1h Imidazole 5 2 Ethyl 2 3 Dihydro 1h Inden 2 Yl
quinoline thiophene imidazole thiazole

1H-imidazole, 5-(2-ethyl-2,3-dihydro-1H-inden-2-yl)-

    Specifications

    HS Code

    227397

    Chemical Formula C16H18N2
    Molecular Weight 238.33 g/mol
    Appearance Solid (predicted, no data on actual color)
    Melting Point No data
    Boiling Point No data
    Solubility In Water Low solubility expected (due to non - polar groups)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (predicted)
    Density No data
    Pka No data
    Logp High logP value expected (due to large non - polar moiety)

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    What are the chemical properties of 1H-imidazole, 5- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -?
    1H-pyrazole, 5- (2-ethyl-2,3-dihydro-1H-indole-2-yl) compound, is an organic compound. Its chemical properties are relatively complex, so let me go into detail.
    From a structural point of view, the 1H-pyrazole ring has a certain aromaticity, and the nitrogen atom on the pyrazole ring makes the part have a certain alkaline, which can react with acids to form corresponding salts. At the same time, the hydrogen atom on the pyrazole ring has a certain activity, and substitution reactions can occur under appropriate conditions. For example, when in contact with an electrophilic reagent, the hydrogen atom on the pyrazole ring can be replaced by other groups to generate different derivatives, which are often used in organic synthesis to construct diverse molecular structures.
    While 5 - (2 - ethyl - 2,3 - dihydro - 1H - indole - 2 - yl) moiety, the presence of 2 - ethyl increases the hydrophobicity of the molecule, making its solubility in some organic solvents may be better than in water. The 2,3 - dihydro - 1H - indole - 2 - yl structure also imparts a special electronic effect to the whole molecule. The indole ring part has a certain conjugate system, which affects the electron cloud distribution of the whole molecule, thereby affecting its chemical reactivity. For example, in some redox reactions, the compound may exhibit unique redox properties due to the conjugate structure of the indole ring.
    In addition, the compound may have certain biological activities. In the field of medicinal chemistry, compounds with similar structures are often studied for their potential pharmacological effects. For example, some compounds containing pyrazole and indole structural fragments have been found to have anti-inflammatory, antibacterial, anti-tumor and other activities. This may be related to their ability to interact with specific targets in organisms, such as binding to the activity check points of certain enzymes, thereby affecting the function of enzymes and exerting corresponding biological effects. < Br >
    This compound is rich in chemical properties and has potential applications in many fields such as organic synthesis and biological activity research.
    What are the common uses of 1H-imidazole, 5- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -?
    1H-pyrazole, 5- (2-ethyl-2,3-dihydro-1H-indole-2-yl) compounds have a wide range of common uses. In the field of medicine, it can serve as a key drug intermediate. In the development of many drugs, with the help of its unique chemical structure, compounds with specific pharmacological activities can be derived, such as some drugs used to treat cardiovascular diseases. This structural fragment can precisely bind to specific receptors to regulate physiological functions in the body and achieve therapeutic effect.
    In the field of pesticides, this compound also plays an important role. The molecular design of some insecticides and fungicides will be integrated into this structure, using its impact on the nervous system of insects or the metabolic pathways of pathogens to achieve efficient pest control, and it is relatively friendly to the environment, with low residues, which can reduce the damage to ecological balance.
    In addition, in the field of materials science, compounds containing this structure can be used to prepare functional materials. For example, in some photoelectric materials, this structure can improve the light absorption and charge transport properties of materials, which can be applied to the research and development of organic solar cells, Light Emitting Diodes and other devices, providing assistance for the progress of energy and display technology. At the same time, in organic synthetic chemistry, it is an important module for building complex organic molecules. Organic chemists can build organic compounds with different functions and structures through various chemical reactions based on their reaction characteristics, thus promoting the development of organic synthetic chemistry.
    What are the synthesis methods of 1H-imidazole, 5- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -?
    To prepare 1H-pyrazole, 5- (2-ethyl-2,3-dihydro-1H-indole-2-yl), the synthesis method is quite complicated. In the past, Fang family followed the ancient method and used various raw materials to obtain it after many twists and turns.
    First take appropriate starting materials, such as indole derivatives containing specific substituents, and pyrazole-related reagents, in a suitable solvent, with a catalyst to make it react. This reaction requires temperature control and control to ensure that it is sufficient and orderly. If the temperature is too high, it is easy to cause a cluster of side reactions; if the temperature is too low, the reaction will be slow and time-consuming.
    There are also improved methods to optimize the reaction steps. Or find new catalysts to improve the reaction rate and increase the purity and yield of the product. Or fine-tune the reaction conditions, such as adjusting the pH, so that the reaction is in a favorable direction.
    And guided by the concept of green synthesis, choose environmentally friendly solvents and reagents to reduce waste and reduce emissions, which is not only suitable for the current time, but also in line with long-term development. These methods are parallel, all of which are for the best way to synthesize this compound, but each has its own advantages and disadvantages, depending on the specific situation. In order to obtain pure and productive products, we need all kinds of tests and repeated scrutiny before we can achieve perfection.
    1H-Imidazole, 5- (2-ethyl-2,3-dihydro-1H-indene-2-yl) - What is the price range in the market?
    I look at your words, but I am inquiring about 1H-pyrazole, 5- (2-ethyl-2,3-dihydro-1H-indene-2-yl) in the market price range. However, the price of these chemical substances is not static and is affected by many factors.
    First, the purity has a great impact. If the purity is extremely high and almost flawless, it is suitable for high-end scientific research, precision pharmaceuticals and other fields, and the price is high. Because the purification process requires exquisite methods, expensive tools, and huge human and material resources. On the contrary, the purity is slightly inferior, and it is only used for general industrial purposes, and the price is relatively easy.
    Second, the trend of supply and demand is also the key. If for a while, many pharmaceutical companies and scientific research institutions are hungry and thirsty for this product, and the supply is limited, such as rare treasures, the price will soar. On the contrary, if the market is abundant and the demand is few, the price will decline.
    Third, the place of production is also related to the transportation route. If the origin is far away, the transportation is difficult, or special methods are required to ensure its quality, the cost will increase, and the price will follow.
    As far as I know, the price of this compound in the market may be between tens of yuan and thousands of yuan per gram. However, this is only an approximate number, and the actual price should be determined according to the specific time, place and quality. For accurate pricing, please consult chemical raw material suppliers, chemical reagent sellers, or professional chemical trading platforms for details.
    What are the manufacturers of 1H-imidazole, 5- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -?
    The producer of 1H-pyrrole, 5- (2-ethyl-2,3-dihydro-1H-indole-2-yl), has been studied by many scholars in ancient times.
    In the past, there were alchemists who accidentally touched on such a combination on the road to longevity. At that time, although it was not clear, it was also a glimpse between the furnace and the cauldron. It may be in the complex ratio of raw materials and the delicate control of the heat, so that all kinds of substances blend with each other, and by chance, this 1H-pyrrole and the like are generated.
    There are also herbal prescribers who also met with objects containing such structures when identifying herbs and processing them for medicine. With their keen observation and practical wisdom, they explored among plants and stones, or found that some plants had been specially treated, and their ingredients contained such 5- (2-ethyl-2,3-dihydro-1H-indole-2-yl) related substances.
    Furthermore, in the exploration of handicraft skills, such as the preparation of pigments and the preparation of fragrances, folk craftsmen may have inadvertently promoted the formation of such substances while constantly trying new formulas and processes. Although they may not know the chemical principles behind it, they have left clues for future generations to explore through experience and experimentation.
    Although people at that time had limited knowledge, their spirit of exploration and accumulation of practice were all later studies on the formation of 1H-pyrrole and 5- (2-ethyl-2,3-dihydro-1H-indole-2-yl), paving the way and becoming the cornerstone of today's in-depth research.