2-(4-fluorophenyl)-1-tosyl-1H-benzoimidazole

2-%284-%E6%B0%9F%E8%8B%AF%E5%9F%BA%29-1-%E7%94%B2%E8%8B%AF%E7%A3%BA%E9%85%B0%E5%9F%BA-1H-%E8%8B%AF%E5%B9%B6%E5%92%AA%E5%94%91%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E6%98%AF%E4%BD%9C%E4%B8%BA%E5%8C%96%E5%AD%A6%E6%9D%90%E6%96%99%E7%94%A8%E4%BA%8E%E5%88%9B%E5%BB%BA%E5%90%84%E7%A7%8D%E5%A4%9A%E5%85%83%E7%B4%A0%E5%8C%96%E5%90%88%E7%89%A9%E3%80%82
This compound plays an important role in the field of chemical synthesis. Among them, the special properties of 2- (4-pyridyl) -1-methylpyridyl chromophore-1H-pyridyl pyrazole make it have a multi-reaction activity center. It can be used as an important medium for the construction of more complex molecules.
In terms of physicochemistry, it can provide a framework for new research. By virtue of the specific properties of this compound, the company can make modifications, such as introducing different substituents at specific locations, and the properties of lipid, lipid, and biological activity of the whole molecule, in order to improve the specific target of the compound. The strength and performance of the target are improved, and the more effective and lower side effects are developed.
In the field of materials science, this compound can be synthesized into materials with special optical, magnetic, and other properties. For example, specific co-complexes can be combined to improve the optical properties of materials, which is expected to be used in optical devices such as optical diodes (OLEDs) to improve the optical efficiency and color resolution of the devices; or through the coordination of gold substrates, the construction of gold-rich frame materials (MOFs) with special magnetic properties can be used in the fields of information storage, magnetic separation, etc.
, 2- (4-pyridyl) -1-methylpyridyl chromophore-1H-pyridyl pyrazole has shown promising applications in chemical synthesis, chemical research, and materials science due to its multi-activity.

To prepare 2- (4-furyl) -1-methylimidazolinyl-1H-imidazolopyridine, the synthesis method is as follows:
First take an appropriate amount of furan derivatives, in a clean reactor, dissolve in a specific organic solvent. This solvent needs to have good solubility and stability, and does not have side reactions with the reactants. Adding an appropriate amount of base as a catalyst requires precise control of the amount and type of base, which has a great impact on the reaction rate and product purity. Warm up to a specific temperature, which depends on the reaction characteristics and the properties of the raw materials. Generally, it is in a moderate high temperature range to fully stir the reaction system, promote intermolecular collision, and accelerate the reaction process.
At the same time, prepare 1-methylimidazoline derivatives. Mix the corresponding raw materials in a certain proportion and pretreat them under suitable reaction conditions to activate the reactants and improve the reactivity.
When both of the above reaction systems reach the ideal reaction state, slowly add 1-methylimidazoline derivative reaction droplets to the furan derivative reaction system. The droplet addition speed should be uniform and slow to prevent the reaction from being too violent. Keep stirring and maintaining a stable temperature to make the two fully react. During the reaction process, closely monitor the reaction process, and observe the consumption of raw materials and the generation of products by means of thin-layer chromatography.
After the reaction is basically completed, the reaction solution should be post-treated. First extract with an appropriate organic solvent to separate the organic phase, remove impurities and unreacted raw materials. Then purify by column chromatography or recrystallization. For column chromatography, suitable fillers and eluents need to be selected, and for recrystallization, suitable solvents and operating conditions need to be selected to obtain high-purity 2- (4-furyl) -1-methylimidazolinyl-1H-imidazolidopyridine products. The whole synthesis process requires strict reaction conditions, raw material proportions and operation details, and a slight error will affect the quality and yield of the product.

2-%284-%E6%B0%9F%E8%8B%AF%E5%9F%BA%29-1-%E7%94%B2%E8%8B%AF%E7%A3%BA%E9%85%B0%E5%9F%BA-1H-%E8%8B%AF%E5%B9%B6%E5%92%AA%E5%94%91%E7%9A%84%E5%88%97%E5%90%8D%E6%9C%89%E8%8B%A5%E5%B9%B2%E5%85%83%E7%B4%A0%E7%BB%84%E6%88%90%E5%90%88%E6%88%90%E7%89%A9%E7%90%86%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E7%9B%B8%E5%BD%93%E7%A7%8D%E7%B1%BB%E4%B8%8D%E5%90%8C%E6%96%B9%E5%BC%8F%E5%90%84%E6%9C%89%E4%B8%8D%E5%90%8C%E5%88%99%E4%B8%8B%E4%B8%BA%E5%85%B6%E7%89%A9%E7%90%86%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E7%9A%84%E6%8F%8F%E8%BF%B0:
2 - (4 - hydroxybenzyl) - 1 - methylbenzyloxycarbonyl - 1H - indole - 3 - formaldehyde and other substances, its physical and chemical properties are quite characteristic. From the appearance, under room temperature or white to light yellow crystalline powder, this is an intuitive and recognizable state. Its melting point has a specific range. Generally speaking, its melting point data can be known by accurate measurement, which is one of the important indicators for determining the purity and characteristics of the substance.
In terms of solubility, in organic solvents, such as common ethanol and acetone, or show some solubility, but in water solubility or poor. This difference in solubility is related to the functional groups in its molecular structure, and the various groups in its structure make it different from different solvent molecules.
In terms of stability, under normal storage conditions, if it is in a cool and dry place away from light, it can maintain a relatively stable state. In case of high temperature, strong light, or a specific chemical environment, or a chemical reaction may be triggered, causing its structure to change. For example, in a strong acid and alkali environment, some chemical bonds in the structure may be destroyed, and reactions such as hydrolysis and addition occur.
Its spectral characteristics are also unique. In infrared spectroscopy, specific functional groups will exhibit characteristic absorption peaks at corresponding wave numbers, such as carbonyl, hydroxyl and other functional groups, which can be analyzed and confirmed. In nuclear magnetic resonance spectroscopy, hydrogen and carbon atoms in different chemical environments will peak at specific chemical shifts, so that the connection mode and spatial position relationship of each atom in the molecule can be clearly analyzed.

I think what you are asking is about the market price range of 2- (4-furanyl) -1-methylfuran-cyanine-1H-furanopyrrole. However, the price of these chemical substances varies greatly depending on the quality, purity, and supply and demand.
If it is of high quality, high purity, and there are many people in the market, and there are few people in supply, its price will be high. On the contrary, if the quality is average, the purity is not high, and the supply is sufficient, and there are few people seeking it, the price may become more affordable.
And such chemicals are mostly used in scientific research and industry, and their transactions are often based on specific channels, and there is an open and uniform price like ordinary goods. For use in scientific research institutions, due to strict requirements on purity, etc., the purchase price should be higher; for industrial production, depending on the scale of mass production and the cost of raw materials, the price is also different.
And the market is changing rapidly, sometimes the price goes up, sometimes the price goes down. Therefore, in order to determine the price, it is necessary to carefully observe the current dynamics of the chemical market, consult the merchants and manufacturers specializing in such chemicals, or refer to relevant industry reports, in order to obtain a more accurate price range. However, it is difficult to determine the exact price range based on the information given.

2-%284-%E6%B0%9F%E8%8B%AF%E5%9F%BA%29-1-%E7%94%B2%E8%8B%AF%E7%A3%BA%E9%85%B0%E5%9F%BA-1H-%E8%8B%AF%E5%B9%B6%E5%92%AA%E5%94%91 related derivatives involved are mostly compounds with specific structures in the field of organic chemistry.
2- (4-hydroxybenzyl) -1-methylimidazolinone, in this compound, hydroxybenzyl is connected to a specific position as a substituent, while methylimidazolinone constitutes the main frame. In its structure, the imidazolinone ring has a specific electron cloud distribution and reactivity check point. Hydroxyl groups on hydroxybenzyl can participate in various reactions, such as nucleophilic substitution, esterification, etc. The benzyl part affects the physicochemical properties of the whole molecule due to the conjugation effect of the benzene ring.
1H-imidazopyridine derivatives, which have imidazopyridine as the core structure. The pyridine ring fuses with the imidazole ring to form a unique rigid structure, giving these compounds special electronic properties and spatial configuration. In terms of biological activity, such derivatives often show the ability to interact with specific biological targets, which has attracted much attention in the field of drug development. For example, some 1H-imidazopyridine derivatives can act as neuroactivity modulators, interacting with neurotransmitter receptors to regulate signal transduction in the nervous system.
The above compounds are often used as key intermediates in the construction of more complex compound structures due to their unique structures in organic synthesis, medicinal chemistry, etc., or directly as lead compounds with potential biological activities. After structural modification and optimization, innovative drugs with specific pharmacological effects are developed.