2-(3,4-Dichlorobenzyl)-1H-benzo[d]imidazole

2-%283%2C4-%E4%BA%8C%E6%B0%AF%E8%8B%84%E5%9F%BA%29-1H-%E8%8B%AF%E5%B9%B6%5Bd%5D%E5%92%AA%E5%94%91, this compound has important uses in many fields.
In the field of medicinal chemistry, it is a key intermediate. Through specific chemical reactions, it can be modified and derivatized as a medicinal active ingredient. In the research and development of many anti-cancer drugs, the 2-%283%2C4-%E4%BA%8C%E6%B0%AF%E8%8B%84%E5%9F%BA%29-1H-%E8%8B%AF%E5%B9%B6%5Bd%5D%E5%92%AA%E5%94%91 structure can introduce drug molecules, and by virtue of its unique spatial configuration and electronic properties, it can enhance the affinity of the drug with specific targets and improve the anti-cancer effect. For example, for specific receptors on the surface of some cancer cells, the modified drug containing this structure can precisely bind, block the growth signal transduction of cancer cells, and inhibit the proliferation of cancer cells.
In the field of materials science, it can be used as a functional material building element. Because of its unique electrical, optical or thermal properties, it can participate in the preparation of organic optoelectronic materials. For example, when preparing organic Light Emitting Diode (OLED), the introduction of this structure can optimize the luminous efficiency and stability of the material. Due to its special electronic transition characteristics, it can efficiently radiate photons when excited, making the OLED display screen clearer and brighter colors. In the design of organic solar cell materials, this structure can also play a role in optimizing the material's light absorption and charge transport capabilities, and improving the photoelectric conversion efficiency of solar cells.
In the field of pesticide chemistry, 2-%283%2C4-%E4%BA%8C%E6%B0%AF%E8%8B%84%E5%9F%BA%29-1H-%E8%8B%AF%E5%B9%B6%5Bd%5D%E5%92%AA%E5%94%91 structure can endow pesticide molecules with specific biological activities. For the nerve conduction or metabolic system of some pests, pesticides containing this structure can interfere with the normal physiological functions of pests, achieve efficient insecticidal and environmentally friendly. Due to its specific effect on pests, it can be designed to reduce the impact on non-target organisms, meeting the development needs of green pesticides.

2-%283%2C4-%E4%BA%8C%E6%B0%AF%E8%8B%84%E5%9F%BA%29-1H-%E8%8B%AF%E5%B9%B6%5Bd%5D%E5%92%AA%E5%94%91 synthesis method often follows the method of organic chemistry, and its steps are complicated and require fine operation.
First, the key intermediate product is constructed with a suitable starting material and a carefully designed reaction path. For example, the precursor containing benzo [d] azole structure and the compound with a specific substituent are selected to interact with each other under suitable reaction conditions. Among them, the reaction conditions are the most critical, such as temperature, pressure, type and dosage of catalyst, which must be carefully regulated.
The control of temperature is related to the reaction rate and product selectivity. If it is too low, the reaction will be slow, and if it is too high, it is easy to cause side reactions. Catalysts can change the rate of chemical reactions, and the selection of catalysts with good activity and selectivity can greatly improve the yield of the target product.
The choice of reaction solvents should not be underestimated, and different solvents affect the reaction process and the purity of the product. Some solvents can promote the dissolution and diffusion of the reactants, which is conducive to the progress of the reaction; however, if the choice is improper, it may make it difficult to separate and purify the product.
When the intermediate product is generated, it needs to go through a series of separation and purification steps, such as extraction, distillation, column chromatography, etc., to obtain high-purity intermediate products. Then based on this intermediate product, 3,4-difluorobenzyl is introduced through further reaction to finally obtain 2- (3,4-difluorobenzyl) -1H-benzo [d] azole.
The separation and purification process also requires careful operation. Select the appropriate extractant during extraction, precisely control the temperature and pressure during distillation, and select the right adsorbent and eluent during column chromatography to obtain a high-purity target product. Throughout the synthesis process, every step needs to be treated strictly, with slight poor pooling, or low yield and impure product.

2-%283%2C4-%E4%BA%8C%E6%B0%AF%E8%8B%84%E5%9F%BA%29-1H-%E8%8B%AF%E5%B9%B6%5Bd%5D%E5%92%AA%E5%94%91, this is a nomenclature for organic compounds. Its physical and chemical properties are quite unique, and it is of great significance for its in-depth investigation in many fields.
From the perspective of physical properties, the state of the substance often varies depending on environmental conditions. Under normal temperature and pressure, it is either a solid state or a liquid state, depending on the strength of its intermolecular forces. If the intermolecular forces are strong, it tends to be a solid state, and the structure is relatively stable; if the forces are weak, it is more likely to be a liquid state, and the molecular activities are relatively free. Its melting and boiling point is also determined by the molecular structure and interaction. There are different forces such as hydrogen bonds and van der Waals forces between molecules, and the magnitude of these forces affects the melting and boiling point. In general, the presence of hydrogen bonds increases the melting boiling point, because more energy is required to break hydrogen bonds.
In terms of chemical properties, specific functional groups in 2-%283%2C4-%E4%BA%8C%E6%B0%AF%E8%8B%84%E5%9F%BA%29-1H-%E8%8B%AF%E5%B9%B6%5Bd%5D%E5%92%AA%E5%94%91 molecules give them unique reactivity. Some chemical bonds it contains, such as carbon-carbon bonds, carbon-hydrogen bonds, etc., can occur under suitable conditions. For example, it may participate in a substitution reaction, that is, an atom or group in the molecule is replaced by another atom or group; addition reactions may also occur, adding other atoms or groups to the unsaturated bond to change the saturation of the molecule. Its chemical stability is also closely related to the molecular structure. If there is a conjugated system in the structure, it will often enhance the stability of the molecule and change the chemical reactivity. In different chemical environments, the substance exhibits different reaction tendencies, which need to be comprehensively considered according to the specific reaction conditions and reactants.

I have not heard of the market price of "2- (3,4-difluorobenzyl) -1H-indole", but I can estimate its price. This is a fine chemical, and its price depends on many.
The price of raw materials is one. If the raw materials for this product are easy to obtain and inexpensive, the cost may be low, and the price may be low; if the raw materials are rare and difficult to obtain, the price must be high.
Synthesis is difficult and heavy. If the synthesis method is difficult, requires multiple steps of reaction, and the conditions are harsh, special reagents and equipment are required, and the cost increases, and the market price must be high. On the contrary, if the synthesis is easy, the price may be close to the people.
Demand and output also affect it. If the market demand for this product is strong, but the output is small, the supply is in short supply, and the price will rise; if the demand is low, the output is large, and the supply exceeds the demand, the price may fall.
In addition, manufacturers, regions, market competition, etc. are all related. Different manufacturers have different costs and pricing strategies, and different prices; different regions have different prices due to factors such as transportation, taxes, etc. Market competition is intense, manufacturers may reduce prices to compete for the market, and prices will fall; competition is slow, and prices may be stable and high.
In summary, the price of "2- (3,4-difluorobenzyl) -1H-indole" may range from several hundred to several thousand yuan per gram, but this is only a guess. To know the exact price, you need to consult chemical raw material suppliers or check market conditions.

There are many manufacturers of 2- (3,4-difluorobenzyl) -1H-indolo [d] pyrimidine, and in the land of China, many capable factories are involved in this industry.
In the Central Plains, there are factories that focus on the research of this compound with exquisite skills. It adheres to the rigor of ancient methods and integrates today's ingenious skills. From the beginning of raw material selection, it uses a strict state to ensure purity and purity. In the reaction kettle, the temperature, duration and ratio are precisely controlled, just like a skilled craftsman carving beautiful jade, and it is necessary to investigate it. The quality of the products produced is high, and it is important for the four sides.
In Jiangnan Water Village, there are also factories involved in this industry. Its local spirit is outstanding, and the craftsman is ingenious. On the basis of craftsmanship, we constantly study and improve, and strive for the ultimate product. Pay attention to the harmony of the environment, and strictly abide by the regulations of the production process, which not only ensures the excellence of the product, but also protects the peace of the world. The 2- (3,4-difluorobenzyl) -1H-indolo [d] pyrimidine produced is quite famous in the industry and is exported to all parties.
There are also manufacturers in the northern part of Saibei. It relies on the benefits of geography, and the raw materials are easily accessible. When producing, it is heroic, but it does not lose its meticulous heart. While ensuring output, the pursuit of quality has never slack off. The products produced are solid and reliable, and are the cornerstone of the industry.
all over the country, inside and outside the Great Wall, many manufacturers have their own advantages in the production of 2- (3,4 -difluorobenzyl) -1H -indolo [d] pyrimidine, each to promote the prosperity of this industry.