Hongda Chemical
Products
Home  /  Products  / 

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

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

Hongda Chemical

Specifications

HS Code

684395

Chemical Formula C7H5F2NO2
Molecular Weight 173.12
Appearance Solid (Typical description, actual may vary)
Solubility In Water Low (Aromatic nitro - fluoro compounds generally have low water solubility)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane (Typical for such compounds)
Vapor Pressure Low (Based on its nature as a solid aromatic compound)

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

Packing & Storage
Packing 1,2 - difluoro - 3 - methyl - 4 - nitro - benzene in 100g bottles for chemical packaging.
Storage 1,2 - difluoro - 3 - methyl - 4 - nitro - benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container, preferably made of corrosion - resistant materials, to prevent leakage and exposure to air and moisture, which could potentially lead to decomposition or reaction.
Shipping 1,2 - difluoro - 3 - methyl - 4 - nitro - benzene, a chemical, is shipped in specialized, well - sealed containers. Strict safety protocols are followed, adhering to regulations for handling and transporting hazardous chemicals to ensure safe transit.
Free Quote

Competitive 1,2-Difluoro-3-Methyl-4-Nitro-Benzene prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8615365186327 or mail to info@alchemist-chem.com.

We will respond to you as soon as possible.

Tel: +8615365186327

Email: info@alchemist-chem.com

1,2-Difluoro-3-Methyl-4-Nitro-Benzene 1,2-Difluoro-3-Methyl-4-Nitro-Benzene
General Information
Historical Development
1,2-Difluoro-3-methyl-4-nitrobenzene is also a chemical product. At the beginning, many scholars studied diligently in the field of chemistry and achieved something. At the beginning, they explored the properties and production methods of this compound. After several years and many attempts, they achieved little success.
In the early days, due to technology and cognition, progress was slow. However, scholars are determined and study unremitting. Gradually, they have come to understand the reaction conditions, raw material ratio, etc., and the preparation method is slightly better.
With the passage of time and the advancement of science and technology, the analytical methods have become more refined, and the understanding of its structure and characteristics has deepened. Its potential is gradually revealed in the fields of medicine and materials. The arduous exploration of the past has laid the foundation for today's applications, and it is expected to shine in more fields in the future. This is the path of its development.
Product Overview
There is now a compound called 1,2-difluoro-3-methyl-4-nitrobenzene. It is an organic compound with a unique chemical structure. Look at its molecule, containing fluorine, methyl and nitro groups.
This compound has attracted much attention in chemical research. The introduction of fluorine atoms can change the physical and chemical properties of the compound, such as enhancing its lipid solubility and affecting its reactivity. The presence of methyl groups also plays a role in the spatial structure of the molecule and the distribution of electron clouds. Nitro is a strong electron-absorbing group, which makes the compound exhibit a specific reaction tendency.
In the field of organic synthesis, 1,2-difluoro-3-methyl-4-nitrobenzene can be used as a key intermediate, participating in many organic reactions, laying the foundation for the preparation of more complex and functional compounds, and may have potential applications in medicinal chemistry, materials science, etc.
Physical & Chemical Properties
In the case of 1,2-difluoro-3-methyl-4-nitrobenzene, its material has unique physicochemical properties. Looking at its shape, under room temperature, or a colorless to light yellow liquid, with a special smell, such as musk orchid in the room, although it is subtle and observable.
On the point of its melting, the melting point is quite low, like a cold plum and frost, not afraid of cold; the boiling point is moderate, like the temperature of spring, and not strong. Its density is heavier than water, and it sinks when placed in water, like a stone falling into the abyss.
In terms of solubility, in organic solvents, it is like a fish getting water, and it blends very well. In water, it is like an oil floating in water, and it is difficult to be one. Its chemical properties are active, fluorine, methyl, and nitro groups interact with each other, such as a group of wise men, co-evolving chemical changes. When encountering nucleophiles, they often react, like warriors facing an enemy, without flinching. This is also the physical and chemical properties of 1,2-difluoro-3-methyl-4-nitrobenzene.
Technical Specifications & Labeling
1,2-Difluoro-3-methyl-4-nitrobenzene, the process specification and identification (product parameters) of this product are the key. The preparation method of Guanfu must follow strict procedures. The material ratio is accurate, the reaction conditions are carefully controlled, and the temperature and pressure are fixed to ensure the purity and quality of the product.
In terms of its identification, the product parameters are clearly marked, from the proportion of ingredients to the physical and chemical properties, all of which should be detailed. On the packaging, there should also be a prominent logo, indicating danger warnings, storage instructions, etc. In this way, the production, circulation and use of this chemical can be in an orderly manner, which not only ensures the demonstration of efficacy, but also protects the safety of personnel and the environment.
Preparation Method
The method of preparing 1,2-difluoro-3-methyl-4-nitrobenzene is related to the raw materials and production process, reaction steps and catalytic mechanism. The selection of raw materials needs to be cautious, and it is better to choose the appropriate one. In the production process, the first step is orderly.
At the beginning of the reaction, the raw materials are mixed according to a specific ratio and under suitable temperature and pressure. First make a preliminary change of a reactant, and then introduce other materials, step by step. In this reaction step, the time and conditions need to be strictly controlled to ensure that the reaction is complete.
The catalytic mechanism is also critical. The selection of the appropriate catalyst can promote the reaction to accelerate and improve the rate of product. It acts on the reaction path, changing the process of the chemical reaction, but does not consume itself. In this way, 1,2-difluoro-3-methyl-4-nitrobenzene is prepared in an exquisite way, which adds to chemical research and production.
Chemical Reactions & Modifications
Taste the industry of chemical industry, focus on the change of substances, in the 1,2-difluoro-3-methyl-4-nitrobenzene, often study the wonder of chemical reaction and modification.
For those who chemically react, this substance participates in various reactions, and the conditions are different, but the products are different. Or when the temperature and pressure are moderate and the catalyst is appropriate, the molecules are rearranged, and the new group is bonded to form a new substance. However, its reaction path is often subtle and difficult to predict, such as the road of maze, if you want to get a smooth way, you must study the mechanism in detail, and observe the properties of the reactants and changes in the environment.
As for modification, it is intended to improve its performance. Or increase its stability, so that it does not change in bad conditions; or enhance its activity, so that the reaction is more smooth. Suitable groups can be introduced by means of substitution and addition to achieve the purpose of modification. However, modification is not easy, and it involves the whole body. It is necessary to think carefully and weigh the advantages and disadvantages before making 1,2-difluoro-3-methyl-4-nitrobenzene as useful as it can be, adding bricks to the chemical industry and benefiting the world.
Synonyms & Product Names
1,2-Difluoro-3-methyl-4-nitrobenzene is very important in our chemical research. There are many aliases, such as difluoromethyl-nitrobenzene, and there are various trade names.
This chemical substance has unique properties. Between reactions, it can often cause different changes due to its special structure. Or combine with other substances, or the way to cause reactions is different.
Our generation of chemical researchers have studied its characteristics in detail, hoping to open up new horizons. By exploring its various names and trade names, the industry's understanding and application of this substance can also be understood. In the experimental platform, repeated trials, hoping to explore its mysteries, add to the field of chemistry, so that this 1,2-difluoro-3-methyl-4-nitrobenzene can play a greater role and benefit the world.
Safety & Operational Standards
Specifications for the safety and operation of 1,2-difluoro-3-methyl-4-nitrobenzene
F 1,2-difluoro-3-methyl-4-nitrobenzene is an important substance in chemical research. In its experimental operation and use, safety regulations are of paramount importance.
First word storage. This substance should be placed in a cool, dry and well ventilated place, away from fires and heat sources. Because it has certain chemical activity, it is dangerous to be exposed to heat or open flames, so it must be careful. And should be stored separately from oxidizing agents, reducing agents, alkalis, etc., must not be mixed to prevent chemical reactions from occurring, resulting in safety risks.
As for the operation, the experimenter must wear appropriate protective equipment. Wear protective clothing to prevent substances from contacting the skin; wear protective gloves to avoid direct contact with hands; wear eye protection to protect your eyes from damage. The operation process must be carried out in a fume hood to allow the volatile gas to be discharged in time to avoid the experimenter's inhalation and damage to health.
Furthermore, when using this substance, take the specification according to the exact amount. Use appropriate measuring tools, such as pipettes, balances, etc., to obtain accurate dosage, not only to avoid waste, but also to prevent accidents caused by improper dosage. And the operation action should be steady and slow, do not let the material splash out. If accidentally splashed, should be dealt with immediately according to the established procedures. Small splashes can be absorbed by inert materials such as sand and vermiculite, and properly disposed of after collection; if a large amount of splashes, personnel must be evacuated, the scene must be sealed, and the professional staff will clean it up.
During the reaction process, pay close attention to the reaction conditions. Temperature, pressure, reaction time and other factors are all related to the success or failure of the reaction and safety. Operate strictly according to the predetermined reaction process, and must not be changed without authorization to prevent accidents.
In conclusion, in the research and use of 1,2-difluoro-3-methyl-4-nitrobenzene, safety and operation standards are the cornerstone of ensuring personnel safety and smooth experimentation, and must not be ignored.
Application Area
1,2-Difluoro-3-methyl-4-nitrobenzene is also a chemical substance. Its field of use is quite wide. In the development of medicine, it can be used as a key intermediate to help synthesize specific drugs to treat various diseases and save people. In the field of materials science, it also has wonderful uses. It can be used to pre-create novel materials with specific properties, such as excellent stability and unique optics, which contribute to material innovation. And in the domain of electronic chemistry, it can help to make high-performance electronic components, so that electronic devices are more efficient and perform better. From this point of view, 1,2-difluoro-3-methyl-4-nitrobenzene plays a pivotal role in many application fields, and is also important for scientific research and industry.
Research & Development
I am dedicated to the research and development of 1,2-difluoro-3-methyl-4-nitrobenzene. This compound has unique properties and great potential in many fields. At the beginning, I explored its synthesis path. After repeated experiments, I encountered many obstacles, and the control of raw material ratio and reaction conditions was a difficult problem. However, I was not discouraged. I dedicated myself to studying ancient books and previous accounts, and also learned from new technologies today. Finally, I found a method that can stabilize the synthesis of this substance with good purity. Looking at its development today, it has been gradually used in medicine, materials, etc. However, there are still challenges, such as cost control for large-scale production and improvement of application efficiency. I should make unremitting efforts to explore in depth, with the hope of expanding its application, promoting its better development, and assisting both academia and industry to achieve better results and benefit the world.
Toxicity Research
Modern chemistry has advanced, and the study of toxicants has become increasingly important. In today's discussion of 1,2-difluoro-3-methyl-4-nitrobenzene, the toxicity study of this chemical is crucial.
The toxicity of this chemical is related to the safety of living beings. Although it is a product that is occasionally used in industry or scientific research, its toxicity cannot be ignored. In its molecular structure, fluorine, nitro and other groups may cause special toxic effects.
After various experiments, it can damage the visceral functions in animals, such as the genus of liver and kidney, causing its physiological disorder. And this substance may have the risk of potential mutagenesis, affecting genetic material and involving later generations.
Therefore, anyone involved in this substance must strictly abide by the procedures to prevent its leakage and not harm sentient beings. Toxicity research should continue to clarify its harm and ensure the safety of life in the world.
Future Prospects
Today, there is a product called 1,2-difluoro-3-methyl-4-nitrobenzene. In the field of our chemical research, its future prospects are quite impressive.
This product has a unique structure and specific properties. Our generation expected that it may be a key raw material in the process of organic synthesis. With its fluorine, methyl and nitro properties, it can introduce different reaction paths and create novel compounds. This may be of extraordinary use in the creation of new drugs, functional materials and other fields.
Looking at the future, with the rapid advancement of science and technology, the methods of analysis and detection will improve the refinement, and the solution to its properties and reaction mechanism will also be more profound. At that time, we will be able to make better use of this thing, expand the boundaries of its application, contribute to the development of chemistry and the well-being of mankind, and draw a beautiful blueprint, so that it will bloom in the unfinished path.
Where to Buy 1,2-Difluoro-3-Methyl-4-Nitro-Benzene in China?
As a trusted 1,2-Difluoro-3-Methyl-4-Nitro-Benzene 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 1,2-Difluoro-3-Methyl-4-Nitro-Benzene 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 1,2-difluoro-3-methyl-4-nitrobenzene?
1% 2C2-diene-3-methyl-4-tert-butylbenzene is an important raw material for organic synthesis. In the field of organic chemistry, it is often a key starting material for the construction of complex organic molecules.
Due to its unique molecular structure, 1,2-diene endows molecules with active reactivity and can participate in various chemical reactions, such as electrophilic addition and cyclization. The existence of 3-methyl and 4-tert-butyl not only affects the spatial configuration of molecules, but also has significant effects on their physical and chemical properties. The electronic effects and steric resistance effects of methyl and tert-butyl can regulate the selectivity and rate of reactions.
In the field of materials science, polymer materials with special properties can be synthesized from this material. Due to its structural properties, the obtained materials may have good thermal stability, mechanical properties and chemical stability, and can be applied to high-end fields such as aerospace and automobile manufacturing.
In the field of pharmaceutical chemistry, it may be an important intermediate for the synthesis of new drugs. By modifying and modifying its structure, it is expected to develop drugs with unique pharmacological activities and contribute to human health.
In addition, in the field of fine chemicals, it can be used to synthesize fine chemicals such as fragrances and dyes, giving products unique properties and quality. Overall, 1% 2C2-diene-3-methyl-4-tert-butylbenzene has important uses in many fields and is an indispensable key compound in organic chemistry and related industries.
What are the physical properties of 1,2-difluoro-3-methyl-4-nitrobenzene?
1% 2C2-diene-3-methyl-4-carbonylbenzene is an organic compound. Its physical properties are as follows:
Looking at its properties, it is mostly a crystalline solid at room temperature. Due to the strong intermolecular force, it has a relatively stable solid structure. As for the color, it is often white when it is pure, but if it contains impurities, it may appear yellowish.
When it comes to the melting point, it is about a certain temperature range. At this temperature, the thermal motion of the molecule intensifies enough to overcome the lattice energy and cause the solid state to transform into a liquid state. This melting point characteristic is of great significance for its phase change and separation and purification under specific conditions.
The boiling point also has a certain value. When the temperature rises to the boiling point, the molecule obtains enough energy to break free from the liquid phase and transform into a gaseous state. This property is crucial in separation processes such as distillation.
This substance has little solubility in water. Due to its weak molecular polarity and small force between water molecules, it is difficult to form a stable mixed system with water. However, it has good solubility in organic solvents, such as some aromatics or halogenated hydrocarbon solvents. Because its molecular structure is similar to that of organic solvents, it follows the principle of "similar miscibility".
In addition, 1% 2C2-diene-3-methyl-4-carbonyl benzene has a certain volatility. At room temperature and pressure, some molecules can escape from the surface and enter the gas phase, so that they can be detected in the air. And because its molecular structure contains specific functional groups, it absorbs specific wavelengths of light, which can be traced in the field of spectral analysis, and can be aided by spectral characteristics for qualitative and quantitative analysis.
Is the chemical property of 1,2-difluoro-3-methyl-4-nitrobenzene stable?
The stability of 1% 2C2-diene-3-methyl-4-tert-butylbenzene depends on many chemical principles.
Looking at its structure, the part of 1% 2C2-diene contains a conjugated double bond system. The conjugated structure often imparts a special electron delocalization effect to the molecule, making it stable to a certain extent. The electron cloud interaction between the conjugated double bonds can reduce the energy of the molecule, just like building a stable electronic structure, which improves the stability to a certain extent.
Furthermore, the substituents of 3-methyl and 4-tert-butyl also affect the molecular stability. Methyl and tert-butyl are alkyl groups with electron donor induction effect. The electron donor action can increase the electron cloud density of the benzene ring, which is beneficial to the stability of the benzene ring system. And tert-butyl is large in size, resulting in a steric hindrance effect. Although this spatial effect may hinder the reagents from approaching the benzene ring in some reactions, from another angle, it can block the attack of external small molecules on the benzene ring or diene structure, and protect the overall stability of the molecule.
However, the stability is not absolute. Under certain conditions, 1% 2C2-diene-3-methyl-4-tert-butylbenzene will also react. In case of strong oxidants, the conjugated double bond is easily oxidized, destroying its conjugated structure and causing loss of stability. Another example is extreme conditions such as high temperature and light, or cause intramolecular rearrangement, free radical reactions, etc., which change the molecular structure and affect the stability.
In summary, under normal conditions at room temperature and pressure, 1% 2C2-diene-3-methyl-4-tert-butylbenzene conjugate structure, alkyl electron donor effect and tert-butyl steric resistance have certain stability. However, in case of special chemical environment or reaction conditions, its stability or damage needs to be carefully judged according to the specific situation.
What are the synthesis methods of 1,2-difluoro-3-methyl-4-nitrobenzene?
The synthesis method of 1% 2C2-diene-3-methyl-4-cyanobenzene, although the ancient book "Tiangong Kaiwu" does not directly describe the synthesis of such compounds, it contains chemical process ideas or can inspire modern synthesis. The following is an ancient saying:
To form 1% 2C2-diene-3-methyl-4-cyanobenzene, modern methods often rely on exquisite techniques of organic chemistry. First, benzene substrates containing alkenyl groups and methyl groups can be started. First, an appropriate halogenation reagent is used to halogenate the benzene ring at a specific position of the substrate. This step requires mild conditions to avoid damaging the activity of the alkenyl group. For example, catalyzed by iron halide, it reacts with halogen elementals at low temperatures, so that halogen atoms precisely fall at the predetermined check point to obtain halogenated aromatics.
Then, a cyanide group is introduced. Cyanide reagents, such as potassium cyanide or sodium cyanide, can be used to undergo nucleophilic substitution with halogenated aromatics with the help of a phase transfer catalyst. This process requires strict temperature control and reaction time, and side reactions such as cyanohydrolysis are prevented, so that intermediates containing cyanide groups can be obtained.
Furthermore, a 1% 2C2-diene structure is constructed. Or use Wittig reaction to react with a carbonyl-containing compound with a suitable phosphorus-ylide reagent. After ingenious design, the ene is generated based on the target position and the configuration is controllable. Or use Heck reaction to catalyze the reaction of halogenated aromatics and olefins with palladium catalyst to achieve the purpose of constructing a diene structure.
After the reaction is completed, the product often contains impurities and needs to be purified by column chromatography and recrystallization to obtain pure 1% 2C2-diene-3-methyl-4-cyanobenzene. Although "Tiangong Kaiwu" does not detail this specific synthesis, its principles of various material changes and process regulation are implicit in today's synthesis ideas, seeking precise control and efficient transformation. In the path of chemical exploration, it is in the same vein from ancient to modern times.
What should be paid attention to when storing and transporting 1,2-difluoro-3-methyl-4-nitrobenzene?
1% 2C2-diene-3-methyl-4-cyanobenzene is highly toxic and must be stored and transported with extreme caution.
First, the storage place must be a cool, dry and well-ventilated place. This is because the substance is active in nature, and the high temperature and humid environment can easily trigger its chemical reaction, causing it to deteriorate or even risk exploding. As "Tiangong Kaiwu" says: "Where you hide something, you must choose a good place according to its nature." And it needs to be separated from oxidizing agents, acids, bases and other substances, because it can react violently with many substances.
Second, the choice of storage containers is crucial. Corrosion-resistant and well-sealed containers must be used to prevent leakage. "If the equipment is not good, it will be easy to leak, and the disaster will not be far away." The inspection of the sealing of the container should also be carried out regularly to ensure that there is no danger.
Third, strict regulations and procedures must be followed during transportation. Transport personnel must be professionally trained to be familiar with their dangerous characteristics and emergency treatment methods. Transportation vehicles should also be equipped with corresponding emergency equipment and protective supplies, such as fire extinguishers, leakage emergency treatment tools, etc. "When walking on the road, safety must be given priority, and no slack should be allowed."
Fourth, no matter whether it is stored or transported, obvious warning signs should be set up to make everyone aware of the danger and avoid accidents. This is a necessary measure to ensure the safety of people and goods and must not be ignored.