6 Methylbenzo B Thiophene
quinoline thiophene imidazole thiazole

6-Methylbenzo[b]thiophene

Taiy Chemical

    Specifications

    HS Code

    285288

    Chemical Formula C9H8S
    Appearance Solid (usually)
    Melting Point Data needed
    Boiling Point Data needed
    Density Data needed
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents
    Odor Characteristic odor (data needed for details)
    Stability Stable under normal conditions
    Flash Point Data needed
    Vapor Pressure Data needed
    Pka Data needed

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    General Information
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    Frequently Asked Questions

    As a leading 6-Methylbenzo[b]thiophene 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 chemical properties of 6-methylbenzo [b] thiophene?
    6-Methylpurino [b] quinoline is an organic compound. Its chemical properties are unique. Its structure contains a fused system of purine and quinoline, and there is a methyl group at the 6th position.
    From the words of acidity and alkalinity, due to the nitrogen atom, it can react with acids to form salts, which is weakly basic. But under different environments, the acidity and alkalinity may change.
    When it comes to reactivity, methyl groups can undergo substitution reactions. If under appropriate conditions, methyl hydrogen can be replaced by halogen atoms, hydroxyl groups, etc. This substitution reaction may generate different products due to differences in reagents and conditions.
    Its conjugate system endows the compound with certain electron delocalization, which affects its stability and reactivity. The conjugated system can make the electron cloud distributed uniformly, make the molecule more stable, and at the same time affect its spectral properties.
    From the perspective of redox, the compound can be oxidized or reduced under specific conditions. Under the action of oxidants, nitrogen atoms or methyl groups may be oxidized; when reducing agents act, the unsaturated bonds in the conjugated system may undergo reduction reactions.
    In addition, the chemical properties of 6-methylpurino [b] quinoline are significantly affected by surrounding substituents, solvents and reaction conditions. Different substituents can change the density of the molecular electron cloud, affecting the reaction check point and activity; solvent polarity also plays a role in its solubility, reaction rate and equilibrium; temperature, pressure, catalyst and other reaction conditions can also regulate the reaction direction and rate.
    What are the common application fields of 6-methylbenzo [b] thiophene
    The common application fields of 6-methylpurino [b] quinazoline are as follows:
    In the field of medicine, this compound is often a key component in the development of anti-cancer drugs. Its unique chemical structure can precisely interact with specific biomacromolecules in cancer cells, or inhibit the activity of key enzymes required for cancer cell proliferation, just like setting up many roadblocks in the growth and reproduction of cancer cells, so as to inhibit the growth and spread of cancer cells. For example, some new anti-cancer drugs targeting specific gene mutations that cause tumors have been developed, 6-methylpurino [b] quinazoline has attracted attention because of its good affinity with mutant protein targets.
    In the field of pesticides, it can be used as the basis for the creation of new insecticides or fungicides. By interfering with the normal physiological and biochemical processes in pests or pathogens, such as destroying the signal transduction of the pest's nervous system, or affecting the cell wall synthesis of pathogens, the purpose of controlling pests and diseases can be achieved. Compared with traditional pesticides, new pesticides developed based on this compound may have higher selectivity and lower environmental toxicity, and have less impact on the ecological environment while protecting crops.
    In the field of materials science, 6-methylpurine [b] quinazoline can participate in the creation of functional materials. Because of its special optoelectronic properties, it may be applied to organic Light Emitting Diode (OLED) materials. In OLED devices, it may improve the luminous efficiency and stability, making the display screen show more brilliant colors and longer service life. In addition, in some semiconductor materials with specific requirements for electron transport properties, the compound may also optimize the electrical properties of the material by virtue of its unique electronic structure, promoting the improvement of semiconductor material properties.
    What are the preparation methods of 6-methylbenzo [b] thiophene?
    The method of making 6-methylpurine and [b] quinazoline has been known for a long time. There are three methods, all of which are very delicate.
    First, purine-based, supplemented by methylation agent. Take an appropriate amount of purine, place it in a clean kettle, and add a specific methylating agent, such as iodomethane. At a suitable temperature, boil it slowly over low heat and stir constantly to make the two fully blend. This process needs to be carefully controlled. If the temperature is high, the reaction will be excessive and the product will be impure; if the temperature is low, the reaction will be slow and take a long time. After the reaction is completed, 6-methylpurine can be obtained by purifying it in a delicate way. Take an appropriate amount of 6-methylpurine, place it in another kettle with the quinazoline precursor, add a suitable catalyst, and react at a specific temperature and pressure to obtain 6-methylpurine and [b] quinazoline. This is a classic method, but it requires quite high operation. If you are not careful, all your efforts will be wasted.
    Second, start with quinazoline. Quinazoline is first prepared, and then methyl and purine structures are introduced in an ingenious way. Take quinazoline, add an active intermediate containing methyl in a specific reaction environment, and use the power of the catalyst to make the methyl cleverly connect to the specific position of quinazoline. Then, through a series of complex reactions, the purine structure is connected to obtain 6-methylpurine and [b] quinazoline. This method requires precise control of the reaction conditions, and the reagents used are also quite special and unusual.
    Third, with a new synthesis strategy, start from the basic small molecules. Take several simple small molecules, such as nitrogen-containing small molecules, carbon-containing small molecules, etc., mix them in a specific ratio, and in a special reaction vessel, under special catalyst and temperature and pressure conditions, gradually construct the skeleton of 6-methylpurine and [b] quinazoline. This is an emerging method. Although the steps are complicated, it has broad prospects because the raw materials used are common and easy to obtain, and the reaction conditions can be adjusted according to the actual situation, or it can become the mainstream method for future preparation.
    What are the precautions for the production of 6-methylbenzo [b] thiophene?
    In the production of 6-methylpurine [b] quinazoline, there are many points to pay attention to.
    First, the selection of raw materials must be cautious. The purity and quality of the raw materials used in the synthesis of this compound have a great impact on the quality of the product. It is necessary to strictly select high-quality raw materials and carefully check their various indicators. If there are too many impurities in the raw materials, not only will the reaction process be disturbed, but also a large number of by-products may be produced, making it extremely difficult to separate and purify the product, and even more will reduce the yield and quality of the product.
    Second, it is crucial to control the reaction conditions. Temperature, pressure, reaction time and catalyst dosage all have a profound impact on the reaction process and product formation. If the temperature is too high, the reaction rate will be accelerated, but it is easy to cause frequent side reactions and reduce the selectivity of the product; if the temperature is too low, the reaction will be slow and take a long time. The same is true for pressure, and the appropriate pressure can ensure the smooth progress of the reaction. The amount of catalyst needs to be accurately weighed. Too much or too little will affect the reaction efficiency and product quality. For example, if the reaction time is not properly controlled, the reaction may be incomplete, or the reaction may be excessive, which will have adverse effects on the product.
    Third, safety protection should not be underestimated. In the process of producing 6-methylpurine and [b] quinazoline, some raw materials, intermediates and products may be toxic, corrosive, or flammable and explosive. Operators must strictly follow safety procedures and wear complete protective equipment, such as protective clothing, gloves, goggles and gas masks. Production sites should be equipped with excellent ventilation facilities and fire equipment to deal with emergencies. At the same time, waste disposal should also be treated strictly, follow environmental regulations, and dispose properly to avoid polluting the environment.
    Fourth, quality monitoring runs through the whole process. From raw material input to product output, strict quality monitoring should be implemented in every link. Appropriate analysis and testing methods, such as chromatography, spectroscopy and other technologies, are used to monitor the reaction process and product quality in real time. Only by promptly detecting and solving quality problems can we ensure that the final product meets the established standards and requirements.
    What are the effects of 6-methylbenzo [b] thiophene on the environment and human health?
    The impact of 6-methylmercaptopurine [b] imidazole on the environment and human health is related to people's livelihood and cannot be ignored.
    Cover this 6-methylmercaptopurine [b] imidazole, in the environment, or there are many complex changes. If it remains between water and soil, it may interact with surrounding substances. Water and soil are the foundation for the growth of all things. If it is affected by this, it may cause soil properties to change and affect vegetation growth. If vegetation is affected by it, the ecological balance will also be shaken. And it may migrate with water currents, spread in water bodies, pollute water sources, and aquatic organisms will not be spared, or cause changes in population numbers and species, and ecological chain disorder.
    As for human health, if 6-methylmercaptopurine [b] imidazole enters the human body through diet, respiration, etc., or interferes with normal physiological functions. The organs and meridians of the human body perform their duties and coordinate with each other. This substance may damage the organs and interfere with the flow of qi and blood. If it acts on the liver, the liver is responsible for dredging and storing blood. If it is harmed by it, the dredging is abnormal, the qi and blood are not smooth, and people may suffer from swelling and pain in the ribs, emotional depression, etc.; when it acts on the kidneys, the kidneys mainly store essence and hold qi, and if they are damaged, the essence and qi will be deficient, the waist and knees will be sore, and they will be exhausted.
    Furthermore, the immune system may also be impacted by Human immunity is like a city wall to defend against the enemy. If 6-methylmercaptopurine [b] imidazole causes immune disorder, external evil is easy to invade, and diseases are plagued. And long-term exposure, or there is a risk of genetic mutation, can cause various difficult diseases, harm life and health. Therefore, the impact of 6-methylmercaptopurine [b] imidazole on the environment and human health should be carefully studied and strictly prevented to ensure people's well-being and ecological harmony.