Ethyl 9 10 Difluoro 3 Methyl 7 Oxo 3 7 Dihydro 2h 1 4 Oxazino 2 3 4 Ij Quinoline 6 Carboxylate
quinoline thiophene imidazole thiazole

ethyl 9,10-difluoro-3-methyl-7-oxo-3,7-dihydro-2h-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate

Taiy Chemical

    Specifications

    HS Code

    283411

    Chemical Formula C19H15F2NO5
    Appearance Typically a solid
    Melting Point Varies, needs experimental determination
    Boiling Point Varies, needs experimental determination
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
    Density Varies, needs experimental determination
    Pka Specific pKa values need experimental determination
    Logp Varies, needs experimental determination
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading ethyl 9,10-difluoro-3-methyl-7-oxo-3,7-dihydro-2h-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate 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 quinoline-6-carboxylate ethyl 9,10-difluoro-3-methyl-7-oxo-3, 7-dihydro-2h- [1,4] oxazino [2,3,4-ij]?
    Ethyl 9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate, one of the organic compounds. The analysis of its chemical structure requires detailed investigation of its naming rules.
    The basic structure of this compound is based on the parent nucleus of quinoline. Quinoline is a nitrogen-containing heterocyclic aromatic compound with a benzene ring fused with a pyridine ring.
    In this compound, 9,10-difluoro (9,10-difluoro) indicates the introduction of fluorine atoms at the 9th and 10th positions of the quinoline parent nucleus. 3-methyl (3-methyl) means that there is a methyl substitution at the 3rd position of the quinoline parent nucleus.
    7-oxo (7-oxo) means that the 7th position of the parent nucleus is carbonyl (C = O). 3,7-dihydro (3,7-dihydro) shows that the double bond of the 3rd and 7th positions is hydrogenated. < Br >
    [1,4] oxazino [2,3,4-ij] quinoline ([1,4] oxazino [2,3,4-ij] quinoline) indicates that the quinoline parent nucleus is fused to the [1,4] oxazine ring. The oxazine ring is a six-membered heterocyclic ring containing one oxygen atom and one nitrogen atom.
    2H in 2H - [1,4] oxazino [2,3,4-ij] quinoline indicates that the second position of the oxazino [2,3,4-ij] quinoline ring is a hydrogen atom.
    And ethyl carboxylate is attached to the 6 position, indicating that the compound is 6-ethoxy carbonyl-9,10-difluoro-3-methyl-7-oxo-3,7-dihydro-2H-[ 1,4] oxazino [2,3,4-ij] quinoline. Its chemical structure generally presents a complex fused ring system, and each substituent is distributed according to a specific position, giving this compound unique chemical and physical properties.
    What are the main uses of ethyl 10-difluoro-3-methyl-7-oxo-3, 7-dihydro-2h- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
    Ethyl 9,10-difluoro-3-methyl-7-oxo-3,7-dihydro-2H-[ 1,4] oxazino [2,3,4-ij] quinoline-6-carboxylic acid ester, which is one of the quinolones. It has a wide range of uses, especially in the field of medicine.
    First of all, it has antibacterial and anti-inflammatory effects. The compound has shown strong inhibition and killing ability against many bacteria. Common pathogens such as Escherichia coli and Staphylococcus aureus are blocked in their growth and reproduction. Therefore, it is often used in the preparation of antibacterial drugs, which have good therapeutic power against various diseases caused by bacterial infections in the human body, such as respiratory tract infections, urinary system infections, etc. When patients suffer from such diseases, drugs containing this ingredient can help them relieve symptoms and promote physical recovery.
    Furthermore, it is also used in the field of veterinary medicine. In the process of livestock and poultry breeding, bacterial infections occur frequently, affecting their health and production performance. This compound can be used in the preparation of veterinary drugs to ensure the health of livestock and poultry, reduce the occurrence of diseases, and is of great significance to the stable development of the breeding industry.
    In addition, in the agricultural field, some plant diseases are caused by bacteria. Ethyl 9,10-difluoro-3-methyl-7-oxo-3,7-dihydro-2H - [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylic acid esters can be rationally prepared, or can be used for the prevention and control of plant bacterial diseases, helping to stabilize crop production and increase income.
    What is the synthesis method of ethyl 10-difluoro-3-methyl-7-oxo-3, 7-dihydro-2h- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
    In view of this question, I am inquiring about the synthesis method of ethyl 9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate. The synthesis of this compound is not easy, and requires delicate methods and meticulous work.
    Generally speaking, the choice of starting materials is crucial. Or a compound containing a quinoline structure can be taken first, and fluorine atoms can be introduced through a specific reaction. The introduction of fluorine atoms can be replaced by a nucleophilic substitution reaction, and fluorine-containing reagents can act on it. If a suitable fluorinating agent is selected, under suitable reaction conditions, the fluorine atom can precisely replace the group at a specific position.
    Furthermore, the [1,4] oxazino ring structure can be constructed, which can be achieved by multi-step reaction. Or first, a compound containing active groups such as hydroxyl groups and amino groups and a compound containing carbonyl groups are condensed to form a cyclization precursor. This process requires strict control of the reaction temperature, pH and reaction time to ensure the smooth progress of the reaction and the purity of the product.
    The introduction of methyl groups can be used at a suitable stage, using methylating reagents, such as iodomethane, etc., under the catalysis of bases, to connect the methyl groups to the target position.
    As for the formation of carboxyl ethyl esters, the intermediate containing carboxyl groups can be prepared first, and then the esterification reaction with ethanol catalyzed by acid can be carried out to obtain the required ethyl 9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate.
    However, the road of synthesis often encounters twists and turns. Every step of the reaction needs to be carefully regulated, and the reaction products need to be carefully separated and purified to obtain high-purity target compounds. The synthesis process is like carving beautiful jade, and it requires the heart of a craftsman to achieve this masterpiece.
    What are the physical properties of quinoline-6-carboxylate ethyl 9,10-difluoro-3-methyl-7-oxo-3, 7-dihydro-2h- [1,4] oxazino [2,3,4-ij]?
    Ethyl 9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate is an organic compound with many physical properties.
    Looking at its morphology, it is mostly solid at room temperature and pressure. Due to the relatively strong intermolecular force, the molecules are arranged in an orderly manner and are stable in the solid state. Its melting point is within a specific range. It is determined by experiments that the melting point is a key indicator to measure the transformation of the compound from solid to liquid state. The melting point is determined by the molecular structure and intermolecular force. The compound has hydrogen bonds, van der Waals forces and other forces between molecules, which enhances the attraction between molecules, so the melting point is high.
    In terms of solubility, the compound has a certain solubility in organic solvents such as dichloromethane and chloroform. Due to the fact that this organic solvent and the compound molecules can form similar intermolecular forces, such as dispersion forces, induction forces, etc., the compound molecules can be dispersed between solvent molecules to achieve dissolution. However, its solubility in water is very small, because water is an extremely polar solvent, and although this compound contains polar groups, the overall polarity is weak, and the intermolecular forces formed with water are difficult to overcome the hydrogen bonds between water molecules, so it is difficult to dissolve in water.
    The density of this compound is also an important physical property. The density reflects the mass of the substance per unit volume, and its specific value can be obtained by experimental measurement. The size of the density is closely related to the molecular structure, and the degree of molecular arrangement, the type and number of atoms will affect the density. In the molecular structure of the compound, the atomic arrangement is relatively compact, resulting in a certain density.
    In addition, the compound has a specific refractive index, which reflects the degree to which the direction of light changes when passing through the compound. The refractive index is related to the electron cloud distribution of the compound molecule and the polarizability of the molecule. Different compounds have different refractive indices due to differences in molecular structure. This property can be used for compound purity identification and structural analysis.
    What is the market outlook for ethyl 10-difluoro-3-methyl-7-oxo-3, 7-dihydro-2h- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
    "Tiangong Kaiwu" is simple and elegant in style. The following is a quaint language for you to describe the market prospects of ethyl 9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate (9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate).
    Looking at this compound today, it has great potential and prospects in the field of medicine. The way of medicine is related to the health of people's livelihood and has always been important to the world. This compound has a unique structure and may be able to show extraordinary effects in antibacterial and antiviral aspects.
    The harm of pathogens has been known in ancient times and is still a serious problem in the world. If this compound can be studied carefully and can be used to make good medicines to overcome pathogens, it will be a blessing for all the people. In the process of scientific research, many scholars are working to explore its pharmacological properties. If they obtain exquisite methods to make its effectiveness apparent, they will surely win the favor of the medical community.
    Looking at the chemical industry, this compound may be the key raw material for synthesizing other things. Chemists are the foundation for the manufacture of all things. If it can be used as the cornerstone of the synthesis of other things and stimulate the industrial chain, it involves a wide range of benefits, and the profits are thick and unlimited.
    However, the market is fickle. Although this compound has great potential, there are also challenges. First, the road of research and development is difficult and dangerous, and it requires huge amounts of capital and manpower to obtain it. Second, the same kind of things may also exist, and the competition must be fierce. To gain a place in the market, you must have outstanding quality, or low cost.
    In summary, ethyl 9,10 - difluoro - 3 - methyl - 7 - oxo - 3,7 - dihydro - 2H - [1,4] oxazino [2,3,4 - ij] quinoline - 6 - carboxylate is like jade in stone, if it is carved and polished, it can be used in the pharmaceutical and chemical markets, or it can shine and achieve an extraordinary career.