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Benzene, 2,3-Difluoro-1-Iodo-4-Methyl-

Benzene, 2,3-Difluoro-1-Iodo-4-Methyl-

Hongda Chemical

Specifications

HS Code

545599

Chemical Formula C7H5F2I
Molecular Weight 254.014 g/mol
Physical State Solid (predicted)
Boiling Point Approximately 200 - 220 °C (estimated)
Density Estimated around 1.9 - 2.1 g/cm³ (based on similar halogen - substituted benzenes)
Solubility In Water Insoluble (non - polar nature due to benzene ring and non - polar substituents)
Solubility In Organic Solvents Soluble in non - polar organic solvents like toluene, chloroform
Vapor Pressure Low (due to relatively high molecular weight and non - volatile nature)

As an accredited Benzene, 2,3-Difluoro-1-Iodo-4-Methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 500g of 2,3 - difluoro - 1 - iodo - 4 - methyl - benzene in a sealed chemical - grade bottle.
Storage Store “Benzene, 2,3 - difluoro - 1 - iodo - 4 - methyl -” in a cool, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container, preferably made of materials resistant to corrosion. As it is a chemical, store it separately from incompatible substances to prevent potential reactions, and ensure proper labeling for easy identification.
Shipping The chemical "Benzene, 2,3 - difluoro - 1 - iodo - 4 - methyl -" should be shipped in well - sealed, corrosion - resistant containers. Ensure compliance with hazardous material regulations, and label containers clearly for safe and proper transportation.
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Benzene, 2,3-Difluoro-1-Iodo-4-Methyl- Benzene, 2,3-Difluoro-1-Iodo-4-Methyl-
General Information
Historical Development
"Historical Development of Benzene, 2,3-Difluoro-1-Iodine-4-Methyl-Product"
The former, the field of organic chemistry, has not been explored. Benzene derivatives are gradually entering the eyes of researchers.
Benzene, 2,3-Difluoro-1-Iodo-4-Methyl-This product, its initial appearance is also, and researchers have used exquisite methods to explore its synthesis. At the beginning, it is limited to technology and knowledge, and progress is difficult. However, people are unremitting, over the years, the method is getting better. Or improve the reaction conditions, or find new reagents, in order to obtain the best method of this product. As a result, the yield has gradually increased, and the purity has also improved.
With the passage of time, this product has gradually shown its use in the fields of medicine and materials. With its special structure, it can be used in the creation of new drugs and the development of new materials. Researchers have increased their emphasis on it, exhausted its properties, expanded its application, and made its historical development path increasingly broad, contributing to the prosperity of chemistry.
Product Overview
"Chemical Description"
Today there is a substance called "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -". This is an organic compound with a unique molecular structure. On the benzene ring, fluorine, iodine and methyl are in their respective positions. Fluorine is two atoms, divided into two or three; iodine atom is the first, and methyl is in four positions.
This substance has the properties of being at room temperature, or in a liquid state, with a special odor. Due to the presence of halogen atoms and methyl groups in its structure, it is chemically active. It can participate in a variety of reactions, such as nucleophilic substitution, and halogen atoms are easily replaced by nucleophilic reagents. It can also undergo an addition reaction under specific conditions to change the unsaturation of the benzene ring. In the field of organic synthesis, it has a wide range of uses and can be used as an intermediate to prepare many compounds with biological activity or special functions, which is beneficial to chemical research and industrial production.
Physical & Chemical Properties
The physical and chemical properties of a substance called "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -" are worth exploring. The form of this substance, whether solid or liquid, depends on the conditions of temperature and pressure. Its color is colorless and transparent, or slightly yellowish, which can be distinguished.
In terms of its solubility, it may be soluble in some organic solvents, such as ethanol and ether, which is related to the intermolecular force and polarity. Its boiling point and melting point are also important characteristics. The boiling point is related to the strength of the attractive force between molecules, and the melting point reflects the characteristics of the crystal structure.
As for chemical properties, due to the presence of fluorine, iodine and other atoms, their reactivity is different. The electronegativity of fluorine atoms is strong, or the density of adjacent electron clouds changes, resulting in different selectivity of chemical reactions. Iodine atoms may also participate in reactions such as substitution and addition, which affect the chemical transformation of this substance. All of these are to be studied in detail by our generation through scientific methods to understand the true meaning of their physical and chemical properties.
Technical Specifications & Labeling
"Technical Specifications and Labeling (Product Parameters) of 2,3-Difluoro-1-Iodine-4-Methylbenzene"
On 2,3-Difluoro-1-Iodine-4-Methylbenzene, the technical specifications are the key. Looking at its shape, it should have a specific state, colorless clarification is appropriate, and there is no obvious impurity. Measure its quality, the purity should be very high, not less than [X]%, and the impurity content is minimal. Its boiling range is also fixed, about between [specific temperature range], which is related to the stability of its physical properties.
As for the logo, on the packaging, the name of the label "2,3-difluoro-1-iodine-4-methylbenzene" should not be ambiguous. And the product parameters, such as purity, molecular weight and other key data, should be marked clearly and clearly identifiable. Warning labels should also be attached to inform the possible dangers, to ensure that users are aware of its nature, aware of its risks, and careful handling, so as to meet the technical specifications and labels.
Preparation Method
To prepare 2,3-difluoro-1-iodine-4-methylbenzene (Benzene, 2,3-Difluoro-1-Iodo-4-Methyl -), the preparation method is the first raw material. 4-methyl-1,2-difluorobenzene can be used as the starting material. This raw material is stable and easy to obtain.
The reaction step is also crucial. First, mix 4-methyl-1,2-difluorobenzene and the iodine substitution reagent in a suitable reaction vessel, add an appropriate amount of catalyst, and adjust the reaction temperature and pressure. If ferric chloride is used as a catalyst, the temperature is controlled at 60-80 degrees Celsius, and the pressure is slightly higher than normal pressure, which prompts the substitution reaction between the two, and the iodine atom replaces the hydrogen atom at a specific position on the benzene ring to form the target product.
In order to ensure the efficient progress of the reaction, a reasonable catalytic mechanism needs to be constructed. A catalyst with high activity and good selectivity can be selected, and the amount of catalyst is precisely controlled. At the same time, the reaction process is closely monitored during the reaction process, and the reaction conditions are adjusted in time to improve the purity and yield of the product. In this way, this product can be obtained.
Chemical Reactions & Modifications
About the chemical reaction and modification of 2,3-difluoro-1-iodine-4-methylbenzene
There is a chemical substance called 2,3-difluoro-1-iodine-4-methylbenzene. In the field of chemistry, the reaction and modification of this substance are quite important to researchers.
Its reaction can vary depending on conditions. Or under a certain reagent or under a certain temperature and pressure, it can combine with other substances to form a new substance. In case of nucleophilic reagents, iodine atoms can be replaced, causing structural changes. This change, or the change of inductive properties and chemical properties. When
is modified, a group can be added to adjust its polarity, boiling point, solubility, etc. If a hydrophilic group is added, its solubility in water can be increased. Studying this reaction and modification can expand its application in the fields of medicine, materials, etc. Make this chemical thing work well and contribute to the progress of the world.
Synonyms & Product Names
A chemist, trying to study a thing, called "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -". The same name and trade name of this thing are quite important in the academic world.
Take the homeland and the same name, so distinguish its nature and clarify its origin. The trade name is related to the world and distribution. In "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -", its same name may vary depending on the order of discovery and the focus of research. Or according to its structure, it is ordered by the ancient chemical law, and has a similar name; or according to its nature, it is called special.
As for the name of the product, merchants want to make it easier to sell it, and also to show its advantages. Either take its utility, or show its quality, in the hope of being known and used by the world. Those who study chemistry in our generation should carefully examine its homonym and the name of the product, so that the whole state of this thing is clear. It is beneficial to the progress of chemistry and the wide use of things.
Safety & Operational Standards
Code of Safety and Operation for Products of 2,3-Difluoro-1-iodine-4-methylbenzene
Fu 2,3-difluoro-1-iodine-4-methylbenzene This substance is of paramount importance in chemical research.
First of all, it is about storage. Store it in a cool, dry and well-ventilated place. Do not be near fire or heat sources to prevent accidents. The cover is exposed to heat or open flame because of its certain chemical activity, and it is dangerous to burn or even explode. The storage device must be made of suitable materials to prevent it from reacting chemically with the wall and causing deterioration of the substance.
Secondly, when operating, all protection must be comprehensive. The operator wears protective clothing, protective gloves and goggles, so as to protect the person from harm. It is especially important to operate in the fume hood, so that the volatile gas can be discharged in time, so as not to accumulate in the room and endanger the person.
Furthermore, the method of use is also stipulated. When measuring this substance, use a precise instrument and take it according to the amount required for the experiment. Do not overdo or underdo it. When mixing, add it slowly and stir constantly to make the reaction uniform and prevent local overheating or overreaction. If the operation is wrong, if it is accidentally splashed, wipe it off with a damp cloth as soon as possible and rinse with plenty of water.
Disposal of waste should not be ignored. It should not be dumped at will, but must be properly handled in accordance with environmental regulations to prevent pollution to the environment.
In short, in the research and application of 2,3-difluoro-1-iodine-4-methylbenzene, safety and operation standards must be kept in mind at all times to ensure the smooth research and protect the safety of people and the environment.
Application Area
Today there is a thing called "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -". It has extraordinary capabilities in various application fields.
In the field of medicine, or with its unique structure, new drugs can be developed to cure various diseases. Because of its molecular properties, it may be able to accurately act on lesions, achieving twice the result with half the effort.
In material science, or can be used as a key component to create materials with special properties. With its chemical properties, it may enhance the stability and heat resistance of materials.
In organic synthesis, it is of great significance. It can provide an important starting material for the synthesis of many complex compounds, lead the expansion of the synthesis path, and open a new chapter in organic chemistry. It is actually a widely used and has infinite potential.
Research & Development
Recently, in my laboratory, I focused on a compound called "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -". This compound has a unique structure and its combination of fluorine, iodine and methyl gives many potential properties.
I first investigated the synthesis path of this compound, and after repeated experiments, optimized the reaction conditions and improved the yield. However, the process is not smooth sailing, and it is often disturbed by reaction by-products, so the ratio, temperature and time of the reactants are carefully adjusted to achieve the desired effect.
Looking forward to its development, if its properties can be further clarified, new specific drugs may be developed in the field of medicine, because the unique structure may be able to accurately act on specific targets. In the field of materials science, it may be possible to prepare materials with special properties, such as high stability and unique optical properties.
I will continue to explore, hoping to unlock more potential of this compound, contribute to scientific research progress, and promote its practical application from the laboratory to the benefit of the world.
Toxicity Research
One of the benzene under study today is called 2,3-difluoro-1-iodine-4-methylbenzene. The study of its toxicity is quite important.
Looking at this substance, the structure is unique, and fluorine, iodine and methyl are attached to the benzene ring. Fluorine and iodine are active in nature, or make this benzene have different biochemical properties. The position of methyl may also affect its toxicological behavior.
Taking the example of all kinds of poisons in the past, such benzene containing halogenated and alkyl groups may enter the organism and disrupt its biochemical order. Or disturb the metabolism of cells, hinder the activity of enzymes, and cause physiological dysfunction. And the existence of halogen atoms, or increase its fat solubility, is easy to penetrate the biofilm and spread in the body, which is even more harmful.
However, if you want to find out its true poison, you need to do more. Observe its damage to cells, observe the response of animal bodies, and analyze its changing state in the environment. After a detailed study, you can know the depth of its poison, which is a basis for protection and treatment, to prevent it from being a disaster to life and protect the ecological safety.
Future Prospects
We are currently researching a substance called "Benzene, 2,3 - Difluoro - 1 - Iodo - 4 - Methyl -". Although it is only visible in its form at present, our generation has seen the dawn of the future. This substance has a unique structure, as if it hides endless mysteries.
We are convinced that on the road of exploration in the future, we will be able to uncover its many wonderful properties. Or it can emerge in the field of medicine, providing new paths for healing various diseases; or it can shine in the world of materials, adding to the construction of novel things. Although there may be thorns in the road ahead, with the heart of research, we will be able to open the door to its potential. Looking to the future, this material will surely bloom on the stage of science, contribute to the well-being of mankind, and achieve a transformation that has never been known.
Where to Buy Benzene, 2,3-Difluoro-1-Iodo-4-Methyl- in China?
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Frequently Asked Questions

As a leading Benzene, 2,3-Difluoro-1-Iodo-4-Methyl- 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 main use of this product 2,3-difluoro-1-iodine-4-methylbenzene?
"Tiangong Kaiwu" says: "The use of this product is related to people's livelihood." However, the "2,3-diene-1-alkyne-4-methylnaphthalene" mentioned in the ancient "Tiangong Kaiwu" has not been described. In today's knowledge, this compound has a wide range of uses.
In the field of organic synthesis, it can be used as a key intermediate. Due to the unique unsaturated bond layout in the molecule, it can be used for a variety of organic reactions, such as nucleophilic addition, cyclization reaction, etc., which can be cleverly designed and transformed into complex organic molecules. This is of great significance in the creation of new drugs, functional materials and other fields. Taking drug synthesis as an example, molecular frameworks with specific biological activities can be constructed according to their structural characteristics, paving the way for the development of specific new drugs.
In the field of materials science, with its conjugated structure and special electronic properties, it may be used to prepare materials with special photoelectric properties. For example, organic Light Emitting Diode (OLED) materials, with their structural modulation, may be able to optimize luminous efficiency and color purity, improve the quality of display technology; in the field of solar cell materials, it may enhance the ability to capture light and charge transport, improve photoelectric conversion efficiency, and contribute to the development of renewable energy.
Although it is difficult for Tiangong Kaiwu to provide details of the uses of this microscopic molecule, today's science and technology are flourishing, and such compounds play a key role in many cutting-edge fields, promoting the continuous progress of human civilization and benefiting the common people.
What are the physical properties of 2,3-difluoro-1-iodine-4-methylbenzene
"Tiangong Kaiwu" said: "Alkanes are gathered in one." Methane is the simplest alkane and has unique physical properties.
First of all, its physical state, under room temperature and pressure, methane is gaseous. Because of the weak force between methane molecules, it is difficult to bind the free movement of molecules, so it mostly exists in the gas phase, colorless and formless, and can only be detected by instruments.
The density of methane is lower than that of air. According to common sense, under the same temperature and pressure, the density of gas is related to molecular weight. The molecular weight of methane is only 16, which is much lower than the average molecular weight of air about 29. It is lighter than air and can float on it.
Furthermore, in terms of its solubility, methane is extremely difficult to dissolve in water. Methane molecules are non-polar molecules, while water molecules are polar molecules. According to the principle of "similarity and dissolution", the polarities of the two are different, and the interaction is weak, causing methane to be insoluble in water and more to escape into bubbles in water.
has a boiling point and a melting point. The boiling point of methane is -161.5 ° C and the melting point is -182.5 ° C, both of which are very low. This is due to the fact that there is only a weak van der Waals force between molecules. With a little energy, the molecules can break free and change from solid to liquid and then to gas, and condense into liquid or solid in a low temperature environment.
In addition, methane is odorless, and it is difficult for ordinary people to smell its taste. However, in natural gas, odorous substances are often added in order to detect leaks. Because natural gas contains methane, it is difficult to detect the leakage of colorless and odorless methane. After adding the odor agent, once it leaks, people can quickly know by smell and prevent problems before they occur.
In summary, methane is gaseous at room temperature and pressure, has a density lower than that of air, is extremely difficult to dissolve in water, has a very low melting point and is odorless. All these physical properties are of great significance for its exploitation, storage, transportation and application. It is used by the world and should be understood in order to avoid its risks.
What are the chemical properties of 2,3-difluoro-1-iodine-4-methylbenzene?
Alas! If you want to know the chemical properties of methylaminopyridine, please listen to me in detail.
Methylaminopyridine is also a nitrogen-containing organic compound. Its molecular structure is unique, and the nitrogen atom is in it, giving it a different chemical activity.
As far as acidity and alkalinity are concerned, methylaminopyridine is weakly basic because the nitrogen atom has a lone pair of electrons. Under appropriate conditions, it can react with acids to form salts. This property makes it a base catalyst in many organic synthesis reactions, helping the reaction to proceed smoothly.
Its nucleophilicity is also worth mentioning. The lone pair electrons on the nitrogen atom make methylaminopyridine nucleophilic and can undergo nucleophilic substitution reactions with electrophilic reagents. In the field of organic synthesis, this property is often used to form new carbon-nitrogen bonds or other chemical bonds, which contribute to the creation of complex organic molecules.
Furthermore, the substituent effect of methylaminopyridine cannot be ignored. The presence of methylamino groups has an impact on the distribution of electron clouds in the pyridine ring, changing its reactivity and selectivity. In the aromatic electrophilic substitution reaction, methylamino groups are the power supply groups, which can increase the density of electron clouds in the adjacent and para-positions of pyridine ring, making it easier for electrophilic reagents to attack these two positions, thus dominating the reaction direction.
In addition, methylaminopyridine can participate in many redox reactions. Under the action of specific oxidants or reducing agents, its pyridine ring or methylamino group can undergo corresponding oxidation or reduction transformation, deriving a variety of chemical products, expanding a broad path for organic synthesis.
In short, methylaminopyridine is rich in chemical properties and has important uses in many fields such as organic synthesis and medicinal chemistry. It is also a key compound in chemical research and application.
What is the production method of 2,3-difluoro-1-iodine-4-methylbenzene?
"Tiangong Kaiwu" is a scientific and technological masterpiece written by Song Yingxing in the Ming Dynasty, and it contains many technological techniques. As for the compound "2,3-diol-1-ether-4-methylphenol", although the book does not directly correspond to the preparation method of modern chemistry, it can be prepared according to the relevant process ideas of the ancients, and traditional raw materials and techniques can be used to deduce its possible preparation methods.
In ancient times, there were many experiences in the preparation of similar organic compounds. Such as distillation, fermentation, extraction, etc. As for "2,3-diol-1-ether-4-methylphenol", plant raw materials rich in phenols and alcohols can be found. In ancient times, plant extracts were widely used, such as obtaining special ingredients from certain trees and herbs.
You can first find plants containing phenolic substances, such as some coniferous plants such as pine and cypress, whose resins or phenolic components. After crushing such plant raw materials, soak them in water or organic solvents such as rice wine, vinegar, etc. This is a common extraction method in ancient times. After soaking, the mixed liquid is obtained, and then separated and purified by distillation. Distillation was also a mature technology in ancient times. By controlling the temperature, the different boiling point components in the mixed liquid are gasified and condensed successively. Distillates containing phenolic components or precursors containing target compounds.
For the alcohol part, it can be prepared by fermentation method. The ancients made good use of grains and fruits to ferment to obtain alcohols such as ethanol. Or the fermentation product can be reacted with the above-mentioned phenol-containing fraction. Although modern precise reaction conditions were not controlled in ancient times, it may be possible to promote its binding by gentle reaction for a long time. For example, the phenol-containing fraction and the alcohol obtained by fermentation are placed in a closed container and left to stand at room temperature or slightly hot environment. During this period, some natural catalysts may need to be added, such as some plant ash, which may contain metal ions, etc. The catalytic reaction can be carried out. After a long time of reaction, it can be distilled and separated for many times, or "2,3-diol-1-ether-4-methylphenol" or its like can be obtained. Although it is difficult to achieve the purity and yield of modern chemistry, according to the idea of "Tiangongkai", traditional raw materials and operations can be used to explore their preparation methods.
What are the precautions for storing and transporting 2,3-difluoro-1-iodine-4-methylbenzene?
Acetyl is used in storage and storage, just as "Tiangong" said, there is a need to pay attention to it.
Acetyl is easy to degrade, which is the first thing to pay attention to. Its chemical activity is easy to start and degrade when it encounters common materials. If the storage environment is not properly controlled, such as the degree and temperature of acetyl are not suitable, and the quality of acetyl is affected. If the degree is high, the molecules will be strong, accelerating the degradation and reaction; if the degree is too large, the water vapor will melt, which will also promote its degradation. Therefore, it is appropriate to keep it dry and cool to maintain its activity.
Furthermore, light also affects acetyl. Light contains energy, which can lead to photochemical reaction. If the acetyl chloride is exposed to light, the molecule may be damaged or destroyed, resulting in a decrease in activity. It can be stored in an opaque container or hidden in the dark.
In addition, the interaction of the acetyl container cannot be ignored. Some materials or their reaction, adsorb acetyl, resulting in a small content. Such as some gold materials, or lead to chemical reactions, change the chemical properties of acetyl. Containers of inert materials, such as specific plastics or glass materials, should be used. The reaction of acetyl is minimal and can be properly stored.
On the way, vibration also takes into account factors. Modify the action of strong vibration or acetyl-causing molecules, affecting their activity. Therefore, it is necessary to take shock-proof measures, such as wrapping with materials, to reduce vibration.
In this regard, acetyl should be used for storage and maintenance, and the factors of caution, accuracy, lighting, equipment and vibration should be used to ensure its activity. As advocated in "Tiangong Wuwu", it is only possible to worry about governance.