2 E 2 5 Nitrofuran 2 Yl Ethenyl Quinoline 4 Carboxylic Acid
quinoline thiophene imidazole thiazole

2-[(E)-2-(5-nitrofuran-2-yl)ethenyl]quinoline-4-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    839694

    Chemical Formula C16H10N2O5
    Molar Mass 310.26 g/mol

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    General Information
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    Frequently Asked Questions

    As a leading 2-[(E)-2-(5-nitrofuran-2-yl)ethenyl]quinoline-4-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.

    What is the chemical structure of 2- [ (E) -2- (5-nitrofuran-2-yl) vinyl] quinoline-4-carboxylic acid?
    My question is about the chemical structure of "2 - [ (E) -2- (5-cyanopyridine-2-yl) ethylboronic acid] tetradecanoic acid-4-carboxylate". The structure of this compound is slightly complicated, and the characteristics of the groups involved need to be studied carefully.
    First, the " (E) 2- (5-cyanopyridine-2-yl) ethylboronic acid" part, in which the pyridine ring is a nitrogen-containing hexaadic ring with a cyano group at the 5-position, and the 2-position is connected to the boronic acid group through the ethyl group. In this structure, the pyridine ring has certain alkalinity and electron cloud distribution characteristics due to the existence of nitrogen atoms; the cyanyl group is a strong electron-absorbing group, which can affect the electron cloud density of the pyridine ring, and then affect its reactivity; the ethyl group acts as a connecting chain, which plays a role in space separation and electron transfer; the boric acid group has various reactivity in organic synthesis, which can participate in coupling reactions.
    Looking at the part of "square acid-4-carboxylate", the square acid is a quaternary cyclic diacid with a special conjugate structure. Its conjugate system makes the molecule have certain stability and electron delocalization characteristics. The existence of 4-bit carboxylates gives molecules ionic properties, which can participate in ionic interactions and have unique behaviors in aqueous solutions or certain polar environments.
    In the overall structure, the 2-bit connects the above two parts in a specific way, and the groups interact with each other, such as electronic effects, space effects, etc., to jointly determine the physicochemical properties and reactivity of the compound. The characteristics of this structure may make it have potential application value in pharmaceutical chemistry, materials science and other fields, such as the use of its special structure and activity to design new drug molecules or functional materials.
    What are the physical properties of 2- [ (E) -2- (5-nitrofuran-2-yl) vinyl] quinoline-4-carboxylic acids?
    2-%5B%28E%29-2-%285-%E7%A1%9D%E5%9F%BA%E5%91%8B%E5%96%83-2-%E5%9F%BA%29%E4%B9%99%E7%83%AF%E5%9F%BA%5D%E5%96%B9%E5%95%89-4-%E7%BE%A7%E9%85%B8%E6%9C%89%E5%93%AA%E4%BA%9B%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%EF%BC%9F%3F
    This is a question about the physical properties of 2- [ (E) -2- (5-furanylpyridine-2-yl) ethylfuranyl] benzyl-4-quinolinic acid. The physical properties of this compound, let me explain in detail.
    Its appearance is often crystalline solid, which is a common state for many such organic compounds. Looking at its color, or white to off-white, the color is pure, reflecting the regularity of its chemical structure.
    Melting point is one of the important physical properties of compounds. The melting point of this 2- [ (E) -2- (5-furanylpyridine-2-yl) ethylfuranyl] benzyl-4-quinolinic acid is within a certain temperature range under specific conditions, which is the key indicator for the identification and purification of this compound. When the temperature rises to the melting point, the compound gradually melts from solid to liquid, and this phase transition process accurately reflects the strength of its intermolecular forces.
    Solubility cannot be ignored either. In organic solvents, such as common ethanol and dichloromethane, this compound exhibits certain solubility. In ethanol, moderate dissolution indicates that there is a certain interaction between it and ethanol molecules, or hydrogen bonds, van der Waals forces, etc. In water, the solubility is poor, because the molecular structure of the compound contains mostly hydrophobic groups, which is quite different from the polarity of water molecules, so it is difficult to dissolve in water.
    In addition, the density of the compound is also one of its physical properties. Although the exact density value needs to be determined by precise experiments, it is inferred that the density is in a specific range according to its molecular structure and similar compound characteristics. This density data is related to material measurement and process design when applied in chemical engineering, materials and other fields.
    In summary, 2- [ (E) -2- (5-furanylpyridine-2-yl) ethylfuranyl] benzyl-4-quinolinic acid has physical properties such as crystalline solid appearance, specific melting point, unique solubility and certain density. All properties are of great significance in chemical research, drug development and related industrial production.
    In what fields are 2- [ (E) -2- (5-nitrofuran-2-yl) vinyl] quinoline-4-carboxylic acids used?
    2-%5B%28E%29-2-%285-%E7%A1%9D%E5%9F%BA%E5%91%8B%E5%96%83-2-%E5%9F%BA%29%E4%B9%99%E7%83%AF%E5%9F%BA%5D%E5%96%B9%E5%95%89-4-%E7%BE%A7%E9%85%B8%E4%B8%8E%E5%A4%A9%E5%B7%A5%E7%94%9F%E6%B4%BB%E4%B8%AD%E8%87%AA%E7%84%B6%E7%94%9F%E6%88%90%E4%B8%8E%E5%8C%BB%E7%96%97%E7%94%A8%E9%87%8F%E5%85%B3%E7%B3%BB%E7%9B%B8%E5%85%B3%E3%80%82
    In the field of medicine, this compound may have unique uses. When synthesizing drugs, it can act as a key intermediate, and with its special structure and properties, the drug can precisely act on the target, improve the efficacy of the drug, and reduce its side effects. For example, when developing targeted drugs for specific diseases, 2-%5B%28E%29-2-%285-%E7%A1%9D%E5%9F%BA%E5%91%8B%E5%96%83-2-%E5%9F%BA%29%E4%B9%99%E7%83%AF%E5%9F%BA%5D%E5%96%B9%E5%95%89-4-%E7%BE%A7%E9%85%B8%E5%8F%AF%E is the cornerstone of building a drug molecular framework, so that the drug can more effectively hit the focus, which is of great significance in the treatment of difficult diseases.
    In the category of natural generation, it may exist in the metabolites of specific plants or microorganisms. Some rare plants, in order to adapt to special environments, have evolved for a long time to synthesize such special compounds in the body. Studying its generation path and regulation mechanism can not only help us understand the subtlety of natural biosynthesis, but also provide ideas for biomimetic synthesis to obtain such compounds in a more efficient and green way.
    And it may also have potential applications in the field of materials science. If it is combined with specific polymer materials, it may improve the properties of materials, such as enhancing the stability, flexibility or endowing them with special optical and electrical properties, and it may open up new application fields in electronic devices, optical materials, etc.
    This compound has shown potential application value in many fields such as medicine, natural science and materials science. It is urgent for our generation to explore in depth to uncover more mysteries and contribute to the development of various fields.
    What are the preparation methods of 2- [ (E) -2- (5-nitrofuran-2-yl) vinyl] quinoline-4-carboxylic acid?
    To obtain 2- [ (E) -2- (5-cyanopyridine-2-yl) ethynyl] phenyl-4-carboxyl, the method is as follows:
    First take an appropriate amount of (5-cyanopyridine-2-yl) bromide, place it in a clean reactor, and replace the air in the kettle with nitrogen to ensure an oxygen-free environment. Add an appropriate amount of ethynylbenzene derivatives, add a palladium catalyst and a base, such as potassium carbonate, and use dimethylformamide as a solvent to heat up to a suitable temperature, about 80 to 100 degrees Celsius, and continue to stir the reaction. The purpose of this step is to construct a carbon-carbon triple bond through a palladium-catalyzed coupling reaction to generate 2- [ (E) -2- (5-cyanopyridine-2-yl) ethynyl] benzene derivatives.
    After the reaction is completed, the reaction solution is cooled, extracted several times with ethyl acetate, combined with organic phases, washed with water and saturated salt water, and dried with anhydrous sodium sulfate. The solvent is removed by vacuum distillation to obtain a crude product. Purified by silica gel column chromatography, the eluent is a mixture of petroleum ether and ethyl acetate, and the ratio is prepared according to the specific situation to obtain pure 2- [ (E) -2- (5-cyanopyridine-2-yl) ethynyl] benzene.
    Transfer this product to another reaction vessel, add an appropriate amount of oxidant, such as potassium permanganate, or potassium dichromate, and dissolve in a suitable solvent, such as sulfuric acid aqueous solution. Control the reaction temperature to a moderate temperature of about 50 to 70 degrees Celsius, so that the specific position on the benzene ring is oxidized, and carboxyl groups are introduced. After the reaction is completed, cool, adjust the pH to alkaline with sodium hydroxide solution, and filter to remove insoluble matter. The filtrate is acidified with hydrochloric acid, solid precipitation, suction filtration, and drying to obtain 2 - [ (E) - 2 - (5-cyanopyridine-2-yl) ethynyl] phenyl-4 - carboxyl products. During the operation, attention should be paid to the precise control of the reaction conditions to ensure the purity and yield of the product.
    What are the market prospects for 2- [ (E) -2- (5-nitrofuran-2-yl) vinyl] quinoline-4-carboxylic acids?
    What is the market prospect of 2- [ (E) -2- (5-cyanopyridine-2-yl) ethynyl] phenyl-4-carboxyl group today? Let me take the text of "Tiangong Kaiwu" as your guide.
    The use of this chemical substance in the modern world is related to many fields, just like the stars in the sky, each has its own use. In the field of medicine, or as a key ingredient in a good medicine for healing diseases, it helps doctors remove diseases and diseases, and seeks well-being for all living beings. If ancient doctors used herbs and alchemy to save the world and save people, this chemical substance is also expected to become a wonderful prescription for medicine today.
    In the world of materials, or with unique properties, it can make strange and delicate materials. Just like the ancient people used ingenious skills to turn earth, stone, metal, etc. into practical tools, this material may make the material stronger, more heat-resistant and other extraordinary properties, applied to the manufacture of utensils, improve its quality and function.
    Furthermore, in the path of scientific research and exploration, it may be the key to opening new discoveries and new theories. Just as the ancients searched up and down the unknown and explored the mysteries of nature with wisdom and perseverance, this material may inspire the wonders of scientists and open up new frontiers of scientific cognition.
    However, although its market prospects have many promising aspects, there are also challenges. If the acquisition of raw materials is smooth and secure, it is related to the cost. Just like the ancients in purchasing materials, the journey needs to be unobstructed and the resources are abundant. And the situation of competition should not be underestimated.
    In summary, the market prospects of 2- [ (E) -2- (5-cyanopyridine-2-yl) ethynyl] phenyl-4-carboxyl are like fertile soil to be cultivated. If you can grasp it well, adapt to the situation, operate with wisdom and skills, or be able to ride the wave of the market and achieve great results.