5 Formylthiophene 3 Boronic Acid
quinoline thiophene imidazole thiazole

5-FORMYLTHIOPHENE-3-BORONIC ACID

    Specifications

    HS Code

    214269

    Name 5-Formylthiophene-3-boronic acid
    Chemical Formula C5H5BO3S
    Molar Mass 154.97 g/mol
    Appearance Solid (usually white or off - white)
    Solubility In Water Moderately soluble in polar solvents like water
    Melting Point 158 - 162 °C
    Purity Typically available in high purity (e.g., 95%+)
    Boiling Point Decomposes before boiling
    Reactivity Reactive towards nucleophiles and electrophiles due to the formyl and boronic acid groups

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    Frequently Asked Questions

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    What are the chemical properties of 5-formylthiophene-3-boronic acid?
    5-Ethylheptyl ether-3-carboxylic acid is an organic compound with unique chemical properties and is widely used in the field of organic synthesis.
    This compound has the characteristics of both ether and carboxylic acid. In terms of ether properties, the ether bond in 5-ethylheptyl ether-3-carboxylic acid is relatively stable, and it has certain resistance to common oxidizing agents, reducing agents and bases. For example, in an alkaline environment, ether bonds are usually not easily broken and can maintain structural stability.
    The carboxylic acid part of the compound exhibits typical acidic characteristics. The compound can neutralize with bases to generate corresponding carboxylate and water. For example, when reacted with sodium hydroxide, 5-ethylheptyl ether-3-carboxylic acid and sodium water are formed. This reaction is often used in organic synthesis to separate and purify mixtures containing this compound. By adjusting the pH, it is converted into water-soluble carboxylic salts, thereby separating it from other organic impurities.
    5-ethylheptyl ether-3-carboxylic acid can also participate in esterification reactions. Under the action of catalysts such as concentrated sulfuric acid, it can react with alcohols to form esters and water. For example, when reacted with ethanol, it will form 5-ethylheptyl ether-3-carboxylic acid ethyl ester and water. This reaction is of great significance in fragrance and drug synthesis, and the ester compounds generated often have unique aromas or biological activities.
    In addition, the carboxyl groups in this compound can also undergo reduction reactions. Under the action of specific reducing agents, the carboxyl groups can be reduced to alcohol hydroxyl groups, which in turn provides more reaction check points and possibilities for subsequent organic synthesis.
    The chemical properties of 5-ethylheptyl ether-3-carboxylic acids are rich and diverse, and these properties have laid a solid foundation for their applications in many fields such as organic synthesis, drug research and development, and materials science.
    What are the main uses of 5-formylthiophene-3-boronic acid?
    5-Ethylheptyl ether-3-carboxylic acid is an organic compound with a wide range of uses and important value in many fields, as detailed below:
    1. ** Pharmaceutical field **: Often a key intermediate in drug synthesis. Drug molecules with specific pharmacological activities can be constructed by combining with other compounds through specific chemical reactions. Due to its unique chemical structure, it can endow drugs with suitable solubility, stability and biological activity, which is of great significance for improving drug efficacy and reducing toxic and side effects. For example, in the development of some anti-inflammatory and antibacterial drugs, this compound can be modified to become an active ingredient, or help the active ingredient to function better.
    2. ** Material Science Field **: Plays an important role in the synthesis of polymer materials. It can be introduced into polymer as a monomer or modifier to change the material properties. For example, when preparing special plastics and rubber, adding an appropriate amount of this compound can enhance the flexibility and corrosion resistance of the material, and broaden the application range of the material. In the field of coatings, it can optimize the film-forming performance of coatings, improve the adhesion, wear resistance and weather resistance of coatings.
    3. ** Fragrance and Flavor Industry **: Because of its unique odor characteristics, it can become a raw material for blending fragrances and flavors. It can add a unique fragrance to the product, and it can be applied in perfumes, air fresheners, detergents and other products to give the product a pleasant aroma and improve the product quality and market competitiveness.
    4. ** Organic synthesis field **: As an important building block for organic synthesis, it provides a basic structural unit for the synthesis of complex organic compounds. Chemists can build more organic compounds with novel structures and unique functions through various organic reactions, such as esterification reactions, substitution reactions, and addition reactions, based on their structures, and promote the development of organic synthesis chemistry.
    What are the synthesis methods of 5-formylthiophene-3-boronic acid?
    There are several methods for synthesizing 5-methylbenzyl ether-3-sulfonic acid. One method can also make 5-methylbenzyl alcohol interact with the sulfonating reagent. First take an appropriate amount of 5-methylbenzyl alcohol and place it in a clean reaction vessel. The device should be made of glass to observe the reaction. Then slowly add the sulfonating reagent, such as concentrated sulfuric acid, etc., with caution and constant stirring to prevent local overheating and side reactions. During the reaction, it is appropriate to control its temperature and place the device in a water bath to maintain the constant temperature. In this way, the sulfonic acid group can be gradually attached to the 5-methylbenzyl group to obtain 5-methylbenzyl ether-3-sulfonic acid.
    Another method can first prepare 5-methylbenzyl halide, such as 5-methylbenzyl chloride. Take 5-methylbenzyl alcohol and a halogenating agent, such as sulfoxide chloride, mix it in an appropriate ratio, and react under suitable conditions. After the reaction is completed, 5-methylbenzyl chloride is purified by conventional methods. Then the halide interacts with the sulfonate phase, such as with the aqueous solution of sodium sulfite, under heating and stirring, the halogen atom is substituted with the sulfonate, and the final product is 5-methylbenzyl ether-3-sulfonic acid.
    There are also those who use 5-methylbenzaldehyde as the starting material. 5-methylbenzaldehyde is first reduced to 5-methylbenzyl alcohol. This reduction can be done by metal hydrides such as sodium borohydride. After obtaining 5-methylbenzyl alcohol, follow the above method of sulfonation, or directly react with the sulfonation reagent, or first prepare the halogen and then react with the sulfonate to form 5-methylbenzyl ether-3-sulfonic acid. All kinds of methods have their own advantages and disadvantages, and it is necessary to choose them carefully depending on the ease of availability of raw materials, the difficulty of operation, and the high or low yield.
    What should be paid attention to when storing and transporting 5-formylthiophene-3-boronic acid?
    5-Methylheptyl ether 3-boronic acid should pay attention to the following things when it is stored in the environment:
    The first environment is dry. Boric acid is easy to absorb, and the moisture content will be changed in the environment, which will affect its chemical properties. The phase of 5-methylheptyl ether is fixed. However, when it is wet, it may also degrade due to reactions such as hydrolysis. Therefore, when it is dry, it is also necessary to prevent it, and it can be used to cover it.
    The control of the second degree. Boric acid may decompose or decompose at high temperatures, resulting in boron trioxide and other substances. 5-Methylheptyl ether has ether properties, and the high temperature increases its rate, and may cause ignition or explosion. It is best to store it in the dark, avoid direct light, and control it in the dark, especially in summer, when the anti-oxidation degree is high.
    Furthermore, both need to be oxidized. Boric acid can be oxidized and changed. 5-Methylheptyl ether encounters oxidation, or causes strong reactions, leading to safety accidents. Store in the dark, do not mix with oxidation.
    In addition, 5-methylheptyl ether is flammable, and it is prohibited to store open flames and fire protection equipment. Packages need to be well sealed to prevent leakage. Once leaked, 5-methylheptyl ether will escape to the air, or cause fire or explosion; Boric acid leakage may also contaminate the environment. It needs to be determined according to the quality of the product, by the manufacturer, the user, the warning, and the emergency management measures.
    What is the market price of 5-formylthiophene-3-boronic acid?
    In today's world, the price of 5-methylfurfural-3-sulfonic acid in the market is a matter of concern to everyone. This compound is important in the chemical industry, medicine and other fields, and its price is also influenced by many reasons.
    The first to bear the brunt is the price of raw materials. The system of 5-methylfurfural-3-sulfonic acid, the raw material of Chang Wai's special decision, if the production of raw materials is affected by changes in weather, geographical conditions, and policies and the price rises, the cost of 5-methylfurfural-3-sulfonic acid will also increase, and the market price will rise.
    Furthermore, the fineness of the process. If the manufacturing process is advanced, the yield is high and the quality is excellent, the unit cost may be reduced, and the market price may tend to be flat; however, the manufacturing process is stagnant, the yield is low and the wear and tear is high, and the price will rise.
    There is also supply and demand in the market. If the demand for this product increases sharply in the chemical, pharmaceutical and other industries, and the supply is small, the price will jump; if the supply exceeds the demand, the price may fall.
    In addition, policy and regulations also have an impact. Environmental protection regulations, quality inspection regulations, etc., can cause changes in production costs, which in turn affect the market price.
    As for the exact price of 5-methylfurfural-3-sulfonic acid in the market, it is difficult to generalize from time to time and from place to place. In the prosperous capital of Dayi, due to the prosperity of demand and the convenience of business flow, the price may be different from remote places; at different times, with the change of supply and demand, the price of raw materials, There are also differences. To know the exact price, when you consult the industry's Jia Shang, research institutions, or observe the real market conditions, you can get a more accurate number.