4 4 Phenyl 5 2 Phenylethyl Sulfanyl 4h 1 2 4 Triazol 3 Yl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

4-{4-phenyl-5-[(2-phenylethyl)sulfanyl]-4H-1,2,4-triazol-3-yl}pyridine

    Specifications

    HS Code

    710437

    Chemical Formula C23H20N4S
    Molecular Weight 384.49 g/mol
    Appearance Solid (usually)
    Melting Point Needs experimental determination
    Boiling Point Needs experimental determination
    Solubility In Water Low (organic compound, likely sparingly soluble)
    Solubility In Organic Solvents Soluble in common organic solvents like chloroform, dichloromethane
    Density Needs experimental determination
    Pka Needs experimental determination
    Uv Vis Absorption Maxima Needs spectroscopic analysis

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    Frequently Asked Questions

    As a leading 4-{4-phenyl-5-[(2-phenylethyl)sulfanyl]-4H-1,2,4-triazol-3-yl}pyridine 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 4- {4-phenyl-5- [ (2-phenylethyl) sulfanyl] -4H-1,2,4-triazol-3-yl} pyridine
    This is a problem of the chemical structure of organic compounds. 4- {4-phenyl-5- [ (2-phenethyl) thio] -4H-1,2,4-triazole-3-yl} pyridine, according to its name, its structure can be gradually analyzed.
    "Pyridine" is the basic structure of a six-membered nitrogen-containing heterocycle and has aromatic properties. In this compound, the pyridine ring is the parent structure. "4 - { }” shows that there is a specific group attached to the 4-carbon of the pyridine ring.
    In this specific group, "4-phenyl" means that there is a phenyl group attached to the 4-carbon of the triazole ring, and the phenyl group is the group left after the benzene ring is removed from a hydrogen atom, with a conjugate system. "5 - [ (2-phenethyl) thio]" means that on the 5-carbon of the triazole ring, a (2-phenethyl) group is connected with a sulfur atom. (2-phenethyl) group, is a phenyl ring attached to the 2-carbon of the ethyl group. " 4H-1,2,4-triazole "is a five-membered heterocyclic ring containing three nitrogen atoms with a specific number, and" 4H "indicates that the hydrogen atom at the fourth position of the triazole ring is involved in bonding.
    Overall, this compound uses the pyridine ring as the parent body, and its 4 positions are connected to a 1,2,4-triazole group containing phenyl and (2-phenethyl) thio groups. Each part is connected by a specific chemical bond to form a unique chemical structure.
    What are the physical properties of 4- {4-phenyl-5- [ (2-phenylethyl) sulfanyl] -4H-1,2,4-triazol-3-yl} pyridine
    4 - {4-Phenyl-5 - [ (2-phenethyl) thio] -4H-1,2,4-triazole-3-yl} pyridine, this is an organic compound. Its physical properties are related to many aspects.
    First, the appearance is white to light yellow crystalline powder, just like the delicate jade chips, and the color of the first flower stamen, which is delicate and pleasing to the eye. From the perspective, the shape is regular, like a carefully carved micro-matter.
    In terms of melting point, it may be in a specific temperature range due to intermolecular forces and structures. Just as the ice melts under the warm sun, when it reaches a certain temperature, the compound will quietly transform from solid to liquid. This melting point is crucial for its identification and purity judgment, just like a precise scale, marking the characteristics of the substance.
    Solubility is also an important physical property. In organic solvents, there may be different manifestations. In some polar organic solvents, such as ethanol, just like fish entering water, it can dissolve well and blend with solvent molecules; in water, due to the polarity difference between its own structure and water, the degree of solubility may be limited, just like water-proof wood, difficult to blend.
    In addition, its density is also characteristic, which is the mass contained in the unit volume, reflecting the close degree of molecular arrangement. The density of this compound is indispensable when measuring the relationship between its mass and volume, like a fixed star, providing accurate data for practical applications.
    Its physical properties are of great significance to the study of the properties, preparation and application of this compound, and are like the key to opening the door to treasure, providing a foundation for exploration in many fields.
    What is the preparation method of 4- {4-phenyl-5- [ (2-phenylethyl) sulfanyl] -4H-1,2,4-triazol-3-yl} pyridine
    To prepare 4- {4-phenyl-5- [ (2-phenethyl) thio] -4H-1,2,4-triazole-3-yl} pyridine, the following method can be used:
    First take an appropriate amount of 4- (4-phenyl-4H-1,2,4-triazole-3-yl) pyridine and place it in a clean reaction vessel. In this container, add an appropriate amount of organic solvent, such as dichloromethane, N, N-dimethylformamide, etc., and stir thoroughly to uniformly disperse the pyridine derivative to form a uniform solution.
    Then, slowly add 2-phenethyl mercaptan. When adding, pay close attention to the changes in the reaction system. After adding, add an appropriate amount of alkali, such as potassium carbonate, sodium carbonate, etc., and the alkali can promote the smooth progress of the reaction. During the reaction process, temperature control is extremely critical. Generally, it is maintained between room temperature and 50 ° C. Continuous stirring allows the reactants to fully contact and react. This reaction may take several hours or even dozens of hours, during which the reaction process can be tracked by thin layer chromatography (TLC). When the raw material point is almost gone, the reaction is basically completed.
    After the reaction is completed, pour the reaction solution into an appropriate amount of water, extract it with an organic solvent, and collect the organic phase. The organic phase is washed with water and saturated salt water successively to remove impurities. After that, the organic phase was dried with anhydrous sodium sulfate, the desiccant was filtered off, and the organic solvent was distilled under reduced pressure to remove the crude product.
    The crude product needs to be further purified. Column chromatography can be used. Silica gel is used as the stationary phase, and the mixture of petroleum ether and ethyl acetate is used as the mobile phase. According to the polarity of the product, a suitable ratio can be prepared for separation and purification. The fraction containing the target product is collected, and the solvent is removed by rotary distillation to obtain a pure 4 - {4-phenyl-5- [ (2-phenethyl) thio] -4H - 1,2,4-triazole-3-yl} pyridine. The entire preparation process requires rigorous operation, and the conditions of each step should be precisely controlled in order to obtain the ideal product.
    What are the application fields of 4- {4-phenyl-5- [ (2-phenylethyl) sulfanyl] -4H-1,2,4-triazol-3-yl} pyridine
    4- {4-Phenyl-5- [ (2-phenethyl) thio] -4H-1,2,4-triazole-3-yl} pyridine is one of the organic compounds. It has potential applications in many fields, and is now referred to as its application field in ancient Chinese.
    In the field of medicinal chemistry, such compounds are often the key to exploring new drugs. Due to their unique chemical structure, they may have the ability to regulate specific targets in organisms. For example, they may act on certain cell receptors and affect cell signaling pathways, providing opportunities for the treatment of specific diseases such as inflammation and tumors. In the development of new drugs, the structural properties of this compound may inspire pharmacists to design more targeted drugs with better efficacy and fewer side effects.
    also shows potential value in materials science. Its chemical properties may enable it to participate in the synthesis and modification of materials. For example, it can be introduced into specific material systems as additives to change the physical and chemical properties of materials, such as improving the stability, conductivity or optical properties of materials. In this way, it may play an important role in the preparation of new functional materials, such as optoelectronic materials, polymer materials, etc., to help materials meet the needs of different application scenarios.
    In the field of agriculture, there are also areas that can be explored. Such compounds may have biological activities such as antibacterial and insecticidal. If confirmed by research, it can be developed as a new type of pesticide for crop pest control. Compared with traditional pesticides, it may be more efficient and environmentally friendly due to its unique mechanism of action, which can not only effectively protect crops, but also reduce the negative impact on the environment and help the sustainable development of agriculture.
    What is the market outlook for 4- {4-phenyl-5- [ (2-phenylethyl) sulfanyl] -4H-1,2,4-triazol-3-yl} pyridine
    In the field of chemical synthesis, it is worth exploring the market prospect of 4-{ 4-phenyl-5- [ (2-phenethyl) thioalkyl] -4H-1,2,4-triazole-3-yl} pyridine.
    covers the field of chemical synthesis, or has unique potential. Its structure fuses benzene ring and triazole and other groups. This unique molecular structure may endow it with diverse physical and chemical properties. In the field of materials science, due to its special structure, it may be used as a key component of new functional materials. For example, in the field of optoelectronic materials, such compounds may exhibit unique optical and electrical properties, and are expected to be used in the preparation of high-performance Light Emitting Diodes, solar cells and other devices. This is because of the broad application prospects in this field, and the market demand may also increase with the progress of science and technology.
    Furthermore, in terms of medicinal chemistry, many compounds containing triazole and benzene ring structures have been proven to have significant biological activities. 4- {4-Phenyl-5- [ (2-phenethyl) thioalkyl] -4H-1,2,4-triazole-3-yl} pyridine or similar properties, such as antibacterial, antiviral, anti-tumor and other biological activities. If the relevant drugs are successfully developed through in-depth research and development, it will be able to meet the needs of the medical market and create considerable economic benefits.
    However, its market prospects are not entirely smooth. During the research and development process, the complexity of the synthesis process may be a major challenge. To achieve large-scale production, it is necessary to optimize the synthesis route, reduce costs and increase yield. And market competition should not be underestimated. Compounds of the same type or similar functions emerge in an endless stream. Only by continuously improving technology and highlighting their own advantages can they occupy a place in the market.
    In summary, 4- {4-phenyl-5- [ (2-phenethyl) thioalkyl] -4H-1,2,4-triazole-3-yl} Pyridine faces challenges, but its potential applications in materials and drugs make it have a considerable market prospect. If it is well developed and utilized, it will be able to bloom in the market.