Benzo B Thiophene 3 Ol
quinoline thiophene imidazole thiazole

Benzo(b)thiophene-3-ol

Taiy Chemical

    Specifications

    HS Code

    411155

    Chemical Formula C8H6OS
    Molar Mass 150.2 g/mol
    Appearance Solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

    As a leading Benzo(b)thiophene-3-ol 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 physical properties of Benzo (b) thiophene-3-ol?
    Benzo (b) thiophene-3-ol is one of the organic compounds. Its physical properties are particularly important and related to the various applications of this compound.
    Looking at its properties, benzo (b) thiophene-3-ol is often in a solid state at room temperature and pressure, due to the intermolecular forces. Its color may be white to light yellow. The appearance of this color is due to the characteristics of molecular structure on light absorption and reflection.
    When it comes to melting point, benzo (b) thiophene-3-ol has a specific melting point value. The melting point is the critical temperature at which a substance changes from a solid state to a liquid state. The melting point of this compound is within a certain range, and this value is crucial for its purification and identification. By measuring the melting point, the purity can be determined. If the melting point is consistent with the theoretical value, the purity is higher; if there is a deviation, it may contain impurities.
    Furthermore, its solubility is also an important physical property. Among common organic solvents, benzo (b) thiophene-3-ol may have a certain solubility. For example, in some polar organic solvents, the degree of solubility varies, which is related to the interaction between the solvent and the solute molecule. Polar solvents and the polar groups of benzo (b) thiophene-3-ol molecules attract each other, so that dissolution can occur. In water, its solubility is poor, due to the weak interaction between water molecules and the compound molecules.
    In addition, the density of benzo (b) thiophene-3-ol also has its own characteristics. The density is the mass of the substance per unit volume, and this value reflects the degree of tight packing of its molecules. The density value is a certain value under specific conditions. In chemical production and experimental operations, it is quite instructive to determine the measurement and mixing ratio of materials.
    In summary, the physical properties of benzo (b) thiophene-3-ol, such as its properties, melting point, solubility, and density, play a key role in its application in chemical synthesis, materials science, and other fields. Only by understanding these properties can we make good use of this compound.
    What are the chemical properties of Benzo (b) thiophene-3-ol?
    Benzo (b) thiophene-3-ol, this is an organic compound with specific chemical properties. It is weakly acidic, because a small amount of hydrogen atoms in the hydroxyl group can be ionized, and can react with bases under specific conditions to form corresponding salts.
    It is nucleophilic, because the oxygen atom in the hydroxyl group contains lone pair electrons, which can attack electron-deficient atoms or groups and act as nucleophilic reagents in nucleophilic substitution reactions. Under suitable conditions, it can react with electrophilic reagents such as halogenated hydrocarbons to form new carbon-oxygen bonds.
    Benzo (b) thiophene-3-ol also has certain aromatic properties. Because the benzothiophene ring is a conjugated system, the electron cloud distribution is uniform, the structure is relatively stable, and the electrophilic substitution reaction like aromatic hydrocarbons can occur, such as halogenation, nitrification, sulfonation, etc. And because the hydroxyl group is an ortho and para-site, the electrophilic substitution reaction mainly occurs in the ortho and para-site of the hydroxyl group.
    In addition, the compound can participate in the addition reaction because it contains multiple unsaturated bonds. For example, under suitable catalyst and reaction conditions with hydrogen, some unsaturated bonds on the benzothiophene ring can be hydrosaturated to achieve structural transformation. Its chemical properties are rich and diverse, and it is widely used in the field of organic synthesis. It can be used as a key intermediate for the synthesis of complex organic compounds, and a series of reactions can be used to construct multi-ring systems or introduce multi-functional groups.
    Where is Benzo (b) thiophene-3-ol used?
    "Tiangong Kaiwu" was written by Song Yingxing in the Ming Dynasty. It is based on the ancient classical Chinese style. Today, I want to answer the question of "Benzo (b) thiophene-3-ol is applied in which fields". It is as follows:
    Benzo (b) thiophene-3-ol is used in various fields. First, in the field of medicinal chemistry, this compound is often the key raw material for the creation of new drugs. Due to its unique chemical structure, it can be used to construct complex drug molecular structures, which can help to develop good drugs for specific diseases, such as anti-inflammatory and anti-tumor drugs, which are expected to cure diseases and benefit the health of the world. < Br >
    Second, materials science, also see its presence. Or it can be used to prepare organic materials with special properties, such as photoelectric materials. Based on this, substances with excellent photoelectric conversion properties can be prepared, which can be used in solar cells and other devices to improve the efficiency of light energy conversion and contribute to the development of new energy; or used to synthesize high-performance fluorescent materials, which shine in optical display, biological imaging, etc., making the image clearer and more gorgeous.
    Third, in the field of organic synthetic chemistry, Benzo (b) thiophene-3-ol is an important synthetic block. Chemists can use their unique reactivity to generate many organic compounds with novel structures and specific functions through various chemical reactions, expanding the boundaries of organic synthesis, opening up new paths for chemical research and industrial production, and promoting the vigorous development of organic chemistry.
    What are the synthesis methods of Benzo (b) thiophene-3-ol?
    There are many different methods for preparing benzo (b) thiophene-3-ol. One common method is to start with benzothiophene and introduce hydroxyl groups through a specific reaction. First, benzothiophene is placed in a suitable solvent, and it is exposed to strong oxidants, such as peroxides, to oxidize the sulfur atom, and then under appropriate conditions, the hydroxyl group is replaced in the 3-position. This process requires precise temperature control, time control, and strict requirements for the reaction environment to avoid side reactions and impure products.
    Another method uses compounds containing sulfur and benzene rings as raw materials and is obtained by multi-step reaction. First, the basic structure of benzothiophene is constructed by condensation reaction, and then the hydroxyl group is placed at the 3-position through selective hydroxylation reaction. In this condensation reaction, a specific catalyst is often required to promote the smooth progress of the reaction. In the hydroxylation step, suitable reagents and conditions need to be selected to achieve the ideal yield and selectivity.
    Others use halogenated benzothiophene as the starting material. First, the halogenated benzothiophene is encountered with a nucleophile, which can carry hydroxyl groups or groups that can be converted into hydroxyl groups through reaction. During the reaction, depending on the activity of the halogen atom, the appropriate reaction conditions need to be selected, or heating or using a phase transfer catalyst to increase the reaction rate and yield. After the reaction is completed, pure benzo (b) thiophene-3-ol can be obtained after subsequent treatment, such as separation and purification.
    All synthesis methods have their own advantages and disadvantages. When choosing the method, the most suitable synthesis path can be found after considering the availability of raw materials, cost, difficulty of reaction and product purity and other factors.
    What are the market prospects for Benzo (b) thiophene-3-ol?
    Wen Jun inquired about the market prospect of benzo (b) thiophene-3-ol. This product has great potential in various fields of chemical industry.
    Looking at the way of medicine, with the advance of medical technology, many new drugs need characteristic intermediates for research and development. Due to its unique structure, benzo (b) thiophene-3-ol may be the key raw material for the creation of new drugs. It may emerge in the exploration of drugs for the treatment of nervous system diseases and tumors, so the rise of pharmaceutical research and development will lead to an increase in demand for this product.
    As for the field of materials, the development of electronic and optical materials is changing with each passing day. Benzo (b) thiophene-3-ol may enter the field of high-end material research and development due to its own photoelectric properties. Such as organic Light Emitting Diode (OLED) materials, if they can be added with optimized performance, the market demand for them will increase significantly.
    Furthermore, in the field of agricultural chemicals, the creation of new pesticides is the general trend. Benzo (b) thiophene-3-ol may be the basis for the development of high-efficiency and low-toxicity pesticides. It is expected to become an important component in the development trend of pesticides that ensure food security and are environmentally friendly, leading to a rise in market demand.
    However, its market also faces challenges. The complexity and high cost of the synthesis process may hinder its large-scale application. If the process is not optimized and the cost is difficult to reduce, it will be difficult to gain an advantage in the market competition. And regulations and regulations are becoming increasingly stringent, and their production and use must be compliant, which is also a concern for the industry.
    In summary, benzo (b) thiophene-3-ol has a bright future, but it needs to break the barriers of processes and regulations. If the industry can make efforts in this way, it will be able to achieve good results in the market.