Phenol 4 4 2 5 Pyridinediyl Bis
pyridine pyrrole pyrazine piperidine piperazine

Phenol, 4,4'-(2,5-pyridinediyl)bis-

    Specifications

    HS Code

    191431

    Chemical Formula C17H12N2O2
    Molar Mass 276.29 g/mol
    Appearance Solid (predicted from structure)
    Boiling Point Estimated high (due to intermolecular forces like hydrogen bonding)
    Melting Point Predicted to be relatively high
    Solubility In Water Low (hydrophobic aromatic rings dominate)
    Solubility In Organic Solvents Good solubility in common organic solvents like dichloromethane, chloroform
    Pka Presence of phenolic -OH groups gives acidic character, pKa around 9 - 10 (estimated for phenolic -OH)
    Density Estimated based on similar aromatic compounds, around 1.2 - 1.3 g/cm³
    Uv Vis Absorption Absorption in the UV region due to aromatic π - π* transitions

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    Frequently Asked Questions

    As a leading Phenol, 4,4'-(2,5-pyridinediyl)bis- 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 Phenol, 4,4 '- (2,5-pyridinediyl) bis-?
    The chemical structure of phenol, 4,4 '- (2,5-pyridyl) bis-this compound is a key research object in the field of organic chemistry. Its structure analysis depends on the basic principles and analytical methods of organic chemistry.
    From the naming, it can be seen that this substance uses phenol as the basic structure. Phenol is a compound in which a hydrogen atom on the phenyl ring is replaced by a hydroxyl group. In this compound, two phenol groups are connected by 2,5-pyridyl diyl. Pyridine, a nitrogen-containing hexagonal heterocyclic compound, is aromatic. In 2,5-pyridyl diyl, the nitrogen atom is located at the 2nd and 5th positions of the pyridine ring.
    Two phenol groups are connected by 2,5-pyridine digroups to construct a unique chemical structure. This connection method allows the molecule to have a specific spatial configuration and electron distribution. From the perspective of electronic effects, the electron cloud of the benzene ring and the pyridine ring can be delocalized due to the conjugation effect, which affects the physical and chemical properties of the molecule.
    In the spatial structure, due to the spatial orientation and interaction of each group, the molecule is either planar or distorted. This spatial structure has a great influence on the intermolecular forces, such as van der Waals force, hydrogen bonds, etc., which in turn affect its physical properties, such as melting point, boiling point, and solubility.
    In summary, the chemical structure of phenol, 4,4 '- (2,5-pyridyl diyl) bis - is composed of phenol groups and 2,5-pyridyl diyl groups. Its electronic effect and spatial structure jointly determine many properties of the compound. It has important theoretical and practical application value in the fields of organic synthesis and materials science.
    What are the physical properties of Phenol, 4,4 '- (2,5-pyridinediyl) bis-?
    Phenol, 4,4 '- (2,5-pyridyl diyl) bis - This substance has a variety of physical properties. Its appearance is often in a specific form, mostly crystalline solids, with a more delicate texture, like a natural crystal. In color, it often appears white to slightly yellow, just like the first light of the morning, pure and soft.
    Looking at its solubility, in organic solvents, such as ethanol, ether, etc., it is like a fish getting water, showing good solubility and being able to blend with it. However, in water, its solubility is relatively limited, as if it maintains a certain distance from water and only slightly dissolves in it.
    When it comes to melting point, this substance has its own specific value. When the temperature gradually rises to a certain precise scale, around [specific melting point value], it is like ice and snow meeting the warm sun, and it begins to slowly change from solid state to liquid state, opening the change of form. The boiling point also has its own unique features. Under a specific pressure environment, when the temperature rises to a corresponding height, about [specific boiling point value], it turns into a gaseous state, showing the wonder of material state transformation.
    Its density is also unique. Compared with common substances, it has a specific density value. In various application scenarios, this density characteristic also plays a key role, determining its position and distribution in different media.
    Furthermore, the substance also has optical properties, and may have a specific refractive index. When light passes through it, it follows a specific law of refraction, adding a mysterious optical color to it. All kinds of physical properties have laid the foundation for its application in different fields, making it unique in chemical industry, scientific research and many other aspects.
    What are the main uses of Phenol, 4,4 '- (2,5-pyridinediyl) bis-?
    Phenol, 4,4 '- (2,5-pyridyl diyl) bis-this substance, its main use is particularly important. It has its uses in various fields.
    In the field of chemical synthesis, it can be used as a key intermediate. Through delicate chemical reactions, it combines with many other compounds to form complex organic macromolecules with unique functions. Just like building a delicate castle, this compound is an indispensable cornerstone, helping chemists build all kinds of novel and useful substances, or with special optical and electrical properties, which bloom in the cutting-edge field of materials science.
    In the process of drug development, it has also emerged. Due to its special chemical structure, it may be able to fit with specific targets in an organism, just like a delicate match between a key and a lock. Researchers can modify and modify it according to this characteristic, in order to create new drugs with significant efficacy and mild side effects, adding to human health and well-being, such as becoming a sharp weapon in the battle against difficult diseases.
    Furthermore, in the field of material surface treatment, phenol, 4,4 '- (2,5-pyridyl diyl) bis - or can play a unique role. It can improve the properties of the surface of the material, such as enhancing its wear resistance and corrosion resistance, so that the material can still maintain good performance for a long time in harsh environments, just like putting a strong armor on the material, prolonging its service life, and is widely used in machinery manufacturing, aerospace and other industries that require strict material properties. In short, phenol, 4,4 '- (2,5-pyridyl diyl) bis - is a rare and important substance in many fields such as chemical industry, medicine, and materials, and has contributed to the progress and development of various industries.
    What are the precautions for the synthesis of Phenol, 4,4 '- (2,5-pyridinediyl) bis?
    When preparing 4,4 '- (2,5-pyridinediyl) bisphenol, many things need to be paid attention to.
    First of all, the selection and treatment of raw materials is crucial. Pyridine derivatives and phenolic compounds must have high purity, and impurities will cause side reactions, which will reduce the purity of the product. Before taking it, the raw materials should be refined by recrystallization, distillation and other methods to ensure a smooth reaction.
    The reaction conditions cannot be ignored. The temperature must be precisely controlled. If the temperature is too low, the reaction rate will be slow and take a long time. If the temperature is too high, it is easy to cause overreaction and produce many by-products. The choice of reaction solvent is also critical, and it is necessary to conform to the solubility and reaction characteristics of the reactants to create a good environment for the reaction. The use of
    catalysts should not be underestimated. Appropriate catalysts can accelerate the reaction process and increase the yield. Pay attention to the type, dosage and timing of addition. If there are too few catalysts, the catalytic effect will be poor; if there are too many, it will increase the cost and may also affect the purity of the product.
    Furthermore, the monitoring of the reaction process is indispensable. TLC, HPLC and other means can be used to gain real-time insight into the reaction progress, so that the reaction conditions can be adjusted in a timely manner to ensure that the reaction is advancing in the expected direction.
    Product separation and purification are also the focus. After the reaction, the product often contains impurities, and suitable separation methods, such as extraction and column chromatography, need to be used to obtain high-purity products. The purification process should take into account the stability of the product to prevent its degradation or deterioration.
    In addition, safety issues must not be forgotten. Many reactants, solvents and catalysts are toxic, corrosive or flammable, and safety procedures must be strictly followed during operation. Wear protective equipment and work in a well-ventilated environment to prevent accidents.
    All these are the key points that should be paid attention to when preparing 4,4 '- (2,5-pyridyl diyl) bisphenol, so as to ensure that the reaction can be carried out efficiently and safely, and the ideal product can be obtained.
    What are the environmental effects of Phenol, 4,4 '- (2,5-pyridinediyl) bis?
    Phenol, 4,4 '- (2,5-pyridyl diyl) bis - The impact of this substance on the environment is quite complex and needs to be explored in detail.
    Phenol compounds have a significant impact on the environment. They are toxic to a certain extent. If they enter the water body in large quantities, they will cause poisoning to aquatic organisms. Fish contact with phenol-containing water bodies will cause breathing difficulties, slow growth and even death. And phenols can cause odor and discoloration in water bodies, affect water quality and reduce the function of water bodies.
    The compounds associated with 4,4' - (2,5-pyridyl diyl) bis - are endowed with unique chemical properties due to the existence of pyridine rings. The stable structure of the pyridine ring makes it more difficult for the substance to degrade in the environment and easy to accumulate in the environment.
    This compound may affect the soil microbial community. Soil microorganisms are essential for soil nutrient cycling and decomposition of organic matter. The existence of this substance may inhibit the growth of some beneficial microorganisms, destroy the soil ecological balance, and then affect plant growth.
    In the atmospheric environment, if the substance evaporates into the air, it may participate in photochemical reactions, affect the air quality, and cause irritation to the human respiratory tract.
    In summary, phenol, 4,4 '- (2,5-pyridyl diyl) bis - may have many adverse effects in water, soil, and atmospheric environments, and its production, use, and emissions need to be treated with caution to reduce the harm to the environment.