2 4 Isopropyl 4 Methyl 5 Oxo 2 Imidazolin 2 Yl Quinoline 3 Carboxylic Acid
quinoline thiophene imidazole thiazole

2-(4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)quinoline-3-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    662157

    Chemical Formula C18H19N3O3
    Molar Mass 325.36 g/mol
    Physical State Solid (usually)
    Appearance May appear as a powder
    Melting Point Data specific to this compound needed
    Boiling Point Data specific to this compound needed
    Solubility In Water Limited solubility likely, being an organic heterocyclic acid
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO
    Acidity Carboxylic acid group imparts acidic properties
    Pka Value Data specific to this compound needed

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    Frequently Asked Questions

    As a leading 2-(4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)quinoline-3-carboxylic acid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    2- (4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) What is the chemical structure of quinoline-3-carboxylic acid
    2-%284-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl%29quinoline-3-carboxylic + acid is resolved as 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl) quinoline-3-carboxylic acid. Its chemical structure is described in the form of ancient Chinese:
    This compound is formed by fusing two parts of quinoline and imidazoline, and is connected with a carboxyl group. The quinoline part is a nitrogen-containing heterocyclic aromatic hydrocarbon, which is formed by fusing a phenyl ring with a pyridine ring. In the third position of quinoline, it is connected with a carboxyl group (-COOH), which gives the compound a certain acidity.
    The imidazoline moiety is a nitrogen-containing five-membered heterocyclic ring, which is a carbonyl group (C = O) at the 5th position, showing its special electron cloud distribution and reactivity. The 4 positions are connected with isopropyl (-CH (CH 🥰) -2) and methyl (-CH 🥰), respectively. Both isopropyl and methyl are alkyl groups, which have the electron cloud effect, which will affect the electron cloud density of the imidazoline ring, and then affect the physicochemical properties of the whole compound.
    The 2-position is connected to the quinoline ring, so that the two parts are related to each other, which together constitute the unique chemical structure of this complex organic compound. The interaction of each part determines the various chemical and physical properties of the compound.
    2- (4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) What are the main uses of quinoline-3-carboxylic acid
    2-%284-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl%29quinoline-3-carboxylic + acid is 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl) quinoline-3-carboxylic acid, which is widely used in the field of pharmaceutical research and development.
    First, it is of great significance in the exploration of anti-tumor drugs. Abnormal proliferation and survival of tumor cells rely on specific signaling pathways and proteins. This compound can target these key targets, such as a specific kinase. By binding to the kinase activity check point, it can change its spatial conformation, inhibit the kinase phosphorylation process, and block the proliferation signal transduction of tumor cells, thereby inhibiting the growth and spread of tumor cells. It provides a new idea and effective way for the creation of anti-tumor drugs.
    Second, it also plays an important role in the research of anti-inflammatory drugs. Inflammation is regulated by many inflammatory mediators and cytokines. The compound can regulate inflammation-related signaling pathways, reduce the release of inflammatory mediators, such as inhibiting the secretion of interleukin, tumor necrosis factor, etc., reducing symptoms such as redness, swelling, heat and pain in inflammatory sites, laying the foundation for the development of high-efficiency and low-toxicity anti-inflammatory drugs.
    Third, it has emerged in the field of drug development for the treatment of neurological diseases. Neurological diseases are often caused by imbalance of neurotransmitters and damage to nerve cells. This compound may regulate neurotransmitter levels and protect nerve cells from damage. It may have potential value in the treatment of neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. It is expected to become an innovative drug for the treatment of such diseases.
    2- (4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) What are the synthesis methods of quinoline-3-carboxylic acid
    To prepare 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl) quinoline-3-carboxylic acid, there are many methods, and each has its own advantages and disadvantages, all of which depend on the required conditions, raw material availability and product purity.
    First, you can start from the precursor containing quinoline and imidazoline structures. First, take a suitable quinoline derivative, and introduce a suitable substituent at its 3-position through a specific reaction to construct the carboxylic acid part. At the same time, prepare imidazoline intermediates containing isopropyl, methyl and carbonyl. Later, by condensation reaction, the two are connected to form the target product. In this process, the reaction conditions must be precisely controlled, such as temperature, pH, and the amount of catalyst, which all have a profound impact on the reaction process and product yield.
    Second, the strategy of gradually constructing heterocycles can also be adopted. First, a simple compound is used to construct a quinoline ring, and then a multi-step reaction is carried out to introduce the imidazoline structure at a suitable location, and modify it into the target 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl). Although this path is complicated, it is beneficial to the selectivity and purity control of each step of the reaction. If properly operated, high-purity products can be obtained. < Br >
    There are also natural products or compounds with similar structures as starting materials, which are structurally modified and directed to target molecules. This approach can often take advantage of the special structure and activity of natural products to reduce the reaction steps, but the source of raw materials may be limited, and the modification process also needs to be carefully designed to achieve the desired structure and purity.
    When synthesizing, the purification step is also indispensable. Recrystallization, column chromatography and other methods are commonly used to remove impurities and improve the purity of the product. Each method must be selected according to the characteristics of the product and the nature of impurities in order to achieve the ideal purification effect. In conclusion, the synthesis of 2 - (4 -isopropyl-4 -methyl-5 -oxo-2 -imidazoline-2 -yl) quinoline-3 -carboxylic acid requires comprehensive consideration of various factors and careful design of routes and conditions.
    2- (4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) What are the physical properties of quinoline-3-carboxylic acid
    This is the substance of 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl) quinoline-3-carboxylic acid, and its physical properties are as follows:
    Appearance is mostly crystalline solid state, looking at its color, it is often white to off-white, this color is pure, just like the whiteness of first snow, and like the elegance of morning mist, under light, crystal clear and no variegated color.
    Its melting point is also an important physical property, but the specific value varies depending on the preparation and purity. Generally speaking, when this substance reaches the melting point, it is like ice and snow meeting the warm sun, slowly melting from the solid state to the liquid state. This process occurs quietly and requires precise instruments and careful observation to detect.
    In terms of solubility, it has a certain degree of dissolution in organic solvents, such as common ethanol and dichloromethane. In ethanol, with the change of temperature, the degree of dissolution also varies. When the temperature rises slightly, just like the spring breeze, this substance gradually dissolves in ethanol to form a uniform system; in water, its solubility is relatively weak, just like the incompatibility of oil and water. Only a very small amount can be dispersed, and most of them remain in the solid state.
    Stability is also the key to consider. In the conventional temperature and humidity environment, this substance is quite stable, just like a calm old man, it can go through time without changing its properties. However, in the case of strong acid and alkali environment, or high temperature and hot topic conditions, its structure will be easily damaged. If a building encounters a strong earthquake, the original stable structure may collapse and undergo a chemical reaction, thus losing its original characteristics.
    Although its density is difficult to visualize with the naked eye, it is an important physical constant. Through precise measurement, it can be seen that its density gives this substance a specific relationship between mass and volume, which is of great significance in the storage, transportation and related applications of substances.
    Such various physical properties are the cornerstones of the understanding and application of this substance. In many fields such as scientific research and production, it is necessary to understand it in detail before it can be used effectively.
    2- (4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) quinoline-3-carboxylic acid market prospects
    The market prospect of Guanfu 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl) quinoline-3-carboxylic acid is quite promising.
    In today's world, pharmaceutical chemistry is booming, and various new compounds have unique potential in the field of pharmaceutical research and development. This compound has an exquisite structure, or contains a special activity check point, which may be the key to drug creation.
    In the search for antimalarial drugs, many studies have focused on molecules containing quinoline structures. This compound contains both quinoline core and has unique effects on the suppression and killing of malaria parasites. If its mechanism of action can be deeply explored and its structure optimized, it may become a new generation of antimalarial drugs, saving thousands of malaria patients from pain, and the market prospect is broad.
    Furthermore, in the process of anti-cancer drug research and development, imidazolinone structures have also attracted a lot of attention. The existence of this structure in this compound may give it the ability to inhibit tumor cell proliferation and induce apoptosis. If properly developed, it is expected to add new power to anti-cancer drugs and gain a place in the cancer treatment market.
    However, it wants to emerge in the market, but also faces many challenges. Research and development costs are high, and huge investment is required from the synthesis of compounds, activity screening, to preclinical and clinical trials. And the road to drug development is full of unknowns and the risk of failure is quite high. In addition, regulations and supervision are becoming increasingly strict, and many stringent standards need to be met in order to obtain marketing approval.
    However, opportunities and challenges coexist. If we can make good use of the power of science and technology, accurately analyze its pharmacology, rationally plan the research and development path, and break through many difficulties, 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2-yl) quinoline-3-carboxylic acid can be used in the pharmaceutical market, or it can create a brilliant situation and contribute to the cause of human health.