1 2 4 Dichlorophenyl 2 1h Imidazole 1 Yl Ethanone
quinoline thiophene imidazole thiazole

1-(2,4-Dichlorophenyl)-2-(1h-imidazole-1-yl) ethanone

    Specifications

    HS Code

    197261

    Chemical Formula C11H8Cl2N2O
    Molecular Weight 255.10
    Appearance White to off - white solid
    Melting Point 140 - 143 °C
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, ethanol
    Odor Odorless or very faint odor
    Density Approx. 1.39 g/cm³
    Stability Stable under normal conditions

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    General Information
    Where to Buy 1-(2,4-Dichlorophenyl)-2-(1h-imidazole-1-yl) ethanone in China?
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    Frequently Asked Questions

    As a leading 1-(2,4-Dichlorophenyl)-2-(1h-imidazole-1-yl) ethanone 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 1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethyl ketone?
    1 - (2,4 - dihydroxyphenyl) - 2 - (1H - indole - 1 - yl) acetic acid, which has the general properties of acid, because it contains carboxyl group (-COOH), can neutralize with bases, such as reacting with sodium hydroxide to form the corresponding carboxylate and water.
    It has a certain degree of acidity, and the hydrogen in the carboxyl group can be partially ionized, which is weakly acidic in aqueous solution. In organic synthesis, the carboxyl group can be converted through various reactions, such as esterification with alcohols to form ester compounds. This reaction requires acid catalysis and is carried out under heating conditions. Esters with specific aromas can be prepared for use in fragrances and other fields. The hydroxyl group is also an important functional group, and the hydroxyl group on the 2,4-dihydroxyphenyl group can participate in the phenolic characteristic reaction. The phenolic hydroxyl group is weakly acidic and can form salts with strong bases. Due to the conjugation system of the benzene ring, the electron cloud density of the phenolic hydroxyl group and the para-site increase, which is prone to electrophilic substitution reactions. If it reacts with bromine water, bromine atoms can be introduced into the o-site and the p-site.
    The 1H-indole-1-yl part endows the compound with unique electronic structure and chemical activity. The indole ring is aromatic, and can be used as a nucleophilic agent in some reactions and can also carry out substitution reactions, which has a great impact on the overall chemical properties and reactivity of the compound. In the field of medicinal chemistry, it may have affinity for specific targets due to structural characteristics and potential biological activity. It can be used as a lead compound for structural modification and optimization to develop drugs with specific pharmacological effects.
    What is the use of 1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethyl ketone?
    1 - (2,4 - dihydroxyphenyl) - 2 - (1H - pyrazole - 1 - yl) ethanol, this compound has important uses in many fields.
    In the field of medicine, it has potential medicinal value. Due to its unique chemical structure, it can interact with specific targets in organisms. For example, in some inflammation-related diseases, drugs with anti-inflammatory activity can be developed by modifying and optimizing their structures. Studies have shown that it may be able to regulate the release of inflammatory factors, thereby reducing the inflammatory response, and bringing new hope for the treatment of inflammatory diseases such as arthritis.
    In materials science, it can be used as a key raw material for the construction of new functional materials. Using its special structure, it is combined with other organic or inorganic materials to prepare materials with special optical and electrical properties. For example, the preparation of materials with fluorescent properties can be used in the field of biological imaging, which can accurately label biomolecules and help biomedical research.
    In the field of agriculture, it also shows potential application prospects. It can be developed as a new type of plant growth regulator to regulate the process of plant growth and development. For example, by affecting the balance of plant hormones, it promotes plant rooting, germination and flowering, and improves crop yield and quality. It may also have certain antibacterial and antiviral activities, play a positive role in the control of crop diseases and pests, reduce the use of chemical pesticides, and achieve sustainable agricultural development.
    What is the preparation method of 1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethyl ketone?
    1 - (2,4 - dihydroxyphenyl) - 2 - (1H - indole - 1 - yl) acetic acid, the preparation method of this product is as follows:
    First take an appropriate amount of starting materials, one of which is a benzene compound containing 2,4 - dihydroxy, and the other is a substance with a 1H - indole - 1 - base structure. Place the two in a suitable reaction vessel, which should be clean and dry to prevent impurities from interfering with the reaction.
    Add an appropriate amount of catalyst to the reaction system. The choice of this catalyst is very critical, and it needs to be able to effectively promote the chemical reaction between the two types of raw materials and accelerate the formation of the target product. The amount of catalyst added is precisely controlled according to the amount of raw materials and reaction characteristics. Too much or too little may affect the process and yield of the reaction. After
    , control the temperature and time of the reaction. The temperature needs to be maintained within a specific range. If it is too low, the reaction rate will be slow, and if it is too high, it may cause side reactions and lead to impure products. After careful exploration and experience summary, in general, the temperature is adjusted to a suitable range to make the reaction proceed smoothly. At the same time, the reaction time is strictly controlled, the process of the reaction is observed regularly, and the consumption of raw materials and the formation of products are monitored by suitable analytical methods, such as thin-layer chromatography. When the reaction reaches the expected level, the reaction is stopped.
    After the reaction is completed, the reaction mixture is separated and purified. Extraction can be used first, and a suitable extractant can be selected to extract the target product from the reaction system. Then the residual impurities are further purified by column chromatography to obtain a pure 1- (2,4-dihydroxyphenyl) -2- (1H-indole-1-yl) acetic acid product. The whole preparation process requires careful operation by the experimenter and attention to the details of each link in order to achieve the ideal preparation effect.
    What is the market outlook for 1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethyl ketone?
    1 - (2,4 - dihydroxyphenyl) - 2 - (1H - indole - 1 - yl) ethyl ketone, which is an organic compound. Its market prospect is quite promising, because it has potential applications in many fields such as medicine and chemical industry.
    In the field of medicine, with the in-depth research on various diseases, many new drug development requires organic compounds with specific structures as raw materials or intermediates. The unique chemical structure of 1- (2,4-dihydroxyphenyl) -2- (1H-indole-1-yl) ethyl ketone may make it a key ingredient for the development of new anti-cancer and anti-inflammatory drugs. Today, there are a large number of patients with cancer and inflammatory diseases, and the market demand for related drugs is huge. If the drugs developed based on this compound can show good efficacy and safety, it will definitely occupy a place in the pharmaceutical market, and the prospects are extremely broad.
    In the chemical field, the compound may be used in the synthesis of fine chemicals. Fine chemicals are widely used in coatings, fragrances, cosmetics and other industries. For example, in the cosmetic industry, consumers have increasingly high requirements for product efficacy and safety. If this compound can be applied to the research and development of cosmetic ingredients, endow the product with unique skin care, antioxidant and other effects, and meet safety standards, it will definitely be welcomed by the market, promote the upgrading of related products, and then expand its market demand.
    Furthermore, the progress of scientific research also provides assistance for its market development. The improvement of analysis and detection technology makes the performance research of the compound more accurate; the optimization of synthesis process may reduce production costs, improve production efficiency, and enhance its market competitiveness. Although the current market size may be limited, with the growth of demand in various fields and technological innovation, 1- (2,4-dihydroxyphenyl) -2- (1H-indole-1-yl) ethyl ketone is expected to usher in a broader market development space.
    What are the precautions for using 1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethyl ketone?
    1 - (2,4 - dihydroxyphenyl) - 2 - (1H - pyrazole - 1 - yl) acetonitrile is a key intermediate in organic synthesis and is widely used in many fields such as medicine and pesticides. When using this compound, pay attention to the following matters:
    First, safety protection must not be neglected. Because it has certain chemical activity, or it may cause harm to the human body. When operating, be sure to wear protective clothing, gloves and protective glasses to prevent skin contact and eye splashing. If you accidentally contact, you need to rinse with a lot of water immediately. If the situation is serious, you should seek medical attention quickly.
    Second, precisely control the reaction conditions. The reaction in which this compound participates requires strict conditions such as temperature, pH, and reaction time. If the temperature is too high or too low, it may cause the reaction rate to change, and even generate by-products. For example, a reaction needs to be carried out efficiently within a specific temperature range. If it deviates from this range, the yield of the product will decrease. Therefore, the reaction conditions should be precisely monitored and regulated with the help of thermometers, pH meters and other instruments.
    Third, pay attention to storage conditions. It should be stored in a dry, cool and well-ventilated place, away from fire sources and oxidants. Due to its active chemical properties, improper storage or deterioration will affect the use effect. Like a humid environment, it may absorb moisture and decompose; if it is close to the fire source, there will be a fire hazard.
    Fourth, do a good job of waste disposal. The waste containing this compound produced by the experiment should not be discarded at will and should be properly disposed of in accordance with relevant regulations. Because it may cause pollution to the environment, it should be collected in a centralized manner and handed over to a professional organization for treatment to reduce the negative impact on the environment.