenzene can be fully demonstrated.
Safety & Operational Standards
Safety and Handling Specifications for 1,3-Difluoro-4-Iodobenzene
Fu 1,3-Difluoro-4-Iodobenzene is a substance commonly used in chemical research. When used, the first priority is safety. Its sex has certain chemical activity, so be careful to avoid fire sources and hot topics. In case of open flame, or cause violent reaction, causing unpredictable disasters.
When operating, appropriate protective equipment is necessary. Protective clothing can protect against its damage to the skin, protective gloves can avoid direct contact with hands, and protective goggles can protect the eyes from accidental spills. It is especially critical to operate in a well-ventilated environment. Due to poor ventilation, the volatile gas of the substance can accumulate in one place, or risk inhalation and damage the respiratory system.
When taking it, the action should be stable and accurate. Measure it with clean utensils, do not cause too much waste, and do not take less wrong experimental process. After measuring, seal the container immediately to prevent it from evaporating and escaping. If it is accidentally spilled, do not panic. Clean it quickly with appropriate materials, such as materials with good adsorption properties, and then dispose of it properly.
Store it in a cool and dry place. Keep it away from oxidants, reducing agents, etc., because it may react with it. Classified storage, clear identification, easy access and management. If there is any discarded 1,3-difluoro-4-iodobenzene, it should not be discarded at will. It should be properly disposed of in accordance with relevant laws and regulations to avoid polluting the environment.
All these are the specifications for the safety and operation of 1,3-difluoro-4-iodobenzene. Follow this to ensure the smooth operation of the experiment, the safety of personnel, and the tranquility of the environment.
Application Area
1,3-Difluoro-4-iodobenzene is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate to help create new drugs. With its unique structure, it can participate in a variety of chemical reactions, or introduce specific functional groups, laying the foundation for the synthesis of drug molecules with unique curative effects.
In the field of materials science, it also has potential. It can be integrated into polymer materials through specific reactions to change the physical and chemical properties of materials, such as improving their electrical and optical properties, opening up new avenues for the research and development of new functional materials.
In organic synthetic chemistry, it is often an important building block for the construction of complex organic molecules. With the activity of fluorine and iodine atoms, chemists can follow ingenious strategies to build various novel organic frameworks and promote the development of organic synthetic chemistry.
Research & Development
In modern times, chemistry has flourished, and in the research of various compounds, it has become increasingly subtle. Today, there is 1,3-difluoro-4-iodobenzene. Its research and development are related to various fields of chemical industry and are quite important.
At the beginning, the study of this compound was aimed at clarifying its physical and chemical properties. After various experiments, analyzing its structure, we know that its molecular arrangement is exquisite, and the position of fluorine and iodine atoms affects its properties greatly. And its stability and reactivity are all important for research.
Then, explore the method of its synthesis. Zhu Xian tried his best and tried different paths. Or start with benzene, go through halogenation, fluorination and other steps, and gradually get this product. However, the process of synthesis is full of difficulties, and the improvement of yield and purity requires ingenuity.
As for development, 1,3-difluoro-4-iodobenzene has potential in the field of medicine and materials. In medicine, it may be the key raw material for the synthesis of new drugs; in materials, it can help create new functional materials. Therefore, our generation should diligently research, promote its better development, and use it for the world.
Toxicity Research
The toxicity of 1,3-difluoro-4-iodobenzene is quite important. This compound has a colorless to light yellow liquid appearance and is increasingly used in the chemical and pharmaceutical fields.
Experiments show that it has certain damage to organisms. Small animals are exposed to it for a long time, or they may have abnormal physiological functions. At the cellular level, it can interfere with the normal metabolic pathway and affect cell proliferation and differentiation.
And its volatility causes the surrounding air to contain a small amount of this substance, which can be inhaled into the human body or damage the respiratory tract and nervous system. Although the current application has not caused serious accidents, toxicity research should not be slack. It is necessary to deeply explore its mechanism of action to clarify the degree of harm, provide a basis for safe use and proper protection in the future, ensure the safety of scientific research and production environment, and avoid personnel from being poisoned by it.
Future Prospects
The use of 1,3-difluoro-4-iodobenzene is also a chemical product. I am currently researching it, and I have high hopes for it in the future. Its characteristics can be used for general chemical and reverse engineering, or it can lead to new research and materials science.
In terms of things, or it can be used for special effects, synthetic special effects, and general diseases, saving the world. In the field of materials, it may also be able to improve the new properties of materials, such as better performance and resistance, to promote high-tech progress.
Our researchers will do our best to keep it secret so that 1,3-difluoro-4-iodobenzene can be used for the benefit of the world before it can be widely used. This is our great goal and has not yet been developed.
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Frequently Asked Questions

As a leading 1,3-Difluoro-4-Iodobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of 1,3-difluoro-4-iodobenzene?
The main uses of 1,3-diene-4-cyanonaphthalene are quite wide. In the context of "Tiangong Kaiwu", this material is often used by all workers.
First, in the dyeing and weaving industry, 1,3-diene-4-cyanonaphthalene can be used as a raw material for dyes. Ancient dyers, in order to obtain a bright and long-lasting color, often sought all kinds of natural and synthetic materials. This substance can produce brilliant colors after ingenious combination and blending. It is applied to silk and hemp, making the fabric bright and lasting, and satisfying the needs of the world for the beauty of clothing.
Second, in the field of medicine, it also has its uses. Ancient physicians studied pharmacology and explored the properties of various things. 1,3-diene-4-cyanonaphthalene has been processed and refined, and may have certain medicinal effects. Although the method at that time was different from today, its potential for conditioning the body and healing diseases has also been observed by physicians, and it may be used to relieve certain diseases and relieve pain for patients.
Third, in the manufacture of exquisite utensils, 1,3-diene-4-cyanonaphthalene may enhance the properties of materials. If the maker wants to make the utensil durable and fine in texture, adding it can change the toughness and hardness of the material, etc., making the utensil more suitable for use, whether it is a daily tool or a delicate handicraft.
In short, 1,3-diene-4-cyanonaphthalene has shown its unique uses in many aspects such as dyeing, weaving, medicine, utensil manufacturing, etc., and has made great contributions to the development of life and craftsmanship at that time.
What are the synthesis methods of 1,3-difluoro-4-iodobenzene?
The synthesis method of 1% 2C3-diene-4-cyanobenzene is not directly related to "Tiangong Kaiwu", but it can be deduced with reference to the wisdom of ancient chemical processes.
Ancient alchemy, metallurgy and other processes involve the transformation of substances, or can be used for reference. To synthesize this substance, the selection of raw materials is quite critical. In ancient times, although there is no fine purification method today, it can be found from natural materials. Cyanobenzene is related, or can be obtained from cyanide-containing plants through complex extraction and transformation, such as bitter almonds and other cyanoside-containing plants, through hydrolysis, oxidation and other steps, or can obtain intermediates containing cyanide groups.
And the diene part can be considered as natural substances such as oils and resins. The oil is saponified, cracked, etc., or unsaturated hydrocarbons are generated, and then double bonds are introduced through clever reactions to construct diene structures.
The reaction process in ancient times often depends on heat and time control. In this synthesis, when setting a suitable reaction environment, or in ceramic or copper vessels. Temperature control can be adjusted according to the size of the charcoal fire and the density of ventilation. The reaction time is measured by hours, and the material changes are closely observed and adjusted in a timely manner.
Separation and purification, ancient also have methods. Or use distillation to separate the target product by taking advantage of the difference in the boiling point of each substance. Or use the method of recrystallization, select a suitable solvent, and make the product crystallize and precipitate in it to achieve the purpose of purification. Although the ancient conditions were simple, with the wisdom and diligence of the ancients, with time, it may be possible to explore a feasible synthesis path, adding a touch of brilliance to the history of chemical technology.
What are the physical properties of 1,3-difluoro-4-iodobenzene?
1% 2C3-diene-4-alkynyleheptane, this is an organic compound with unique physical properties.
It is a liquid at room temperature and pressure. Due to the unsaturated carbon-carbon double and triple bonds in the molecule, the intermolecular forces are affected, and the melting boiling point has its own characteristics. Generally speaking, high levels of unsaturation will cause the intermolecular forces to weaken, and the melting boiling point is relatively low for saturated hydrocarbons with the same number of carbon atoms. For example, compared with heptane, heptane is a saturated alkane with a relatively high melting boiling point, while 1% 2C3-diene-4-alkynyleheptane has a lower melting boiling point.
The compound is less dense than water and will float on the water surface. This is related to its molecular structure and composition, and the type of atoms and the spatial arrangement determine its density characteristics.
In terms of solubility, it is insoluble in water, because it is an organic matter, and water is a polar molecule. According to the principle of "similar miscibility", it is difficult to dissolve if the polarity difference is large. However, it is easily soluble in organic solvents, such as common ether, carbon tetrachloride, etc. Organic solvents are mostly non-polar or weakly polar, and are similar in structure and polarity to 1% 2C3-diene-4-alkyleheptane, so they are miscible. In addition, 1% 2C3-diene-4-alkynyleheptane has high chemical activity due to its multiple unsaturated bonds, and can undergo various chemical reactions such as addition and polymerization under suitable conditions, which also affects its physical property stability to a certain extent. During different chemical reactions, the physical state and other properties may change accordingly.
Is the chemical properties of 1,3-difluoro-4-iodobenzene stable?
The chemical properties of 1% 2C3-diene-4-cyanobenzene are quite stable. In this substance, the structure of carbon-carbon double bonds and cyanobenzene groups affects each other's checks and balances, making it have unique chemical stability.
Although the carbon-carbon double bond has certain activity, due to the electron-absorbing effect of the cyanyl group, the electron cloud distribution changes, so that the electron cloud density of the double bond decreases, and the activity also decreases. In this way, under common general conditions, the double bond is not easy to undergo addition reactions as easily as ordinary olefins.
As a strong electron-absorbing group, the cyanyl group is conjugated with the benzene ring to further enhance the stability of the molecule. The benzene ring itself is structurally stable, with a large π bond. After the cyano group is conjugated with it, the electron delocalization range expands and the energy of the system decreases, thereby significantly improving the chemical stability of the whole molecule.
From the perspective of reactivity, in order to make 1% 2C3-diene-4-cyanobenzene react, more severe conditions or specific catalysts are often required to assist the reaction. This stability makes the substance less prone to chemical reactions and deterioration in storage and general use environments, and can maintain its chemical structure and properties for a long time. Therefore, in general, the chemical properties of 1% 2C3-diene-4-cyanobenzene are relatively stable.
What is the price range of 1,3-difluoro-4-iodobenzene in the market?
For 1% 2C3-diene-4-chloronaphthalene, in the market, the price range is difficult to determine. The level of the cover price often depends on various reasons.
First, it depends on its quality. If the quality is excellent and pure, and there are few impurities, the price will be high; if the quality is poor and many defects, and there are many impurities, the price will be low.
Second, it is related to supply and demand. If there are many people in the market who want it, but there are few people who supply it, the price will tend to rise; if there are few people who want it, and the supply exceeds the demand, the price will be downward.
Third, the difficulty of control is also involved. If the production process is complicated, the required materials are rare, labor-intensive and time-consuming, the price will be high; if the production is easy, the materials are widely available, the labor is time-saving and the effort is small, the price will be flat.
Fourth, the profit of the business, the distance of the land, the amount of tax, etc., are also variables of the price. If the business wants a lot of profit, the price will increase; if the land is far away, the transportation cost will be expensive, and the price will also be high; if the tax is heavy, the cost will increase, and the price will rise.
To sum up, the price of 1% 2C3-diene-4-chloronaphthalene in the market is about tens of gold to hundreds of gold. However, this is only a rough estimate. To obtain a definite price, it is necessary to examine the situation of the time and city in detail, and consult the industry and businesspeople to obtain a more accurate number.