4 Methylthiophene 2 Boronic Acid
quinoline thiophene imidazole thiazole

4-Methylthiophene-2-boronic acid

    Specifications

    HS Code

    954174

    Chemical Formula C5H7BO2S
    Molecular Weight 141.98
    Appearance White to off - white solid
    Melting Point 135 - 140 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, tetrahydrofuran
    Purity Typically high - purity products are 95%+
    Boiling Point Decomposes before boiling

    As an accredited 4-Methylthiophene-2-boronic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive 4-Methylthiophene-2-boronic acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: info@alchemist-chem.com

    General Information
    Where to Buy 4-Methylthiophene-2-boronic acid in China?
    As a trusted 4-Methylthiophene-2-boronic acid 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 4-Methylthiophene-2-boronic acid 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 chemistry of 4-Methylthiophene-2-boronic acid?
    4-Methylthiophene-2-boronic acid, which is active and easy to react in contact with water. Appearance is often white to light yellow crystalline powder, which can maintain a certain stability in the air, but when the humidity is high, it is easy to interact with water and cause deterioration.
    This product has the typical properties of boric acid, is weakly acidic, and can produce borate esters with alcohols. Due to the existence of thiophene ring and methyl group, it also has special electronic properties and spatial structure. Thiophene ring is rich in electrons, which increases its adjacent and para-site activity, and the methyl donator effect also affects the distribution of molecular electron clouds and enhances its electrophilic substitution reaction activity.
    In organic synthesis, 4-methylthiophene-2-boronic acid is an important angle and is often used as an intermediate. By the Suzuki-Miyaura coupling reaction, it is connected with halogenated aromatics or halogenated olefins to form carbon-carbon bonds and combine complex organic molecules. Due to the excellent properties of thiophene rings in materials science, such as good photoelectric properties, the compounds are reacted into polymers or functional materials to produce materials with special photoelectric properties. When storing, it is necessary to avoid water and moisture, and it should be stored in a dry and cool place to maintain its chemical stability, prevent deterioration-induced activity loss, and play its due role in organic synthesis and material preparation.
    What are the main uses of 4-Methylthiophene-2-boronic acid?
    4-Methylthiophene-2-boronic acid, which has a wide range of uses. In the field of organic synthesis, it is often a key intermediate. Gein boric acid groups have unique reactivity and can react with many organic halides, alkenyl halides, etc., through Suzuki coupling reaction to form carbon-carbon bonds. In this way, organic compounds with diverse structures can be synthesized, such as complex aromatics and heteroaromatics. In the field of medicinal chemistry, it helps to develop new drug molecules and provides a path for the creation of compounds with specific biological activities.
    Furthermore, in the field of materials science, it is also indispensable. Through Suzuki coupling reaction, organic materials with specific photoelectric properties can be prepared. For example, the synthesis of conjugated polymer materials, which exhibit excellent optoelectronic properties in organic Light Emitting Diode (OLED), organic solar cells and other devices, can improve the performance and efficiency of the device.
    In addition, in the field of pesticide chemistry, it also plays an important role. It can be used to synthesize pesticide ingredients with high insecticidal, bactericidal or herbicidal activities. By constructing a specific molecular structure, the effect of pesticides on target organisms is enhanced, while reducing the adverse impact on the environment, which is in line with the current trend of green pesticide development. In conclusion, 4-methylthiophene-2-boronic acid has important uses in many chemical-related fields due to its unique reactivity, promoting the development and innovation of various fields.
    What is the synthesis method of 4-Methylthiophene-2-boronic acid?
    In the synthesis of 4-methylthiophene-2-boronic acid, there are several important ones. One method is to use 4-methylthiophene as the starting material. First, 4-methylthiophene is interacted with a halogenating agent. If bromine ($Br_2 $) is used in an inert solvent under suitable reaction conditions, at low temperature and in the presence of a catalyst, a halogenation reaction can occur, so that halogen atoms are introduced into a specific position on the thiophene ring to generate 4-methyl-2-halothiophene. This halogenation reaction needs to be carefully controlled. Too high or too low temperature may affect the selectivity and yield of the reaction. < Br >
    The obtained 4-methyl-2-halothiophene is then reacted with a metal reagent. If it is reacted with magnesium chips in an ether solvent such as anhydrous ether or tetrahydrofuran, through the action of an initiator, the Grignard reagent 4-methyl-2-thiophenyl magnesium bromide can be formed. The preparation of this Grignard reagent has strict requirements on the anhydrous and oxygen-free reaction system. Because the Grignard reagent is extremely active, it is easy to decompose in contact with water or oxygen, resulting in the failure of the reaction.
    Then, 4-methyl-2-thiophenylmagnesium bromide is reacted with a borate ester, such as trimethyl borate ($B (OCH_3) _3 $). The reaction is initiated at a low temperature, gradually warmed to a suitable temperature and maintained for a certain period of time. After the reaction is completed, the borate ester can be converted into the target product 4-methylthiophene-2-boric acid after the hydrolysis step and treated with a dilute acid solution. The concentration and reaction time of the acid during hydrolysis also need to be precisely controlled to avoid side reactions or decomposition of the product.
    Another method can use the coupling reaction catalyzed by palladium. In the presence of palladium catalysts such as tetra (triphenylphosphine) palladium ($Pd (PPh_3) _4 $) and suitable bases, such as potassium carbonate ($K_2CO_3 $), the reaction is heated in an organic solvent using 4-methylthiophene-2-halide and diphenylthiophene-2-borate as raw materials. This reaction requires high activity of palladium catalyst, amount of base and reaction temperature control. After the reaction is completed, pure 4-methylthiophene-2-boronic acid can be obtained through separation and purification steps such as column chromatography with suitable eluent. Although the steps of this synthesis are more complicated, the yield and selectivity may be considerable, and it is also a commonly used method in the field of organic synthesis.
    What are the precautions for 4-Methylthiophene-2-boronic acid during storage and transportation?
    4-Methylthiophene-2-boronic acid is a commonly used reagent in organic synthesis. When storing and transporting, many things must be paid attention to.
    When storing, the first environment is dry. This substance is prone to react in contact with water and cause it to deteriorate, so it should be stored in a dry and ventilated place, away from water sources and moisture. In addition, the temperature needs to be controlled. Generally speaking, it should be stored in a cool environment to avoid high temperature. High temperature may cause it to decompose or accelerate the deterioration process.
    During transportation, the packaging must be sturdy. To prevent damage to the packaging due to vibration and collision, so that the material can leak. The packaging materials used must have good sealing and corrosion resistance to resist possible chemical reactions. It is necessary to prevent moisture during transportation. If it is transported in humid weather, effective moisture-proof measures must be taken, such as using moisture-proof packaging or placing desiccant in the transportation vehicle.
    In addition, because of its certain chemical activity, transportation and storage should avoid contact with strong oxidants, strong bases and other substances to prevent violent chemical reactions and endanger safety. It is necessary to strictly follow the specifications and standards for the storage and transportation of relevant chemical substances, so as to ensure the stability and safety of 4-methylthiophene-2-boronic acid during storage and transportation, and avoid damage to its quality or safety accidents due to improper operation.
    What is the market price of 4-Methylthiophene-2-boronic acid?
    4-Methylthiophene-2-boronic acid, the price of this product in the market often changes due to many reasons. If we take the ancient style of "Tiangong Kaiwu", the price of all things in the world is determined by the balance of supply and demand, the difficulty of making, and the quality.
    As far as 4-methylthiophene-2-boronic acid is concerned, if the preparation method is complex and the materials used are thin, the price will be high. Such as the ancient rare utensils, which require exquisite craftsmanship, take a long time, and require rare materials, their price is naturally high. If the preparation of this acid is simple and the materials used are common, the price will be low. < Br >
    And the situation of market supply and demand is also the main reason. If there are many people in need, and there are few suppliers, such as water in a dry time, the price will rise; if the supply exceeds the demand, it will be like the valley of abundant years, and the price will decline.
    Furthermore, the quality of its quality is also related to the price. Those who are of high quality, such as carefully selected beautiful jade, have a high price; those who are of inferior quality, such as mixed stones, have a low price.
    If you want to know its market price, you still need to observe the current chemical market, consult merchants, and compare prices before you can obtain an approximate value. It cannot be based on common sense speculation alone, but must be based on actual investigation.