Benzo B Thiophene 2 Carbaldehyde
quinoline thiophene imidazole thiazole

Benzo[b]thiophene-2-carbaldehyde

Taiy Chemical

    Specifications

    HS Code

    109330

    Chemical Formula C9H6OS
    Molar Mass 162.21 g/mol
    Appearance Yellow to orange solid
    Melting Point 37 - 41 °C
    Boiling Point 150 - 152 °C at 11 mmHg
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Flash Point 110 °C
    Density 1.309 g/cm³
    Pka No significant acidic hydrogens (no common pKa value applicable in normal conditions)
    Odor Characteristic odor

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    General Information
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    Frequently Asked Questions

    As a leading Benzo[b]thiophene-2-carbaldehyde 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 Benzo [b] thiophene-2-carbaldehyde?
    Benzo [b] thiophene-2-formaldehyde, which has an aldehyde group, is an active functional group, causing it to have many unique chemical properties.
    First, it is oxidizing. The aldehyde group can be oxidized. In case of weak oxidant Torun reagent (silver ammonia solution), a silver mirror reaction can occur. The aldehyde group is oxidized to a carboxyl group to precipitate silver elemental. This reaction is often used for the identification of aldose. In case of strong oxidants such as potassium permanganate, it can also be oxidized, and the product is usually benzo [b] thiophene-2-formic acid.
    Second, it is reducing. The carbon and oxygen double bonds in the aldehyde group can be reduced, and hydrogen is used as a reducing agent. Under the action of suitable catalysts such as nickel and palladium, the aldehyde group can be reduced to a hydroxyl group to generate benzo [b] thiophene-2-methanol.
    Third, nucleophilic addition reaction can occur. The carbon and oxygen double bonds in the aldehyde group make the carbon atom partially positive due to the strong electronegativity of the oxygen atom, making it vulnerable to attack by nucleophilic reagents. For example, under acid catalysis with alcohols, semi-acetals are formed first, and then acetals are formed. Addition with hydrocyanic acid can obtain cyanoalcohol products, and this reaction can grow the carbon chain.
    Fourth, can participate in the condensation reaction. With compounds containing active hydrogen, such as ketones, esters, etc., under alkali catalysis, condensation reactions such as hydroxyaldehyde condensation can occur to generate products with carbon-carbon double bonds, which are important methods for building carbon skeletons in organic synthesis.
    In short, benzo [b] thiophene-2-formaldehyde is chemically active due to the presence of aldehyde groups, and is widely used in the field of organic synthesis. Various organic compounds can be prepared through various reactions.
    What are the synthesis methods of Benzo [b] thiophene-2-carbaldehyde
    The method of preparing benzo [b] thiophene-2-formaldehyde has been explored by many scholars in the past, and each has shown his wisdom, so several ways have been formed.
    First, benzo [b] thiophene is used as the starting material, and the bromination reaction is first carried out to introduce benzo [b] thiophene into the bromine atom at a specific position. In this bromination method, liquid bromine or N-bromosuccinimide (NBS) can be selected as the bromine source. In an appropriate solvent, such as dichloromethane, supplemented by light or an initiator, the reaction can proceed smoothly to obtain bromobenzo [b] thiophene. Then, the brominated product is interacted with metal magnesium to make Grignard reagent. This Grignard reagent has good activity, and then reacts with N, N-dimethylformamide (DMF). After hydrolysis, benzo [b] thiophene-2-formaldehyde can be obtained. Although this path is slightly complicated, the reaction conditions of each step are relatively mild and the yield is considerable.
    Second, starting from o-aminophenol, it is first reacted with maleic anhydride, and then cyclized and dehydrated to form benzo [b] thiophene-2-carboxylic acid derivatives. Subsequently, this carboxylic acid derivative is reduced, and strong reducing agents such as lithium aluminum hydride can be used to reduce the carboxyl group to the aldehyde group, so as to obtain the target product. The starting material of this method is relatively easy to obtain, but the reduction step needs to be carefully operated. Due to the high activity of lithium aluminum hydride, it is easy to react violently in contact with water.
    Third, using thiopheno [2,3-b] pyridine as raw material, through appropriate oxidation and rearrangement reaction, benzo [b] thiophene-2-formaldehyde can also be prepared. This route uses the activity of the pyridine ring to skillfully guide the reaction, but the reaction mechanism is relatively complex, and the control of the reaction conditions is strict. It is necessary to precisely adjust the parameters such as temperature and pH to obtain satisfactory results.
    All these methods have advantages and disadvantages. Experimenters should consider various factors such as the cost of raw materials, the difficulty of reaction, and the high or low yield according to their own needs, and choose the most suitable method to achieve the preparation process.
    Benzo [b] thiophene-2-carbaldehyde in which areas
    Benzo [b] thiophene-2-formaldehyde is useful in various fields.
    In the field of medicine, it can be used as a key raw material for the synthesis of many drugs. Due to the unique chemical structure of benzo [b] thiophene-2-formaldehyde, specific functional groups can be introduced by organic synthesis to create compounds with special pharmacological activities. If used to synthesize anti-tumor drugs, its structure modification can enable the drug to precisely act on specific targets of tumor cells and inhibit the proliferation and metastasis of tumor cells; in the development of antibacterial drugs, it can be used to build core structures, endow drugs with antibacterial effect, fight against various pathogenic bacteria, and provide effective drugs for clinical treatment of infectious diseases.
    In the field of materials science, it can also be seen. It can be used to prepare organic materials with special functions. Due to its structural characteristics, through specific reactions and treatments, materials with excellent optical properties can be prepared, such as those used in organic Light Emitting Diodes (OLEDs). In OLED materials, compounds derived from benzo [b] thiophene-2-formaldehyde can be used as light-emitting layer materials. With its unique electronic structure, high-efficiency electroluminescence can be achieved, and the luminous efficiency and color purity of OLEDs can be improved. It contributes to the development of display technology.
    In addition, in the field of pesticide chemistry, there is no shortage of its applications. It can be used as an important intermediate for the synthesis of new pesticides. Through chemical synthesis, it is converted into pesticide components that have high-efficiency poisoning effects on pests or growth regulation functions on crops. It can accurately target the physiological characteristics of specific pests, interfere with their normal physiological activities, achieve green and efficient pest control, ensure the yield and quality of crops, and play an important role in agricultural production.
    In short, benzo [b] thiophene-2-formaldehyde has shown important application value in many fields such as medicine, materials, and pesticides, promoting technological innovation and development in various fields.
    What is the market price of Benzo [b] thiophene-2-carbaldehyde
    There is a question today, what is the market price of benzo [b] thiophene-2-formaldehyde. This is an organic chemical, and its market price is variable and difficult to determine.
    First, it is related to the production process. If the preparation method is exquisite and the cost is controlled, the price may be stable and suitable. If an efficient catalytic synthesis path is used, the raw material utilization rate is high, the side reactions are few, and the cost can be reduced, and the price may be close to the people. However, if the process is complicated, expensive reagents and harsh conditions are required, and the price must be high.
    Second, the price of raw materials is the main factor. In the synthesis of benzo [b] thiophene-2-formaldehyde, the price of raw materials fluctuates, and its price also follows. If raw materials are scarce, or their acquisition is difficult, the supply is small and there are many people seeking them, and the price will increase. If the special sulfur source and benzene source used are used, if the market supply is tight, the price will increase, and the price of this compound will also increase.
    Third, the supply and demand of the market is the key. If many industries, such as pharmaceutical research and development, material preparation, etc., the demand for benzo [b] thiophene-2-formaldehyde is strong, but the supply is limited, and the price will rise. On the contrary, if the demand is weak, manufacturers will build up inventory and reduce prices for promotion.
    Fourth, regional differences also have an impact. Different places have different prices due to differences in economy, logistics, policies, etc. Prosperous cities, with strong demand, smooth materials, or high prices; remote places, with less demand, inconvenient transportation, or low prices.
    Fifth, the quality is divided into different prices. High purity is suitable for high-end scientific research and pharmaceutical production, and the price is high; ordinary purity is used in general industry, and the price is low.
    To sum up, in order to know the exact price of benzo [b] thiophene-2-formaldehyde, it is necessary to carefully examine the production process, raw material price, supply and demand status, local differences and quality, etc., in order to understand its general outline.
    What are the storage conditions for thiophene-2-carbaldehyde?
    This thiophene-2-formaldehyde is a kind of organic compound. Its storage principle is quite important.
    When stored, the first thing is the dryness of the environment. This thing is afraid of moisture, and if it is in a wet environment, it is easy to deteriorate. Cover dampness can cause its hydrolysis and isochemical reaction, which will damage its quality. Therefore, it must be placed in a dry place, and it can be accompanied by a dry agent to maintain its dry state.
    Second, temperature is also critical. It should be stored in a cool place to avoid hot topics. Because hot topics can promote their separation or risk ignition and explosion. Generally speaking, it is suitable for storage in a freezer at 2-8 ° C. If this temperature cannot be reached, it should be controlled at a slightly lower room temperature and should not be exposed to sunlight. Light can actinize and damage its structure.
    Furthermore, the choice of receptacle should not be ignored. It should be stored in a glass or plastic bottle, and it must be well sealed. Glass and plastic can be separated from external objects, so as not to contact with air, water, etc. Sealing can prevent its volatilization, keep it thick, and avoid responding to external objects.
    In addition, the storage place must be good. If the gas does not flow, the volatile gas of this object can accumulate, which can cause explosion. And it can reduce the harm of its gas to the things and people in the storage.
    Repeat, this thing should be stored separately from other things. Do not store it with strong oxygen agents, acids, alkalis, etc. Cover it or play with it, leading to a dangerous scene.
    In short, if you want to store benzo [b] thiophene-2-formaldehyde well, you must observe the rules of dryness, coolness, sealing, communication and sub-storage, so as to protect its quality and avoid danger.