3 4 Thiophenedicarboxylic Acid Diethyl Ester
quinoline thiophene imidazole thiazole

3,4-Thiophenedicarboxylic acid, diethyl ester

Taiy Chemical

    Specifications

    HS Code

    975247

    Chemical Formula C10H12O4S
    Molar Mass 228.27 g/mol
    Appearance Solid (usually white or off - white)
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform
    Boiling Point Approximately 320 - 325 °C (decomposes)
    Melting Point 64 - 66 °C
    Density 1.224 g/cm³
    Odor Faint, characteristic odor
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 3,4-Thiophenedicarboxylic acid, diethyl ester 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 diethyl 3,4-thiophenediformate?
    3,4-Dihydroxybenzophenone dimethyl ether, its main uses are as follows:
    This substance has important applications in many fields. In the field of medicine, it is often used as a key intermediate in the synthesis of many drugs. Due to its special chemical structure, it can participate in the construction of various drug molecules and help synthesize compounds with specific pharmacological activities, thus providing effective drugs for the treatment of diseases.
    In the field of materials science, its uses are also quite extensive. It can be added to a variety of polymer materials, such as plastics, rubber, etc. as an ultraviolet absorber. Because it can effectively absorb ultraviolet rays, thereby protecting these materials from ultraviolet radiation damage, prolonging the service life of materials, and improving the weather resistance of materials. For example, for plastic products used outdoors, the addition of this substance can significantly reduce the aging, discoloration, and brittleness caused by ultraviolet radiation.
    Furthermore, in the field of organic synthesis, it is an extremely important reaction raw material. With its unique functional group characteristics, it can participate in many organic chemical reactions, such as nucleophilic substitution reactions, condensation reactions, etc., providing the possibility for the synthesis of more complex organic compounds, which helps organic chemists to develop more organic materials with novel structures and properties.
    In summary, 3,4-dihydroxybenzophenone dimethyl ether plays an indispensable role in the fields of medicine, materials science, and organic synthesis, and is of great significance to promoting the development of related fields.
    What are the physical properties of diethyl 3,4-thiophenediformate
    3,4-Diethyl dichlorodiacetate is one of the organic compounds. Its physical properties are quite characteristic, and let me tell them one by one.
    Looking at its properties, it is usually a colorless to light yellow transparent liquid with a clear appearance, no obvious impurities, and may appear soft and shiny under light. Its smell is specific and irritating, and it can alert the senses. This smell can be one of the clues to identify the substance in a specific environment or operation.
    When it comes to solubility, this compound exhibits good affinity in organic solvents, such as ethanol, ether, acetone, and other common organic solvents, which can be miscible with it. This property makes it in organic synthesis and related chemical operations. It can be prepared and used by suitable organic solvents, which is convenient for reaction or substance treatment. However, its solubility in water is poor, and when it encounters water, it is often in a layered state. The upper layer is either the aqueous phase, and the lower layer is the organic liquid. This is closely related to the difference in the force between water molecules and the compound molecules.
    The boiling point is an important physical parameter of the substance. The boiling point of diethyl 3,4-dichlorodiacetate is within a specific range and boils at about a certain temperature. This boiling point characteristic is crucial in the separation and purification process. It can be effectively separated from the mixture by means of distillation and other means according to the difference in boiling points. Similarly, the melting point is also a significant property. At a specific temperature, the substance changes from a solid state to a liquid state. This transition temperature is of great significance for setting its storage, transportation and processing conditions.
    In terms of density, it is larger than water. It is placed in water and naturally settles at the bottom. This density characteristic can be used as an important basis for operators to judge the distribution and separation method of substances in some processes involving liquid-liquid separation or stratification operations.
    In addition, although its volatility is not very high, some molecules will still escape into the air under certain temperatures and environments. This characteristic requires that when storing and using, attention should be paid to ventilation and other conditions to ensure environmental safety and prevent potential hazards.
    In summary, the physical properties of 3,4-diethyl dichlorodiacetate cover many aspects such as properties, odor, solubility, boiling point, melting point, density and volatility. All properties are interrelated. Its production, application, storage and transportation all play a key role and must be familiar to chemical practitioners and related researchers.
    Is diethyl 3,4-thiophenediformate chemically stable?
    The chemical stability of 3% 2C4-diethyl dichlorodiacetate is related to many reasons. This compound has a specific structure and functional group, which are very powerful in the shaping of its chemical properties.
    Looking at its molecular structure, the existence of chlorine atoms and ester groups gives it unique reactivity. Chlorine atoms are electronegative, which can change the distribution of molecular electron clouds and affect their chemical behavior. Ester groups are often involved in hydrolysis, alcoholysis and other reactions.
    When it comes to stability, 3% 2C4-diethyl dichlorodiacetate can maintain certain stability at room temperature and pressure without external factors. In case of high temperature, strong acid, strong base or specific catalyst, its stability may be destroyed.
    Under high temperature, the kinetic energy of molecules increases, and the reactivity also rises, or causes reactions such as decomposition and rearrangement. In strong acids and strong bases, ester groups are easy to hydrolyze. When catalyzed by acid, the proton binds to the carbonyl oxygen of the ester group, and increases the positive electricity of the carbonyl carbon, which promotes the nucleophilic attack of water, causing the hydrolysis of esters into acids and alcohols; when catalyzed by bases, hydroxide ions directly attack carbonyl carbons, which also lead to ester hydrolysis, and the products are carboxylic salts and alcohols.
    In addition, the presence of light or specific oxidants and reducing agents may also affect its stability. Light can cause chlorine atoms to initiate free radical reactions and make molecular structures easier. In case of strong oxidizing agents, molecules may be oxidized; in case of strong reducing agents, or organic reduction reactions.
    Therefore, the chemical properties of 3% 2C4 -diethyl dichlorodiacetate can be said to be stable under specific conditions. However, under suitable reaction conditions, it is also prone to chemical changes and is not absolutely stable.
    What are the synthesis methods of diethyl 3,4-thiophenediformate?
    The synthesis of diethyl 3,4-dichlorodiacetate is an important issue in organic synthesis. There are many methods, each with its advantages and disadvantages, which will be described in detail today.
    First, the esterification reaction is carried out with dichloroacetic acid and ethanol as raw materials under the catalysis of concentrated sulfuric acid. This is a common method, the raw materials are easy to purchase, and the reaction conditions are not harsh. However, concentrated sulfuric acid is highly corrosive and easy to cause side reactions, such as dehydration of ethanol to form ethylene, etc., and the subsequent product separation and purification is slightly more complex. The reaction is roughly as follows: Dichloroacetic acid and ethanol are mixed in an appropriate proportion, an appropriate amount of concentrated sulfuric acid is added, and the reaction is stirred at a certain temperature. After the reaction is completed, the product is neutralized in sodium bicarbonate solution, and then the product is obtained < Br >
    Second, dichloroacetyl chloride and ethanol are used as raw materials. This method has high reactivity, fast reaction rate, and relatively few side reactions. However, dichloroacetyl chloride is active, irritating and corrosive, and special care is required for storage and handling. During the reaction, dichloroacetyl chloride is slowly dropped into ethanol to control the reaction temperature, so as to avoid violent reaction. After the reaction is completed, the product can be obtained after simple treatment, such as removing unreacted raw materials and drying.
    Third, the phase transfer catalysis method is used. This method allows the reaction to be carried out under mild conditions and improves the reaction efficiency. Usually suitable phase transfer catalysts, such as quaternary ammonium salts, are selected. In the reaction system, the catalyst can promote the rapid mass transfer of the reactants in the two phases and accelerate the reaction. This method can overcome some of the shortcomings of the traditional method, such as harsh reaction conditions and many side reactions. However, the selection and recovery of the catalyst are very critical, which is related to cost and environmental protection.
    The above synthesis methods have their own advantages. In practical application, it is necessary to comprehensively consider factors such as product purity, cost, reaction conditions and other factors, and make careful choices to achieve the best synthesis effect.
    What is the price range of diethyl 3,4-thiophenediformate in the market?
    In today's world, in the market, the price of diethyl 3,4-dichlorodiacetate is what everyone asks. However, the price of this product often changes due to factors such as current situation, origin, and quality, and it is difficult to determine.
    In the past, when the market was stable and the supply was full, its price hovered between tens and hundreds of dollars per catty. At that time, all kinds of workshops took it on demand, and they all felt that this price was still affordable.
    If in times of chaos or natural disasters, the place of origin is damaged and the supply of goods is scarce, its price will skyrocket. Or to hundreds of dollars per catty, or even thousands of dollars. At that time, all the merchants frowned, lamenting the rarity of the goods and the high price.
    Or due to the improvement of the production method, the cost has dropped slightly, and the price may also drop. Or drop to a low level of tens of dollars per catty to attract all kinds of users.
    On the quality side, the price of the excellent product is higher than that of the regular product. Its price may be more expensive than the usual product. It ranges from ten or even dozens of dollars.
    Therefore, if you want to know the current market price of 3,4-dichlorodiacetate, you must go to the market in person and consult various merchants to get an accurate number. You must not judge today's market according to the price of the past.