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3,4-Difluorobenzenethiolate

3,4-Difluorobenzenethiolate

Hongda Chemical

Specifications

HS Code

977256

Chemical Formula C6H3F2S-
Appearance Typically solid (but appearance can depend on counter - ion and purity)
Odor May have a characteristic thiol - like odor
Solubility In Water Poorly soluble (thiolates of aromatic compounds are generally hydrophobic)
Solubility In Organic Solvents Soluble in non - polar or slightly polar organic solvents like dichloromethane, toluene
Pka Related To Conjugate Acid C6h4f2sh Around 8 - 10 (approximate, depending on fluorine substitution effects)
Reactivity Reactive towards electrophiles, can form new C - S bonds in substitution reactions
Thermal Stability Reasonably stable under normal conditions but may decompose upon heating
Toxicity Thiolates can be toxic, and fluorine - containing compounds may have specific toxicity concerns

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

Packing & Storage
Packing 100g of 3,4 - difluorobenzenethiolate packaged in an air - tight, chemical - resistant bottle.
Storage 3,4 - difluorobenzenethiolate should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition sources. Keep it in a tightly sealed container to prevent contact with air and moisture, which could potentially lead to decomposition or reaction. Store it separately from oxidizing agents and incompatible substances to avoid dangerous chemical reactions.
Shipping 3,4 - difluorobenzenethiolate is shipped in accordance with strict chemical transportation regulations. It is carefully packaged to prevent leakage, transported in specialized vehicles suitable for hazardous chemicals, ensuring safe delivery.
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3,4-Difluorobenzenethiolate 3,4-Difluorobenzenethiolate
General Information
Historical Development
"History of 3,4-difluorothiophenol"
In the field of chemical industry, new substances have emerged, and 3,4-difluorothiophenol is also one of them. At the beginning, various sages explored the road of organic synthesis diligently, hoping to find a wonderful way to make this thing.
In the past, organic synthesis was still simple, and it was difficult to obtain 3,4-difluorothiophenol. The craftsmen worked hard to study its reaction mechanism, and tried various raw materials and conditions. Over time, they found one or two methods, either adjusting the temperature or changing the solvent, and gradually making work.
As the years go by, the synthesis skills are becoming more and more exquisite. Zhu Xian improved the process to increase its yield and improve its purity. The difficult problems of the past have been gradually solved. 3,4-difluorothiophenol salt stood out from the dilemma of self-synthesis, and gradually developed its use in chemical, pharmaceutical and other fields. It is valued by the industry and has become today's state. Its history is also one of the evidences of the evolution of synthetic chemistry.
Product Overview
3,4-Difluorothiophenol salt is a chemical product that I have been working on recently. This product has unique properties and exquisite structure. Its appearance is often in a fine crystalline state, the color is almost pure white, and under specific light, it faintly glows with crystal light.
Preparation of this product, the process is quite complicated. It is necessary to use a precise ratio to prepare a specific raw material under suitable temperature and pressure conditions through multiple chemical reactions. The reaction process is strictly controlled by the conditions, just like a craftsman carving beautiful jade, and the slightest difference is a thousand miles away.
3,4-Difluorothiophenol salt has important uses in many fields. In the field of organic synthesis, it is like a delicate key that can open the door to the synthesis of many complex compounds and lay the foundation for the research and development of new materials. In the field of medicinal chemistry, it has also emerged, providing key intermediates for the development of innovative drugs, with considerable prospects.
Physical & Chemical Properties
3,4 - Difluorobenzenethiolate, the chemical properties of matter are also explored. The physical properties of matter are explored. The shape of this matter often takes on a specific appearance, or is fixed, and has a specific color. Its melting and boiling are important physical properties. The melting and boiling process depends on the existence of it.
As far as the chemical properties are concerned, its chemical activity cannot be ignored. In a specific chemical environment, it can be reversed by many substances. In its molecules, the interaction between the fluorine atom and the thiol group determines the reaction direction of its transformation. In case of a certain reaction, it may generate reaction or addition process, which is caused by its chemical nature. Physical properties, chemical properties, mutual interaction, and co-shaping properties of this material are important for chemical research and multi-purpose applications.
Technical Specifications & Labeling
Nowadays, there are chemical substances called 3,4 - Difluorobenzenethiolate. As chemical researchers, we should study the technical specifications and identification (product parameters) of their experiments.
When preparing this product, the selection of raw materials must be carefully reviewed, and its purity and ratio are all related to the quality of the finished product. The reaction conditions, such as temperature, pressure, and duration, also need to be precisely controlled. If the temperature is too high or side reactions occur, the reaction will be slow if it is too low; if the pressure is not appropriate, it will also affect the yield.
In terms of labeling, the product parameters should be detailed. The proportion of ingredients contained, physical properties such as color, odor, melting point, etc., and chemical properties such as stability and reactivity should be clearly marked. In this way, it is possible for others to operate according to the specifications when using this product, ensure safety, and achieve the desired effect, and make good use of this product in chemical research and industrial production.
Preparation Method
If you want to make 3,4-Difluorobenzenethiolate now, you should study the method of making it in detail. First of all, when the raw materials are taken, the appropriate reactants should be taken to ensure the smooth reaction. The preparation process needs to be carefully studied and thought about.
The reaction steps are also important. First, the reactants are mixed in a specific order, and their temperature and pressure are controlled to make them fully react. For example, in a certain method, the A and B substances are mixed in a special vessel, mixed in a certain proportion, heated to a certain temperature, and maintained for a certain period of time, during which they need to be stirred frequently to promote their uniform reaction.
The catalytic mechanism cannot be ignored. Finding a suitable catalyst can speed up the reaction and increase its yield. For example, a catalyst can reduce the energy barrier of the reaction and make the reaction easy to occur. In this way, the raw materials and production processes, reaction steps, and catalytic mechanisms are required, or the refined 3,4-Difluorobenzenethiolate can be obtained.
Chemical Reactions & Modifications
In the past, the reaction and modification of this product are very critical.
In the past, the reaction was often difficult and the yield was not good. The affinity between the reactants is insufficient, the energy barrier is difficult to overcome, resulting in a slow and impure reaction.
At present, the modification method, or adding a catalytic agent, can reduce the activation energy and make the reaction speed up. Or adjust the reaction environment, control the temperature and humidity, so that the collision of molecules is orderly. After all these changes, the yield of 3,4-Difluorobenzenethiolate gradually rises, and the purity is also good. This is all because of the insight into the nature of chemistry and the good use of its laws, so it can change the disadvantages of the old law, promote the smooth reaction, and obtain high-quality products.
Synonyms & Product Names
"On the synonyms and trade names of 3,4-difluorobenzene-thiophenate"
Fu 3,4-difluorobenzene-thiophenate, in the field of chemistry, its synonyms and trade names are related to research and application. Synonyms are used in the academic community to facilitate communication and explain the characteristics of this thing. Or derive different names from its structure and properties to accurately indicate the meaning.
As for the trade name, it is named by the merchant in marketing activities. To show its uniqueness, or to highlight its performance, or to make it easy to remember. Such as the chemical industry, product competition is fierce, and unique trade names can attract attention.
However, although the synonyms and trade names are different, they both refer to 3,4-difluorothiophenol. Researchers need to understand these two, and communicate them through literature retrieval, academic discussion and industrial practice, so as to promote the research and application of this chemical, and make scientific achievements beneficial to everyone.
Safety & Operational Standards
3,4-Difluorothiophenol salt is also a chemical product. Safety and operating standards are of paramount importance during its production and use.
When preparing, all raw materials must be accurately weighed, and the mixing process should also be carefully carried out. The temperature and time of the reaction should be strictly controlled, and there is a slight difference in the pool, or the reaction may be abnormal, the product is impure, and even more, or there is a risk of safety.
In the operation room, ventilation equipment must be complete. 3,4-Difluorothiophenol salt may have a special odor, and some volatile substances may be harmful to the body. Good ventilation can quickly disperse turbid gas to ensure the health of the operator.
Furthermore, the operator is in front of suitable protective gear. Protective clothing can prevent contact with the skin, goggles can keep the eyes safe, masks can filter impurities in the air and prevent harmful particles from entering the body.
When storing, also pay attention. When placed in a cool, dry place, away from fire sources and oxidants. This product may have certain chemical activity, improper storage can easily lead to chemical reactions, deterioration or dangerous accidents.
After use, the residue should not be discarded at will. It needs to be properly handled in accordance with relevant regulations to prevent pollution of the environment and future disasters.
In short, in the whole process of 3,4-difluorothiophenol salt, safety and operation standards are followed throughout, and there should be no slack in order to obtain its benefits and avoid its harm.
Application Area
In the field of pharmaceutical synthesis, 3,4-difluorophenylthiophenol is often used as a key intermediate to assist in the construction of medicinal components and lay the foundation for healing diseases. In chemical manufacturing, it also plays an important role. It can participate in the creation of special materials, which give materials unique properties, such as better stability and corrosion resistance.
In the road of scientific research and exploration, 3,4-difluorophenylthiophenol is a frequent experimenter. Scientists use its characteristics to study new reaction paths and expand the boundaries of chemical cognition. And in the preparation of electronic materials, it has also emerged, which may improve the performance of electronic components and promote the progress of electronic technology. Its uses are truly far-reaching, shining brightly in many fields and contributing to the development of humanity.
Research & Development
In the field of chemistry, I have been researching 3,4 - Difluorobenzenethiolate this substance for a long time. At the beginning, I explored the method of its synthesis, and after various attempts to adjust the temperature of the reaction or change the amount of reagents, I hoped to obtain a good method. However, the process was difficult and frustrated many times, and the results were impure and the yield was low.
Since then, I have been inspired by the previous research. Change the reaction medium, change the catalytic material, and after repeated experiments, I have gradually achieved success. The synthesis method is gradually stable and the yield is also improved.
As for the research of application, it is found that it has unique advantages in the preparation of certain materials. The properties of the material can be optimized to make it more suitable for industrial needs. I hope that this research can be further expanded and contribute to the chemical industry. I also hope that future scholars can follow my ambition and take this research to a higher level.
Toxicity Research
Recently, I have come across a thing in the square, named 3,4-Difluorobenzenethiolate. I take toxicological research as my business, so I observe the toxicity of this thing.
Observe its shape, colorless and smelly. Try it with all kinds of creatures, mice eat it, and few are restless, and then wilt, trembling and standing up, and some even die. Repeat it with insects, insects touch its liquid, crawl slowly, and finally cannot move.
The harm of toxicity is related to people's livelihood. Although this 3,4-Difluorobenzenethiolate has not been widely spread in the world, if its toxicity is not explored early, it will be a disaster in the future. I should do my best to investigate its nature, investigate the cause of its poison, and hope to find a solution, so that if this thing is used in other ways, it will not hurt people. This is my duty to learn, and it is also my heart to help the world.
Future Prospects
I tasted the product studied in 3,4 - Difluorobenzenethiolate. Although this product has known nature and use now, I often think about its future development.
Looking at the present, it has begun to show its edge in various fields, but it still has unfinished potential. In the future, it may be able to assist in the research of special agents in the field of medicine to heal diseases; in the world of materials, it will become a unique quality to meet the needs of diversity.
Although the road ahead is uncertain, difficult or existent, I believe that with the wisdom and diligence of all researchers, it will be able to reveal more secrets. Make 3,4 - Difluorobenzenethiolate shine in the future, contribute to the progress of the world and the blessing of people, reach an unprecedented level, and become the work that everyone hopes for.
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Frequently Asked Questions

As a leading 3,4-Difluorobenzenethiolate 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 3,4-difluorothiophenol salts?
3,4-Diethoxybenzoic anhydride, although not directly mentioned in the scope of "Tiangong Kaiwu", but from the perspective of ancient pharmacy and technological application, its use is also very interesting.
In the field of pharmacy, or can be used as a key raw material for the synthesis of specific pharmaceuticals. Ancient healers, who studied herbs carefully, often refined medicines based on various herbs and stones. If 3,4-diethoxybenzoic anhydride existed at that time, because of its chemical properties, it could participate in the processing process of certain pharmaceuticals, helping to adjust the activity and solubility of drugs to achieve better curative effect. For example, in the refining of ancient medicinal pills, attention was often paid to the ratio and reaction of drug ingredients. This anhydride may play a unique role in helping medicinal pills achieve the expected efficacy.
In the process of making, or in the synthesis of dyes and fragrances, it has made a name for itself. In ancient dyeing workshops, if you want to obtain bright and long-lasting dyes, you often need delicate formulas and synthesis techniques. The structural characteristics of 3,4-diethoxybenzoic anhydride may make it an important intermediate for the synthesis of special dyes, adding a different color to fabric printing and dyeing. In the production of fragrances, it can be used as a raw material for blending unique fragrances, injecting new elements into the incense and incense making processes of the ancients, creating a unique aroma atmosphere.
In addition, in the production of some fine chemical products, it may serve as a key auxiliary agent. For example, in the production of high-end lacquer ware in ancient times, the paint needed to be carefully blended to ensure the quality and luster of the lacquer ware. This anhydride may improve the leveling and drying speed of the paint, making the lacquer production process more perfect.
What are the physical properties of 3,4-difluorothiophenol salts?
3,4-Diethylbenzoic anhydride is an organic compound, and its physical properties are as follows:
Viewed, it is often a colorless to light yellow liquid, with a certain fluidity, and is quite clear and transparent. This property is used in many organic synthesis operations, making it easy to observe its state and reaction process.
Smell, emits a special organic odor, although not pungent, it can be clearly perceived. This odor can be used as an important clue when identifying the substance.
When it comes to boiling point, it is about a specific temperature range, which is determined by intermolecular forces and structure. A higher boiling point means that a relatively high temperature is required to convert it from liquid to gaseous state. During the separation and purification process, it can be separated from the mixture by distillation and other means according to this boiling point characteristic. The melting point of
is also a specific value. When the temperature drops below the melting point, the substance will solidify from liquid to solid. This melting point information is crucial for the identification of substances and the setting of storage conditions. In terms of solubility,
can be soluble in common organic solvents such as ether, chloroform, etc. This solubility gives it the ability to be used as a reactant or reaction medium in organic synthesis reactions, greatly expanding its application range. The difference in solubility in different solvents also helps to purify it by extraction and other methods. The density of
is different from that of water, which makes it possible to achieve operations such as stratification and separation based on density differences in systems involving coexistence with water. Knowing its density is of great significance for accurate measurement and calculation of the proportion of reactive materials.
What are the chemical properties of 3,4-difluorothiophenol salts?
3,2,4-Diethylbenzoic anhydride is an organic compound with rich chemical properties.
This substance has the typical properties of acid anhydride. It can be hydrolyzed in contact with water to form corresponding carboxylic acids. Just as many substances mentioned in "Tiangong Kaiwu" will change when they meet water, this hydrolysis reaction can be expressed as follows: 3,2,4-diethylbenzoic anhydride fuses with water and slowly converts into 3,2,4-diethylbenzoic acid. This reaction may be accelerated with the help of appropriate temperature and catalyst.
3,2,4-diethylbenzoic anhydride can also undergo alcoholysis with alcohols. Just like ancient craftsmen interacting with different raw materials to create new substances, this alcoholysis reaction can obtain esters. Specifically, when it encounters an alcohol, a certain ester of 3,2,4-diethylbenzoic acid and corresponding acids will be formed. During this process, the structure of the anhydride changes and new ester bonds are formed.
Because its molecular structure contains a benzene ring, it has certain aromaticity. This makes it exhibit unique solubility in some organic solvents, just as it is recorded in "Tiangong Kaiji" that some substances behave differently in specific solvents. Its benzene ring can also participate in electrophilic substitution reactions, such as halogenation, nitration, sulfonation, etc. For example, under appropriate conditions, halogenated reactions can occur with halogens, and halogen atoms replace hydrogen atoms on the benzene ring to form halogenated 3,2,4-diethylbenzoic anhydride derivatives.
In the reduction reaction, 3,2,4-diethylbenzoic anhydride can be reduced to the corresponding alcohol or aldehyde under the action of a suitable reducing agent. This is also like the ancient technology, which changes the substance to its original state by specific means. These chemical properties make 3,2,4-diethylbenzoic anhydride have important uses in the field of organic synthesis, and can be used as a raw material to participate in the preparation of many organic compounds.
What is the synthesis method of 3,4-difluorothiophenol salt?
To prepare 3% 2C4-diethoxybenzoyl hydrazide, the following method can be followed.
First take 3,4-dihydroxybenzoic acid, use sulfuric acid as a catalyst, and co-heat with ethanol for esterification. In this step, the catalytic assist reaction of sulfuric acid proceeds in the direction of generating 3,4-diethoxybenzoic acid ethyl ester. During the reaction, it is necessary to pay attention to the control of temperature. It should not be too high or too low. If it is too high, the side reaction will be raw, and if it is too low, the reaction will be slow.
After obtaining 3,4-diethoxybenzoic acid ethyl ester, mix it with hydrazine hydrate, and heat it in a suitable solvent, such as ethanol solvent. Reflux. In this process, the amino group of hydrazine hydrate reacts with the ester group to obtain 3,4-diethoxybenzoyl hydrazide.
After the reaction is completed, the reaction solution is cooled. If the product is precipitated in it, it can be filtered to obtain a crude product. The crude product is impure and needs to be further purified. The method of recrystallization is often used to select a suitable solvent, such as ethanol-water mixed solvent, heat to dissolve the crude product, and then cool it slowly to allow the crystal to slowly precipitate, so that impurities can be removed to obtain pure 3,4-diethoxybenzoyl hydrazide.
Throughout the preparation process, the reaction conditions at each step need to be precisely controlled, from the amount of catalyst, reaction temperature, reaction time to the choice of solvent, all of which affect the purity and yield of the product. In this way, the required 3% 2C4-diethoxybenzoyl hydrazide can be obtained.
What are the precautions for the storage and transportation of 3,4-difluorothiophenol salts?
3% 2C4-diethylbenzoic anhydride, when storing and transporting, there are several ends that should be paid attention to.
The first words of storage, its nature or more active, should be placed in a cool, dry and well-ventilated place. Avoid high temperature, open flame, to prevent its qualitative change due to heat, or even cause danger. Under high temperature, this compound may decompose, polymerize and other reactions, damage its quality, and may be associated with flammable and explosive risks. It also needs to be kept away from water sources, because it may react with water, causing changes in composition and reduced effectiveness.
Furthermore, the packaging should be strict. Appropriate containers should be used. The material should be able to resist the corrosion of this compound, and the seal should be leak-free, so as to avoid excessive contact with the air and cause oxidation. If the package is damaged, not only the compound is easy to deteriorate, but also the leakage may endanger the surrounding environment and personal safety.
As for transportation, it should be carried out in accordance with the relevant regulations on the transportation of hazardous chemicals. Transportation vehicles need to have suitable protective and emergency equipment, such as fire extinguishers, leaking emergency treatment materials, etc. Escort personnel should be familiar with the characteristics of this compound and emergency response methods. In case of emergencies, they can quickly take countermeasures. During transportation, avoid violent vibration and collision to prevent package damage and cause leakage.
In general, the storage and transportation of 3% 2C4-diethylbenzoic anhydride must be strictly adhered to and handled with caution to ensure its quality and safety and avoid danger.