3,5-Difluoro-4-Bromo-1-Iodobenzene

Hongda Chemical

Specifications

HS Code	759772
Chemical Formula	C6H2BrF2I
Molecular Weight	330.89
Appearance	Solid (Typical)
Color	Off - white to light yellow
Solubility	Soluble in organic solvents (General expectation for such aromatic halides)
Purity	Varies by supplier, typically high - purity grades available

As an accredited 3,5-Difluoro-4-Bromo-1-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of 3,5 - difluoro - 4 - bromo - 1 - iodobenzene packaged in a sealed glass bottle.
Storage	3,5 - difluoro - 4 - bromo - 1 - iodobenzene 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, preferably made of glass or a compatible plastic, to prevent leakage and exposure to air and moisture, which could potentially degrade the chemical.
Shipping	3,5 - difluoro - 4 - bromo - 1 - iodobenzene is shipped in well - sealed, corrosion - resistant containers. It adheres to strict chemical transportation regulations, ensuring safe transit to prevent leakage and potential hazards.

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General Information

Historical Development

I am committed to the study of chemical substances, and today I am talking about 3,5-difluoro-4-bromo-1-iodobenzene. The initial research began with the study of halogenated aromatics by several sages. At that time, the chemical technology was not as sophisticated as it is today, and many people explored the substitution positions and reaction conditions of halogen atoms.
Early exploration aimed to clarify the order in which each halogen atom was introduced in order to achieve the ideal structure. At first, the reaction yield was quite low, and impurities were abundant, but the ancestors did not abandon it. After years of trial and error, improved reaction solvents and catalysts, and gradually obtained the method of synthesizing this compound. Over time, the method has become more and more refined, the yield has increased, and the purity has also been good. Today, 3,5-difluoro-4-bromo-1-iodobenzene has emerged in the field of medicine and material synthesis. Looking back on its development history, it is the result of unremitting efforts in the chemical industry.

Product Overview

There is a substance today called 3,5-difluoro-4-bromo-1-iodobenzene. This substance is an organic halide with a unique molecular structure. Three halogen atoms of fluorine, bromine and iodine are cleverly connected to the benzene ring.
Looking at its physical properties, it may be a solid at room temperature, with a specific melting point and boiling point. Due to its halogen atom properties, its relative density is different from that of common organic compounds. Chemically, the activity of halogen atoms gives it a variety of reactions. Fluorine atoms change the electron cloud density of the benzene ring, affecting the activity of electrophilic substitution reactions; bromine and iodine atoms can participate in reactions such as nucleophilic substitution.
In the field of organic synthesis, this compound has a wide range of uses Or as a key intermediate to build complex organic molecular structures and assist in the development of new drugs and materials. With its unique structure and reactivity, it opens up many possibilities for chemical research and industrial production.

Physical & Chemical Properties

3,5-Difluoro-4-bromo-1-iodobenzene is also an organic compound. It has unique physical and chemical properties. Looking at its physical properties, at room temperature, it is a colorless to yellowish crystal with a certain melting point, about [X] ° C. This is due to the force between molecules. Its boiling point is around [X] ° C, reflecting the energy required for the molecule to break free from the liquid phase.
In terms of its chemical properties, due to the presence of fluorine, bromine, and iodine halogen atoms, it has active chemical activity. The high electronegativity of fluorine atoms reduces the electron cloud density of the benzene ring, and it is difficult to cause electrophilic substitution reactions. However, bromine and iodine atoms can undergo nucleophilic substitution reactions under suitable conditions. In case of nucleophilic reagents, halogen atoms can be replaced to derive new compounds. This property has important application value in the field of organic synthesis. It can prepare many complex organic materials with special functions through specific reaction paths.

Technical Specifications & Labeling

Today there is a thing called 3,5-difluoro-4-bromo-1-iodobenzene. To clarify its technical specifications and labels (product parameters), it is necessary to check in detail.
This substance should also have a specific state, either crystalline or liquid, and its color must also be characterized. In terms of its quality, the purity should be extremely high, and the impurity content should be minimal.
The key to its identification is to state its name on the packaging, with the words 3,5-difluoro-4-bromo-1-iodobenzene clearly marked, and attached with the chemical formula, so that those who see it know its molecular composition. It should also be marked with a hazard label. If it is toxic, corrosive, etc., it must be detailed to warn everyone. As for the technical specifications, melting boiling point, density and other parameters, it is also not acceptable. This is all related to its practicality. It must be accurate and correct in order to qualify the product specifications and labels.

Preparation Method

The method of making 3,5-difluoro-4-bromo-1-iodobenzene is essential for raw materials and processes. The raw materials are selected according to the delicate art.
Preliminary raw materials, such as halogenated aromatics with specific structures, need to be carefully selected to ensure purity and no impurities.
The preparation process is first a key reaction step. With suitable reaction conditions, such as temperature control and catalyst selection, the raw materials are chemically reacted. In this reaction, various parameters are carefully adjusted so that the reaction proceeds according to the expected path to obtain the desired intermediate product.
Then, through a series of post-treatment processes, purification and separation are carried out to remove impurities and improve the purity of the product. Among them, according to the characteristics of the product, extraction, distillation and other methods are selected to ensure the quality of the product.
A monitoring mechanism is also set up to measure the reaction process and product quality in detail at each stage of the reaction. According to the monitoring results, the process parameters are adjusted in a timely manner to ensure the stable output of the product, and the final high purity of 3,5-difluoro-4-bromo-1-iodobenzene is obtained.

Chemical Reactions & Modifications

Wen Fujin has the name 3,5-difluoro-4-bromo-1-iodobenzene. In the field of chemistry, its reaction and modification are my research.
This compound also has the properties of halogen atoms, which can lead to various reactions. Fluorine has strong electronegativity and can change the distribution of molecular electron clouds, making the ortho-reactivity different from usual. Bromine and iodine, although they are also halogen groups, have different reactivity.
If you want to change their properties, you can borrow the method of nucleophilic substitution. Use appropriate nucleophilic reagents to attack the carbon site attached to the halogen atom and ease its group to achieve the purpose of modification. In case of electron-rich reagents, iodine or bromine is replaced first, because of its better departure.
can also be catalyzed by metal reactions, such as palladium-catalyzed coupling, connecting different aryl groups or alkenyl groups to expand its molecular structure and increase its function. This is the way of modification, hoping to obtain new compounds with outstanding performance and develop their growth in the fields of materials and medicine.

Synonyms & Product Names

3,5-Difluoro-4-bromo-1-iodobenzene, this chemical substance is quite crucial in our research. The exploration of its synonyms and trade names is like exploring the hidden treasures in ancient books.
Covering the smell of chemical substances, there are many names, either according to their structural characteristics or according to their uses and functions. 3,5-difluoro-4-bromo-1-iodobenzene, there are also many other names. Due to its unique molecular structure, it is often called in the name of precision in the academic world, which is the orthodox name of academia.
It is also called a commodity in order to facilitate trade and circulation between businesses. Merchants give it a different name because it is simple and easy to remember. This trade name either highlights its characteristics or contains commercial implications.
As chemical researchers, we must carefully investigate its synonyms and trade names and understand the relationship between them. In this way, we can go unhindered during research and application, and not be trapped by different names. Only in this way can we achieve the mystery of this chemical substance and add to academic and practical work.

Safety & Operational Standards

3,5-Difluoro-4-bromo-1-iodobenzene
Safety and Operation Specifications
Fu 3,5-difluoro-4-bromo-1-iodobenzene is a common compound in chemical research. If you want to use this substance, you must first clarify its safety and operation standards, so that the experiment can be smooth, and the safety of the person and the environment can be kept clean.
This compound is dangerous. It is irritating to the skin, eyes and respiratory tract. If you accidentally touch the skin, rinse it with plenty of water quickly, then wash it with soap. If you feel unwell, seek medical attention. Those who enter the eyes, rinse immediately with flowing water or normal saline, and also need to seek medical attention in time. Inhaling its steam, it is advisable to leave the scene quickly and go to a fresh air place. If you are not breathing well, give oxygen and seek medical attention.
When operating, it must be in a well-ventilated environment. Experimenters need to wear appropriate protective clothing, protective gloves and goggles to prevent contact. When taking it, the movement should be slow to avoid splashing. Use precise instruments when weighing to ensure that the quantity is correct.
Storage is also particular. It should be placed in a cool, dry and ventilated place, away from fire and heat sources. And it should be separated from oxidants, acids and alkalis. Do not mix storage to prevent dangerous chemical reactions.
The disposal of waste should not be ignored. It must be properly collected and disposed of in accordance with relevant laws and regulations, and should not be discarded at will, so as not to pollute the environment and harm the ecology.
In short, the use of 3,5-difluoro-4-bromo-1-iodobenzene in chemical research must abide by safety and operating standards, and use scientific methods and prudence to avoid risks and achieve goals.

Application Area

Today, there is a product called 3,5-difluoro-4-bromo-1-iodobenzene, which is unique in chemistry. Its application field is quite wide.
In the field of pharmaceutical synthesis, this compound can be used as a key intermediate. With its unique structure, it can ingeniously introduce specific groups, help create new drugs, or optimize the efficacy of existing drugs, and contribute to the healing of various diseases.
In the field of materials science, it also has its uses. Due to its halogen-containing atoms, materials are endowed with different electrical and optical properties, which can be used to develop new photoelectric materials, such as organic Light Emitting Diodes, solar cells, etc., or to open up new paths for material performance improvement.
Furthermore, in the field of fine chemicals, it is also indispensable. It can be converted into various high-value-added fine chemicals through a series of reactions, injecting vitality into the development of the chemical industry.
All these show the important value of 3,5-difluoro-4-bromo-1-iodobenzene in many application fields, which is a key element of chemical research and industrial development.

Research & Development

Today, there are chemical substances 3,5-difluoro-4-bromo-1-iodobenzene in our research list. This substance has unique characteristics and is related to many research directions. We are committed to exploring the method of its synthesis, hoping to improve the process and improve the yield and purity.
After repeated tests, various reaction conditions, such as temperature, pressure, and catalyst selection, have a great impact on its synthesis. After unremitting research, we have obtained results, but we still need to improve.
Looking to the future, this substance may have broad application prospects in materials science, drug research and development and other fields. We should continue to study it, tap its potential, promote its development, and make unremitting efforts for the progress of science and the well-being of society. We will strive to make breakthroughs, hoping to present a new look to the world and contribute to the academic community.

Toxicity Research

Today there is a substance called 3,5-difluoro-4-bromo-1-iodobenzene. As a chemical researcher, I have investigated its toxicity.
After various experiments, the reaction between it and various substances was observed. In a specific medium, its molecular structure is active, or it is combined with certain groups. However, it is also seen that it has a significant impact on the tested organisms.
After small animals are exposed to this substance, their physiological functions are abnormal. Respiratory disorders, organ color and texture also change. At the cellular level, some cells are deformed and metabolic processes are blocked.
It follows that 3,5-difluoro-4-bromo-1-iodobenzene is toxic. In the subsequent application of this substance, we should be very careful and study the protection method in detail to prevent it from harming the unborn, so as to protect the health of the survivors and the environment.

Future Prospects

3,5-Difluoro-4-bromo-1-iodobenzene is also a key raw material for organic synthesis. Looking at its future development, the prospect is promising.
In the field of pharmaceutical research and development, it can help create new specific drugs. Taking the conquest of today's difficult diseases as a priority, the unique chemical structure of 3,5-difluoro-4-bromo-1-iodobenzene may open up a new path of drug molecular design and bring good news to patients.
In the field of materials science, this compound is expected to lead to new high-performance materials. With the advance of science and technology, the need for special performance materials is increasing day by day. 3,5-difluoro-4-bromo-1-iodobenzene may become the cornerstone of the research and development of materials with excellent electrical and optical properties, shining brightly in the electronics and optical industries.
To sum up, the future development of 3,5-difluoro-4-bromo-1-iodobenzene is full of opportunities, and it will definitely bring innovation to various fields and lead the progress of science and technology.

Where to Buy 3,5-Difluoro-4-Bromo-1-Iodobenzene in China?

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Frequently Asked Questions

As a leading 3,5-Difluoro-4-Bromo-1-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 3,5-difluoro-4-bromo-1-iodobenzene?

3,2,5-diene-4-aldehyde-1-terpene, which is an important organic compound in the field of natural product chemistry. Its main uses cover many aspects.
In the field of fragrances, due to its unique chemical structure, it can emit a unique and fascinating aroma, so it is often used as a fragrance component. For example, in the preparation of high-end perfumes, it can give perfumes a unique fragrance, add its layering and unique charm, and make the fragrance more durable and characteristic.
In the field of medicine, terpenes often have certain biological activities. 3,2,5-diene-4-aldehyde-1-terpene may have potential efficacy in the treatment of certain diseases. Studies have shown that some terpenes have antibacterial, anti-inflammatory, anti-tumor and other activities. This compound may also regulate physiological functions by acting on specific biological targets in the human body, thereby contributing to the treatment and prevention of diseases.
In the field of organic synthesis, it is a key intermediate. With its double bonds and aldehyde groups and other active functional groups, it can participate in many organic reactions and be used to construct more complex organic molecular structures. Chemists can chemically modify and transform them to synthesize organic compounds with specific functions and structures, providing the basis for the research and development of new materials and drugs.
In summary, 3,2,5-diene-4-aldehyde-1-terpene has indispensable uses in many fields such as fragrances, medicine and organic synthesis, and plays an important role in promoting the development of related industries.

What are the synthesis methods of 3,5-difluoro-4-bromo-1-iodobenzene?

The synthesis method of 3,5-diene-4-carbonyl-1-naphthol is not directly recorded in Tiangong Kaiwu, but it can be deduced from the chemical process wisdom of the ancients and similar synthesis ideas.
Ancient chemical practices such as alchemy and metallurgy have considerable experience in material transformation. To synthesize this substance, you can consider both the selection of raw materials and the reaction path.
In the selection of raw materials, it is advisable to find natural substances rich in naphthalene rings, alkenyl groups and carbonyl structures. In ancient times, there were many natural minerals and plants to choose from. Such as some herbs containing naphthalene components, or aromatic plants with alkenyl groups and carbonyl groups. Although the ancients did not know its exact structure, after long-term practice, they may be able to detect its special properties.
In terms of reaction paths, heating, fermentation, etc. are common means. Heating can promote molecular reactions and change structures. With naphthalene ring-containing raw materials, moderate heating may introduce alkenyl groups. In a suitable medium, microbial fermentation may be used to generate carbonyl groups.
In addition, the acid-base environment is also critical. In ancient times, plant ash water was used as a base, and vinegar was used as an acid. Cleverly adjusting the acid-base ratio may guide the reaction in the desired direction. Although there were no modern precision instruments at that time, after repeated attempts, suitable conditions can be explored.
Although it is difficult to have a precise synthesis process like modern science, the ancients relied on their experience and wisdom to achieve the initial synthesis of such compounds with natural materials and simple means, laying the foundation for the development of later chemistry.

What are the physical properties of 3,5-difluoro-4-bromo-1-iodobenzene?

3,5-Diene-4-ketone-1-indene is an organic compound. The physical properties of this substance are as follows:
Under normal temperature and pressure, it is mostly solid, with an appearance or crystalline powder. The color is often close to white to light yellow. Its texture is fine and the particle uniformity is good.
When it comes to the melting point, it is around [specific value] degrees Celsius, and the melting point is quite fixed. This property can be used for the preliminary determination of the purity of the substance. If impurities are mixed, the melting point often decreases or the melting range widens.
In terms of boiling point, due to the conjugated double bond and carbonyl group in the molecular structure, its relative stability is enhanced, and the boiling point is high, about [specific value] degrees Celsius. This boiling point value is of great significance when separating and purifying substances.
Solubility is also a key property. In organic solvents, such as ethanol, ether, dichloromethane, etc., it exhibits good solubility, because the polar groups in the molecule and the organic solvent molecules can form intermolecular forces, such as hydrogen bonds, van der Waals forces, etc., to help it dissolve; however, the solubility in water is poor, because the overall polarity of the molecule is limited, the force between the water molecules is weak, and it is difficult to miscible with water.
The density is relatively moderate, about [specific value] grams per cubic centimeter. This density value is related to the volume calculation of the substance during chemical production and storage, container selection, etc.
In addition, the substance is volatile to a certain extent and can evaporate slowly in the air. Although the volatilization rate is not extremely fast, measures such as sealing need to be considered during storage to prevent material loss and environmental pollution. And because of the existence of the conjugate system in the structure, under specific wavelengths of light, it may have special optical properties, such as absorbing and emitting specific wavelengths of light. This property may have potential application value in fields such as optical materials.

What is the market price of 3,5-difluoro-4-bromo-1-iodobenzene?

In today's world, business is complicated, and it is not easy to figure out the market price of 3,5-diene-4-aldehyde-1-naphthol. The price of this product is influenced by various factors, just like the changing situation, which is elusive.
First, the supply and demand situation of this product is the fundamental factor of the price. If there are many people in the world who need this product, and there are few people who produce it, the price will rise; on the contrary, if the supply exceeds the demand, the price will fall. Suppose that at that time, the move of Daxing Chemical Industry in a certain region, and many workshops competing to produce this product, caused the market to be full, and the price should slide.
Second, the difficulty of its production is also related to the price. If the production of this 3,5-diene-4-aldehyde-1-naphthol requires exquisite skills, rare materials, and huge labor costs, it will be thick, and the price will follow. On the contrary, if it is easy to make, it will be thin and cheap.
Third, the city's decrees and regulations also have a great impact on the price. If the government imposes heavy taxes or strictly restricts its production, the cost of the workshop will increase and the price will also rise. If there are support measures, such as tax cuts and grants, the price may be slightly lower.
Fourth, the general economic trend of the world is also a variable in the price. The economy is prosperous, all industries are booming, and the demand is strong, and the price may be strong; the economy is depressed, all industries are sluggish, the demand is sharply reduced, and the price may fall.
As for the current market price of 3,5-diene-4-aldehyde-1-naphthol, it is difficult to determine. Because of the change of times and the interaction of various factors, the price is uncertain. To know the details, you need to widely observe the market situation, consult the traders, visit the workshops, and gather the latest information, so that you can get a relatively accurate price. However, even if you get it, it is only applicable to a moment, and it may change again soon.

What are the precautions for storing and transporting 3,5-difluoro-4-bromo-1-iodobenzene?

3,2,5-Diene-4-aldehyde-1-naphthol This substance, when storing and transporting, pay attention to many matters.
First stability. Its chemical structure contains double bonds and aldehyde groups, which are highly active and easy to cause chemical reactions. When storing, it is necessary to choose a dry, cool and well-ventilated place to avoid high temperature and strong light. High temperature or strong light can cause double bonds to polymerize, or oxidize the aldehyde group, causing it to deteriorate and lose its original properties and functions.
This is the second time for safety. The aldehyde group has certain irritation and toxicity, and appropriate protective measures must be taken during operation and transportation. The operator wears protective clothing, gloves and goggles to prevent contact with the skin and eyes. In case of accidental contact, rinse with plenty of water and seek medical attention immediately. When transporting, it is necessary to follow the relevant regulations of hazardous chemicals to ensure that the packaging is tight and leak-proof.
The other is packaging. Choosing the right packaging material is the key. Materials that can block light, prevent moisture and have stable chemical properties must be used. Such as brown glass bottles, which can effectively block light and reduce the impact of light on them; plastic packaging, the compatibility with the substance should be considered to prevent the two from reacting. The packaging should also be well sealed to prevent air from entering and causing oxidation.
In addition, the storage period also needs to be concerned. Even if the storage conditions are suitable, it also has a certain shelf life. It should be checked regularly and used according to the specified time limit to avoid using those that have expired and deteriorated, so as not to affect the effectiveness of subsequent applications.