2 9 Bis 4 Methoxyphenyl Methyl Anthra 2 1 9 Def 6 5 10 D E F Diisoquinoline 1 3 8 10 2h 9h Tetrone
quinoline thiophene imidazole thiazole

2,9-bis[(4-methoxyphenyl)methyl]-Anthra[2,1,9-def:6,5,10-d',e',f'-]diisoquinoline-1,3,8,10(2H,9H)-tetrone

Taiy Chemical

    Specifications

    HS Code

    173470

    Chemical Formula C48H34N2O6
    Molecular Weight 738.79 g/mol
    Appearance Typically solid (description may vary)
    Solubility In Water Low (organic compound, likely hydrophobic)
    Solubility In Organic Solvents Soluble in common organic solvents like chloroform, dichloromethane (general prediction for aromatic compounds)
    Uv Vis Absorption Absorption in the UV - visible region due to aromatic chromophores (specific wavelengths need experimental determination)
    Fluorescence Properties May exhibit fluorescence due to conjugated aromatic structure (intensity and wavelength need experimental determination)

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    General Information
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    As a trusted 2,9-bis[(4-methoxyphenyl)methyl]-Anthra[2,1,9-def:6,5,10-d',e',f'-]diisoquinoline-1,3,8,10(2H,9H)-tetrone manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2,9-bis[(4-methoxyphenyl)methyl]-Anthra[2,1,9-def:6,5,10-d',e',f'-]diisoquinoline-1,3,8,10(2H,9H)-tetrone 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 main use of 2,9-bis [ (4-methoxyphenyl) methyl] -anthracene [2,1,9-def: 6,5,10-d'e'f '] -diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone
    2% 2C9 - bis [ (4-methoxybenzyl) methyl] - matte [2% 2C1% 2C9 - def% 3A6% 2C5% 2C10 - d'e'f '] - diisosquanoic acid - 1% 2C3% 2C8% 2C10 (2H% 2C9H) - tetraketone This compound is not detailed in the book "Tiangong Kaiwu". However, according to the current chemical understanding, such compounds may have various uses.
    One, in the field of materials science, may be used as a building block for functional materials. The special molecular structure of this compound may endow the material with unique photoelectric properties, such as the conductivity and fluorescence properties of the modulated material, etc., which may have potential application value in the research and development of optoelectronic devices such as organic Light Emitting Diode (OLED) and organic photovoltaic cells, and help improve the performance and efficiency of the device.
    Second, in the field of pharmaceutical chemistry, such compounds with complex structures may exhibit biological activity after reasonable modification and modification. Its unique chemical structure or fit specific biological targets can be used as lead compounds for drug developers to explore in depth to develop new therapeutic drugs to deal with diseases such as tumors and inflammation.
    Third, in the field of organic synthetic chemistry, it can be used as a key intermediate. By means of organic synthesis, using this compound as the starting material, more complex and functional organic molecules can be derived, the variety of organic compounds can be enriched, the paths and methods of organic synthesis can be expanded, and the progress and development of organic synthetic chemistry can be promoted.
    What are the chemical properties of 2,9-bis [ (4-methoxyphenyl) methyl] -anthracene [2,1,9 - def: 6,5,10 - d'e'f '] -diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone
    2% 2C9 - bis [ (4-methoxybenzyl) methyl] -iodine [2,1,9 - def: 6,5,10 - d'e'f '] -diisosacrine - 1,3,8,10 (2H, 9H) -tetraketone This compound has the following chemical properties:
    This compound exhibits unique chemical activity due to the presence of multiple specific functional groups. Among them, the methoxybenzyl moiety, the methoxy group acts as the power supply group, which can enhance the electron cloud density at the connection of the benzyl group with other groups, affecting the nucleophilic or electrophilic reactivity of the compound. For example, in the electrophilic substitution reaction, it may make the benzyl o-para-position more susceptible to attack by electrophilic reagents. The introduction of
    iodine atoms, on the one hand, increases the molecular weight and polarity of the compound, and changes its physical properties such as solubility; on the other hand, iodine atoms can undergo substitution reactions under appropriate conditions, which is a potential check point for the introduction of other functional groups, such as coupling reactions with organoboronic acids under metal catalysis, so as to modify the structure of the molecule.
    Diisoscalic acid structural units have strong acidity, and their two carboxyl groups can undergo acid-base reactions, which can react with bases to form corresponding salts. Moreover, the conjugated system in the isoscalic acid structure makes this part have certain electron delocalization, which can participate in the electron transfer process and exhibit specific properties in redox reactions. The carbonyl groups in the structure of
    1,3,8,10 (2H, 9H) -tetraketone have typical carbonyl properties and can undergo nucleophilic addition reactions, such as condensation with alcohols to form ketals, or reaction with amines to form imines. At the same time, the conjugated system of the tetraketone structure also affects the electron distribution and stability of the whole molecule, which in turn affects its chemical properties.
    This compound may have potential application value in organic synthesis, materials science and other fields due to the synergistic effect of its various functional groups. It can be constructed by chemical transformation of these functional groups to construct more complex and unique compounds.
    What is the preparation method of 2,9-bis [ (4-methoxyphenyl) methyl] -anthracene [2,1,9-def: 6,5,10-d'e'f '] -diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone
    To prepare 2,9-bis [ (4-methoxybenzyl) methyl] -naphthalene [2,1,9-def: 6,5,10-d'e'f '] -diisoprazene-1,3,8,10 (2H, 9H) -tetraketone, according to the following ancient method:
    Preparation of various drugs requires an appropriate amount of raw materials with a specific structure. This raw material relates to the combination of methoxybenzyl and methyl, and the substitution of specific positions of naphthalene rings.
    In a clean kettle, add an appropriate amount of reactants at a precisely controlled temperature. At the beginning, it is appropriate to slowly heat up to make the contents of the kettle gradually merge. During this period, it is necessary to use delicate methods to control the reaction rate, and do not make it too hasty or too slow. When the contents of the kettle are of a specific color, and based on the ancient method, an appropriate amount of another reactant is added. This reactant is closely related to the formation of diisoprene and tetraketone.
    Continue to keep the heat warm, and add stirring from time to time to make the contents uniform. After several hours, observe closely during this period, and fine-tune the heat according to the changes in the contents of the kettle. When the reaction is asymptotically over, the product is analyzed by the ancient method, and the impurities are removed, and the pure 2,9-bis [ (4-methoxybenzyl) methyl] -naphthalene [2,1,9 - def: 6,5,10 - d'e'f '] -diisoprene-1,3,8,10 (2H, 9H) -tetraketone can be obtained. The whole process needs to strictly abide by the rules of the ancient law. If there is a slight difference, the product may be impure or the amount may be small.
    2,9-Bis [ (4-methoxyphenyl) methyl] -anthracene [2,1,9-def: 6,5,10-d'e'f '] -diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone in which areas are used
    2% 2C9 -bis [ (4 -ethoxybenzyl) ethyl] -naphthalene [2,1,9 -def: 6,5,10 -d'e'f '] -didixuangguang-1,3,8,10 (2H, 9H) -tetraketone This substance has many application fields, and listen to me one by one.
    In the field of medicinal chemistry, it may have unique biological activities and can be used as a lead compound. Due to its unique structure, it may be able to cooperate with specific biological targets, such as certain enzymes or receptors, by interacting with the target, it regulates the physiological and pathological processes in the organism, which is of great significance for the development of new therapeutic drugs, such as anti-cancer, anti-inflammatory or neurological diseases.
    The field of materials science also has its own figures. Due to its special chemical structure and physical properties, it can be used to prepare functional materials. For example, its outstanding optical properties can be used to fabricate optoelectronic devices such as optical sensors and Light Emitting Diodes. After structural modification, the light absorption, emission and electron transmission properties can be optimized to meet the needs of different optoelectronic devices.
    In the field of organic synthetic chemistry, 2% 2C9-bis [ (4-ethoxybenzyl) ethyl] -naphthalene [2,1,9-def: 6,5,10-d'e'f '] -diisoquaternion-1,3,8,10 (2H, 9H) -tetraketone can be used as a key intermediate. Organic synthesis aims to build complex organic molecules, which are complex in structure and have multiple reaction check points. Organic chemists can use them to carry out various organic reactions, such as nucleophilic substitution, addition, redox, etc., to synthesize more complex and functional organic compounds, which contribute to the development of organic synthesis chemistry.
    What are the market prospects for 2,9-bis [ (4-methoxyphenyl) methyl] -anthracene [2,1,9-def: 6,5,10-d'e'f '] -diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone?
    Looking at the market prospects of 2,9-bis [ (4-ethoxybenzyl) ethyl] -naphthalene [2,1,9-def: 6,5,10-d'e'f '] -diisocubic ether-1,3,8,10 (2H, 9H) -tetraketone, it is worth further investigation.
    This object is among the many ingenious techniques and exquisite materials involved in "Tiangong Kaiwu". Although no exact trace of it can be found, it may be inferred from the development of ancient techniques and facts, or there is something to be explored. In ancient times, craftsmen refined craftsmanship, and the ratio, synthesis and application of materials were all secrets. Although there was no such fine chemical analysis and synthesis method as modern ones at that time, the accumulation of experience and the application of wisdom are also unique.
    If you talk about the market prospect of this compound, you should consider the field involved. In today's world, chemical synthetic materials are widely used, or they can find their place in medicine, materials science and many other aspects. Medicine is related to the health of people's livelihood. If this material can be studied to obtain its unique pharmacological activity for the treatment and prevention of diseases, it will surely emerge in the pharmaceutical market and have unlimited prospects. In materials science, its unique molecular structure may endow materials with novel properties, such as excellent optical and electrical properties, and it is also expected to occupy a place in the field of high-end material manufacturing.
    It is not easy to make it shine in the market. Rigorous scientific research is required to clarify its properties and application potential, and to break through the difficulties of the synthesis process and reduce production costs in order to be accepted by the market and realize its value. In this way, the market prospect of this compound, although there are opportunities and challenges, depends on the diligent research of future generations to see what it is.